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- Use and Patient-Reported Outcomes of Clinical Multigene Panel Testing for Cancer Susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study.
- Hall MJ, Patrick-Miller LJ, Egleston BL, Domchek SM, Daly MB, Ganschow P, Grana G, Olopade OI, Fetzer D, Brandt A, Chambers R, Clark DF, Forman A, Gaber R, Gulden C, Horte J, Long JM, Lucas T, Madaan S, Mattie K, McKenna D, Montgomery S, Nielsen S, Powers J, Rainey K, Rybak C, Savage M, Seelaus C, Stoll J, Stopfer JE, Yao XS, Bradbury AR.
- JCO Precis Oncol. 2018;2. doi: 10.1200/PO.18.00199. Epub 2018 Dec 18.
- PMID: 31819920
- PubMed abstract
- Source abstract
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- Contribution of MUTYH Variants to Male Breast Cancer Risk: Results From a Multicenter Study in Italy.
- Rizzolo P, Silvestri V, Bucalo A, Zelli V, Valentini V, Catucci I, Zanna I, Masala G, Bianchi S, Spinelli AM, Tommasi S, Tibiletti MG, Russo A, Varesco L, Coppa A, Calistri D, Cortesi L, Viel A, Bonanni B, Azzollini J, Manoukian S, Montagna M, Radice P, Palli D, Peterlongo P, Ottini L.
- Front Oncol. 2018 Dec 4;8:583. doi: 10.3389/fonc.2018.00583. eCollection 2018.
- PMID: 30564557
- PubMed abstract
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- Cancer Risk Estimates for Study of Multiple-Gene Testing After Diagnosis of Breast Cancer.
- Narod SA.
- JAMA Oncol. 2018 Dec 1;4(12):1787-1788. doi: 10.1001/jamaoncol.2018.4931.
- PMID: 30383137
- PubMed abstract
- Source abstract
Original Research:
Uptake, Results, and Outcomes of Germline Multiple-Gene Sequencing After Diagnosis of Breast Cancer.
- PMID: 29801090
- PubMed abstract
- Source abstract
Letter, reply:
Cancer Risk Estimates for Study of Multiple-Gene Testing After Diagnosis of Breast Cancer—Reply
- PMID: 30383131
- PubMed abstract
- Source abstract
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- A portrait of germline mutation in Brazilian at-risk for hereditary breast cancer.
- de Souza Timoteo AR, Gonçalves AÉMM, Sales LAP, Albuquerque BM, de Souza JES, de Moura PCP, de Aquino MAA, Agnez-Lima LF, Lajus TBP.
- Breast Cancer Res Treat. 2018 Dec;172(3):637-646. doi: 10.1007/s10549-018-4938-0. Epub 2018 Aug 29.
- PMID: 30159786
- PubMed abstract
- Source abstract
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- New insights into the performance of multigene panel testing: Two novel nonsense variants in BRIP1 and TP53 in a young woman with breast cancer.
- Castillo-Guardiola V, Sarabia-Meseguer MD, Marín-Vera M, Sánchez-Bermúdez AI, Alonso-Romero JL, Noguera-Velasco JA, Ruiz-Espejo F.
- Cancer Genet. 2018 Dec;228-229:1-4. doi: 10.1016/j.cancergen.2018.06.002. Epub 2018 Jun 23.
- PMID: 30553462
- PubMed abstract
- Source abstract
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- BRCA-analyzer: Automatic workflow for processing NGS reads of BRCA1 and BRCA2 genes.
- Kechin A, Khrapov E, Boyarskikh U, Kel A, Filipenko M.
- Comput Biol Chem. 2018 Dec;77:297-306. doi: 10.1016/j.compbiolchem.2018.10.012. Epub 2018 Oct 23.
- PMID: 30408727
- PubMed abstract
- Source abstract
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- Prevalence of pathogenic variants and variants of unknown significance in patients at high risk of breast cancer: A systematic review and meta-analysis of gene-panel data.
- van Marcke C, Collard A, Vikkula M, Duhoux FP.
- Crit Rev Oncol Hematol. 2018 Dec;132:138-144. doi: 10.1016/j.critrevonc.2018.09.009. Epub 2018 Sep 14.
- PMID: 30447919
- PubMed abstract
- Source abstract
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- Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations.
- Pujol P, Vande Perre P, Faivre L, Sanlaville D, Corsini C, Baertschi B, Anahory M, Vaur D, Olschwang S, Soufir N, Bastide N, Amar S, Vintraud M, Ingster O, Richard S, Le Coz P, Spano JP, Caron O, Hammel P, Luporsi E, Toledano A, Rebillard X, Cambon-Thomsen A, Putois O, Rey JM, Hervé C, Zorn C, Baudry K, Galibert V, Gligorov J, Azria D, Bressac-de Paillerets B, Burnichon N, Spielmann M, Zarca D, Coupier I, Cussenot O, Gimenez-Roqueplo AP, Giraud S, Lapointe AS, Niccoli P, Raingeard I, Le Bidan M, Frebourg T, Rafii A, Geneviève D.
- Eur J Hum Genet. 2018 Dec;26(12):1732-1742. doi: 10.1038/s41431-018-0224-1. Epub 2018 Aug 8.
- PMID: 30089825
- PubMed abstract
- Source abstract
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- Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families.
- Castéra L, Harter V, Muller E, Krieger S, Goardon N, Ricou A, Rousselin A, Paimparay G, Legros A, Bruet O, Quesnelle C, Domin F, San C, Brault B, Fouillet R, Abadie C, Béra O, Berthet P; French Exome Project Consortium, Frébourg T, Vaur D.
- Genet Med. 2018 Dec;20(12):1677-1686. doi: 10.1038/s41436-018-0005-9. Epub 2018 Jul 10.
- PMID: 29988077
- PubMed abstract
- Source abstract
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- Germline pathogenic variants identified in women with ovarian tumors.
- Carter NJ, Marshall ML, Susswein LR, Zorn KK, Hiraki S, Arvai KJ, Torene RI, McGill AK, Yackowski L, Murphy PD, Xu Z, Solomon BD, Klein RT, Hruska KS.
- Gynecol Oncol. 2018 Dec;151(3):481-488. doi: 10.1016/j.ygyno.2018.09.030. Epub 2018 Oct 12.
- PMID: 30322717
- PubMed abstract
- Source abstract
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- Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings.
- Bonache S, Esteban I, Moles-Fernández A, Tenés A, Duran-Lozano L, Montalban G, Bach V, Carrasco E, Gadea N, López-Fernández A, Torres-Esquius S, Mancuso F, Caratú G, Vivancos A, Tuset N, Balmaña J, Gutiérrez-Enríquez S, Diez O.
- J Cancer Res Clin Oncol. 2018 Dec;144(12):2495-2513. doi: 10.1007/s00432-018-2763-9. Epub 2018 Oct 10.
- PMID: 30306255
- PubMed abstract
- Source abstract
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- Cancer Susceptibility Genetic Testing in a High-Risk Cohort of Urban Ashkenazi Jewish Individuals.
- Nielsen SM, De Simone LM, Olopade OI.
- J Genet Couns. 2018 Dec;27(6):1405-1410. doi: 10.1007/s10897-018-0269-x. Epub 2018 Jun 26.
- PMID: 29946849
- PubMed abstract
- Source abstract
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- A narrative overview of the patients’ outcomes after multigene cancer panel testing: Thorough evaluation of its implications for genetic counselling.
- Estebana I, Lopez-Fernandez A, Balmaña J.
- Eur J Med Genet. 2018 Nov 23. pii: S1769-7212(18)30422-1. doi: 10.1016/j.ejmg.2018.11.027. [Epub ahead of print]
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- Utility of Expedited Hereditary Cancer Testing in the Surgical Management of Patients with a New Breast Cancer Diagnosis.
- Theobald KA, Susswein LR, Marshall ML, Roberts ME, Mester JL, Speyer D, Williams RNW, Knapke SC, Solomon SR, Murphy PD, Klein RT, Hruska KS, Solomon BD.
- Ann Surg Oncol. 2018 Nov;25(12):3556-3562. doi: 10.1245/s10434-018-6581-8. Epub 2018 Aug 30.
- PMID: 30167906
- PubMed abstract
- Source abstract
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- High Prevalence of Hereditary Cancer Syndromes and Outcomes in Adults with Early-Onset Pancreatic Cancer.
- Bannon SA, Montiel MF, Goldstein JB, Dong W, Mork ME, Borras E, Hasanov M, Varadhachary GR, Maitra A, Katz MH, Feng L, Futreal A, Fogelman DR, Vilar E, McAllister F.
- Cancer Prev Res (Phila). 2018 Nov;11(11):679-686. doi: 10.1158/1940-6207.CAPR-18-0014. Epub 2018 Oct 1.
- PMID: 30274973
- PubMed abstract
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- Hereditary cancer gene panel test reports: wide heterogeneity suggests need for standardization.
- Makhnoon S, Shirts BH, Bowen DJ, Fullerton SM.
- Genet Med. 2018 Nov;20(11):1438-1445. doi: 10.1038/gim.2018.23. Epub 2018 Mar 1.
- PMID: 29493582
- PubMed abstract
- Source abstract
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- Association of Germline Genetic Test Type and Results With Patient Cancer Worry After Diagnosis of Breast Cancer.
- Katz SJ, Ward KC, Hamilton AS, Abrahamse P, Hawley ST, Kurian AW.
- JCO Precis Oncol. 2018 Nov;2018. doi: 10.1200/PO.18.00225. Epub 2018 Dec 19.
- PMID: 30656245
- PubMed abstract
- Source abstract
Research news: Genetic testing does not cause undue worry for breast cancer patients. (Rogel Cancer Center. Michigan Medicine)
Press: Multi-Gene Panel Breast Cancer Tests Don't Faze Women. (Medscape Oncology)
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- Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece.
- Konstanta I, Fostira F, Apostolou P, Stratikos E, Kalfakakou D, Pampanos A, Kollia P, Papadimitriou C, Konstantopoulou I, Yannoukakos D.
- J Hum Genet. 2018 Nov;63(11):1149-1158. doi: 10.1038/s10038-018-0498-8. Epub 2018 Aug 15.
- PMID: 30111881
- PubMed abstract
- Source abstract
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- Hereditary cancer screening: Case reports and review of literature on ten Ashkenazi Jewish founder mutations.
- Cox DM, Nelson KL, Clytone M, Collins DL.
- Mol Genet Genomic Med. 2018 Nov;6(6):1236-1242. doi: 10.1002/mgg3.460. Epub 2018 Aug 27.
- PMID: 30152102
- PubMed abstract
- Source abstract
- Case report, Review
- Free PMC article
- Free Full Text
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- Hereditary Cancer Risk Assessment and Genetic Testing in the Community-Practice Setting.
- DeFrancesco MS, Waldman RN, Pearlstone MM, Karanik D, Bernhisel R, Logan J, Alico L, Adkins RT.
- Obstet Gynecol. 2018 Nov;132(5):1121-1129. doi: 10.1097/AOG.0000000000002916.
- PMID: 30303907
- PubMed abstract
- Source abstract
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- Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) Clinical Working Group.
- Nielsen SM, Eccles DM, Romero IL, Al-Mulla F, Balmaña J, Biancolella M, Bslok R, Caligo MA, Calvello M, Capone GL, Cavalli P, Chan TLC, Claes KBM, Cortesi L, Couch FJ, de la Hoya M, De Toffol S, Diez O, Domchek SM, Eeles R, Efremidis A, Fostira F, Goldgar D, Hadjisavvas A, Hansen TVO, Hirasawa A, Houdayer C, Kleiblova P, Krieger S, Lázaro C, Loizidou M, Manoukian S, Mensenkamp AR, Moghadasi S, Monteiro AN, Mori L, Morrow A, Naldi N, Nielsen HR, Olopade OI, Pachter NS, Palmero EI, Pedersen IS, Piane M, Puzzo M, Robson M, Rossing M, Sini MC, Solano A, Soukupova J, Tedaldi G, Teixeira M, Thomassen M, Tibiletti MG, Toland A, Törngren T, Vaccari E, Varesco L, Vega A, Wallis Y, Wappenschmidt B, Weitzel J, Spurdle AB, De Nicolo A, Gómez-García EB.
- JCO Precis Oncol. 2018;2. doi: 10.1200/PO.18.00091. Epub 2018 Oct 26.
- PMID: 31517176
- PubMed abstract
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- Identification of Incidental Germline Mutations in Patients With Advanced Solid Tumors Who Underwent Cell-Free Circulating Tumor DNA Sequencing.
- Slavin TP, Banks KC, Chudova D, Oxnard GR, Odegaard JI, Nagy RJ, Tsang KWK, Neuhausen SL, Gray SW, Cristofanilli M, Rodriguez AA, Bardia A, Leyland-Jones B, Janicek MF, Lilly M, Sonpavde G, Lee CE, Lanman RB, Meric-Bernstam F, Kurzrock R, Weitzel JN.
- J Clin Oncol. 2018 Oct 19:JCO1800328. doi: 10.1200/JCO.18.00328. [Epub ahead of print]
- PMID: 30339520
- PubMed abstract
- Source abstract
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- A Devastatingly "Minor" Relationship Between Male Breast Cancer and Prostate Cancer.
- Kolli S, Asarian A, Genato R, Xiao P.
- Cureus. 2018 Oct 17;10(10):e3463. doi: 10.7759/cureus.3463.
- PMID: 30564542
- PubMed abstract
- Case report
- Free PMC article
- Free Full Text
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- Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls.
- Momozawa Y, Iwasaki Y, Parsons MT, Kamatani Y, Takahashi A, Tamura C, Katagiri T, Yoshida T, Nakamura S, Sugano K, Miki Y, Hirata M, Matsuda K, Spurdle AB, Kubo M.
- Nat Commun. 2018 Oct 4;9(1):4083. doi: 10.1038/s41467-018-06581-8.
- PMID: 30287823
- PubMed abstract
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- The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent.
- Brovkina OI, Shigapova L, Chudakova DA, Gordiev MG, Enikeev RF, Druzhkov MO, Khodyrev DS, Shagimardanova EI, Nikitin AG, Gusev OA.
- Front Oncol. 2018 Oct 2;8:421. doi: 10.3389/fonc.2018.00421. eCollection 2018.
- PMID: 30333958
- PubMed abstract
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- Prospective Evaluation of Germline Alterations in Patients With Exocrine Pancreatic Neoplasms.
- Lowery MA, Wong W, Jordan EJ, Lee JW, Kemel Y, Vijai J, Mandelker D, Zehir A, Capanu M, Salo-Mullen E, Arnold AG, Yu KH, Varghese AM, Kelsen DP, Brenner R, Kaufmann E, Ravichandran V, Mukherjee S, Berger MF, Hyman DM, Klimstra DS, Abou-Alfa GK, Tjan C, Covington C, Maynard H, Allen PJ, Askan G, Leach SD, Iacobuzio-Donahue CA, Robson ME, Offit K, Stadler ZK, O'Reilly EM.
- J Natl Cancer Inst. 2018 Oct 1;110(10):1067-1074. doi: 10.1093/jnci/djy024.
- PMID: 29506128
- PubMed abstract
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- [The French Genetic and Cancer Consortium guidelines for multigene panel analysis in hereditary breast and ovarian cancer predisposition].
- Moretta J, Berthet P, Bonadona V, Caron O, Cohen-Haguenauer O, Colas C, Corsini C, Cusin V, De Pauw A, Delnatte C, Dussart S, Jamain C, Longy M, Luporsi E, Maugard C, Nguyen TD, Pujol P, Vaur D, Andrieu N, Lasset C, Noguès C; Groupe Génétique et Cancer d’Unicancer.
- Bull Cancer. 2018 Oct;105(10):907-917. doi: 10.1016/j.bulcan.2018.08.003. Epub 2018 Sep 27.
- PMID: 30268633
- PubMed abstract
- Source abstract
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- Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate risk.
- West AH, Blazer KR, Stoll J, Jones M, Weipert CM, Nielsen SM, Kupfer SS, Weitzel JN, Olopade OI.
- Fam Cancer. 2018 Oct;17(4):495-505. doi: 10.1007/s10689-018-0070-x.
- PMID: 29445900
- PubMed abstract
- Source abstract
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- BRCA germline mutations in an unselected nationwide cohort of Chinese patients with ovarian cancer and healthy controls.
- Li A, Xie R, Zhi Q, Deng Y, Wu Y, Li W, Yang L, Jiao Z, Luo J, Zi Y, Sun G, Zhang J, Shi Y, Liu J.
- Gynecol Oncol. 2018 Oct;151(1):145-152. doi: 10.1016/j.ygyno.2018.07.024. Epub 2018 Aug 2.
- PMID: 30078507
- PubMed abstract
- Source abstract
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- Detection of novel germline mutations in six breast cancer predisposition genes by targeted next-generation sequencing.
- Dong L, Wu N, Wang S, Cheng Y, Han L, Zhao J, Long X, Mu K, Li M, Wei L, Wang W, Zhang W, Cao Y, Liu J, Yu J, Hao X.
- Hum Mutat. 2018 Oct;39(10):1442-1455. doi: 10.1002/humu.23597. Epub 2018 Aug 2.
- PMID: 30039884
- PubMed abstract
- Source abstract
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- Whole exome sequencing of breast cancer (TNBC) cases from India: association of MSH6 and BRIP1 variants with TNBC risk and oxidative DNA damage.
- Aravind Kumar M, Naushad SM, Narasimgu N, Nagaraju Naik S, Kadali S, Shanker U, Lakshmi Narasu M.
- Mol Biol Rep. 2018 Oct;45(5):1413-1419. doi: 10.1007/s11033-018-4307-4. Epub 2018 Aug 22.
- PMID: 30136158
- PubMed abstract
- Source abstract
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- Comprehensive Analysis of Germline Variants in Mexican Patients with Hereditary Breast and Ovarian Cancer Susceptibility.
- Quezada Urban R, Díaz Velásquez CE, Gitler R, Rojo Castillo MP, Sirota Toporek M, Figueroa Morales A, Moreno García O, García Esquivel L, Torres Mejía G, Dean M, Delgado Enciso I, Ochoa Díaz López H, Rodríguez León F, Jan V, Garzón Barrientos VH, Ruiz Flores P, Espino Silva PK, Haro Santa Cruz J, Martínez Gregorio H, Rojas Jiménez EA, Romero Cruz LE, Méndez Catalá CF, Álvarez Gómez RM, Fragoso Ontiveros V, Herrera LA, Romieu I, Terrazas LI, Chirino YI, Frecha C, Oliver J, Perdomo S, Vaca Paniagua F.
- Cancers (Basel). 2018 Sep 27;10(10). pii: E361. doi: 10.3390/cancers10100361.
- PMID: 30262796
- PubMed abstract
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- Addition of triple negativity of breast cancer as an indicator for germline mutations in predisposing genes increases sensitivity of clinical selection criteria.
- Hoyer J, Vasileiou G, Uebe S, Wunderle M, Kraus C, Fasching PA, Thiel CT, Hartmann A, Beckmann MW, Lux MP, Reis A.
- BMC Cancer. 2018 Sep 26;18(1):926. doi: 10.1186/s12885-018-4821-8.
- PMID: 30257646
- PubMed abstract
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- Exome Sequencing–Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
- Manickam K, Buchanan AH, Schwartz MLB, Hallquist MLG, Williams JL, Rahm AK, Heather Rocha H, Savatt JM, Evans AE, Butry LM, Lazzeri AL, Lindbuchler DM, Flansburg CN, Leeming R, Vogel VG, Lebo MS, Mason-Suares HM, Hoskinson DC, Abul-Husn NS, Dewey FE, Overton JD, Reid JG, Baras A, Willard HF, McCormick CZ, Krishnamurthy SB, Hartzel DN, Kost KA, Lavage DR, Sturm AC, Frisbie LR, Person TN, Metpally RP, Giovanni MA, Lowry LE, Leader JB, Ritchie MD, Carey DJ, Justice AE, Kirchner HL, Faucett WA, Williams MS, Ledbetter DH, Murray MF.
- JAMA Netw Open. 2018 Sep 21;1(5): e182140. doi: 10.1001/jamanetworkopen.2018.2140.
Research news: Can population-based DNA sequencing identify those at risk for hereditary cancers? (FORCE. XRAYS.)
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- Cascade Genetic Testing of Relatives for Hereditary Cancer Risk: Results of an Online Initiative.
- Caswell-Jin JL, Zimmer AD, Stedden W, Kingham KE, Zhou AY, Kurian AW.
- J Natl Cancer Inst. 2018 Sep 18. doi: 10.1093/jnci/djy147. [Epub ahead of print]
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- Rapid detection of copy number variations and point mutations in BRCA1/2 genes using a single workflow by ion semiconductor sequencing pipeline.
- Germani A, Libi F, Maggi S, Stanzani G, Lombardi A, Pellegrini P, Mattei M, De Marchis L, Amanti C, Pizzuti A, Torrisi MR, Piane M.
- Oncotarget. 2018 Sep 14;9(72):33648-33655. doi: 10.18632/oncotarget.26000. eCollection 2018 Sep 14.
- PMID: 30263092
- PubMed abstract
- Source abstract
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- Exome Sequencing-Based Screening for BRCA1/2 Expected Pathogenic Variants Among Adult Biobank Participants.
- Manickam K, Buchanan AH, Schwartz MLB, Hallquist MLG, Williams JL, Rahm AK, Rocha H, Savatt JM, Evans AE, Butry LM, Lazzeri AL, Lindbuchler DM, Flansburg CN, Leeming R, Vogel VG, Lebo MS, Mason-Suares HM, Hoskinson DC, Abul-Husn NS, Dewey FE, Overton JD, Reid JG, Baras A, Willard HF, McCormick CZ, Krishnamurthy SB, Hartzel DN, Kost KA, Lavage DR, Sturm AC, Frisbie LR, Person TN, Metpally RP, Giovanni MA, Lowry LE, Leader JB, Ritchie MD, Carey DJ, Justice AE, Kirchner HL, Faucett WA, Williams MS, Ledbetter DH, Murray MF.
- JAMA Netw Open. 2018 Sep 7;1(5):e182140. doi: 10.1001/jamanetworkopen.2018.2140.
- PMID: 30646163
- PubMed abstract
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- Population based germline testing for primary cancer prevention.
- Manchanda R, Legood R.
- Oncotarget. 2018 Sep 4;9(69):33062-33063. eCollection 2018 Sep 4.
- Commentary
- Free Full Text (PDF)
Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population Women.
- PMID: 29361001
- PubMed abstract
- Free Full Text
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- Prospective study of germline genetic testing in incident cases of pancreatic adenocarcinoma.
- Brand R, Borazanci E, Speare V, Dudley B, Karloski E, Peters MLB, Stobie L, Bahary N, Zeh H, Zureikat A, Hogg M, Lee K, Tsung A, Rhee J, Ohr J, Sun W, Lee J, Moser AJ, DeLeonardis K, Krejdovsky J, Dalton E, LaDuca H, Dolinsky J, Colvin A, Lim C, Black MH, Tung N.
- Cancer. 2018 Sep 1;124(17):3520-3527. doi: 10.1002/cncr.31628. Epub 2018 Aug 1.
- PMID: 30067863
- PubMed abstract
- Source abstract
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- Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results.
- Bradbury AR, Patrick-Miller LJ, Egleston BL, Hall MJ, Domchek SM, Daly MB, Ganschow P, Grana G, Olopade OI, Fetzer D, Brandt A, Chambers R, Clark DF, Forman A, Gaber R, Gulden C, Horte J, Long JM, Lucas T, Madaan S, Mattie K, McKenna D, Montgomery S, Nielsen S, Powers J, Rainey K, Rybak C, Savage M, Seelaus C, Stoll J, Stopfer JE, Yao XS.
- J Natl Cancer Inst. 2018 Sep 1;110(9):985-993. doi: 10.1093/jnci/djy015.
- PMID: 29490071
- PubMed abstract
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- Surgery in ovarian cancer - Brazilian Society of Surgical Oncology consensus.
- Tsunoda AT, Ribeiro R, Reis RJ, da Cunha Andrade C, Moretti Marques R, Baiocchi G, Fin F, Zanvettor PH, Falcao D, Batista TP, Azevedo B, Guitmann G, Pessini SA, Nunes JS, Campbell LM, Linhares JC, Carneiro V, Coimbra F.
- BJOG. 2018 Sep;125(10):1243-1252. doi: 10.1111/1471-0528.15328. Epub 2018 Jul 18.
- PMID: 29900651
- PubMed abstract
- Source abstract
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- A Clinical Decision Support Tool to Predict Cancer Risk for Commonly Tested Cancer-Related Germline Mutations.
- Braun D, Yang J, Griffin M, Parmigiani G, Hughes KS.
- J Genet Couns. 2018 Sep;27(5):1187-1199. doi: 10.1007/s10897-018-0238-4. Epub 2018 Mar 2.
- PMID: 29500626
- PubMed abstract
- Source abstract
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- How Should Genetic Counseling for Ovarian Cancer Be Implemented in a Middle-Income Country? An Insight Based on the Brazilian Scenario.
- Koike Folgueira MAA, Maistro S, Teixeira N, Mourits MJE, Chammas R, Hendrika de Bock G.
- J Glob Oncol. 2018 Sep;4:1-3. doi: 10.1200/JGO.17.00230.
- PMID: 30241261
- PubMed abstract
- Source abstract
- Commentary
- Free PMC article
- Free Full Text
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- Validation and Implementation of BRCA1/2 Variant Screening in Ovarian Tumor Tissue.
- de Jonge MM, Ruano D, van Eijk R, van der Stoep N, Nielsen M, Wijnen JT, Ter Haar NT, Baalbergen A, Bos MEMM, Kagie MJ, Vreeswijk MPG, Gaarenstroom KN, Kroep JR, Smit VTHBM, Bosse T, van Wezel T, van Asperen CJ.
- J Mol Diagn. 2018 Sep;20(5):600-611. doi: 10.1016/j.jmoldx.2018.05.005. Epub 2018 Jun 21.
- PMID: 29936257
- PubMed abstract
- Source abstract
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- Identification of a novel breast cancer-causing mutation in the BRCA1 gene by targeted next generation sequencing: A case report.
- Wang Y, Jiang D, Zhao Q, Huang H, Zhang X, Cui Y, Liu J, Wu J, Lin K, Chen W, Xiang J, Jin H, Peng Z, Banerjee S.
- Oncol Lett. 2018 Sep;16(3):3913-3916. doi: 10.3892/ol.2018.9139. Epub 2018 Jul 12.
- PMID: 30128007
- PubMed abstract
- Source abstract
- Case report
- Free PMC article
- Free Full Text
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- Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity.
- Penkert J, Schmidt G, Hofmann W, Schubert S, Schieck M, Auber B, Ripperger T, Hackmann K, Sturm M, Prokisch H, Hille-Betz U, Mark D, Illig T, Schlegelberger B, Steinemann D.
- Breast Cancer Res. 2018 Aug 7;20(1):87. doi: 10.1186/s13058-018-1011-1.
- PMID: 30086788
- PubMed abstract
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- Genetic testing for hereditary prostate cancer: Current status and limitations.
- Zhen JT, Syed J, Nguyen KA, Leapman MS, Agarwal N, Brierley K, Llor X, Hofstatter E, Shuch B.
- Cancer. 2018 Aug 1;124(15):3105-3117. doi: 10.1002/cncr.31316. Epub 2018 Apr 18.
- PMID: 29669169
- PubMed abstract
- Source abstract
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- Uptake, Results, and Outcomes of Germline Multiple-Gene Sequencing After Diagnosis of Breast Cancer.
- Kurian AW, Ward KC, Hamilton AS, Deapen DM, Abrahamse P, Bondarenko I, Li Y, Hawley ST, Morrow M, Jagsi R, Katz SJ.
- JAMA Oncol. 2018 Aug 1;4(8):1066-1072. doi: 10.1001/jamaoncol.2018.0644.
- PMID: 29801090
- PubMed abstract
- Source abstract
Press: Multigene Sequencing Rapidly Replacing BRCA Tests. (Medscape Oncology)
Letter, Comment:
Cancer Risk Estimates for Study of Multiple-Gene Testing After Diagnosis of Breast Cancer.
- PMID: 30383137
- PubMed abstract
- Source abstract
Letter, Reply:
Cancer Risk Estimates for Study of Multiple-Gene Testing After Diagnosis of Breast Cancer-Reply.
- PMID: 30383131
- PubMed abstract
- Source abstract
-
- Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing.
- Shimelis H, LaDuca H, Hu C, Hart SN, Na J, Thomas A, Akinhanmi M, Moore RM, Brauch H, Cox A, Eccles DM, Ewart-Toland A, Fasching PA, Fostira F, Garber J, Godwin AK, Konstantopoulou I, Nevanlinna H, Sharma P, Yannoukakos D, Yao S, Feng BJ, Tippin Davis B, Lilyquist J, Pesaran T, Goldgar DE, Polley EC, Dolinsky JS, Couch FJ.
- J Natl Cancer Inst. 2018 Aug 1;110(8):855-862. doi: 10.1093/jnci/djy106.
- PMID: 30099541
- PubMed abstract
Research news:
New triple-negative breast cancer risk genes identified.
- PMID: 30122618
- PubMed abstract
- Source abstract
Research news: Triple-negative: Genes associated with risk for aggressive breast cancer. (Science Daily)
Research news: Triple-Negative Breast Cancer Risk Linked to Germline Variants in Several Cancer Genes. (Precision Oncology News)
Research news: Study identifies genes associated with risk of triple-negative breast cancer. (FORCE. XRAYS.)
-
- Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing.
- Rana HQ, Gelman R, LaDuca H, McFarland R, Dalton E, Thompson J, Speare V, Dolinsky JS, Chao EC, Garber JE.
- J Natl Cancer Inst. 2018 Aug 1;110(8):863-870. doi: 10.1093/jnci/djy001.
- PMID: 29529297
- PubMed abstract
- Source abstract
Editorial:
Testing Positive on a Multigene Panel Does Not Suffice to Determine Disease Risks.
- PMID: 29529278
- PubMed abstract
- Free Full Text
-
- FFPE breast tumour blocks provide reliable sources of both germline and malignant DNA for investigation of genetic determinants of individual tumour responses to treatment.
- Wilkins A, Chauhan R, Rust A, Pearson A, Daley F, Manodoro F, Fenwick K, Bliss J, Yarnold J, Somaiah N.
- Breast Cancer Res Treat. 2018 Aug;170(3):573-581. doi: 10.1007/s10549-018-4798-7. Epub 2018 Feb 22.
- PMID: 29700676
- PubMed abstract
-
- Beyond BRCA: A Case Series Examining the Advent of Multigene Panel Testing.
- Reap L, Ahsan S, Saleh M.
- Clin Breast Cancer. 2018 Aug;18(4):e431-e439. doi: 10.1016/j.clbc.2018.03.015. Epub 2018 Apr 6.
- PMID: 29739691
- PubMed abstract
- Source abstract
-
- Breast Cancer Genetics and Indications for Prophylactic Mastectomy.
- Krontiras H, Farmer M, Whatley J.
- Surg Clin North Am. 2018 Aug;98(4):677-685. doi: 10.1016/j.suc.2018.03.004. Epub 2018 May 30.
- PMID: 30005767
- PubMed abstract
- Source abstract
-
- Sputum Detection of Predisposing Genetic Mutations in Women with Pulmonary Nontuberculous Mycobacterial Disease.
- Philley JV, Hertweck KL, Kannan A, Brown-Elliott BA, Wallace RJ Jr, Kurdowska A, Ndetan H, Singh KP, Miller EJ, Griffith DE, Dasgupta S.
- Sci Rep. 2018 Jul 27;8(1):11336. doi: 10.1038/s41598-018-29471-x.
- PMID: 30054559
- PubMed abstract
-
- Multigene Hereditary Cancer Panels Reveal High-Risk Pancreatic Cancer Susceptibility Genes.
- Hu C, LaDuca H, Shimelis H, Polley EC, Lilyquist J, Hart SN, Na J, Thomas A, Lee KY, Davis BT, Black MH, Pesaran T, Goldgar DE, Dolinsky JS, Couch FJ.
- JCO Precis Oncol. 2018;2. doi: 10.1200/PO.17.00291. Epub 2018 Jul 25.
- PMID: 31497750
- PubMed abstract
-
- BRCA1 founder mutations and beyond in the Polish population: A single-institution BRCA1/2 next-generation sequencing study.
- Kowalik A, Siołek M, Kopczyński J, Krawiec K, Kalisz J, Zięba S, Kozak-Klonowska B, Wypiórkiewicz E, Furmańczyk J, Nowak-Ozimek E, Chłopek M, Macek P, Smok-Kalwat J, Góźdź S.
- PLoS One. 2018 Jul 24;13(7):e0201086. doi: 10.1371/journal.pone.0201086. eCollection 2018.
- PMID: 30040829
- PubMed abstract
-
- Identification of a BRCA2 mutation in a Turkish family with early-onset breast cancer.
- Celik E, Ermis Tekkus K, Akcay IM, Alkurt Sal G, Ezberci F, Dinler Doganay G, Doganay L.
- Clin Case Rep. 2018 Jul 17;6(9):1751-1755. doi: 10.1002/ccr3.1625. eCollection 2018 Sep.
- PMID: 30214756
- PubMed abstract
- Source abstract
- Case report
- Free PMC article
- Free Full Text
-
- Clinical genetic testing outcome with multi-gene panel in Asian patients with multiple primary cancers.
- Chan GHJ, Ong PY, Low JJH, Kong HL, Ow SGW, Tan DSP, Lim YW, Lim SE, Lee SC.
- Oncotarget. 2018 Jul 17;9(55):30649-30660. doi: 10.18632/oncotarget.25769. eCollection 2018 Jul 17.
- PMID: 30093976
- PubMed abstract
- Source abstract
-
- NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) — Genetic/Familial High-Risk Assessment: Breast and Ovarian
- Daly MB, Pilarski R, Berry M, Buys SS, Friedman S, Garber JE, Hutton ML, Kauff ND, Khan S, Klein C, Kohlmann W, Kurian A, Laronga C, Litton JK, Madlensky L, Mac JS, Merajver SD, Offit K, Pal T, Peterson HJ, Reiser G, Shannon KM, Thaker P, Visvanathan K, Weitzel JN, Wick MJ, Wisinski KB, Darlow S.
- NCCN.org. 2018 Jul 11. Version 1.2019.
- Guidelines
- Free Full Text (PDF - Registration required)
-
- Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes.
- Whitworth J, Smith PS, Martin JE, West H, Luchetti A, Rodger F, Clark G, Carss K, Stephens J, Stirrups K, Penkett C, Mapeta R, Ashford S, Megy K, Shakeel H, Ahmed M, Adlard J, Barwell J, Brewer , Casey , Armstrong R, Cole T, Evans DG, Fostira F, Greenhalgh L, Hanson H, Henderson A, Hoffman J, Izatt L, Kumar A, Kwong A, Lalloo F, Ong KR, Paterson J, Park SM, Chen-Shtoyerman R, Searle C, Side L, Skytte AB, Snape K, Woodward ER; NIHR BioResource Rare Diseases Consortium, Tischkowitz MD, Maher ER.
- Am J Hum Genet. 2018 Jul 5;103(1):3-18. doi: 10.1016/j.ajhg.2018.04.013. Epub 2018 Jun 14.
- PMID: 29909963
- PubMed abstract
-
- Breast cancer in an 18-year-old female: A fatal case report and literature review.
- Jóźwik M, Posmyk R, Jóźwik M, Semczuk A, Gogiel-Shields M, Kuś-Słowińska M, Garbowicz M, Klukowski M, Wojciechowicz J.
- Cancer Biol Ther. 2018 Jul 3;19(7):543-548. doi: 10.1080/15384047.2017.1416931.
- PMID: 29723101
- PubMed abstract
-
- Testing Ashkenazi Jewish Women for Mutations Predisposing to Breast Cancer in Genes Other Than BRCA1 and BRCA2.
- Narod S, Sopik V, Cybulski C.
- JAMA Oncol. 2018 Jul 1;4(7):1012. doi: 10.1001/jamaoncol.2018.0595.
- PMID: 29801022
- PubMed abstract
- Source abstract
Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women.
- PMID: 28727877
- PubMed abstract
- Free Full Text
Letter, Reply:
Testing Ashkenazi Jewish Women for Mutations Predisposing to Breast Cancer in Genes Other Than BRCA1 and BRCA2—Reply.
- PMID: 29800948
- PubMed abstract
- Source abstract
-
- Cost-effectiveness of Population-Based BRCA1, BRCA2, RAD51C, RAD51D, BRIP1, PALB2 Mutation Testing in Unselected General Population Women.
- Manchanda R, Patel S, Gordeev VS, Antoniou AC, Smith S, Lee A, Hopper JL, MacInnis RJ, Turnbull C, Ramus SJ, Gayther SA, Pharoah PDP, Menon U, Jacobs I, Legood R.
- J Natl Cancer Inst. 2018 Jul 1;110(7):714-725. doi: 10.1093/jnci/djx265.
- PMID: 29361001
- PubMed abstract
Editorial:
Population Testing for High Penetrance Genes: Are We There Yet?
- PMID: 29401305
- PubMed abstract
- Source abstract
Commentary:
Population based germline testing for primary cancer prevention.
- PMID: 29361001
- PubMed abstract
- Free Full Text (PDF)
-
- Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations.
- Singh J, Thota N, Singh S, Padhi S, Mohan P, Deshwal S, Sur S, Ghosh M, Agarwal A, Sarin R, Ahmed R, Almel S, Chakraborti B, Raina V, DadiReddy PK, Smruti BK, Rajappa S, Dodagoudar C, Aggarwal S, Singhal M, Joshi A, Kumar R, Kumar A, Mishra DK, Arora N, Karaba A, Sankaran S, Katragadda S, Ghosh A, Veeramachaneni V, Hariharan R, Mannan AU.
- Breast Cancer Res Treat. 2018 Jul;170(1):189-196. doi: 10.1007/s10549-018-4726-x. Epub 2018 Feb 22.
- PMID: 29470806
- PubMed abstract
- Source abstract
-
- Detection of Germline Mutations in Patients with Epithelial Ovarian Cancer Using Multi-gene Panels: Beyond BRCA1/2.
- Eoh KJ, Kim JE, Park HS, Lee ST, Park JS, Han JW, Lee JY, Kim S, Kim SW, Kim JH, Kim YT, Nam EJ.
- Cancer Res Treat. 2018 Jul;50(3):917-925. doi: 10.4143/crt.2017.220. Epub 2017 Sep 27.
- PMID: 29020732
- PubMed abstract
-
- Increased access to TP53 analysis through breast cancer multi-gene panels: clinical considerations.
- Azzollini J, Mariani M, Peissel B, Manoukian S.
- Fam Cancer. 2018 Jul;17(3):317-319. doi: 10.1007/s10689-017-0020-z.
- PMID: 28681140
- PubMed abstract
- Letter
- Free PMC article
- Free Full Text
Next generation sequencing is informing phenotype: a TP53 example.
- PMID: 28509937
- PubMed abstract
- Source abstract
-
- Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine.
- Myszka A, Nguyen-Dumont T, Karpinski P, Sasiadek MM, Akopyan H, Hammet F, Tsimiklis H, Park DJ, Pope BJ, Slezak R, Kitsera N, Siekierzynska A, Southey MC.
- Fam Cancer. 2018 Jul;17(3):345-349. doi: 10.1007/s10689-017-0050-6.
- PMID: 29052111
- PubMed abstract
-
- Heterogeneity and Uncertainties Specific to Genome-Based Health Technological Assessments.
- Petelin L, Liew D, Mitchell G, James PA, Trainer AH.
- Value Health. 2018 Jul;21(7):891-893. doi: 10.1016/j.jval.2018.02.009. Epub 2018 May 16.
- PMID: 30005762
- PubMed abstract
- Source abstract
A Multigene Test Could Cost-Effectively Help Extend Life Expectancy for Women at Risk of Hereditary Breast Cancer.
- PMID: 28407996
- PubMed abstract
- Free Full Text
Letter:
A multigene test could cost-effectively help extend life expectancy for women at risk of hereditary breast cancer-Reply to letter to the editor by Petelin et al.
- PMID: 30005763
- PubMed abstract
- Source abstract
-
- A multigene test could cost-effectively help extend life expectancy for women at risk of hereditary breast cancer-Reply to letter to the editor by Petelin et al.
- Li Y, Devlin JJ.
- Value Health. 2018 Jul;21(7):893-894. doi: 10.1016/j.jval.2018.02.010. Epub 2018 Apr 5.
- PMID: 30005763
- PubMed abstract
- Source abstract
Letter:
Heterogeneity and Uncertainties Specific to Genome-Based Health Technological Assessments.
- PMID: 30005762
- PubMed abstract
- Source abstract
Original Research:
A Multigene Test Could Cost-Effectively Help Extend Life Expectancy for Women at Risk of Hereditary Breast Cancer.
- PMID: 28407996
- PubMed abstract
- Free Full Text
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- Evaluation of some direct-to-consumer genetic testing reveals inaccuracies and misinterpretations.
- [No author given]
- FORCE. XRAYS. 2018 Jun 28.
- Research news
- Free Full Text
False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
- PMID: 29565420
- PubMed abstract
- Free Full Text
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- Pancreatic cancer as a sentinel for hereditary cancer predisposition.
- Young EL, Thompson BA, Neklason DW, Firpo MA, Werner T, Bell R, Berger J, Fraser A, Gammon A, Koptiuch C, Kohlmann WK, Neumayer L, Goldgar DE, Mulvihill SJ, Cannon-Albright LA, Tavtigian SV.
- BMC Cancer. 2018 Jun 27;18(1):697. doi: 10.1186/s12885-018-4573-5.
- PMID: 29945567
- PubMed abstract
-
- Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.
- Hu C, Hart SN, Polley EC, Gnanaolivu R, Shimelis H, Lee KY, Lilyquist J, Na J, Moore R, Antwi SO, Bamlet WR, Chaffee KG, DiCarlo J, Wu Z, Samara R, Kasi PM, McWilliams RR, Petersen GM, Couch FJ.
- JAMA. 2018 Jun 19;319(23):2401-2409. doi: 10.1001/jama.2018.6228.
- PMID: 29922827
- PubMed abstract
- Source abstract
Editorial:
Germline Genetic Testing for Pancreatic Ductal Adenocarcinoma at Time of Diagnosis.
- PMID: 29922810
- PubMed abstract
- Source abstract
Press: Genetic Testing in Relatives of Pancreatic Cancer Patients? (Medscape Oncology)
Press: Six Germline Mutations Uncovered of Increased Pancreatic Cancer Risk. (Clinical Omics)
-
- Exome sequencing and case-control analyses identify RCC1 as a candidate breast cancer susceptibility gene.
- Riahi A, Radmanesh H, Schürmann P, Bogdanova N, Geffers R, Meddeb R, Kharrat M, Dörk T.
- Int J Cancer. 2018 Jun 15;142(12):2512-2517. doi: 10.1002/ijc.31273. Epub 2018 Feb 5.
- PMID: 29363114
- PubMed abstract
- Source abstract
-
- The ICR639 CPG NGS validation series: A resource to assess analytical sensitivity of cancer predisposition gene testing.
- Mahamdallie S, Ruark E, Holt E, Poyastro-Pearson E, Renwick A, Strydom A, Seal S, Rahman N.
- Wellcome Open Res. 2018 Jun 12;3:68. doi: 10.12688/wellcomeopenres.14594.1. eCollection 2018.
- PMID: 30175241
- PubMed abstract
-
- [Chinese consensus on next generation sequencing-based BRCA testing].
- Working group of Chinese consensus on next generation sequencing-based BRCA testing.
- Zhonghua Bing Li Xue Za Zhi. 2018 Jun 8;47(6):401-406. doi: 10.3760/cma.j.issn.0529-5807.2018.06.003.
- PMID: 29886581
- PubMed abstract
-
- XRAYS Follow Up: Does expanded genetic testing benefit Jewish women with breast cancer?
- [No author given]
- FORCE. XRAYS. 2018 Jun 7.
- Research review, Commentary
- Free Full Text
Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women.
- PMID: 28727877
- PubMed abstract
- Free Full Text
Research review, Commentary: Does expanded genetic testing benefit Jewish women diagnosed with breast cancer? (FORCE. XRAYS. 2017 Sep 13.)
-
- High frequency of pathogenic non-founder germline mutations in BRCA1 and BRCA2 in families with breast and ovarian cancer in a founder population.
- Maksimenko J, Irmejs A, Trofimovičs G, Bērziņa D, Skuja E, Purkalne G, Miklaševičs E, Gardovskis J.
- Hered Cancer Clin Pract. 2018 Jun 5;16:12. doi: 10.1186/s13053-018-0094-0. eCollection 2018.
- PMID: 29928469
- PubMed abstract
-
- Mutations in Known and Novel cancer Susceptibility Genes in Young Patients with Pancreatic Cancer.
- Alimirzaie S, Mohamadkhani A, Masoudi S, Sellars E, Boffetta P, Malekzadeh R, Akbari MR, Pourshams A.
- Arch Iran Med. 2018 Jun 1;21(6):228-233.
- PMID: 29940740
- PubMed abstract
- Source abstract
-
- Contralateral prophylactic mastectomy rate and predictive factors among patients with breast cancer who underwent multigene panel testing for hereditary cancer.
- Elsayegh N, Webster RD, Gutierrez Barrera AM, Lin H, Kuerer HM, Litton JK, Bedrosian I, Arun BK.
- Cancer Med. 2018 Jun;7(6):2718-2726. doi: 10.1002/cam4.1519. Epub 2018 May 7.
- PMID: 29733510
- PubMed abstract
- Source abstract
-
- Cancer gene-panel testing identifies two loss-of-function alleles in PALB2 and PTEN.
- Avgerinou C, Fostira F, Economopoulou P, Psyrri A.
- Clin Genet. 2018 Jun;93(6):1250-1251. doi: 10.1111/cge.13138. Epub 2018 Feb 11.
- PMID: 29430632
- PubMed abstract
- Source abstract
-
- Mutational analysis of RAD51C and RAD51D genes in hereditary breast and ovarian cancer families from Murcia (southeastern Spain).
- Sánchez-Bermúdez AI, Sarabia-Meseguer MD, García-Aliaga Á, Marín-Vera M, Macías-Cerrolaza JA, Henaréjos PS, Guardiola-Castillo V, Peña FA, Alonso-Romero JL, Noguera-Velasco JA, Ruiz-Espejo F.
- Eur J Med Genet. 2018 Jun;61(6):355-361. doi: 10.1016/j.ejmg.2018.01.015. Epub 2018 Feb 2.
- PMID: 29409816
- PubMed abstract
- Source abstract
-
- Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group.
- Taylor A, Brady AF, Frayling IM, Hanson H, Tischkowitz M, Turnbull C, Side L; UK Cancer Genetics Group (UK-CGG).
- J Med Genet. 2018 Jun;55(6):372-377. doi: 10.1136/jmedgenet-2017-105188. Epub 2018 Apr 16.
- PMID: 29661970
- PubMed abstract
- Guideline
- Free PMC article
- Free Full Text
-
- Effects of Cancer Genetic Panel Testing on at-Risk Individuals.
- Frost AS, Toaff M, Biagi T, Stark E, McHenry A, Kaltman R.
- Obstet Gynecol. 2018 Jun;131(6):1103-1110. doi: 10.1097/AOG.0000000000002531.
- PMID: 29742654
- PubMed abstract
- Source abstract
-
- Breast Cancer Family History and Contralateral Breast Cancer Risk in Young Women: An Update From the Women's Environmental Cancer and Radiation Epidemiology Study.
- Reiner AS, Sisti J, John EM, Lynch CF, Brooks JD, Mellemkjær L, Boice JD, Knight JA, Concannon P, Capanu M, Tischkowitz M, Robson M, Liang X, Woods M, Conti DV, Duggan D, Shore R, Stram DO, Thomas DC, Malone KE, Bernstein L; WECARE Study Collaborative Group, Bernstein JL.
- J Clin Oncol. 2018 May 20;36(15):1513-1520. doi: 10.1200/JCO.2017.77.3424. Epub 2018 Apr 5.
- PMID: 29620998
- PubMed abstract
- Source abstract
-
- Genetics of breast cancer in African populations: a literature review.
- Abbad A, Baba H, Dehbi H, Elmessaoudi-Idrissi M, Elyazghi Z, Abidi O, Radouani F.
- Glob Health Epidemiol Genom. 2018 May 11;3:e8. doi: 10.1017/gheg.2018.8. eCollection 2018.
- PMID: 30263132
- PubMed abstract
- Source abstract
-
- Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer.
- Torrezan GT, de Almeida FGDSR, Figueiredo MCP, Barros BDF, de Paula CAA, Valieris R, de Souza JES, Ramalho RF, da Silva FCC, Ferreira EN, de Nóbrega AF, Felicio PS, Achatz MI, de Souza SJ, Palmero EI, Carraro DM.
- Front Genet. 2018 May 7;9:161. doi: 10.3389/fgene.2018.00161. eCollection 2018.
- PMID: 29868112
- PubMed abstract
-
- Germline deleterious mutations in genes other than BRCA2 are infrequent in male breast cancer.
- Fostira F, Saloustros E, Apostolou P, Vagena A, Kalfakakou D, Mauri D, Tryfonopoulos D, Georgoulias V, Yannoukakos D, Fountzilas G, Konstantopoulou I.
- Breast Cancer Res Treat. 2018 May;169(1):105-113. doi: 10.1007/s10549-018-4661-x. Epub 2018 Jan 15.
- PMID: 29335925
- PubMed abstract
- Source abstract
-
- A comprehensive BRCA1/2 NGS pipeline for an immediate Copy Number Variation (CNV) detection in breast and ovarian cancer molecular diagnosis.
- Concolino P, Rizza R, Mignone F, Costella A, Guarino D, Carboni I, Capoluongo E, Santonocito C, Urbani A, Minucci A.
- Clin Chim Acta. 2018 May;480:173-179. doi: 10.1016/j.cca.2018.02.012. Epub 2018 Feb 16.
- PMID: 29458049
- PubMed abstract
- Source abstract
-
- Risk, Prediction and Prevention of Hereditary Breast Cancer - Large-Scale Genomic Studies in Times of Big and Smart Data.
- Wunderle M, Olmes G, Nabieva N, Häberle L, Jud SM, Hein A, Rauh C, Hack CC, Erber R, Ekici AB, Hoyer J, Vasileiou G, Kraus C, Reis A, Hartmann A, Schulz-Wendtland R, Lux MP, Beckmann MW, Fasching PA.
- Geburtshilfe Frauenheilkd. 2018 May;78(5):481-492. doi: 10.1055/a-0603-4350. Epub 2018 Jun 4.
- PMID: 29880983
- PubMed abstract
- Source abstract
- Review
- Free PMC article
- Free Full Text
-
- Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants.
- Buchanan AH, Manickam K, Meyer MN, Wagner JK, Hallquist MLG, Williams JL, Rahm AK, Williams MS, Chen ZE, Shah CK, Garg TK, Lazzeri AL, Schwartz MLB, Lindbuchler DM, Fan AL, Leeming R, Servano PO 3rd, Smith AL, Vogel VG, Abul-Husn NS, Dewey FE, Lebo MS, Mason-Suares HM, Ritchie MD, Davis FD, Carey DJ, Feinberg DT, Faucett WA, Ledbetter DH, Murray MF.
- Genet Med. [2018 May;]20(5):554-558. doi: 10.1038/gim.2017.145. Epub 2017 Oct 26.
- PMID: 29261187
- PubMed abstract
-
- Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
- Rebbeck TR, Friebel TM, Friedman E, Hamann U, Huo D, Kwong A, Olah E, Olopade OI, Solano AR, Teo SH, Thomassen M, Weitzel JN, Chan TL, Couch FJ, Goldgar DE, Kruse TA, Palmero EI, Park SK, Torres D, van Rensburg EJ, McGuffog L, Parsons MT, Leslie G, Aalfs CM, Abugattas J, Adlard J, Agata S, Aittomäki K, Andrews L, Andrulis IL, Arason A, Arnold N, Arun BK, Asseryanis E, Auerbach L, Azzollini J, Balmaña J, Barile M, Barkardottir RB, Barrowdale D, Benitez J, Berger A, Berger R, Blanco AM, Blazer KR, Blok MJ, Bonadona V, Bonanni B, Bradbury AR, Brewer C, Buecher B, Buys SS, Caldes T, Caliebe A, Caligo MA, Campbell I, Caputo SM, Chiquette J, Chung WK, Claes KBM, Collée JM, Cook J, Davidson R, de la Hoya M, De Leeneer K, de Pauw A, Delnatte C, Diez O, Ding YC, Ditsch N, Domchek SM, Dorfling CM, Velazquez C, Dworniczak B, Eason J, Easton DF, Eeles R, Ehrencrona H, Ejlertsen B; EMBRACE, Engel C, Engert S, Evans DG, Faivre L, Feliubadaló L, Ferrer SF, Foretova L, Fowler J, Frost D, Galvão HCR, Ganz PA, Garber J, Gauthier-Villars M, Gehrig A; GEMO Study Collaborators, Gerdes AM, Gesta P, Giannini G, Giraud S, Glendon G, Godwin AK, Greene MH, Gronwald J, Gutierrez-Barrera A, Hahnen E, Hauke J; HEBON, Henderson A, Hentschel J, Hogervorst FBL, Honisch E, Imyanitov EN, Isaacs C, Izatt L, Izquierdo A, Jakubowska A, James P, Janavicius R, Jensen UB, John EM, Vijai J, Kaczmarek K, Karlan BY, Kast K, Investigators K, Kim SW, Konstantopoulou I, Korach J, Laitman Y, Lasa A, Lasset C, Lázaro C, Lee A, Lee MH, Lester J, Lesueur F, Liljegren A, Lindor NM, Longy M, Loud JT, Lu KH, Lubinski J, Machackova E, Manoukian S, Mari V, Martínez-Bouzas C, Matrai Z, Mebirouk N, Meijers-Heijboer HEJ, Meindl A, Mensenkamp AR, Mickys U, Miller A, Montagna M, Moysich KB, Mulligan AM, Musinsky J, Neuhausen SL, Nevanlinna H, Ngeow J, Nguyen HP, Niederacher D, Nielsen HR, Nielsen FC, Nussbaum RL, Offit K, Öfverholm A, Ong KR, Osorio A, Papi L, Papp J, Pasini B, Pedersen IS, Peixoto A, Peruga N, Peterlongo P, Pohl E, Pradhan N, Prajzendanc K, Prieur F, Pujol P, Radice P, Ramus SJ, Rantala J, Rashid MU, Rhiem K, Robson M, Rodriguez GC, Rogers MT, Rudaitis V, Schmidt AY, Schmutzler RK, Senter L, Shah PD, Sharma P, Side LE, Simard J, Singer CF, Skytte AB, Slavin TP, Snape K, Sobol H, Southey M, Steele L, Steinemann D, Sukiennicki G, Sutter C, Szabo CI, Tan YY, Teixeira MR, Terry MB, Teulé A, Thomas A, Thull DL, Tischkowitz M, Tognazzo S, Toland AE, Topka S, Trainer AH, Tung N, van Asperen CJ, van der Hout AH, van der Kolk LE, van der Luijt RB, Van Heetvelde M, Varesco L, Varon-Mateeva R, Vega A, Villarreal-Garza C, von Wachenfeldt A, Walker L, Wang-Gohrke S, Wappenschmidt B, Weber BHF, Yannoukakos D, Yoon SY, Zanzottera C, Zidan J, Zorn KK, Hutten Selkirk CG, Hulick PJ, Chenevix-Trench G, Spurdle AB, Antoniou AC, Nathanson KL.
- Hum Mutat. 2018 May;39(5):593-620. doi: 10.1002/humu.23406. Epub 2018 Mar 12.
- PMID: 29446198
- PubMed abstract
- Source abstract
-
- Somatic BRCA1 mutations in clinically sporadic breast cancer with medullary histological features.
- Rechsteiner M, Dedes K, Fink D, Pestalozzi B, Sobottka B, Moch H, Wild P, Varga Z.
- J Cancer Res Clin Oncol. 2018 May;144(5):865-874. doi: 10.1007/s00432-018-2609-5. Epub 2018 Feb 17.
- PMID: 29453630
- PubMed abstract
-
- Evaluation of the relative effectiveness of the 2017 updated Manchester scoring system for predicting BRCA1/2 mutations in a Southeast Asian country.
- Chew W, Moorakonda RB, Courtney E, Soh H, Li ST, Chen Y, Shaw T, Allen JC, Evans DGR, Ngeow J.
- J Med Genet. 2018 May;55(5):344-350. doi: 10.1136/jmedgenet-2017-105073. Epub 2017 Dec 23.
- PMID: 29275357
- PubMed abstract
- Source abstract
-
- Frequency of pathogenic germline mutations in cancer susceptibility genes in breast cancer patients.
- Kaur RP, Shafi G, Benipal RPS, Munshi A.
- Med Oncol. 2018 Apr 26;35(6):81. doi: 10.1007/s12032-018-1143-2.
- PMID: 29700634
- PubMed abstract
- Source abstract
-
- Challenges in recruiting African-American women for a breast cancer genetics study.
- Compadre AJ, Simonson ME, Gray K, Runnells G, Kadlubar S, Zorn KK.
- Hered Cancer Clin Pract. 2018 Apr 24;16:8. doi: 10.1186/s13053-018-0091-3. eCollection 2018.
- PMID: 29760829
- PubMed abstract
-
- Prevalence and Spectrum of BRCA1/2 Germline Mutations in Women with Breast Cancer in China Based on Next-Generation Sequencing.
- Liang Y, Yang X, Li H, Zhu A, Guo Z, Li M.
- Med Sci Monit. 2018 Apr 23;24:2465-2475.
- PMID: 29681614
- PubMed abstract
- Source abstract
-
- Germline mutation prevalence in individuals with pancreatic cancer and a history of previous malignancy.
- Dudley B, Karloski E, Monzon FA, Singhi AD, Lincoln SE, Bahary N, Brand RE.
- Cancer. 2018 Apr 15;124(8):1691-1700. doi: 10.1002/cncr.31242. Epub 2018 Jan 23.
- PMID: 29360161
- PubMed abstract
- Source abstract
-
- Main implications related to the switch to BRCA1/2 tumor testing in ovarian cancer patients: a proposal of a consensus.
- Capoluongo E, Scambia G, Nabholtz JM.
- Oncotarget. 2018 Apr 13;9(28):19463-19468. doi: 10.18632/oncotarget.24728. eCollection 2018 Apr 13.
- PMID: 29731958
- PubMed abstract
- Source abstract
- Review, Commentary
- Free PMC article
- Free Full Text
-
- Ascertainment Bias and Estimating Penetrance.
- Sorscher S.
- JAMA Oncol. 2018 Apr 1;4(4):587. doi: 10.1001/jamaoncol.2017.4573.
- PMID: 29285541
- PubMed abstract
- Letter, Comment
- Free Full Text
Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.
- PMID: 28418444
- PubMed abstract
- Free Full Text
-
- A possible role of FANCM mutations in male breast cancer susceptibility: Results from a multicenter study in Italy.
- Silvestri V, Rizzolo P, Zelli V, Valentini V, Zanna I, Bianchi S, Tibiletti MG, Varesco L, Russo A, Tommasi S, Coppa A, Capalbo C, Calistri D, Viel A, Cortesi L, Manoukian S, Bonanni B, Montagna M, Palli D, Radice P, Peterlongo P, Ottini L.
- Breast. 2018 Apr;38:92-97. doi: 10.1016/j.breast.2017.12.013. Epub 2018 Jan 4.
- PMID: 29287190
- PubMed abstract
- Source abstract
-
- High prevalence of deleterious BRCA1 and BRCA2 germline mutations in arab breast and ovarian cancer patients.
- Alhuqail AJ, Alzahrani A, Almubarak H, Al-Qadheeb S, Alghofaili L, Almoghrabi N, Alhussaini H, Park BH, Colak D, Karakas B.
- Breast Cancer Res Treat. 2018 Apr;168(3):695-702. doi: 10.1007/s10549-017-4635-4. Epub 2018 Jan 2.
- PMID: 29297111
- PubMed abstract
- Source abstract
-
- Gene panel testing of 5589 BRCA1/2-negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer.
- Hauke J, Horvath J, Groß E, Gehrig A, Honisch E, Hackmann K, Schmidt G, Arnold N, Faust U, Sutter C, Hentschel J, Wang-Gohrke S, Smogavec M, Weber BHF, Weber-Lassalle N, Weber-Lassalle K, Borde J, Ernst C, Altmüller J, Volk AE, Thiele H, Hübbel V, Nürnberg P, Keupp K, Versmold B, Pohl E, Kubisch C, Grill S, Paul V, Herold N, Lichey N, Rhiem K, Ditsch N, Ruckert C, Wappenschmidt B, Auber B, Rump A, Niederacher D, Haaf T, Ramser J, Dworniczak B, Engel C, Meindl A, Schmutzler RK, Hahnen E.
- Cancer Med. 2018 Apr;7(4):1349-1358. doi: 10.1002/cam4.1376. Epub 2018 Mar 9.
- PMID: 29522266
- PubMed abstract
- Source abstract
-
- The spectrum of genetic variants in hereditary pancreatic cancer includes Fanconi anemia genes.
- Slavin TP, Neuhausen SL, Nehoray B, Niell-Swiller M, Solomon I, Rybak C, Blazer K, Adamson A, Yang K, Sand S, Guerrero-Llamas N, Castillo D, Herzog J, Wu X, Tao S, Raja S, Chung V, Singh G, Nadesan S, Brown S, Cruz-Correa M, Petersen GM, Weitzel J; Clinical Cancer Genomics Community Research Network (CCGCRN).
- Fam Cancer. 2018 Apr;17(2):235-245. doi: 10.1007/s10689-017-0019-5.
- PMID: 28687971
- PubMed abstract
- Source abstract
-
- Impact of Multigene Panel Testing on Surgical Decision Making in Breast Cancer Patients.
- Pederson HJ, Gopalakrishnan D, Noss R, Yanda C, Eng C, Grobmyer SR.
- J Am Coll Surg. 2018 Apr;226(4):560-565. doi: 10.1016/j.jamcollsurg.2017.12.037. Epub 2018 Jan 31.
- PMID: 29360614
- PubMed abstract
- Source abstract
-
- BRCA1/BRCA2 Germline Mutation Carriers and Sporadic Pancreatic Ductal Adenocarcinoma.
- Blair AB, Groot VP, Gemenetzis G, Wei J, Cameron JL, Weiss MJ, Goggins M, Wolfgang CL, Yu J, He J.
- J Am Coll Surg. 2018 Apr;226(4):630-637.e1. doi: 10.1016/j.jamcollsurg.2017.12.021. Epub 2018 Jan 5.
- PMID: 29309945
- PubMed abstract
- Source abstract
-
- Rare germline mutations in African American men diagnosed with early-onset prostate cancer.
- Beebe-Dimmer JL, Zuhlke KA, Johnson AM, Liesman D, Cooney KA.
- Prostate. 2018 Apr;78(5):321-326. doi: 10.1002/pros.23464. Epub 2018 Jan 21.
- PMID: 29356034
- PubMed abstract
- Source abstract
-
- Intraductal/ductal histology and lymphovascular invasion are associated with germline DNA-repair gene mutations in prostate cancer.
- Isaacsson Velho P, Silberstein JL, Markowski MC, Luo J, Lotan TL, Isaacs WB, Antonarakis ES.
- Prostate. 2018 Apr;78(5):401-407. doi: 10.1002/pros.23484. Epub 2018 Jan 25.
- PMID: 29368341
- PubMed abstract
- Source abstract
-
- False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
- Tandy-Connor S, Guiltinan J, Krempely K, LaDuca H, Reineke P, Gutierrez S, Gray P, Tippin Davis B.
- Genet Med. 2018 Mar 22. doi: 10.1038/gim.2018.38. [Epub ahead of print]
- PMID: 29565420
- PubMed abstract
Commentary:
Attention: Direct-To-Consumer patrons: Proceed with caution.
- PMID: 29713001
- PubMed abstract
- Source abstract
Research news: Evaluation of some direct-to-consumer genetic testing reveals inaccuracies and misinterpretations (FORCE. XRAYS.)
Press: Wrangle Over DTC Results—Ambry Study Highlights 40% False Positives, 23andMe Defends Tests, and Experts Weigh In. (Clinical OMICs)
Press: Ambry and My Gene Counsel Team Up on Tests to Confirm DTC Results, Counseling. (Clinical OMICs)
-
- ABC4 Consensus: Assessment by a German Group of Experts.
- Harbeck N, Lüftner D, Marschner N, Untch M, Augustin D, Briest S, Ettl J, Haidinger R, Müller L, Müller V, Ruckhäberle E, Wuerstlein R, Thomssen C.
- Breast Care (Basel). 2018 Mar;13(1):48-58. doi: 10.1159/000486722. Epub 2018 Feb 15.
- PMID: 29950968
- PubMed abstract
- Source abstract
- Conference report
- Free Full Text
-
- Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication.
- Pelttari LM, Shimelis H, Toiminen H, Kvist A, Törngren T, Borg Å, Blomqvist C, Bützow R, Couch F, Aittomäki K, Nevanlinna H.
- Clin Genet. 2018 Mar;93(3):595-602. doi: 10.1111/cge.13123. Epub 2018 Jan 12.
- PMID: 28802053
- PubMed abstract
- Source abstract
-
- Homozygous loss of function BRCA1 variant causing a fanconi-anemia-like phenotype, a clinical report and review of previous patients.
- Freire BL, Homma TK, Funari MFA, Lerario AM, de Medeiros Leal A, Rodrigues Pereira Velloso ED, Malaquias AC, Jorge AAL.
- Eur J Med Genet. 2018 Mar;61(3):130-133. doi: 10.1016/j.ejmg.2017.11.003. Epub 2017 Nov 10.
- PMID: 29133208
- PubMed abstract
- Source abstract
-
- A5 Relatively high incidence of non-founder brca1/2 mutation carriers among familial breast cancer cases in Latvia.
- Irmejs A, Maksimenko J, Trofimovičs G, Bērziņa D, Skuja E, Purkalne G, Miklaševičs E, Gardovskis J
- Hered Cancer Clin Pract. 2018 Feb 28;16(Suppl 1):A5. Meeting abstracts from Clinical Genetics of Cancer 2017; Szczecin, Poland. 21-22 September 2017. doi: 10.1186/s13053-018-0087-z.
-
- Identification of a novel truncating mutation in PALB2 gene by a multigene sequencing panel for mutational screening of breast cancer risk-associated and related genes.
- Guacci A, Cordella A, Rocco T, Giurato G, Nassa G, Rizzo F, Carlomagno C, Pepe S, Tarallo R, Weisz A.
- J Clin Lab Anal. 2018 Feb 27. doi: 10.1002/jcla.22418. [Epub ahead of print]
- PMID: 29484706
- PubMed abstract
- Source abstract
-
- With Regard to PTEN Promoter Testing for Hereditary Cancer Risk Assessment.
- fMester JL, Hruska KS.
- JCO Precis Oncol. 2018 Feb 23;2018. doi: 10.1200/PO.17.00280. Epub 2018 Feb 23.
PTEN Promoter Variants Are Not Associated With Common Cancers: Implications for Multigene Panel Testing.
-
- Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices.
- Toland AE, Forman A, Couch FJ, Culver JO, Eccles DM, Foulkes WD, Hogervorst FBL, Houdayer C, Levy-Lahad E, Monteiro AN, Neuhausen SL, Plon SE, Sharan SK, Spurdle AB, Szabo C, Brody LC; BIC Steering Committee.
- NPJ Genom Med. 2018 Feb 15;3:7. doi: 10.1038/s41525-018-0046-7. eCollection 2018.
- PMID: 29479477
- PubMed abstract
-
- Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?
- Nguyen-Dumont T, Teo ZL, Hammet F, Roberge A, Mahmoodi M, Tsimiklis H, Park DJ, Pope BJ, Lonie A, Kapuscinski MK, Mahmood K; ABCFR, Goldgar DE, Giles GG, Winship I, Hopper JL, Southey MC.
- BMC Cancer. 2018 Feb 8;18(1):165. doi: 10.1186/s12885-018-4028-z.
- PMID: 29422015
- PubMed abstract
-
- The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.
- Reuter MS, Walker S, Thiruvahindrapuram B, Whitney J, Cohn I, Sondheimer N, Yuen RKC, Trost B, Paton TA, Pereira SL, Herbrick JA, Wintle RF, Merico D, Howe J, MacDonald JR, Lu C, Nalpathamkalam T, Sung WWL, Wang Z, Patel RV, Pellecchia G, Wei J, Strug LJ, Bell S, Kellam B, Mahtani MM, Bassett AS, Bombard Y, Weksberg R, Shuman C, Cohn RD, Stavropoulos DJ, Bowdin S, Hildebrandt MR, Wei W, Romm A, Pasceri P, Ellis J, Ray P, Meyn MS, Monfared N, Hosseini SM, Joseph-George AM, Keeley FW, Cook RA, Fiume M, Lee HC, Marshall CR, Davies J, Hazell A, Buchanan JA, Szego MJ, Scherer SW.
- CMAJ. 2018 Feb 5;190(5):E126-E136. doi: 10.1503/cmaj.171151.
- PMID: 29431110
- PubMed abstract
-
- Role of Genetic Testing for Inherited Prostate Cancer Risk: Philadelphia Prostate Cancer Consensus Conference 2017.
- Giri VN, Knudsen KE, Kelly WK, Abida W, Andriole GL, Bangma CH, Bekelman JE, Benson MC, Blanco A, Burnett A, Catalona WJ, Cooney KA, Cooperberg M, Crawford DE, Den RB, Dicker AP, Eggener S, Fleshner N, Freedman ML, Hamdy FC, Hoffman-Censits J, Hurwitz MD, Hyatt C, Isaacs WB, Kane CJ, Kantoff P, Karnes RJ, Karsh LI, Klein EA, Lin DW, Loughlin KR, Lu-Yao G, Malkowicz SB, Mann MJ, Mark JR, McCue PA, Miner MM, Morgan T, Moul JW, Myers RE, Nielsen SM, Obeid E, Pavlovich CP, Peiper SC, Penson DF, Petrylak D, Pettaway CA, Pilarski R, Pinto PA, Poage W, Raj GV, Rebbeck TR, Robson ME, Rosenberg MT, Sandler H, Sartor O, Schaeffer E, Schwartz GF, Shahin MS, Shore ND, Shuch B, Soule HR, Tomlins SA, Trabulsi EJ, Uzzo R, Vander Griend DJ, Walsh PC, Weil CJ, Wender R, Gomella LG.
- J Clin Oncol. 2018 Feb 1;36(4):414-424. doi: 10.1200/JCO.2017.74.1173. Epub 2017 Dec 13.
- PMID: 29236593
- PubMed abstract
- Source abstract
- [Conference report]
- Free Full Text
-
- Racial/ethnic differences in multiple-gene sequencing results for hereditary cancer risk.
- Caswell-Jin JL, Gupta T, Hall E, Petrovchich IM, Mills MA, Kingham KE, Koff R, Chun NM, Levonian P, Lebensohn AP, Ford JM, Kurian AW.
- Genet Med. 2018 Feb;20(2):234-239. doi: 10.1038/gim.2017.96. Epub 2017 Jul 27.
- PMID: 28749474
- PubMed abstract
-
- Rapid detection of BRCA1/2 recurrent mutations in Chinese breast and ovarian cancer patients with multiplex SNaPshot genotyping panels.
- Kwong A, Ho JCW, Shin VY, Kurian AW, Tai E, Esserman LJ, Weitzel JN, Lin PH, Field M, Domchek SM, Lo J, Ngan HYS, Ma ESK, Chan TL, Ford JM.
- Oncotarget. 2017 Dec 20;9(8):7832-7843. doi: 10.18632/oncotarget.23471. eCollection 2018 Jan 30.
- PMID: 29487695
- PubMed abstract
- Source abstract
-
- Gene aberration profile of tumors of adolescent and young adult females.
- Kanke Y, Shimomura A, Saito M, Honda T, Shiraishi K, Shimada Y, Watanabe R, Yoshida H, Yoshida M, Shimizu C, Takahashi K, Totsuka H, Ogiwara H, Hirose S, Kono K, Tamura K, Okamoto A, Kinoshita T, Kato T, Kohno T.
- Oncotarget. 2017 Dec 29;9(5):6228-6237. doi: 10.18632/oncotarget.23765. eCollection 2018 Jan 19.
- PMID: 29464067
- PubMed abstract
- Source abstract
-
- Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
- Lata S, Marasa M, Li Y, Fasel DA, Groopman E, Jobanputra V, Rasouly H, Mitrotti A, Westland R, Verbitsky M, Nestor J, Slater LM, D'Agati V, Zaniew M, Materna-Kiryluk A, Lugani F, Caridi G, Rampoldi L, Mattoo A, Newton CA, Rao MK, Radhakrishnan J, Ahn W, Canetta PA, Bomback AS, Appel GB, Antignac C, Markowitz GS, Garcia CK, Kiryluk K, Sanna-Cherchi S, Gharavi AG.
- Ann Intern Med. 2018 Jan 16;168(2):100-109. doi: 10.7326/M17-1319. Epub 2017 Dec 5.
- PMID: 29204651
- PubMed abstract
- Source abstract
-
- Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer.
- Park JS, Lee ST, Nam EJ, Han JW, Lee JY, Kim J, Kim TI, Park HS.
- BMC Cancer. 2018 Jan 16;18(1):83. doi: 10.1186/s12885-017-3940-y.
- PMID: 29338689
- PubMed abstract
-
- Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds.
- Dominguez-Valentin M, Evans DGR, Nakken S, Tubeuf H, Vodak D, Ekstrøm PO, Nissen AM, Morak M, Holinski-Feder E, Martins A, Møller P, Hovig E.
- Hered Cancer Clin Pract. 2018 Jan 15;16:4. doi: 10.1186/s13053-018-0086-0. eCollection 2018.
- PMID: 29371908
- PubMed abstract
-
- Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory.
- Gardner SA, Weymouth KS, Kelly WS, Bogdanova E, Chen W, Lupu D, Suhl J, Zeng Q, Geigenmüller U, Boles D, Okamoto PM, McDowell G, Hayden MA, Nagan N.
- Hered Cancer Clin Pract. 2018 Jan 4;16:1. doi: 10.1186/s13053-017-0083-8. eCollection 2018.
- PMID: 29308099
- PubMed abstract
-
- Optimizing the identification of risk-relevant mutations by multigene panel testing in selected hereditary breast/ovarian cancer families.
- Coppa A, Nicolussi A, D'Inzeo S, Capalbo C, Belardinilli F, Colicchia V, Petroni M, Zani M, Ferraro S, Rinaldi C, Buffone A, Bartolazzi A, Screpanti I, Ottini L, Giannini G.
- Cancer Med. 2018 Jan;7(1):46-55. doi: 10.1002/cam4.1251. Epub 2017 Dec 22.
- PMID: 29271107
- PubMed abstract
- Source abstract
-
- Comparison of Ion Personal Genome Machine Platforms for the Detection of Variants in BRCA1 and BRCA2.
- Hwang SM, Lee KC, Lee MS, Park KU.
- Cancer Res Treat. 2018 Jan;50(1):255-264. doi: 10.4143/crt.2017.062. Epub 2017 Apr 7.
- PMID: 28392550
- PubMed abstract
-
- Mutation Screening of 10 Cancer Susceptibility Genes in Unselected Breast Cancer Patients.
- Xie Y, Guoli L, Chen M, Guo X, Tang L, Luo X, Wang S, Yi W, Dai L, Wang J.
- Clin Genet. 2018 Jan;93(1):41-51. doi: 10.1111/cge.13063. Epub 2017 Sep 25.
- PMID: 28580595
- PubMed abstract
- Source abstract
-
- The importance of a well-structured pancreatic screening program for familial and hereditary pancreatic cancer.
- Vasen HFA.
- Fam Cancer. 2018 Jan;17(1):1-3. doi: 10.1007/s10689-017-0066-y.
- PMID: 29204967
- PubMed abstract
- Editorial
- Free Full Text
Development of a high risk pancreatic screening clinic using 3.0 T MRI.
- PMID: 29101607
- PubMed abstract
- Source abstract
-
- A multi-gene panel study in hereditary breast and ovarian cancer in Colombia.
- Cock-Rada AM, Ossa CA, Garcia HI, Gomez LR.
- Fam Cancer. 2018 Jan;17(1):23-30. doi: 10.1007/s10689-017-0004-z.
- PMID: 28528518
- PubMed abstract
- Source abstract
-
- Potentially pathogenic germline CHEK2 c.319+2T>A among multiple early-onset cancer families.
- Dominguez-Valentin M, Nakken S, Tubeuf H, Vodak D, Ekstrøm PO, Nissen AM, Morak M, Holinski-Feder E, Martins A, Møller P, Hovig E.
- Fam Cancer. 2018 Jan;17(1):141-153. doi: 10.1007/s10689-017-0011-0.
- PMID: 28608266
- PubMed abstract
- Source abstract
-
- A single visit multidisciplinary model for managing patients with mutations in moderate and high-risk genes in a community practice setting.
- O'Leary MP, Goldner BS, Abboy S, Mercado PD, Plurad HY.
- Fam Cancer. 2018 Jan;17(1):175-178. doi: 10.1007/s10689-017-0010-1.
- PMID: 28600699
- PubMed abstract
- Source abstract
-
- Prevalence of germ-line mutations in cancer genes among pancreatic cancer patients with a positive family history.
- Chaffee KG, Oberg AL, McWilliams RR, Majithia N, Allen BA, Kidd J, Singh N, Hartman AR, Wenstrup RJ, Petersen GM.
- Genet Med. 2018 Jan;20(1):119-127. doi: 10.1038/gim.2017.85. Epub 2017 Jul 20.
- PMID: 28726808
- PubMed abstract
- Source abstract
-
- Breadth of Genetic Testing Selected by Patients at Risk of Hereditary Breast and Ovarian Cancer.
- Szender JB, Kaur J, Clayback K, Hutton ML, Mikkelson J, Odunsi K, Dresbold C.
- Int J Gynecol Cancer. 2018 Jan;28(1):26-33. doi: 10.1097/IGC.0000000000001122.
- PMID: 28930807
- PubMed abstract
- Source abstract
-
- Preferences for multigene panel testing for hereditary breast cancer risk among ethnically diverse BRCA-uninformative families.
- Vicuña B, Delaney HD, Flores KG, Ballinger L, Royce M, Dayao Z, Pal T, Kinney AY.
- J Community Genet. 2018 Jan;9(1):81-92. doi: 10.1007/s12687-017-0322-8. Epub 2017 Oct 2.
- PMID: 28971318
- PubMed abstract
- Source abstract
-
- Multi-gene Panel Testing in Breast Cancer Management.
- Fountzilas C, Kaklamani VG.
- Cancer Treat Res. 2018;173:121-140. doi: 10.1007/978-3-319-70197-4_8.
- PMID: 29349761
- PubMed abstract
- Source abstract
-
- Simultaneous detection of genetic and copy number alterations in BRCA1/2 genes.
- Hirotsu Y, Ooka Y, Sakamoto I, Nakagomi H, Omata M.
- Oncotarget. 2017 Dec 6;8(70):114463-114473. doi: 10.18632/oncotarget.22962. eCollection 2017 Dec 29.
- PMID: 29383094
- PubMed abstract
- Source abstract
-
- Prevalence of pathogenic germline variants detected by multigene sequencing in unselected Japanese patients with ovarian cancer.
- Hirasawa A, Imoto I, Naruto T, Akahane T, Yamagami W, Nomura H, Masuda K, Susumu N, Tsuda H, Aoki D.
- Oncotarget. 2017 Nov 28;8(68):112258-112267. doi: 10.18632/oncotarget.22733. eCollection 2017 Dec 22.
- PMID: 29348823
- PubMed abstract
- Source abstract
-
- Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women.
- Walsh T, Mandell JB, Norquist BM, Casadei S, Gulsuner S, Lee MK, King MC.
- JAMA Oncol. 2017 Dec 1;3(12):1647-1653. doi: 10.1001/jamaoncol.2017.1996.
- PMID: 28727877
- PubMed abstract
Audio Interview: Breast Cancer Due to Non–BRCA1 and Non–BRCA2 Mutations in Ashkenazi Jewish Women. (The JAMA Network)
Letter:
Testing Ashkenazi Jewish Women for Mutations Predisposing to Breast Cancer in Genes Other Than BRCA1 and BRCA2
- PMID: 29801022
- PubMed abstract
- Source abstract
Letter, Reply:
Testing Ashkenazi Jewish Women for Mutations Predisposing to Breast Cancer in Genes Other Than BRCA1 and BRCA2—Reply
- PMID: 29800948
- PubMed abstract
- Source abstract
Research review, Commentary: Does expanded genetic testing benefit Jewish women diagnosed with breast cancer? (FORCE. XRAYS. 2017 Sep 13.)
Research review, Commentary: XRAYS Follow Up: Does expanded genetic testing benefit Jewish women with breast cancer? (FORCE. XRAYS. 2018 Jun 7.)
-
- The Multifaceted Experience of Multigene Panel Testing for Breast Cancer.
- Daly M, Azvolinsky A.
- OncoTherapy Network. 2017 Dec 1.
- Interview, Audio
- Free Full Text
Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.
- PMID: 28418444
- PubMed abstract
- Free Full Text
Editorial:
Multigene Panel Testing and Breast Cancer Risk: Is It Time to Scale Down?
- PMID: 28418452
- PubMed abstract
- Source abstract
-
- Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families.
- Li J, Li H, Makunin I; kConFab Investigators, Thompson BA, Tao K, Young EL, Lopez J, Camp NJ, Tavtigian SV, John EM, Andrulis IL, Khanna KK, Goldgar D, Chenevix-Trench G.
- Breast Cancer Res Treat. 2017 Dec;166(3):937-949. doi: 10.1007/s10549-017-4469-0. Epub 2017 Aug 24.
- PMID: 28840378
- PubMed abstract
- Source abstract
-
- Clinical testing with a panel of 25 genes associated with increased cancer risk results in a significant increase in clinically significant findings across a broad range of cancer histories.
- Rosenthal ET, Bernhisel R, Brown K, Kidd J, Manley S.
- Cancer Genet. 2017 Dec;218-219:58-68. doi: 10.1016/j.cancergen.2017.09.003. Epub 2017 Sep 25.
- PMID: 29153097
- PubMed abstract
- Source abstract
-
- The use of panel testing in familial breast and ovarian cancer.
- Prapa M, Solomons J, Tischkowitz M.
- Clin Med (Lond). 2017 Dec;17(6):568-572. doi: 10.7861/clinmedicine.17-6-568.
- PMID: 29196360
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- Cancer Genetic Counseling and Testing in an Era of Rapid Change.
- Hooker GW, Clemens KR, Quillin J, Vogel Postula KJ, Summerour P, Nagy R, Buchanan AH.
- J Genet Couns. 2017 Dec;26(6):1244-1253. doi: 10.1007/s10897-017-0099-2. Epub 2017 Apr 22.
- PMID: 28434142
- PubMed abstract
- Source abstract
-
- Genetics of Breast and Gynecologic Cancers (PDQ®): Health Professional Version. Multigene (Panel) Testing.
- PDQ Cancer Genetics Editorial Board.
- PDQ Cancer Information Summaries [Internet]. Bethesda, MD: National Cancer Institute. Updated 2017 Nov 30. Accessed 2017 Dec 8.
- PMID: 26389210
- PubMed abstract
- Section link
-
- Fast Detection of a BRCA2 Large Genomic Duplication by Next Generation Sequencing as a Single Procedure: A Case Report.
- Nunziato M, Starnone F, Lombardo B, Pensabene M, Condello C, Verdesca F, Carlomagno C, De Placido S, Pastore L, Salvatore F, D'Argenio V.
- Int J Mol Sci. 2017 Nov 22;18(11). pii: E2487. doi: 10.3390/ijms18112487.
- PMID: 29165356
- PubMed abstract
- Source abstract
- Case report
- Free Full Text
-
- Germline BRCA2 mutations detected in pediatric sequencing studies impact parents' evaluation and care.
- Walsh MF, Kennedy J, Harlan M, Kentsis A, Shukla N, Musinsky J, Roberts S, Kung AL, Robson M, Kushner BH, Meyers P, Offit K.
- Cold Spring Harb Mol Case Stud. 2017 Nov 21;3(6). pii: a001925. doi: 10.1101/mcs.a001925. Print 2017 Nov.
- PMID: 28655807
- PubMed abstract
- Source abstract
- Case report
- Free Full Text
-
- Hereditary diffuse gastric cancer and lynch syndromes in a BRCA1/2 negative breast cancer patient.
- Njoroge SW, Burgess KR, Cobleigh MA, Alnajar HH, Gattuso P, Usha L.
- Breast Cancer Res Treat. 2017 Nov;166(1):315-319. doi: 10.1007/s10549-017-4393-3. Epub 2017 Jul 12.
- PMID: 28702897
- PubMed abstract
- Source abstract
-
- Combined tumor genomic profiling and exome sequencing in a breast cancer family implicates ATM in tumorigenesis: a proof of principle study.
- Bubien V, Bonnet F, Dupiot-Chiron J, Barouk-Simonet E, Jones N, de Reynies A, MacGrogan G, Sevenet N, Letouzé E, Longy M.
- Genes Chromosomes Cancer. 2017 Nov;56(11):788-799. doi: 10.1002/gcc.22482. Epub 2017 Aug 16.
- PMID: 28691344
- PubMed abstract
- Source abstract
-
- Frequency of mutations in a large series of clinically ascertained ovarian cancer cases tested on multi-gene panels compared to reference controls.
- Lilyquist J, LaDuca H, Polley E, Davis BT, Shimelis H, Hu C, Hart SN, Dolinsky JS, Couch FJ, Goldgar DE.
- Gynecol Oncol. 2017 Nov;147(2):375-380. doi: 10.1016/j.ygyno.2017.08.030. Epub 2017 Sep 7.
- PMID: 28888541
- PubMed abstract
- Source abstract
-
- Next-Generation Sequencing-Based Detection of Germline Copy Number Variations in BRCA1/BRCA2: Validation of a One-Step Diagnostic Workflow.
- Schmidt AY, Hansen TVO, Ahlborn LB, Jønson L, Yde CW, Nielsen FC.
- J Mol Diagn. 2017 Nov;19(6):809-816. doi: 10.1016/j.jmoldx.2017.07.003. Epub 2017 Aug 17.
- PMID: 28822785
- PubMed abstract
- Source abstract
-
- Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1).
- Harter P, Hauke J, Heitz F, Reuss A, Kommoss S, Marmé F, Heimbach A, Prieske K, Richters L, Burges A, Neidhardt G, de Gregorio N, El-Balat A, Hilpert F, Meier W, Kimmig R, Kast K, Sehouli J, Baumann K, Jackisch C, Park-Simon TW, Hanker L, Kröber S, Pfisterer J, Gevensleben H, Schnelzer A, Dietrich D, Neunhöffer T, Krockenberger M, Brucker SY, Nürnberg P, Thiele H, Altmüller J, Lamla J, Elser G, du Bois A, Hahnen E, Schmutzler R.
- PLoS One. 2017 Oct 20;12(10):e0186043. doi: 10.1371/journal.pone.0186043. eCollection 2017.
- PMID: 29053726
- PubMed abstract
-
- Cancer Status Bests Family History for BRCA Testing.
- Neil Osterweil.
- Medscape. Conference News. 2017 Oct 19.
- Conference report
- Free Full Text
-
- Clinical implications of germline mutations in breast cancer: TP53.
- Schon K, Tischkowitz M.
- Breast Cancer Res Treat. 2017 Oct 16. doi: 10.1007/s10549-017-4531-y. [Epub ahead of print]
- PMID: 29039119
- PubMed abstract
- Review
- Free Full Text
-
- Germline genetic variants in men with prostate cancer and one or more additional cancers.
- Pilié PG, Johnson AM, Hanson KL, Dayno ME, Kapron AL, Stoffel EM, Cooney KA.
- Cancer. 2017 Oct 15;123(20):3925-3932. doi: 10.1002/cncr.30817. Epub 2017 Jun 28.
- PMID: 28657667
- PubMed abstract
- Source abstract
-
- PTEN Promoter Variants Are Not Associated With Common Cancers: Implications for Multigene Panel Testing.
- Black MH, Li S, Pesaran T, LaDuca H, Karam R, Clifford J, Smith B, Pilarski R.
- JCO Precis Oncol. 2017 Oct 9;2017. doi: 10.1200/PO.17.00108. Epub 2017 Oct 9.
Letter:
With Regard to PTEN Promoter Testing for Hereditary Cancer Risk Assessment.
-
- Expanding the spectrum of germline variants in cancer.
- Siraj AK, Masoodi T, Bu R, Parvathareddy SK, Al-Badawi IA, Al-Sanea N, Ashari LH, Abduljabbar A, Alhomoud S, Al-Sobhi SS, Tulbah A, Ajarim D, Alzoman K, Aljuboury M, Yousef HB, Al-Dawish M, Al-Dayel F, Alkuraya FS, Al-Kuraya KS.
- Hum Genet. 2017 Oct 3. doi: 10.1007/s00439-017-1845-0. [Epub ahead of print]
- PMID: 28975465
- PubMed abstract
- Source abstract
-
- Genetic Testing: Challenges and Changes in Testing for Hereditary Cancer Syndromes.
- King E, Mahon SM.
- Clin J Oncol Nurs. 2017 Oct 1;21(5):589-598. doi: 10.1188/17.CJON.589-598.
- PMID: 28945723
- PubMed abstract
- Source abstract
-
- Preoperative Panel Testing for Hereditary Cancer Syndromes Does Not Significantly Impact Time to Surgery for Newly Diagnosed Breast Cancer Patients Compared with BRCA1/2 Testing.
- Murphy AE, Hussain L, Ho C, Dunki-Jacobs E, Lee D, Tameron A, Huelsman K, Rice C, Wexelman BA.
- Ann Surg Oncol. 2017 Oct;24(10):3055-3059. doi: 10.1245/s10434-017-5957-5. Epub 2017 Aug 1.
- PMID: 28766202
- PubMed abstract
- Source abstract
-
- Expanded Gene Panel Use for Women With Breast Cancer: Identification and Intervention Beyond Breast Cancer Risk.
- O'Leary E, Iacoboni D, Holle J, Michalski ST, Esplin ED, Yang S, Ouyang K.
- Ann Surg Oncol. 2017 Oct;24(10):3060-3066. doi: 10.1245/s10434-017-5963-7. Epub 2017 Aug 1./cite>
- PMID: 28766213
- PubMed abstract
-
- Identification of pathogenic retrotransposon insertions in cancer predisposition genes.
- Qian Y, Mancini-DiNardo D, Judkins T, Cox HC, Brown K, Elias M, Singh N, Daniels C, Holladay J, Coffee B, Bowles KR, Roa BB.
- Cancer Genet. 2017 Oct;216-217:159-169. doi: 10.1016/j.cancergen.2017.08.002. Epub 2017 Aug 24.
- PMID: 29025590
- PubMed abstract
- Source abstract
-
- Inherited DNA repair gene mutations detected by tumor next generation sequencing in urinary tract cancers.
- Gupta S, Greenberg S, Grimmett J, Gaston D, Agarwal N, Lowrance W, Schiffman J, Kohlmann W.
- Fam Cancer. 2017 Oct;16(4):545-550. doi: 10.1007/s10689-017-9980-2.
- PMID: 28315974
- PubMed abstract
- Case report
- Free Full Text
-
- Impact of germline and somatic BRCA1/2 mutations: Tumor spectrum and detection platforms.
- Wu H, Wu X, Liang Z.
- Gene Ther. 2017 Oct;24(10):601-609. doi: 10.1038/gt.2017.73. Epub 2017 Aug 3.
- PMID: 28771233
- PubMed abstract
- Source abstract
-
- Analysis of BRCA1/2 mutation spectrum and prevalence in unselected Chinese breast cancer patients by next-generation sequencing.
- Li G, Guo X, Tang L, Chen M, Luo X, Peng L, Xu X, Wang S, Xiao Z, Yi W, Dai L, Wang J.
- J Cancer Res Clin Oncol. 2017 Oct;143(10):2011-2024. doi: 10.1007/s00432-017-2465-8. Epub 2017 Jun 29.
- PMID: 28664449
- PubMed abstract
- Source abstract
-
- Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients.
- Lumish HS, Steinfeld H, Koval C, Russo D, Levinson E, Wynn J, Duong J, Chung WK.
- J Genet Couns. 2017 Oct;26(5):1116-1129. doi: 10.1007/s10897-017-0090-y. Epub 2017 Mar 29.
- PMID: 28357778
- PubMed abstract
- Source abstract
Letter:
Anxiety and Hereditary Testing Results.
- PMID: 28540620
- PubMed abstract
- Source abstract
Letter, Reply:
Response to Dr. Sorscher.
- PMID: 28536924
- PubMed abstract
- Free Full Text
-
- Anxiety and Hereditary Testing Results.
- Sorscher S.
- J Genet Couns. 2017 Oct;26(5):1162–1163. doi: 10.1007/s10897-017-0109-4. Epub 2017 May 24.
- PMID: 28540620
- PubMed abstract
- Source abstract
Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients.
- PMID: 28357778
- PubMed abstract
- Source abstract
Letter, Reply:
Response to Dr. Sorscher.
- PMID: 28536924
- PubMed abstract
- Free Full Text
-
- Identification and Management of TP53 Gene Carriers Detected Through Multigene Panel Testing.
- Pal T, Brzosowicz J, Valladares A, Wiesner GL, Laronga C.
- South Med J. 2017 Oct;110(10):643-648. doi: 10.14423/SMJ.0000000000000711.
- PMID: 28973705
- PubMed abstract
- Source abstract
-
- The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels.
- Sung PL, Wen KC, Chen YJ, Chao TC, Tsai YF, Tseng LM, Qiu JT, Chao KC, Wu HH, Chuang CM, Wang PH, Huang CF.
- PLoS One. 2017 Sep 29;12(9):e0185615. doi: 10.1371/journal.pone.0185615. eCollection 2017.
- PMID: 28961279
- PubMed abstract
-
- Contralateral Prophylactic Mastectomy.
- Ramaswami R, Morrow M, Jagsi R.
- N Engl J Med. 2017 Sep 28;377(13):1288-1291. doi: 10.1056/NEJMclde1708293.
- PMID: 28953446
- PubMed abstract
- Case report, Clinical Decision Poll
- Free Full Text
-
- Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing.
- Mandelker D, Zhang L, Kemel Y, Stadler ZK, Joseph V, Zehir A, Pradhan N, Arnold A, Walsh MF, Li Y, Balakrishnan AR, Syed A, Prasad M, Nafa K, Carlo MI, Cadoo KA, Sheehan M, Fleischut MH, Salo-Mullen E, Trottier M, Lipkin SM, Lincoln A, Mukherjee S, Ravichandran V, Cambria R, Galle J, Abida W, Arcila ME, Benayed R, Shah R, Yu K, Bajorin DF, Coleman JA, Leach SD, Lowery MA, Garcia-Aguilar J, Kantoff PW, Sawyers CL, Dickler MN, Saltz L, Motzer RJ, O'Reilly EM, Scher HI, Baselga J, Klimstra DS, Solit DB, Hyman DM, Berger MF, Ladanyi M, Robson ME, Offit K.
- JAMA. 2017 Sep 5;318(9):825-835. doi: 10.1001/jama.2017.11137.
- PMID: 28873162
- PubMed abstract
- Source abstract
Editorial:
The Potential and Challenges of Expanded Germline Testing in Clinical Oncology.
- PMID: 28873143
- PubMed abstract
- Source abstract
Press: Study Shows More Cancer Mutations Detected by Universal Sequencing. (Clinical Omics)
Press: Expanding Germline Analyses to Prevent and Treat Cancers. (Medscape)
-
- Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.
- Couch FJ, Shimelis H, Hu C, Hart SN, Polley EC, Na J, Hallberg E, Moore R, Thomas A, Lilyquist J, Feng B, McFarland R, Pesaran T, Huether R, LaDuca H, Chao EC, Goldgar DE, Dolinsky JS.
- JAMA Oncol. 2017 Sep 1;3(9):1190-1196. doi: 10.1001/jamaoncol.2017.0424.
- PMID: 28418444
- PubMed abstract
Editorial:
Multigene Panel Testing and Breast Cancer Risk: Is It Time to Scale Down?
- PMID: 28418452
- PubMed abstract
- Source abstract
Letter, Comment:
Ascertainment Bias and Estimating Penetrance.
- PMID: 29285541
- PubMed abstract
- Free Full Text
Interview, Audio: The Multifaceted Experience of Multigene Panel Testing for Breast Cancer. (OncoTherapy Network)
-
- Current Challenges Associated With Next-Generation Sequencing of Breast Cancer.
- Sorscher S.
- JAMA Oncol. 2017 Sep 1;3(9):1283-1284. doi: 10.1001/jamaoncol.2017.0659.
- PMID: 28520831
- PubMed abstract
- Source abstract
Review:
The Role of Genetic Testing in the Selection of Therapy for Breast Cancer: A Review.
- PMID: 27560719
- PubMed abstract
- Source abstract
Letter, Reply:
Current Challenges Associated With Next-Generation Sequencing of Breast Cancer-Reply.
- PMID: 28520826
- PubMed abstract
- Source abstract
-
- Application of Panel-Based Tests for Inherited Risk of Cancer.
- Shah PD, Nathanson KL.
- Annu Rev Genomics Hum Genet. 2017 Aug 31;18:201-227. doi: 10.1146/annurev-genom-091416-035305. Epub 2017 May 15.
- PMID: 28504904
- PubMed abstract
- Source abstract
-
- A comparative study of germline BRCA1 and BRCA2 mutation screening methods in use in 20 European clinical diagnostic laboratories.
- Ellison G, Wallace A, Kohlmann A, Patton S.
- Br J Cancer. 2017 Aug 22;117(5):710-716. doi: 10.1038/bjc.2017.223. Epub 2017 Jul 27.
- PMID: 28751759
- PubMed abstract
- Source abstract
-
- Implementation and utilization of the molecular tumor board to guide precision medicine.
- Harada S, Arend R, Dai Q, Levesque JA, Winokur TS, Guo R, Heslin MJ, Nabell L, Nabors LB, Limdi NA, Roth KA, Partridge EE, Siegal GP, Yang ES.
- Oncotarget. 2017 Jun 14;8(34):57845-57854. doi: 10.18632/oncotarget.18471. eCollection 2017 Aug 22.
- PMID: 28915716
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
-
- [The progress and prospect of application of genetic testing technology-based gene detection technology in the diagnosis and treatment of hereditary cancer].
- He JX, Jiang YF.
- Zhonghua Yu Fang Yi Xue Za Zhi. 2017 Aug 6;51(8):772-776. doi: 10.3760/cma.j.issn.0253-9624.2017.08.022.
- PMID: 28763932
- PubMed abstract
-
- Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
- Espenschied CR, LaDuca H, Li S, McFarland R, Gau CL, Hampel H.
- J Clin Oncol. 2017 Aug 1;35(22):2568-2575. doi: 10.1200/JCO.2016.71.9260. Epub 2017 May 17.
- PMID: 28514183
- PubMed abstract
- Source abstract
-
- Frequency of Germline BRCA1/2 Mutations in Unselected Patients With Colorectal Cancer.
- Daniels MS, Bannon SA, Mork ME.
- J Clin Oncol. 2017 Aug 1;35(22):2588. doi: 10.1200/JCO.2017.72.7222. Epub 2017 May 16.
- PMID: 28510492
- PubMed abstract
- Letter
- Free Full Text
Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
- PMID: 28135145
- PubMed abstract
- Free Full Text
Letter, Reply:
Reply to M.S. Daniels et al.
- PMID: 28510494
- PubMed abstract
- Free Full Text
-
- Contribution of germline mutations in cancer predisposition genes to tumor etiology in young women diagnosed with invasive breast cancer.
- Rummel SK, Lovejoy L, Shriver CD, Ellsworth RE.
- Breast Cancer Res Treat. 2017 Aug;164(3):593-601. doi: 10.1007/s10549-017-4291-8. Epub 2017 May 13.
- PMID: 28503720
- PubMed abstract
- Source abstract
-
- Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
- Sun J, Meng H, Yao L, Lv M, Bai J, Zhang J, Wang L, Ouyang T, Li J, Wang T, Fan Z, Fan T, Lin B, Xie Y.
- Clin Cancer Res. 2017 Jul 19. pii: clincanres.3227.2016. doi: 10.1158/1078-0432.CCR-16-3227. [Epub ahead of print]
- PMID: 28724667
- PubMed abstract
- Source abstract
-
- Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer.
- Tedaldi G, Tebaldi M, Zampiga V, Danesi R, Arcangeli V, Ravegnani M, Cangini I, Pirini F, Petracci E, Rocca A, Falcini F, Amadori D, Calistri D.
- Oncotarget. 2017 Jul 18;8(29):47064-47075. doi: 10.18632/oncotarget.16791.
- PMID: 28423363
- PubMed abstract
- Source abstract
-
- Detection of false positive mutations in BRCA gene by next generation sequencing.
- Suryavanshi M, Kumar D, Panigrahi MK, Chowdhary M, Mehta A.
- Fam Cancer. 2017 Jul;16(3):311-317. doi: 10.1007/s10689-016-9955-8.
- PMID: 27848044
- PubMed abstract
- Source abstract
-
- Outcomes of retesting BRCA negative patients using multigene panels.
- Yadav S, Reeves A, Campian S, Paine A, Zakalik D.
- Fam Cancer. 2017 Jul;16(3):319-328. doi: 10.1007/s10689-016-9956-7.
- PMID: 27878467
- PubMed abstract
- Source abstract
-
- Multigene panels in Ashkenazi Jewish patients yield high rates of actionable mutations in multiple non-BRCA cancer-associated genes.
- Frey MK, Sandler G, Sobolev R, Kim SH, Chambers R, Bassett RY, Martineau J, Sapra KJ, Boyd L, Curtin JP, Pothuri B, Blank SV.
- Gynecol Oncol. 2017 Jul;146(1):123-128. doi: 10.1016/j.ygyno.2017.04.009. Epub 2017 May 8.
- PMID: 28495237
- PubMed abstract
- Source abstract
-
- Prospective Genomic Profiling of Prostate Cancer Across Disease States Reveals Germline and Somatic Alterations That May Affect Clinical Decision Making.
- Abida W, Armenia J, Gopalan A, Brennan R, Walsh M, Barron D, Danila D, Rathkopf D, Morris M, Slovin S, McLaughlin B, Curtis K, Hyman DM, Durack JC, Solomon SB, Arcila ME, Zehir A, Syed A, Gao J, Chakravarty D, Vargas HA, Robson ME, Joseph V, Offit K, Donoghue MTA, Abeshouse AA, Kundra R, Heins ZJ, Penson AV, Harris C, Taylor BS, Ladanyi M, Mandelker D, Zhang L, Reuter VE, Kantoff PW, Solit DB, Berger MF, Sawyers CL, Schultz N, Scher HI.
- JCO Precis Oncol. 2017 Jul;2017. doi: 10.1200/PO.17.00029. Epub 2017 May 31.
- PMID: 28825054
- PubMed abstract
- Source abstract
-
- Germline and somatic mutations in homologous recombination genes among Chinese ovarian cancer patients detected using next-generation sequencing.
- Zhao Q, Yang J, Li L, Cao D, Yu M, Shen K; BGI Group.
- J Gynecol Oncol. 2017 Jul;28(4):e39. doi: 10.3802/jgo.2017.28.e39.
- PMID: 28541631
- PubMed abstract
- Source abstract
-
- Breast and Ovarian Cancer Penetrance Estimates Derived From Germline Multiple-Gene Sequencing Results in Women.
- Kurian AW, Hughes E, Handorf EA, Gutin A, Allen B, Hartman AR, Hall MJ.
- JCO Precis Oncol. 2017 Nov [Epub 2017 Jun 27];1:1-12. doi: 10.1200/PO.16.00066.
- PMID: 35172496
- PubMed abstract
- Source abstract
-
- Development and validation of a variant detection workflow for BRCA1 and BRCA2 genes and its clinical application based on the Ion Torrent technology.
- Buzolin AL, Moreira CM, Sacramento PR, Oku AY, Fornari ARDS, Antonio DSM, Quaio CRDAC, Baratela WR, Mitne-Neto M.
- Hum Genomics. 2017 Jun 26;11(1):14. doi: 10.1186/s40246-017-0110-x.
- PMID: 28651617
- PubMed abstract
-
- The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.
- Slavin TP, Maxwell KN, Lilyquist J, Vijai J, Neuhausen SL, Hart SN, Ravichandran V, Thomas T, Maria A, Villano D, Schrader KA, Moore R, Hu C, Wubbenhorst B, Wenz BM, D'Andrea K, Robson ME, Peterlongo P, Bonanni B, Ford JM, Garber JE, Domchek SM, Szabo C, Offit K, Nathanson KL, Weitzel JN, Couch FJ.
- NPJ Breast Cancer. 2017 Jun 9;3:22. doi: 10.1038/s41523-017-0024-8. eCollection 2017.
- PMID: 28649662
- PubMed abstract
-
- Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability.
- Stafford JL, Dyson G, Levin NK, Chaudhry S, Rosati R, Kalpage H, Wernette C, Petrucelli N, Simon MS, Tainsky MA.
- PLoS One. 2017 Jun 7;12(6):e0178450. doi: 10.1371/journal.pone.0178450. eCollection 2017.
- PMID: 28591191
- PubMed abstract
-
- High frequency of the recurrent c.1310_1313delAAGA BRCA2 mutation in the North-East of Morocco and implication for hereditary breast-ovarian cancer prevention and control.
- Laarabi FZ, Ratbi I, Elalaoui SC, Mezzouar L, Doubaj Y, Bouguenouch L, Ouldim K, Benjaafar N, Sefiani A.
- BMC Res Notes. 2017 Jun 2;10(1):188. doi: 10.1186/s13104-017-2511-2.
- PMID: 28577564
- PubMed abstract
-
- High-risk patients with breast cancer may not receive genetic testing.
- Printz C
- Cancer. 2017 Jun 1;123(11):1887. doi: 10.1002/cncr.30774.
- Research news
- Free Full Text
Letter, Comment:
Genetic Testing and Counseling Among Patients With Newly Diagnosed Breast Cancer.
- PMID: 28170472
- PubMed abstract
- Source abstract
-
- Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.
- Crawford B, Adams SB, Sittler T, van den Akker J, Chan S, Leitner O, Ryan L, Gil E, van 't Veer L.
- Breast Cancer Res Treat. 2017 Jun;163(2):383-390. doi: 10.1007/s10549-017-4181-0. Epub 2017 Mar 9.
- PMID: 28281021
- PubMed abstract
-
- Factors Associated with Interest in Gene-Panel Testing and Risk Communication Preferences in Women from BRCA1/2 Negative Families.
- Flores KG, Steffen LE, McLouth CJ, Vicuña BE, Gammon A, Kohlmann W, Vigil L, Dayao ZR, Royce ME, Kinney AY.
- J Genet Couns. 2017 Jun;26(3):480-490. doi: 10.1007/s10897-016-0001-7. Epub 2016 Aug 6.
- PMID: 27496122
- PubMed abstract
- Source abstract
-
- Information Topics of Greatest Interest for Return of Genome Sequencing Results among Women Diagnosed with Breast Cancer at a Young Age.
- Seo J, Ivanovich J, Goodman MS, Biesecker BB, Kaphingst KA.
- J Genet Couns. 2017 Jun;26(3):511-521. doi: 10.1007/s10897-016-0006-2. Epub 2016 Aug 20.
- PMID: 27542972
- PubMed abstract
- Source abstract
-
- A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data.
- Melloni GEM, Mazzarella L, Bernard L, Bodini M, Russo A, Luzi L, Pelicci PG, Riva L.
- Breast Cancer Res. 2017 May 31;19(1):63. doi: 10.1186/s13058-017-0854-1.
- PMID: 28569218
- PubMed abstract
-
- Comprehensive detection of germline variants by MSK-IMPACT, a clinical diagnostic platform for solid tumor molecular oncology and concurrent cancer predisposition testing.
- Cheng DT, Prasad M, Chekaluk Y, Benayed R, Sadowska J, Zehir A, Syed A, Wang YE, Somar J, Li Y, Yelskaya Z, Wong D, Robson ME, Offit K, Berger MF, Nafa K, Ladanyi M, Zhang L.
- BMC Med Genomics. 2017 May 19;10(1):33. doi: 10.1186/s12920-017-0271-4.
- PMID: 28526081
- PubMed abstract
-
- 5 Big Questions (and Answers) on Inherited Prostate Cancer Testing.
- Nick Mulcahy
- Medscape. Coverage from the American Urological Association (AUA) 2017 Annual Meeting. 2017 May 18.
- News, Conference report
- Free Full Text
-
- A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes.
- Buys SS, Sandbach JF, Gammon A, Patel G, Kidd J, Brown KL, Sharma L, Saam J, Lancaster J, Daly MB.
- Cancer. 2017 May 15;123(10):1721-1730. doi: 10.1002/cncr.30498. Epub 2017 Jan 13.
- PMID: 28085182
- PubMed abstract
- Source abstract
-
- Inherited Mutations in Men Undergoing Multigene Panel Testing for Prostate Cancer: Emerging Implications for Personalized Prostate Cancer Genetic Evaluation.
- Giri VN, Obeid E, Gross L, Bealin L, Hyatt C, Hegarty SE, Montgomery S, Forman A, Bingler R, Kelly WK, Dicker AP, Winheld S, Trabulsi EJ, Chen DYT, Lallas CD, Allen BA, Daly MB, Gomella LG.
- JCO Precis Oncol. 2017 May 4;1:PO.16.00039. doi: 10.1200/PO.16.00039.
- PMID: 34164591
- PubMed abstract
- Source abstract
Commentary:
Genetic Testing for Prostate Cancer in Clinical Practice.
- PMID: 35172486
- PubMed abstract
- Free Full Text
-
- Genomic Testing and Precision Medicine in Cancer Care.
- West HJ, Miller G.
- Medscape. News & Perspective. 2017 May 2.
-
- Multigene Testing for Hereditary Cancer: When, Why, and How.
- Offit K.
- J Natl Compr Canc Netw. 2017 May 1;15(5 Suppl):741-743.
-
- Next-generation sequencing of BRCA1/2 in breast cancer patients: potential effects on clinical decision-making using rapid, high-accuracy genetic results.
- Park HS, Park SJ, Kim JY, Kim S, Ryu J, Sohn J, Park S, Kim GM, Hwang IS, Choi JR, Kim SI.
- Ann Surg Treat Res. 2017 May;92(5):331-339. doi: 10.4174/astr.2017.92.5.331. Epub 2017 Apr 27.
- PMID: 28480178
- PubMed abstract
- Source abstract
-
- Next-Generation Sequencing Reveals a Nonsense Mutation (p.Arg364Ter) in MRE11A Gene in an Indian Patient with Familial Breast Cancer.
- Sharma Bhai P, Sharma D, Saxena R, Verma IC.
- Breast Care (Basel). 2017 May;12(2):114-116. doi: 10.1159/000457786. Epub 2017 Mar 21.
- PMID: 28559769
- PubMed abstract
- Source abstract
- Case report
- Free PMC article
- Free Full Text
-
- The Changing Landscape of Genetic Testing for Inherited Breast Cancer Predisposition.
- Afghahi A, Kurian AW.
- Curr Treat Options Oncol. 2017 May;18(5):27. doi: 10.1007/s11864-017-0468-y.
- PMID: 28439798
- PubMed abstract
- Free Full Text
-
- High-risk epithelial ovarian cancer patients for hereditary ovarian cancer.
- Chirasophon S, Manchana T, Teerapakpinyo C.
- J Obstet Gynaecol Res. 2017 May;43(5):929-934. doi: 10.1111/jog.13287. Epub 2017 Feb 11.
- PMID: 28188963
- PubMed abstract
- Source abstract
-
- Next Generation Sequencing and Multi-Gene Panel Testing: Implications for the Oncology Nurse.
- Kelly PA.
- Semin Oncol Nurs. 2017 May;33(2):208-218. doi: 10.1016/j.soncn.2017.02.007. Epub 2017 Apr 5.
- PMID: 28390840
- PubMed abstract
- Source abstract
-
- A novel molecular diagnostics platform for somatic and germline precision oncology.
- Cabanillas R, Diñeiro M, Castillo D, Pruneda PC, Penas C, Cifuentes GA, de Vicente Á, Durán NS, Álvarez R, Ordóñez GR, Cadiñanos J.
- Mol Genet Genomic Med. 2017 Apr 23;5(4):336-359. doi: 10.1002/mgg3.291. eCollection 2017 Jul.
- PMID: 28717660
- PubMed abstract
- Source abstract
-
- Next Generation Sequencing Reveals High Prevalence of BRCA1 and BRCA2 Variants of Unknown Significance in Early-Onset Breast Cancer in African American Women.
- Ricks-Santi L, McDonald JT, Gold B, Dean M, Thompson N, Abbas M, Wilson B, Kanaan Y, Naab TJ, Dunston G.
- Ethn Dis. 2017 Apr 20;27(2):169-178. doi: 10.18865/ed.27.2.169. eCollection 2017 Spring.
- PMID: 28439188
- PubMed abstract
- Source abstract
-
- Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
- Yurgelun MB, Kulke MH, Fuchs CS, Allen BA, Uno H, Hornick JL, Ukaegbu CI, Brais LK, McNamara PG, Mayer RJ, Schrag D, Meyerhardt JA, Ng K, Kidd J, Singh N, Hartman AR, Wenstrup RJ, Syngal S.
- J Clin Oncol. 2017 Apr 1;35(10):1086-1095. doi: 10.1200/JCO.2016.71.0012. Epub 2017 Jan 30.
- PMID: 28135145
- PubMed abstract
- Source abstract
Letter, Comments:
Frequency of Germline BRCA1/2 Mutations in Unselected Patients With Colorectal Cancer.
- PMID: 28510492
- PubMed abstract
- Free Full Text
Letter, Reply:
Reply to M.S. Daniels et al.
- PMID: 28510494
- PubMed abstract
- Free Full Text
-
- Increased Identification of Candidates for High-Risk Breast Cancer Screening Through Expanded Genetic Testing.
- Rosenthal ET, Evans B, Kidd J, Brown K, Gorringe H, van Orman M, Manley S.
- J Am Coll Radiol. 2017 Apr;14(4):561-568. doi: 10.1016/j.jacr.2016.10.003. Epub 2016 Dec 20.
- PMID: 28011157
- PubMed abstract
- Source abstract
-
- A Multigene Test Could Cost-Effectively Help Extend Life Expectancy for Women at Risk of Hereditary Breast Cancer.
- Li Y, Arellano AR, Bare LA, Bender RA, Strom CM, Devlin JJ.
- Value Health. 2017 Apr;20(4):547-555. doi: 10.1016/j.jval.2017.01.006. Epub 2017 Feb 23.
- PMID: 28407996
- PubMed abstract
- Source abstract
- Free Full Text
News: Advantage of Multigene Test for Women at Risk of Hereditary Breast Cancer. (OncoTherapy Network)
Letter:
Heterogeneity and Uncertainties Specific to Genome-Based Health Technological Assessments.
- PMID: 30005762
- PubMed abstract
- Source abstract
Letter:
A multigene test could cost-effectively help extend life expectancy for women at risk of hereditary breast cancer-Reply to letter to the editor by Petelin et al.
- PMID: 30005763
- PubMed abstract
- Source abstract
-
- Identification, genetic testing, and management of hereditary melanoma.
- Leachman SA, Lucero OM, Sampson JE, Cassidy P, Bruno W, Queirolo P, Ghiorzo P.
- Cancer Metastasis Rev. 2017 Mar;36(1):77-90. doi: 10.1007/s10555-017-9661-5.
- PMID: 28283772
- PubMed abstract
- Review
- Free Full Text
-
- Homologous recombination deficiency (HRD) testing in ovarian cancer clinical practice: a review of the literature.
- Frey MK, Pothuri B.
- Gynecol Oncol Res Pract. 2017 Feb 22;4:4. doi: 10.1186/s40661-017-0039-8. eCollection 2017.
- PMID: 28250960
- PubMed abstract
- Review
- Free Full Text
-
- Exome Sequencing in a Family with Luminal-Type Breast Cancer Underpinned by Variation in the Methylation Pathway.
- van der Merwe N, Peeters AV, Pienaar FM, Bezuidenhout J, van Rensburg SJ, Kotze MJ.
- Int J Mol Sci. 2017 Feb 22;18(2). pii: E467. doi: 10.3390/ijms18020467.
- PMID: 28241424
- PubMed abstract
- Source abstract
-
- Genetic Testing and Counseling Among Patients With Newly Diagnosed Breast Cancer .
- Kurian AW, Griffith KA, Hamilton AS, Ward KC, Morrow M, Katz SJ, Jagsi R.
- JAMA. 2017 Feb 7;317(5):531-534. doi: 10.1001/jama.2016.16918.
- PMID: 28170472
- PubMed abstract
- Source abstract
Viewpoint:
Multigene Panel Testing in Oncology Practice: How Should We Respond?
- PMID: 26181167
- PubMed abstract
- Free Full Text
Research news: High-risk patients with breast cancer may not receive genetic testing. (Cancer)
Press: Shortage of Genetic Counselors in Face of Growing Need. (Medscape Conference News)
-
- The Role of Genetic Testing in the Selection of Therapy for Breast Cancer: A Review.
- Niravath P, Cakar B, Ellis M.
- JAMA Oncol. 2017 Feb 1;3(2):262-268. doi: 10.1001/jamaoncol.2016.2719.
- PMID: 27560719
- PubMed abstract
- Source abstract
Letter, Comment:
Current Challenges Associated With Next-Generation Sequencing of Breast Cancer.
- PMID: 28520831
- PubMed abstract
- Source abstract
Letter, Reply:
Current Challenges Associated With Next-Generation Sequencing of Breast Cancer-Reply.
- PMID: 28520826
- PubMed abstract
- Source abstract
-
- Retesting BRCA1/BRCA2 mutation negative male breast cancer patients using next generation sequencing technologies.
- Rizzolo P, Silvestri V, Ottini L.
- Breast Cancer Res Treat. 2017 Feb;162(1):199-200. doi: 10.1007/s10549-017-4108-9. Epub 2017 Jan 16.
- PMID: 28091860
- PubMed abstract
- Source abstract
-
- Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.
- Pritzlaff M, Summerour P, McFarland R, Li S, Reineke P, Dolinsky JS, Goldgar DE, Shimelis H, Couch FJ, Chao EC, LaDuca H.
- Breast Cancer Res Treat. 2017 Feb;161(3):575-586. doi: 10.1007/s10549-016-4085-4. Epub 2016 Dec 22.
- PMID: 28008555
- PubMed abstract
-
- Almost 2% of Spanish breast cancer families are associated to germline pathogenic mutations in the ATM gene.
- Tavera-Tapia A, Pérez-Cabornero L, Macías JA, Ceballos MI, Roncador G, de la Hoya M, Barroso A, Felipe-Ponce V, Serrano-Blanch R, Hinojo C, Miramar-Gallart MD, Urioste M, Caldés T, Santillan-Garzón S, Benitez J, Osorio A.
- Breast Cancer Res Treat. 2017 Feb;161(3):597-604. doi: 10.1007/s10549-016-4058-7. Epub 2016 Dec 2.
- PMID: 27913932
- PubMed abstract
- Source abstract
-
- Cost Comparison of Genetic Testing Strategies in Women With Epithelial Ovarian Cancer.
- Foote JR, Lopez-Acevedo M, Buchanan AH, Secord AA, Lee PS, Fountain C, Myers ER, Cohn DE, Reed SD, Havrilesky LJ.
- J Oncol Pract. 2017 Feb;13(2):e120-e129. doi: 10.1200/JOP.2016.011866. Epub 2017 Jan 3.
- PMID: 28045615
- PubMed abstract
- Source abstract
Comments from NSGC Discussion Forum Cancer SIG
Subject: Always Handy
-
- The Clinical Utility of Next Generation Sequencing Results in a Community-Based Hereditary Cancer Risk Program.
- Bunnell AE, Garby CA, Pearson EJ, Walker SA, Panos LE, Blum JL.
- J Genet Couns. 2017 Feb;26(1):105-112. doi: 10.1007/s10897-016-9985-2. Epub 2016 Jun 9.
- PMID: 27276934
- PubMed abstract
- Source abstract
-
- [Clinical significance and distribution of BRCA genes mutation in sporadic high grade serous ovarian cancer].
- Liu WL, Wang ZZ, Zhao JZ, Hou YY, Wu XX, Li W, Dong B, Tong TT, Guo YJ.
- Zhonghua Fu Chan Ke Za Zhi. 2017 Jan 25;52(1):26-31. doi: 10.3760/cma.j.issn.0529-567X.2017.01.007.
- PMID: 28190312
- PubMed abstract
-
- Characterization of BRCA1/2 mutations in patients with family history of breast cancer in Armenia.
- Atshemyan S, Chavushyan A, Berberian N, Sahakyan A, Zakharyan R, Arakelyan A.
- F1000Res. 2017 Jan 10;6:29. doi: 10.12688/f1000research.10434.1. eCollection 2017.
- PMID: 28357044
- PubMed abstract
-
- The transfer of multigene panel testing for hereditary breast and ovarian cancer to healthcare: What are the implications for the management of patients and families?
- Arnould L, Delignette A, Padéano MM, Lepage C, Raichon-Patru G, Boudrant A, Bône-Lépinoy MC, Villing AL, Charpin A, Peignaux K, Chevrier S, Vegran F, Ghiringhelli F, Boidot R, Sevenet N, Lizard S, Faivre L.
- Oncotarget. 2017 Jan 10;8(2):1957-1971. doi: 10.18632/oncotarget.12699.
- PMID: 27779110
- PubMed abstract
- Source abstract
-
- A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape.
- Castellanos E, Gel B, Rosas I, Tornero E, Santín S, Pluvinet R, Velasco J, Sumoy L, Del Valle J, Perucho M, Blanco I, Navarro M, Brunet J, Pineda M, Feliubadaló L, Capellá G, Lázaro C, Serra E.
- Sci Rep. 2017 Jan 4;7:39348. doi: 10.1038/srep39348.
- PMID: 28051113
- PubMed abstract
-
- Gene panel sequencing in familial Breast/Ovarian Cancer patients identifies multiple novel mutations also in genes others than BRCA1/2.
- Kraus C, Hoyer J, Vasileiou G, Wunderle M, Lux MP, Fasching PA, Krumbiegel M, Uebe S, Reuter M, Beckmann MW, Reis A.
- Int J Cancer. 2017 Jan 1;140(1):95-102. doi: 10.1002/ijc.30428. Epub 2016 Sep 23.
- PMID: 27616075
- PubMed abstract
- Source abstract
-
- Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel.
- Moran O, Nikitina D, Royer R, Poll A, Metcalfe K, Narod SA, Akbari MR, Kotsopoulos J.
- Breast Cancer Res Treat. 2017 Jan;161(1):135-142. doi: 10.1007/s10549-016-4038-y. Epub 2016 Oct 31.
- PMID: 27798748
- PubMed abstract
- Source abstract
-
- Multi-gene panel testing for hereditary cancer susceptibility in a rural Familial Cancer Program.
- Hermel DJ, McKinnon WC, Wood ME, Greenblatt MS.
- Fam Cancer. 2017 Jan;16(1):159-166. doi: 10.1007/s10689-016-9913-5.
- PMID: 27401692
- PubMed abstract
- Source abstract
Letter:
Patients with negative multi-gene panel testing: a back to the future paradox?
- PMID: 28258424
- PubMed abstract
- Free Full Text
Letter:
Placing negative multi-gene panel results into clinical context.
- PMID: 28455554
- PubMed abstract
- Free Full Text
-
- Molecular analysis of BRCA1 and BRCA2 genes by next generation sequencing and ultrastructural aspects of breast tumor tissue.
- Mihalcea CE, Moroşanu AM, Murăraşu D, Puiu L, Cinca SA, Voinea SC, Mirancea N.
- Rom J Morphol Embryol. 2017;58(2):445-455.
- PMID: 28730229
- PubMed abstract
- ToC
-
- A Novel Pathogenic BRCA1 Splicing Variant Produces Partial Intron Retention in the Mature Messenger RNA.
- Esposito MV, Nunziato M, Starnone F, Telese A, Calabrese A, D'Aiuto G, Pucci P, D'Aiuto M, Baralle F, D'Argenio V, Salvatore F.
- Int J Mol Sci. 2016 Dec 21;17(12). pii: E2145. doi: 10.3390/ijms17122145.
- PMID: 28009814
- PubMed abstract
- Source abstract
- Case report
- Free Full Text
-
- Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records.
- He KY, Zhao Y, McPherson EW, Li Q, Xia F, Weng C, Wang K, He MM.
- PLoS One. 2016 Dec 8;11(12):e0167847. doi: 10.1371/journal.pone.0167847. eCollection 2016.
- PMID: 27930734
- PubMed abstract
-
- Next-generation sequencing: advances and applications in cancer diagnosis.
- Serratì S, De Summa S, Pilato B, Petriella D, Lacalamita R, Tommasi S, Pinto R.
- Onco Targets Ther. 2016 Dec 2;9:7355-7365. eCollection 2016.
- PMID: 27980425
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- Time to incorporate germline multigene panel testing into breast and ovarian cancer patient care.
- Graffeo R, Livraghi L, Pagani O, Goldhirsch A, Partridge AH, Garber JE.
- Breast Cancer Res Treat. 2016 Dec;160(3):393-410. Epub 2016 Oct 12.
- PMID: 27734215
- PubMed abstract
- Source abstract
-
- Breast Cancer: Genetics and Risk Assessment.
- Tejada-Bergés T.
- Clin Obstet Gynecol. 2016 Dec;59(4):673-687.
- PMID: 27749364
- PubMed abstract
- Source abstract
-
- Routine use of gene panel testing in hereditary breast cancer should be performed with caution.
- van Marcke C, De Leener A, Berlière M, Vikkula M, Duhoux FP.
- Crit Rev Oncol Hematol. 2016 Dec;108:33-39. doi: 10.1016/j.critrevonc.2016.10.008. Epub 2016 Oct 29.
- PMID: 27931838
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- Incorporating truncating variants in PALB2, CHEK2, and ATM into the BOADICEA breast cancer risk model.
- Lee AJ, Cunningham AP, Tischkowitz M, Simard J, Pharoah PD, Easton DF, Antoniou AC.
- Genet Med. 2016 Dec;18(12):1190-1198. doi: 10.1038/gim.2016.31. Epub 2016 Apr 14.
- PMID: 27464310
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: PALB2 breast cancer recurrence
Subject: article request
-
- Conflicting Interpretation of Genetic Variants and Cancer Risk by Commercial Laboratories as Assessed by the Prospective Registry of Multiplex Testing.
- Balmaña J, Digiovanni L, Gaddam P, Walsh MF, Joseph V, Stadler ZK, Nathanson KL, Garber JE, Couch FJ, Offit K, Robson ME, Domchek SM.
- J Clin Oncol. 2016 Dec;34(34):4071-4078. Epub 2016 Sep 30.
- PMID: 27621404
- PubMed abstract
- Source abstract
Letter:
Clinical Genetics Testing Laboratories Have a Remarkably Low Rate of Clinically Significant Discordance When Interpreting Variants in Hereditary Cancer Syndrome Genes.
- PMID: 28135136
- PubMed abstract
- Free Full Text
Letter:
Reply to R. Nussbaum et al and J. Dolinsky et al.
- PMID: 28135137
- PubMed abstract
- Free Full Text
-
- Germline mutations in Japanese familial pancreatic cancer patients.
- Takai E, Yachida S, Shimizu K, Furuse J, Kubo E, Ohmoto A, Suzuki M, Hruban RH, Okusaka T, Morizane C, Furukawa T.
- Oncotarget. 2016 Nov 8;7(45):74227-74235. doi: 10.18632/oncotarget.12490.
- PMID: 27732944
- PubMed abstract
- Source abstract
-
- Sensitivity of BRCA1/2 testing in high-risk breast/ovarian/male breast cancer families: little contribution of comprehensive RNA/NGS panel testing.
- Byers H, Wallis Y, van Veen EM, Lalloo F, Reay K, Smith P, Wallace AJ, Bowers N, Newman WG, Evans DG.
- Eur J Hum Genet. 2016 Nov;24(11):1591-1597. doi: 10.1038/ejhg.2016.57. Epub 2016 Jun 8.
- PMID: 27273131
- PubMed abstract
- Source abstract
-
- Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort.
- Ring KL, Bruegl AS, Allen BA, Elkin EP, Singh N, Hartman AR, Daniels MS, Broaddus RR.
- Mod Pathol. 2016 Nov;29(11):1381-1389. doi: 10.1038/modpathol.2016.135. Epub 2016 Jul 22.
- PMID: 27443514
- PubMed abstract
- Source abstract
-
- Prevention and Screening in Hereditary Breast and Ovarian Cancer.
- Zeichner SB, Stanislaw C, Meisel JL.
- Oncology (Williston Park). 2016 Oct 15;30(10). pii: 219285.
- PMID: 27753056
- PubMed abstract
- Source website
- Review
- Free Full Text
Commentary
Clinical Hereditary Cancer Syndromes and Gene Panel Testing.
- PMID: 27753057
- PubMed abstract
- Free Full Text
-
- Assessing, Counseling, and Treating Patients at High Risk for Breast Cancer.
- Clifford E, Hughes KS, Roberts M, Pirzadeh-Miller S, McLaughlin SA.
- Ann Surg Oncol. 2016 Oct;23(10):3128-32. doi: 10.1245/s10434-016-5399-5. Epub 2016 Jul 11.
- PMID: 27401444
- PubMed abstract
- Source abstract
-
- Identification of germline alterations in breast cancer predisposition genes among Malaysian breast cancer patients using panel testing.
- Ng PS, Wen WX, Fadlullah MZ, Yoon SY, Lee SY, Thong MK, Yip CH, Mohd Taib NA, Teo SH.
- Clin Genet. 2016 Oct;90(4):315-23. doi: 10.1111/cge.12735. Epub 2016 Feb 3.
- PMID: 26757417
- PubMed abstract
- Source abstract
-
- Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patients.
- Lhota F, Zemankova P, Kleiblova P, Soukupova J, Vocka M, Stranecky V, Janatova M, Hartmannova H, Hodanova K, Kmoch S, Kleibl Z.
- Clin Genet. 2016 Oct;90(4):324-33. doi: 10.1111/cge.12748. Epub 2016 Mar 4.
- PMID: 26822949
- PubMed abstract
- Source abstract
-
- Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes.
- Dobbins SE, Broderick P, Chubb D, Kinnersley B, Sherborne AL, Houlston RS.
- Fam Cancer. 2016 Oct;15(4):593-9. doi: 10.1007/s10689-016-9914-4.
- PMID: 27356891
- PubMed abstract
-
- BRCA1-2 diagnostic workflow from next-generation sequencing technologies to variant identification and final report.
- Pilato B, Pinto R, De Summa S, Petriella D, Lacalamita R, Danza K, Virgilio Paradiso A, Tommasi S.
- Genes Chromosomes Cancer. 2016 Oct;55(10):803-13. doi: 10.1002/gcc.22383. Epub 2016 Jul 4.
- PMID: 27225819
- PubMed abstract
- Source abstract
-
- Updates on breast cancer genetics: Clinical implications of detecting syndromes of inherited increased susceptibility to breast cancer.
- Cobain EF, Milliron KJ, Merajver SD.
- Semin Oncol. 2016 Oct;43(5):528-535. doi: 10.1053/j.seminoncol.2016.10.001. Epub 2016 Oct 8.
- PMID: 27899183
- PubMed abstract
- Source abstract
-
- Consensus Guideline on Hereditary Genetic Testing for Patients With and Without Breast Cancer
- ASBS Research committee
- The American Society of Breast Surgeons. www.breastsurgeons.org. 2016 Sep 13.
- Practice Guideline
- Free Full Text (PDF)
Comments on NSGC Discussion Forum Cancer SIG
Subject: American Society of Breast Surgeons Consenus Guidelines on Genetic Testing
Subject: American Society of Breast Surgeons Consenus Guidelines on Genetic Testing
-
- Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.
- Pinto P, Paulo P, Santos C, Rocha P, Pinto C, Veiga I, Pinheiro M, Peixoto A, Teixeira MR.
- Breast Cancer Res Treat. 2016 Sep;159(2):245-56. doi: 10.1007/s10549-016-3948-z. Epub 2016 Aug 23.
- PMID: 27553368
- PubMed abstract
- Source abstract
-
- Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriers.
- Leedom TP, LaDuca H, McFarland R, Li S, Dolinsky JS, Chao EC.
- Cancer Genet. 2016 Sep;209(9):403-407. doi: 10.1016/j.cancergen.2016.08.005. Epub 2016 Aug 15.
- PMID: 27751358
- PubMed abstract
- Source abstract
-
- Prevalence of Hispanic BRCA1 and BRCA2 mutations among hereditary breast and ovarian cancer patients from Brazil reveals differences among Latin American populations.
- Alemar B, Herzog J, Brinckmann Oliveira Netto C, Artigalás O, Schwartz IV, Matzenbacher Bittar C, Ashton-Prolla P, Weitzel JN.
- Cancer Genet. 2016 Sep;209(9):417-422. doi: 10.1016/j.cancergen.2016.06.008. Epub 2016 Jun 20.
- PMID: 27425403
- PubMed abstract
- Source abstract
-
- New challenges for BRCA testing: a view from the diagnostic laboratory.
- Wallace AJ.
- Eur J Hum Genet. 2016 Sep;24 Suppl 1:S10-8. doi: 10.1038/ejhg.2016.94.
- PMID: 27514839
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- A Review of Whole Exome Sequencing Efforts Toward Hereditary Breast Cancer Susceptibility Gene Discovery.
- Chandler MR, Bilgili EP, Merner ND.
- Hum Mutat. 2016 Sep;37(9):835-46. doi: 10.1002/humu.23017. Epub 2016 Jun 27.
- PMID: 27226120
- PubMed abstract
- Source abstract
-
- Clinical Next-Generation Sequencing Pipeline Outperforms a Combined Approach Using Sanger Sequencing and Multiplex Ligation-Dependent Probe Amplification in Targeted Gene Panel Analysis.
- Schenkel LC, Kerkhof J, Stuart A, Reilly J, Eng B, Woodside C, Levstik A, Howlett CJ, Rupar AC, Knoll JH, Ainsworth P, Waye JS, Sadikovic B.
- J Mol Diagn. 2016 Sep;18(5):657-67. doi: 10.1016/j.jmoldx.2016.04.002. Epub 2016 Jul 2.
- PMID: 27376475
- PubMed abstract
- Source abstract
-
- Next-Generation Sequencing: Role in Gynecologic Cancers.
- Evans T, Matulonis U.
- J Natl Compr Canc Netw. 2016 Sep;14(9):1165-73.
- PMID: 27587626
- PubMed abstract
- Source abstract
-
- Multigene Panel Tests Yield Clues to Breast and Ovarian Cancer Risk.
- Greg Kennelty.
- Oncology Nursing News. 2016 Aug 3.
- Conference report
- Free full text
-
- Primary Peritoneal Carcinoma in a BRCA1/2-negative, PALB2-positive patient.
- Kahn R, Garcia-Soto A, Silva-Smith R, Pinto A, George SH.
- Gynecol Oncol Rep. 2016 Aug 2;17:93-5. doi: 10.1016/j.gore.2016.08.001. eCollection 2016.
- PMID: 27547810
- PubMed abstract
- Source abstract
- Case report
- Free PMC article
- Free Full Text
-
- Are genetic testing criteria redundant in the light of next generation sequencing technologies?
- Charlotte Warren-Gash.
- PHG Foundation. 2016 July 29.
- News
- Free Full Text
Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study.
- PMID: 27252788
- PubMed abstract
-
- Genomics in Clinical Practice, Part 1: The Rise of Multiplex Gene Testing for Cancer.
- Kate M. O'Rourke
- Medscape Oncology. Coverage from the American Society of Clinical Oncology (ASCO) 2016 Annual Meeting. 2016 Jul 20.
-
- Prioritizing Variants in Complete Hereditary Breast and Ovarian Cancer Genes in Patients Lacking Known BRCA Mutations.
- Caminsky NG, Mucaki EJ, Perri AM, Lu R, Knoll JH, Rogan PK.
- Hum Mutat. 2016 Jul;37(7):640-52. doi: 10.1002/humu.22972. Epub 2016 Mar 18.
- PMID: 26898890
- PubMed abstract
- Source abstract
-
- Detection of Germline Mutation in Hereditary Breast and/or Ovarian Cancers by Next-Generation Sequencing on a Four-Gene Panel.
- Kwong A, Shin VY, Au CH, Law FB, Ho DN, Ip BK, Wong AT, Lau SS, To RM, Choy G, Ford JM, Ma ES, Chan TL.
- J Mol Diagn. 2016 Jul;18(4):580-94. doi: 10.1016/j.jmoldx.2016.03.005. Epub 2016 May 5.
- PMID: 27157322
- PubMed abstract
- Source abstract
-
- Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing.
- Kang HP, Maguire JR, Chu CS, Haque IS, Lai H, Mar-Heyming R, Ready K, Vysotskaia VS, Evans EA.
- PeerJ. 2016 Jun 28;4:e2162. doi: 10.7717/peerj.2162. eCollection 2016.
- PMID: 27375968
- PubMed abstract
-
- Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study.
- Warren-Gash C, Kroese M, Burton H, Pharoah P.
- Hered Cancer Clin Pract. 2016 Jun 1;14:12. doi: 10.1186/s13053-016-0052-7. eCollection 2016.
- PMID: 27252788
- PubMed abstract
Press: Are genetic testing criteria redundant in the light of next generation sequencing technologies? (PHG Foundation)
-
- Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India.
- Mannan AU, Singh J, Lakshmikeshava R, Thota N, Singh S, Sowmya TS, Mishra A, Sinha A, Deshwal S, Soni MR, Chandrasekar A, Ramesh B, Ramamurthy B, Padhi S, Manek P, Ramalingam R, Kapoor S, Ghosh M, Sankaran S, Ghosh A, Veeramachaneni V, Ramamoorthy P, Hariharan R, Subramanian K.
- J Hum Genet. 2016 Jun;61(6):515-22. doi: 10.1038/jhg.2016.4. Epub 2016 Feb 25.
- PMID: 26911350
- PubMed abstract
- Source abstract
Letter
Estimating risk using multi-gene panel testing; do negative results change the risk?
- PMID: 27734838
- PubMed abstract
- Source abstract
-
- Multigene testing of moderate-risk genes: be mindful of the missense.
- Young EL, Feng BJ, Stark AW, Damiola F, Durand G, Forey N, Francy TC, Gammon A, Kohlmann WK, Kaphingst KA, McKay-Chopin S, Nguyen-Dumont T, Oliver J, Paquette AM, Pertesi M, Robinot N, Rosenthal JS, Vallee M, Voegele C, Hopper JL, Southey MC, Andrulis IL, John EM, Hashibe M, Gertz J; Breast Cancer Family Registry, Le Calvez-Kelm F, Lesueur F, Goldgar DE, Tavtigian SV.
- J Med Genet. 2016 Jun;53(6):366-76. doi: 10.1136/jmedgenet-2015-103398. Epub 2016 Jan 19.
- PMID: 26787654
- PubMed abstract
- Source abstract
-
- Testing for Hereditary Predisposition in Patients with Gynecologic Cancers, Quo Vadis?
- Mitchell G, Schrader KA.
- Surg Pathol Clin. 2016 Jun;9(2):301-6. doi: 10.1016/j.path.2016.01.009. Epub 2016 Apr 11.
- PMID: 27241110
- PubMed abstract
- Source abstract
-
- Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer.
- Maxwell KN, Hart SN, Vijai J, Schrader KA, Slavin TP, Thomas T, Wubbenhorst B, Ravichandran V, Moore RM, Hu C, Guidugli L, Wenz B, Domchek SM, Robson ME, Szabo C, Neuhausen SL, Weitzel JN, Offit K, Couch FJ, Nathanson KL.
- Am J Hum Genet. 2016 May 5;98(5):801-817. doi: 10.1016/j.ajhg.2016.02.024.
- PMID: 27153395
- PubMed abstract
- Source abstract
-
- Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.
- Parsons DW, Roy A, Yang Y, Wang T, Scollon S, Bergstrom K, Kerstein RA, Gutierrez S, Petersen AK, Bavle A, Lin FY, López-Terrada DH, Monzon FA, Hicks MJ, Eldin KW, Quintanilla NM, Adesina AM, Mohila CA, Whitehead W, Jea A, Vasudevan SA, Nuchtern JG, Ramamurthy U, McGuire AL, Hilsenbeck SG, Reid JG, Muzny DM, Wheeler DA, Berg SL, Chintagumpala MM, Eng CM, Gibbs RA, Plon SE.
- JAMA Oncol. 2016 May 1;2(5):616-624. doi: 10.1001/jamaoncol.2015.5699.
- PMID: 26822237
- PubMed abstract
Editorial
Precision Therapy for Pediatric Cancers.
- PMID: 26822032
- PubMed abstract
- Source abstract
Press: Lessons From Genetic Testing in Pediatric Cancers. (Medscape Oncology)
-
- Panel Testing Is Not a Panacea.
- Axilbund JE.
- J Clin Oncol. 2016 May 1;34(13):1433-5. doi: 10.1200/JCO.2015.65.5522. Epub 2016 Mar 14.
- PMID: 26976416
- PubMed abstract
- Editorial / Commentary
- Free Full Text
Letter
Multigene Panels to Evaluate Hereditary Cancer Risk: Reckless or Relevant?
- PMID: 27551136
- PubMed abstract
- Free article
-
- Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
- Thompson ER, Rowley SM, Li N, McInerny S, Devereux L, Wong-Brown MW, Trainer AH, Mitchell G, Scott RJ, James PA, Campbell IG.
- J Clin Oncol. 2016 May 1;34(13):1455-9. doi: 10.1200/JCO.2015.63.7454. Epub 2016 Jan 19.
- PMID: 26786923
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: Article request
Subject: Article request
Press: Caution Urged in Interpreting Breast Cancer Gene Panels at Individual Level (Medscape/Reuters)
-
- Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
- Tung N, Lin NU, Kidd J, Allen BA, Singh N, Wenstrup RJ, Hartman AR, Winer EP, Garber JE.
- J Clin Oncol. 2016 May 1;34(13):1460-8. doi: 10.1200/JCO.2015.65.0747. Epub 2016 Mar 14.
- PMID: 26976419
- PubMed abstract
- Source abstract
Letter
Next-Generation Sequencing of Tumors to Better Estimate the Clinical Significance of Non-BRCA Germline Deleterious Mutations.
- PMID: 27551129
- PubMed abstract
- Free article
-
- How Far Do We Go With Genetic Evaluation? Gene, Panel, and Tumor Testing.
- Lynce F, Isaacs C.
- Am Soc Clin Oncol Educ Book. 2016 May;(36):e72-e78. doi: 10.1200/EDBK_160391.
- PMID: 30372286
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- Incidental germline variants in 1000 advanced cancers on a prospective somatic genomic profiling protocol.
- Meric-Bernstam F, Brusco L, Daniels M, Wathoo C, Bailey AM, Strong L, Shaw K, Lu K, Qi Y, Zhao H, Lara-Guerra H, Litton J, Arun B, Eterovic AK, Aytac U, Routbort M, Subbiah V, Janku F, Davies MA, Kopetz S, Mendelsohn J, Mills GB, Chen K.
- Ann Oncol. 2016 May;27(5):795-800. doi: 10.1093/annonc/mdw018. Epub 2016 Jan 19.
- PMID: 26787237
- PubMed abstract
- Source abstract
-
- No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing.
- Easton DF, Lesueur F, Decker B, Michailidou K, Li J, Allen J, Luccarini C, Pooley KA, Shah M, Bolla MK, Wang Q, Dennis J, Ahmad J, Thompson ER, Damiola F, Pertesi M, Voegele C, Mebirouk N, Robinot N, Durand G, Forey N, Luben RN, Ahmed S, Aittomäki K, Anton-Culver H, Arndt V; Australian Ovarian Cancer Study Group, Baynes C, Beckman MW, Benitez J, Van Den Berg D, Blot WJ, Bogdanova NV, Bojesen SE, Brenner H, Chang-Claude J, Chia KS, Choi JY, Conroy DM, Cox A, Cross SS, Czene K, Darabi H, Devilee P, Eriksson M, Fasching PA, Figueroa J, Flyger H, Fostira F, García-Closas M, Giles GG, Glendon G, González-Neira A, Guénel P, Haiman CA, Hall P, Hart SN, Hartman M, Hooning MJ, Hsiung CN, Ito H, Jakubowska A, James PA, John EM, Johnson N, Jones M, Kabisch M, Kang D; kConFab Investigators, Kosma VM, Kristensen V, Lambrechts D, Li N; Lifepool Investigators, Lindblom A, Long J, Lophatananon A, Lubinski J, Mannermaa A, Manoukian S, Margolin S, Matsuo K, Meindl A, Mitchell G, Muir K; NBCS Investigators, Nevelsteen I, van den Ouweland A, Peterlongo P, Phuah SY, Pylkäs K, Rowley SM, Sangrajrang S, Schmutzler RK, Shen CY, Shu XO, Southey MC, Surowy H, Swerdlow A, Teo SH, Tollenaar RA, Tomlinson I, Torres D, Truong T, Vachon C, Verhoef S, Wong-Brown M, Zheng W, Zheng Y, Nevanlinna H, Scott RJ, Andrulis IL, Wu AH, Hopper JL, Couch FJ, Winqvist R, Burwinkel B, Sawyer EJ, Schmidt MK, Rudolph A, Dörk T, Brauch H, Hamann U, Neuhausen SL, Milne RL, Fletcher O, Pharoah PD, Campbell IG, Dunning AM, Le Calvez-Kelm F, Goldgar DE, Tavtigian SV, Chenevix-Trench G.
- J Med Genet. 2016 May;53(5):298-309. doi: 10.1136/jmedgenet-2015-103529. Epub 2016 Feb 26.
- PMID: 26921362
- PubMed abstract
- Source abstract
Commentary
Risky business: getting a grip on BRIP.
- PMID: 26921361
- PubMed abstract
- Source abstract
-
- BRCA 1/2-negative patients who receive counseling after genetic testing have lower anxiety.
- Printz C.
- Cancer. 2016 Apr 15;122(8):1149. doi: 10.1002/cncr.30002.
- PMID: 27061519
- PubMed abstract
- Conference Report
- Free Full Text
-
- A new paradigm of genetic testing for hereditary breast/ovarian cancers.
- Kwong A, Chen JW, Shin VY.
- Hong Kong Med J. 2016 Apr;22(2):171-7. doi: 10.12809/hkmj154634. Epub 2016 Mar 14.
- PMID: 26980575
- PubMed abstract
- Review
- Free Full Text
-
- Gene panel testing for hereditary breast cancer.
- Winship I, Southey MC.
- Med J Aust. 2016 Mar 21;204(5):188-90.
- PMID: 26985847
- PubMed abstract
- Review
- Free Full Text
-
- Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 Variant.
- Schrader KA, Stratton KL, Murali R, Laitman Y, Cavallone L, Offit L, Wen YH, Thomas T, Shah S, Rau-Murthy R, Manschreck C, Salo-Mullen E, Otegbeye E, Corines M, Zhang L, Norton L, Hudis C, Klein RJ, Kauff ND, Robson M, Stadler ZK, Haber DA, Lipkin SM, Friedman E, Foulkes WD, Altshuler D, Vijai J, Offit K.
- J Clin Oncol. 2016 Mar 10;34(8):e61-7. doi: 10.1200/JCO.2013.50.0272. Epub 2014 Jun 30.
- PMID: 24982446
- PubMed abstract
- Case report
- Free Full Text
-
- Medical implications of technical accuracy in genome sequencing.
- Goldfeder RL, Priest JR, Zook JM, Grove ME, Waggott D, Wheeler MT, Salit M, Ashley EA.
- Genome Med. 2016 Mar 2;8(1):24. doi: 10.1186/s13073-016-0269-0.
- PMID: 26932475
- PubMed abstract
-
- Comparison of Targeted Next-Generation and Sanger Sequencing for the BRCA1 and BRCA2 Mutation Screening.
- Park J, Jang W, Chae H, Kim Y, Chi HY, Kim M.
- Ann Lab Med. 2016 Mar;36(2):197-201. doi: 10.3343/alm.2016.36.2.197.
- PMID: 26709275
- PubMed abstract
- Source abstract
-
- Genetic testing in a cohort of young patients with HER2-amplified breast cancer.
- Eccles DM, Li N, Handwerker R, Maishman T, Copson ER, Durcan LT, Gerty SM, Jones L, Evans DG, Haywood L, Campbell I.
- Ann Oncol. 2016 Mar;27(3):467-73. doi: 10.1093/annonc/mdv592. Epub 2015 Dec 17.
- PMID: 26681682
- PubMed abstract
- Source abstract
-
- Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.
- Kaphingst KA, Ivanovich J, Biesecker BB, Dresser R, Seo J, Dressler LG, Goodfellow PJ, Goodman MS.
- Clin Genet. 2016 Mar;89(3):378-84. doi: 10.1111/cge.12597. Epub 2015 May 5.
- PMID: 25871653
- PubMed abstract
- Source abstract
-
- Beyond BRCA: Testing negative and living in the 'gray zone' for cancer risk.
- [No author given]
- My Gene Counsel. 2016 Feb 16.
- Blog post
- Free Full Text
-
- Multiple gene sequencing for risk assessment in patients with early-onset or familial breast cancer.
- Lin PH, Kuo WH, Huang AC, Lu YS, Lin CH, Kuo SH, Wang MY, Liu CY, Cheng FT, Yeh MH, Li HY, Yang YH, Hsu YH, Fan SC, Li LY, Yu SL, Chang KJ, Chen PL, Ni YH, Huang CS.
- Oncotarget. 2016 Feb 16;7(7):8310-20. doi: 10.18632/oncotarget.7027.
- PMID: 26824983
- PubMed abstract
- Source abstract
-
- Whole Genome Sequencing Defines the Genetic Heterogeneity of Familial Pancreatic Cancer.
- Roberts NJ, Norris AL, Petersen GM, Bondy ML, Brand R, Gallinger S, Kurtz RC, Olson SH, Rustgi AK, Schwartz AG, Stoffel E, Syngal S, Zogopoulos G, Ali SZ, Axilbund J, Chaffee KG, Chen YC, Cote ML, Childs EJ, Douville C, Goes FS, Herman JM, Iacobuzio-Donahue C, Kramer M, Makohon-Moore A, McCombie RW, McMahon KW, Niknafs N, Parla J, Pirooznia M, Potash JB, Rhim AD, Smith AL, Wang Y, Wolfgang CL, Wood LD, Zandi PP, Goggins M, Karchin R, Eshleman JR, Papadopoulos N, Kinzler KW, Vogelstein B, Hruban RH, Klein AP.
- Cancer Discov. 2016 Feb;6(2):166-75. doi: 10.1158/2159-8290.CD-15-0402. Epub 2015 Dec 9.
- PMID: 26658419
- PubMed abstract
- Source abstract
-
- Genetic characterization of early onset ovarian carcinoma.
- Bernards SS, Norquist BM, Harrell MI, Agnew KJ, Lee MK, Walsh T, Swisher EM.
- Gynecol Oncol. 2016 Feb;140(2):221-225. doi: 10.1016/j.ygyno.2015.12.017. Epub 2015 Dec 21.
- PMID: 26718727
- PubMed abstract
- Source abstract
-
- Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
- Daly MB, Pilarski R, Axilbund JE, Berry M, Buys SS, Crawford B, Farmer M, Friedman S, Garber JE, Khan S, Klein C, Kohlmann W, Kurian A, Litton JK, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Rana H, Reiser G, Robson ME, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wick MJ, Wiesner GL, Dwyer M, Kumar R, Darlow S.
- J Natl Compr Canc Netw. 2016 Feb;14(2):153-62.
- PMID: 26850485
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
-
- Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.
- Mantere T, Winqvist R, Kauppila S, Grip M, Jukkola-Vuorinen A, Tervasmäki A, Rapakko K, Pylkäs K.
- PLoS Genet. 2016 Jan 28;12(1):e1005816. doi: 10.1371/journal.pgen.1005816. eCollection 2016.
- PMID: 26820313
- PubMed abstract
-
- Inherited breast cancer predisposition in Asians: multigene panel testing outcomes from Singapore.
- Wong ESY, Shekar S, Met-Domestici M, Chan C, Sze M, Yap YS, Rozen SG, Tan MH, Ang P, Ngeow J, Lee ASG.
- NPJ Genom Med. 2016 Jan 13;1:15003. doi: 10.1038/npjgenmed.2015.3. eCollection 2016.
- PMID: 29263802
- PubMed abstract
-
- Precision medicine in heritable cancer: when somatic tumour testing and germline mutations meet.
- Ngeow J, Eng C.
- NPJ Genom Med. 2016 Jan 13;1:15006. doi: 10.1038/npjgenmed.2015.6. eCollection 2016.
- PMID: 29263804
- PubMed abstract
- Editorial
- Free PMC article
- Free Full Text
-
- BRCA somatic and germline mutation detection in paraffin embedded ovarian cancers by next-generation sequencing.
- Mafficini A, Simbolo M, Parisi A, Rusev B, Luchini C, Cataldo I, Piazzola E, Sperandio N, Turri G, Franchi M, Tortora G, Bovo C, Lawlor RT, Scarpa A.
- Oncotarget. 2016 Jan 12;7(2):1076-83. doi: 10.18632/oncotarget.6834.
- PMID: 26745875
- PubMed abstract
- Source abstract
-
- Prevalence of Pathogenic Mutations in Cancer Predisposition Genes among Pancreatic Cancer Patients.
- Hu C, Hart SN, Bamlet WR, Moore RM, Nandakumar K, Eckloff BW, Lee YK, Petersen GM, McWilliams RR, Couch FJ.
- Cancer Epidemiol Biomarkers Prev. 2016 Jan;25(1):207-11. doi: 10.1158/1055-9965.EPI-15-0455. Epub 2015 Oct 19.
- PMID: 26483394
- PubMed abstract
-
- Genetic screening for gynecological cancer: where are we heading?
- Manchanda R, Jacobs I.
- Future Oncol. 2016 Jan;12(2):207-20. doi: 10.2217/fon.15.278. Epub 2015 Dec 7.
- PMID: 26638726
- PubMed abstract
- Source abstract
-
- Patient feedback and early outcome data with a novel tiered-binned model for multiplex breast cancer susceptibility testing.
- Bradbury AR, Patrick-Miller LJ, Egleston BL, DiGiovanni L, Brower J, Harris D, Stevens EM, Maxwell KN, Kulkarni A, Chavez T, Brandt A, Long JM, Powers J, Stopfer JE, Nathanson KL, Domchek SM.
- Genet Med. 2016 Jan;18(1):25-33. doi: 10.1038/gim.2015.19. Epub 2015 Apr 2.
- PMID: 25834950
- PubMed abstract
- Source abstract
-
- Targeted massively parallel sequencing of a panel of putative breast cancer susceptibility genes in a large cohort of multiple-case breast and ovarian cancer families.
- Li J, Meeks H, Feng BJ, Healey S, Thorne H, Makunin I, Ellis J; kConFab Investigators, Campbell I, Southey M, Mitchell G, Clouston D, Kirk J, Goldgar D, Chenevix-Trench G.
- J Med Genet. 2016 Jan;53(1):34-42. doi: 10.1136/jmedgenet-2015-103452. Epub 2015 Nov 3.
- PMID: 26534844
- PubMed abstract
- Source abstract
-
- Breast Cancer Risk Assessment: Moving Beyond BRCA 1 and 2.
- Scalia-Wilbur J, Colins BL, Penson RT, Dizon DS.
- Semin Radiat Oncol. 2016 Jan;26(1):3-8. doi: 10.1016/j.semradonc.2015.09.004. Epub 2015 Sep 4.
- PMID: 26617204
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- Refining Breast Cancer Risk Stratification: Additional Genes, Additional Information.
- Kurian AW, Antoniou AC, Domchek SM.
- Am Soc Clin Oncol Educ Book. 2016;35:44-56. doi: 10.14694/EDBK_158817.
- PMID: 27249685
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- How Far Do We Go With Genetic Evaluation? Gene, Panel, and Tumor Testing.
- Lynce F, Isaacs C.
- Am Soc Clin Oncol Educ Book. 2016;35:e72-e78. doi: 10.14694/EDBK_160391.
- PMID: 27249773
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- Performance Characterization and Validation of Saliva as an Alternative Specimen Source for Detecting Hereditary Breast Cancer Mutations by Next Generation Sequencing.
- Meghnani V, Mohammed N, Giauque C, Nahire R, David T.
- Int J Genomics. 2016;2016:2059041. Epub 2016 Oct 13.
- PMID: 27818992
- PubMed abstract
- Source abstract
-
- 2016 Genetics Toolkit
- Society of Gynecologic Oncology
- Society of Gynecologic Oncology. 2016.
- Review. Toolkit.
- Free Full Text
News: New Toolkit Can Help Debunk Myths About Genetic Testing for Gynecologic Cancer. (Cure)
-
- Identification of novel hereditary cancer genes by whole exome sequencing.
- Sokolenko AP, Suspitsin EN, Kuligina ESh, Bizin IV, Frishman D, Imyanitov EN.
- Cancer Lett. 2015 Dec 28;369(2):274-88. doi: 10.1016/j.canlet.2015.09.014. Epub 2015 Sep 30.
- PMID: 26427841
- PubMed abstract
- Source abstract
-
- The Science -- Or Lack Of It -- Behind Genetic Tests Offered In The Workplace.
- David Shaywitz.
- Forbes. 2015 Dec 18.
- Press article
- Free Full Text
-
- UK BRCA mutation testing in patients with ovarian cancer.
- George A.
- Br J Cancer. 2015 Dec 15;113(S1):S17-S21. doi: 10.1038/bjc.2015.396.
- PMID: 26669451
- PubMed abstract
- Source abstract
-
- Germline Mutations in Predisposition Genes in Pediatric Cancer.
- Zhang J, Walsh MF, Wu G, Edmonson MN, Gruber TA, Easton J, Hedges D, Ma X, Zhou X, Yergeau DA, Wilkinson MR, Vadodaria B, Chen X, McGee RB, Hines-Dowell S, Nuccio R, Quinn E, Shurtleff SA, Rusch M, Patel A, Becksfort JB, Wang S, Weaver MS, Ding L, Mardis ER, Wilson RK, Gajjar A, Ellison DW, Pappo AS, Pui CH, Nichols KE, Downing JR.
- N Engl J Med. 2015 Dec 10;373(24):2336-2346. Epub 2015 Nov 18.
- PMID: 26580448
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: Ewing Sarcoma and early onset pancreatic cancer?
Subject: Exome for Cancer LMN
Editorial
Defining Why Cancer Develops in Children.
- PMID: 26580096
- PubMed abstract
- Free full text
Letter
Germline Mutations in Predisposition Genes in Pediatric Cancer.
- PMID: 27050225
- PubMed abstract
- Free full text
Reply / Letter
Germline Mutations in Predisposition Genes in Pediatric Cancer.
- PMID: 27050224
- PubMed abstract
- Free full text
Research Highlight
Cancer predisposition: Searching for early events.
- PMID: 26694933
- PubMed abstract
- Source abstract
News
Genetic mutations in paediatric cancer.
- PMID: 26631830
- PubMed abstract
- Source abstract
Press: Why Some Children Get Cancer: Germline Mutations Found (Medscape)
News: Destiny or chance? (Science Translational Medicine)
-
- [Germline mutations of TP53 gene among Chinese families with high risk for breast cancer].
- Yang X, Hu Z, Wu J, Liu G, Di G, Chen C, Hou Y, Huang X, Liu Z, Shen Z, Shao Z.
- Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Dec 10;32(6):761-5. doi: 10.3760/cma.j.issn.1003-9406.2015.06.001.
- PMID: 26663043
- PubMed abstract
- Source abstract
-
- [Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute].
- Macháčková E, Hazova J, Sťahlová Hrabincová E, Vašíčková P, Navrátilová M, Svoboda M, Foretová L.
- Klin Onkol. 2015 Winter;29 Suppl 1:35-45.
- PMID: 26691941
- PubMed abstract
- Source abstract
-
- Utilization of Next Generation Multi-gene Panels Versus Single Gene Testing.
- Zenas Chang, Jenny Backman, Sara Carroll, M. Heather Einstein.
- Gynecologic Oncology. 2015 Dec;139(3):584. 2015 NEAGO ABSTRACTS. doi: 10.1016/j.ygyno.2015.09.023.
-
- Clinical Practice Guideline for the prevention and early detection of breast and ovarian cancer in women from HBOC (hereditary breast and ovarian cancer) families.
- Singer CF, Tea MK, Pristauz G, Hubalek M, Rappaport C, Riedl CC, Helbich TH.
- Wien Klin Wochenschr. 2015 Dec;127(23-24):981-6. doi: 10.1007/s00508-015-0880-x. Epub 2015 Nov 2.
- PMID: 26525377
- PubMed abstract
- Source abstract
-
- Next-Generation Gene Sequencing: Looking Beyond Hereditary Breast and Ovarian Cancer.
- Estrada SS, LeGrazie B, McKamie T2, Montgomery S.
- Oncol Nurs Forum. 2015 Nov 1;42(6):691-4. doi: 10.1188/15.ONF.691-694.
- PMID: 26488839
- PubMed abstract
- Source abstract
-
- Genetic risk assessment and prevention: the role of genetic testing panels in breast cancer.
- Lerner-Ellis J, Khalouei S, Sopik V, Narod SA.
- Expert Rev Anticancer Ther. 2015 Nov;15(11):1315-26. doi: 10.1586/14737140.2015.1090879. Epub 2015 Nov 2.
- PMID: 26523341
- PubMed abstract
- Source abstract
-
- More genes, more problems? Benefits and risks of multiplex genetic testing.
- Norquist BM, Swisher EM.
- Gynecol Oncol. 2015 Nov;139(2):209-210. doi: 10.1016/j.ygyno.2015.10.013.
- PMID: 26521152
- PubMed abstract
- Source abstract
-
- Rescreening for genetic mutations using multi-gene panel testing in patients who previously underwent non-informative genetic screening.
- Frey MK, Kim SH, Bassett RY, Martineau J, Dalton E, Chern JY, Blank SV.
- Gynecol Oncol. 2015 Nov;139(2):211-215. doi: 10.1016/j.ygyno.2015.08.006. Epub 2015 Aug 18.
- PMID: 26296696
- PubMed abstract
- Source abstract
-
- Usefulness of Multigene Testing: Catching the Train That's Left the Station.
- Swisher EM.
- JAMA Oncol. 2015 Oct 1;1(7):951-952. doi: 10.1001/jamaoncol.2015.2699.
- PMID: 26270409
- PubMed abstract
- Source abstract
Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
- PMID: 26270727
- PubMed abstract
- Free full text
Press: Testing for more breast cancer genes offers useful information (Reuters Health)
-
- Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
- Desmond A, Kurian AW, Gabree M, Mills MA, Anderson MJ, Kobayashi Y, Horick N, Yang S, Shannon KM, Tung N, Ford JM, Lincoln SE, Ellisen LW.
- JAMA Oncol. 2015 Oct 1;1(7):943-951. doi: 10.1001/jamaoncol.2015.2690.
- PMID: 26270727
- PubMed abstract
Comment
Usefulness of Multigene Testing: Catching the Train That's Left the Station.
- PMID: 26270409
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: Article Requestp
Press: Multigene Panel Test Finds Mutations in BRCA-Negative Individuals. (Medscape Oncology)
Press: Testing for more breast cancer genes offers useful information. (Reuters Health)
Press: Monitoring Techniques for Hereditary Breast and Ovarian Cancer Being Developed. (Targeted Oncology)
-
- Initial Results of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer and Lynch Syndrome.
- Howarth DR, Lum SS, Esquivel P, Garberoglio CA, Senthil M, Solomon NL.
- Am Surg. 2015 Oct;81(10):941-4.
- PMID: 26463285
- PubMed abstract
- Source abstract
-
- Multigene Panel Testing Detects Equal Rates of Pathogenic BRCA1/2 Mutations and has a Higher Diagnostic Yield Compared to Limited BRCA1/2 Analysis Alone in Patients at Risk for Hereditary Breast Cancer.
- Kapoor NS, Curcio LD, Blakemore CA, Bremner AK, McFarland RE, West JG, Banks KC.
- Ann Surg Oncol. 2015 Oct;22(10):3282-8. doi: 10.1245/s10434-015-4754-2. Epub 2015 Jul 29.
- PMID: 26219241
- PubMed abstract
- Source abstract
-
- Clinical impact on ovarian cancer patients of massive parallel sequencing for BRCA mutation detection: the experience at Gemelli hospital and a literature review.
- Minucci A, Scambia G, Santonocito C, Concolino P, Canu G, Mignone F, Saggese I, Guarino D, Costella A, Molinario R, De Bonis M, Ferrandina G, Petrillo M, Scaglione GL, Capoluongo E.
- Expert Rev Mol Diagn. 2015 Oct;15(10):1383-403. doi: 10.1586/14737159.2015.1081059. Epub 2015 Aug 26.
- PMID: 26306726
- PubMed abstract
- Source abstract
-
- Double Heterozygosity of BRCA2 and STK11 in Familial Breast Cancer Detected by Exome Sequencing.
- Ataei-Kachouei M, Nadaf J, Akbari MT, Atri M, Majewski J, Riazalhosseini Y, Garshasbi M.
- Iran J Public Health. 2015 Oct;44(10):1348-1352.
- PMID: 26576347
- PubMed abstract
- Source abstract
-
- Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories.
- Saam J, Arnell C, Theisen A, Moyes K, Marino I, Roundy KM, Wenstrup RJ.
- Oncology. [2015 Oct;]89(5):288-93. doi: 10.1159/000437307. Epub 2015 Aug 28.
- PMID: 26315041
- PubMed abstract
-
- Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management.
- Slavin TP, Niell-Swiller M, Solomon I, Nehoray B, Rybak C, Blazer KR, Weitzel JN.
- Front Oncol. 2015 Sep 29;5:208. doi: 10.3389/fonc.2015.00208. eCollection 2015.
- PMID: 26484312
- PubMed abstract
-
- Treatment Decision Making and Genetic Testing for Breast Cancer: Mainstreaming Mutations.
- Katz SJ, Kurian AW, Morrow M.
- JAMA. 2015 Sep 8;314(10):997-998. doi: 10.1001/jama.2015.8088.
- PMID: 26203642
- PubMed abstract
- Source abstract
-
- Availability and payer coverage of BRCA1/2 tests and gene panels.
- Clain E, Trosman JR, Douglas MP, Weldon CB, Phillips KA.
- Nat Biotechnol. 2015 Sep 8;33(9):900-2. doi: 10.1038/nbt.3322.
- PMID: 26348951
- PubMed abstract
- Source abstract
-
- Detection of novel germline mutations for breast cancer in non-BRCA1/2 families.
- Aloraifi F, McDevitt T, Martiniano R, McGreevy J, McLaughlin R, Egan CM, Cody N, Meany M, Kenny E, Green AJ, Bradley DG, Geraghty JG, Bracken AP.
- FEBS J. 2015 Sep;282(17):3424-37. doi: 10.1111/febs.13352. Epub 2015 Jul 14.
- PMID: 26094658
- PubMed abstract
- Source abstract
-
- Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
- Yurgelun MB, Allen B, Kaldate RR, Bowles KR, Judkins T, Kaushik P, Roa BB, Wenstrup RJ, Hartman AR, Syngal S.
- Gastroenterology. 2015 Sep;149(3):604-613.e20. doi: 10.1053/j.gastro.2015.05.006. Epub 2015 May 14.
- PMID: 25980754
- PubMed abstract
- Source abstract
Editorial
Next Generation Multigene Panel Testing: The Next Step for Identification of Hereditary Colorectal Cancer Syndromes?
- PMID: 26226575
- PubMed abstract
- Source abstract
-
- A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Genes in More Than 1000 Patients.
- Lincoln SE, Kobayashi Y, Anderson MJ, Yang S, Desmond AJ, Mills MA, Nilsen GB, Jacobs KB, Monzon FA, Kurian AW, Ford JM, Ellisen LW.
- J Mol Diagn. 2015 Sep;17(5):533-44. doi: 10.1016/j.jmoldx.2015.04.009. Epub 2015 Jul 22.
- PMID: 26207792
- PubMed abstract
- Source abstract
-
- Multigene panel analysis identified germline mutations of DNA repair genes in breast and ovarian cancer.
- Hirotsu Y, Nakagomi H, Sakamoto I, Amemiya K, Oyama T, Mochizuki H, Omata M.
- Mol Genet Genomic Med. 2015 Sep;3(5):459-66. doi: 10.1002/mgg3.157. Epub 2015 May 12.
- PMID: 26436112
- PubMed abstract
- Source abstract
-
- "The BRCA Responder" on Genetic Testing, Family Histories, and Why Counseling Is Key.
- Kelly Johnson.
- Oncology Nursing News. 2015 Aug 31.
- Press article
- Free Full Text
-
- Genetic Testing Can Lead to Insights — Or Uncertainty.
- Lauren M. Green.
- Cure. 2015 Aug 13.
- Press article
- Free Full Text
-
- Prevalence of mutations in a panel of breast cancer susceptibility genes in BRCA1/2-negative patients with early-onset breast cancer.
- Maxwell KN, Wubbenhorst B, D'Andrea K, Garman B, Long JM, Powers J, Rathbun K, Stopfer JE, Zhu J, Bradbury AR, Simon MS, DeMichele A, Domchek SM, Nathanson KL.
- Genet Med. 2015 Aug;17(8):630-638. doi: 10.1038/gim.2014.176. Epub 2014 Dec 11.
- PMID: 25503501
- PubMed abstract
- Source abstract
-
- Testing for Hereditary Breast Cancer: Panel or Targeted Testing? Experience from a Clinical Cancer Genetics Practice.
- Doherty J, Bonadies DC, Matloff ET.
- J Genet Couns. 2015 Aug;24(4):683-7. doi: 10.1007/s10897-014-9796-2. Epub 2014 Dec 5.
- PMID: 25475920
- PubMed abstract
- Source abstract
-
- Video: Genetic Testing for only $249?
- [No author given].
- My Gene Counsel. 2015 Jul 21.
- Blog post, Video
- Free Full Text
-
- Genetics of breast cancer: a topic in evolution.
- Shiovitz S, Korde LA.
- Ann Oncol. 2015 Jul;26(7):1291-9. doi: 10.1093/annonc/mdv022. Epub 2015 Jan 20.
- PMID: 25605744
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- HBOC multi-gene panel testing: comparison of two sequencing centers.
- Schroeder C, Faust U, Sturm M, Hackmann K, Grundmann K, Harmuth F, Bosse K, Kehrer M, Benkert T, Klink B, Mackenroth L, Betcheva-Krajcir E, Wimberger P, Kast K, Heilig M, Nguyen HP, Riess O, Schröck E, Bauer P, Rump A.
- Breast Cancer Res Treat. 2015 Jul;152(1):129-36. doi: 10.1007/s10549-015-3429-9. Epub 2015 May 29.
- PMID: 26022348
- PubMed abstract
- Source abstract
-
- Two novel frameshift mutations in BRCA2 gene detected by next generation sequencing in a survey of Spanish patients of breast cancer.
- Hernan I, Mañé B, Borràs E, de Sousa Dias M, Llort G, Yagüe C, Gamundi MJ, Arcusa À, Carballo M.
- Clin Transl Oncol. 2015 Jul;17(7):576-80. doi: 10.1007/s12094-014-1271-x. Epub 2015 Jan 14.
- PMID: 25586199
- PubMed abstract
- Source abstract
-
- The Challenges of Incorporating Gene Panels Into Clinical Practice.
- Kate M. O'Rourke.
- Medscape Oncology. American Society of Clinical Oncology (ASCO) 2015 Annual Meeting. 2015 Jun 22.
- Conference report
- Free Full Text
-
- Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
- Karageorgos I, Mizzi C, Giannopoulou E, Pavlidis C, Peters BA, Zagoriti Z, Stenson PD, Mitropoulos K, Borg J, Kalofonos HP, Drmanac R, Stubbs A, van der Spek P, Cooper DN, Katsila T, Patrinos GP.
- Hum Genomics. 2015 Jun 20;9:12. doi: 10.1186/s40246-015-0034-2.
- PMID: 26092435
- PubMed abstract
-
- The molecular analysis of BRCA1 and BRCA2: Next-generation sequencing supersedes conventional approaches.
- D'Argenio V, Esposito MV, Telese A, Precone V, Starnone F, Nunziato M, Cantiello P, Iorio M, Evangelista E, D'Aiuto M, Calabrese A, Frisso G, D'Aiuto G, Salvatore F.
- Clin Chim Acta. 2015 Jun 15;446:221-5. doi: 10.1016/j.cca.2015.03.045. Epub 2015 Apr 17.
- PMID: 25896959
- PubMed abstract
-
- Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk.
- Easton DF, Pharoah PD, Antoniou AC, Tischkowitz M, Tavtigian SV, Nathanson KL, Devilee P, Meindl A, Couch FJ, Southey M, Goldgar DE, Evans DG, Chenevix-Trench G, Rahman N, Robson M, Domchek SM, Foulkes WD.
- N Engl J Med. 2015 Jun 4;372(23):2243-2257. Epub 2015 May 27.
- PMID: 26014596
- PubMed abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: Excellent review paper in NEJM
Comment / Letter
ClinGen and Genetic Testing.
- PMID: 26422737
- PubMed abstract
- Free article
-
- Germ-Line, Other Actionable Mutations Reported with Next-Generation Sequencing.
- [No author given]
- ASCO Daily News. 2015 ASCO Annual Meeting. 2015 Jun 1.
- Conference report, Video
- Free Full Text
-
- Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer.
- Marikkannu R, Aravidis C, Rantala J, Picelli S, Adamovic T, Keihas M, Liu T, Kontham V, Nilsson D, Lindblom A.
- Anticancer Res. 2015 Jun;35(6):3155-65.
- PMID: 26026075
- PubMed abstract
- Source abstract
-
- Exome sequencing in a breast cancer family without BRCA mutation.
- Noh JM, Kim J, Cho DY, Choi DH, Park W, Huh SJ.
- Radiat Oncol J. 2015 Jun;33(2):149-54. doi: 10.3857/roj.2015.33.2.149. Epub 2015 Jun 30.
- PMID: 26157685
- PubMed abstract
-
- Gene analysis techniques and susceptibility gene discovery in non-BRCA1/BRCA2 familial breast cancer.
- Aloraifi F, Boland MR, Green AJ, Geraghty JG.
- Surg Oncol. 2015 Jun;24(2):100-9. doi: 10.1016/j.suronc.2015.04.003. Epub 2015 Apr 13.
- PMID: 25936246
- PubMed abstract
- Source abstract
-
- New recurrent BRCA1/2 mutations in Polish patients with familial breast/ovarian cancer detected by next generation sequencing.
- Kluska A, Balabas A, Paziewska A, Kulecka M, Nowakowska D, Mikula M, Ostrowski J.
- BMC Med Genomics. 2015 May 7;8:19. doi: 10.1186/s12920-015-0092-2.
- PMID: 25948282
- PubMed abstract
-
- New Study on 'Very Hot Topic' in BRCA Testing.
- Roxanne Nelson.
- Medscape Medical News. American Society of Breast Surgeons (ASBS) 16th Annual Meeting. 2015 May 4.
- Conference report
- Free Full Text
-
- Mutational analysis of BRCA1/2 in a group of 134 consecutive ovarian cancer patients. Novel and recurrent BRCA1/2 alterations detected by next generation sequencing.
- Ratajska M, Krygier M, Stukan M, Kuźniacka A, Koczkowska M, Dudziak M, Śniadecki M, Dębniak J, Wydra D, Brozek I, Biernat W, Borg A, Limon J, Wasąg B.
- J Appl Genet. 2015 May;56(2):193-8. doi: 10.1007/s13353-014-0254-5. Epub 2014 Nov 1.
- PMID: 25366421
- PubMed abstract
-
- Genetic tests to identify risk for breast cancer.
- Lynch JA, Venne V, Berse B.
- Semin Oncol Nurs. 2015 May;31(2):100-7. doi: 10.1016/j.soncn.2015.02.007. Epub 2015 Feb 26.
- PMID: 25951739
- PubMed abstract
- Source abstract
-
- For $249, Shouldn’t We All Have the Cancer Gene Panel?
- [No author given]
- My Gene Counsel. 2015 Apr 28.
- Blog post
- Free Full Text
-
- Affordable access to a new genetic test for cancer.
- Andrea.
- Brave Bosom. 2015 Apr 21.
- Blog post
- Free Full Text
-
- Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk.
- Judkins T, Leclair B, Bowles K, Gutin N, Trost J, McCulloch J, Bhatnagar S, Murray A, Craft J, Wardell B, Bastian M, Mitchell J, Chen J, Tran T, Williams D, Potter J, Jammulapati S, Perry M, Morris B, Roa B, Timms K.
- BMC Cancer. 2015 Apr 2;15:215. doi: 10.1186/s12885-015-1224-y.
- PMID: 25886519
- PubMed abstract
-
- Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2.
- Minion LE, Dolinsky JS, Chase DM, Dunlop CL, Chao EC, Monk BJ.
- Gynecol Oncol. 2015 Apr;137(1):86-92. doi: 10.1016/j.ygyno.2015.01.537. Epub 2015 Jan 23.
- PMID: 25622547
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: RAD50 Positive Letter
-
- The Promise and Peril of Panel Genetic Testing for Inherited Cancer Susceptibility.
- Jill Stopfer.
- FORCE. Be Empowered Webinars. 2015 Mar 24.
- Webinar
- Free video
-
- Identification of a breast cancer family double heterozygote for RAD51C and BRCA2 gene mutations.
- Ahlborn LB, Steffensen AY, Jønson L, Djursby M, Nielsen FC, Gerdes AM, Hansen TV.
- Fam Cancer. 2015 Mar;14(1):129-33. doi: 10.1007/s10689-014-9747-y.
- PMID: 25154786
- PubMed abstract
- Source abstract
-
- Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.
- Grant RC, Selander I, Connor AA, Selvarajah S, Borgida A, Briollais L, Petersen GM, Lerner-Ellis J, Holter S, Gallinger S.
- Gastroenterology. 2015 Mar;148(3):556-64. doi: 10.1053/j.gastro.2014.11.042. Epub 2014 Dec 2.
- PMID: 25479140
- PubMed abstract
- Source abstract
Comment
Inherited susceptibility to pancreatic cancer in the era of next-generation sequencing.
- PMID: 25613311
- PubMed abstract
- Source abstract
Introductory Journal Article
Covering the Cover
- PMID: 25625760
- PubMed abstract
- Source abstract
CME Activities: Exam 2: Prevalence of Germline Mutations in Cancer Predisposition Genes in Patients With Pancreatic Cancer (Gastroenterology)
-
- Next-Generation Sequencing of the BRCA1 and BRCA2 Genes for the Genetic Diagnostics of Hereditary Breast and/or Ovarian Cancer.
- Trujillano D, Weiss ME, Schneider J, Köster J, Papachristos EB, Saviouk V, Zakharkina T, Nahavandi N, Kovacevic L, Rolfs A.
- J Mol Diagn. 2015 Mar;17(2):162-70. doi: 10.1016/j.jmoldx.2014.11.004. Epub 2014 Dec 31.
- PMID: 25556971
- PubMed abstract
- Source abstract
-
- Detection of BRCA1 and BRCA2 germline mutations in Japanese population using next-generation sequencing.
- Hirotsu Y, Nakagomi H, Sakamoto I, Amemiya K, Mochizuki H, Omata M.
- Mol Genet Genomic Med. 2015 Mar;3(2):121-9. doi: 10.1002/mgg3.120. Epub 2014 Dec 4.
- PMID: 25802882
- PubMed abstract
- Source abstract
-
- Low-level constitutional mosaicism of a de novoBRCA1 gene mutation.
- Friedman E, Efrat N, Soussan-Gutman L, Dvir A, Kaplan Y, Ekstein T, Nykamp K, Powers M, Rabideau M, Sorenson J, Topper S.
- Br J Cancer. 2015 Feb 17;112(4):765-768. doi: 10.1038/bjc.2015.14. Epub 2015 Jan 29.
- PMID: 25633036
- PubMed abstract
- Source abstract
- Case Report
- Free PMC article
- Free Full Text
-
- Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer.
- Couch FJ, Hart SN, Sharma P, Toland AE, Wang X, Miron P, Olson JE, Godwin AK, Pankratz VS, Olswold C, Slettedahl S, Hallberg E, Guidugli L, Davila JI, Beckmann MW, Janni W, Rack B, Ekici AB, Slamon DJ, Konstantopoulou I, Fostira F, Vratimos A, Fountzilas G, Pelttari LM, Tapper WJ, Durcan L, Cross SS, Pilarski R, Shapiro CL, Klemp J, Yao S, Garber J, Cox A, Brauch H, Ambrosone C, Nevanlinna H, Yannoukakos D, Slager SL, Vachon CM, Eccles DM, Fasching PA.
- J Clin Oncol. 2015 Feb 1;33(4):304-11. doi: 10.1200/JCO.2014.57.1414. Epub 2014 Dec 1.
- PMID: 25452441
- PubMed abstract
- Source abstract
Evolution of genetic testing for inherited susceptibility to breast cancer.
- PMID: 25512463
- PubMed abstract
- Free full text
-
- Genetic risk assessment for breast and gynecological malignancies.
- Profato JL, Arun BK.
- Curr Opin Obstet Gynecol. 2015 Feb;27(1):1-5. doi: 10.1097/GCO.0000000000000142.
- PMID: 25502427
- PubMed abstract
- Source abstract
-
- Next-generation sequencing for hereditary breast and gynecologic cancer risk assessment.
- Kurian AW, Kingham KE, Ford JM.
- Curr Opin Obstet Gynecol. 2015 Feb;27(1):23-33. doi: 10.1097/GCO.0000000000000141.
- PMID: 25502425
- PubMed abstract
- Source abstract
-
- Multiplex genetic testing: reconsidering utility and informed consent in the era of next-generation sequencing.
- Bradbury AR, Patrick-Miller L, Domchek S.
- Genet Med. 2015 Feb;17(2):97-98. doi: 10.1038/gim.2014.85. Epub 2014 Jul 17.
- PMID: 25032987
- PubMed abstract
- Letter, Editorial / Commentary
- Free PMC article
- Free Full Text
-
- Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
- Tung N, Battelli C, Allen B, Kaldate R, Bhatnagar S, Bowles K, Timms K, Garber JE, Herold C, Ellisen L, Krejdovsky J, DeLeonardis K, Sedgwick K, Soltis K, Roa B, Wenstrup RJ, Hartman A.
- Cancer. 2015 Jan 1;121(1):25-33. doi: 10.1002/cncr.29010. Epub 2014 Sep 3.
- PMID: 25186627
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: Slides/Data from NSGC
-
- Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.
- Foley SB, Rios JJ, Mgbemena VE, Robinson LS, Hampel HL, Toland AE, Durham L, Ross TS.
- EBioMedicine. 2015 Jan;2(1):74-81.
- PMID: 26023681
- PubMed abstract
- Source abstract
-
- A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
- Hampel H, Bennett RL, Buchanan A, Pearlman R, Wiesner GL.
- Genet Med. 2015 Jan;17(1):70-87. doi: 10.1038/gim.2014.147. Epub 2014 Nov 13.
- PMID: 25394175
- PubMed abstract
- Source abstract
Addendum:
Addendum: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
-
- Hereditary breast cancer syndromes and genetic testing.
- Rich TA, Woodson AH, Litton J, Arun B.
- J Surg Oncol. 2015 Jan;111(1):66-80. doi: 10.1002/jso.23791. Epub 2014 Nov 7.
- PMID: 25381882
- PubMed abstract
- Source abstract
-
- The importance to update the guidelines for the use of genetic testing in noncancer patients in Brazil.
- Lajus TB.
- Rev Saude Publica. 2015;49:71. doi: 10.1590/S0034-8910.2015049005988. Epub 2015 Oct 13.
- PMID: 26465663
- PubMed abstract
- Source abstract
-
- Rapid and cost effective screening of breast and ovarian cancer genes using novel sequence capture method in clinical samples.
- Arvai K, Horváth P, Balla B, Tőkés AM, Tobiás B, Takács I, Nagy Z, Lakatos P, Kósa JP.
- Fam Cancer. 2014 Dec;13(4):583-9. doi: 10.1007/s10689-014-9730-7.
- PMID: 24853695
- PubMed abstract
- Source abstract
-
- Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes.
- Castéra L, Krieger S, Rousselin A, Legros A, Baumann JJ, Bruet O, Brault B, Fouillet R, Goardon N, Letac O, Baert-Desurmont S, Tinat J, Bera O, Dugast C, Berthet P, Polycarpe F, Layet V, Hardouin A, Frébourg T, Vaur D.
- Eur J Hum Genet. 2014 Nov;22(11):1305-13. doi: 10.1038/ejhg.2014.16. Epub 2014 Feb 19.
- PMID: 24549055
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: RAD50 Positive Letter
-
- Panel testing for inherited susceptibility to breast, ovarian, and colorectal cancer.
- Domchek SM, Nathanson KL.
- Genet Med. 2014 Nov;16(11):827-9. doi: 10.1038/gim.2014.56. Epub 2014 Jul 3.
- PMID: 24991876
- PubMed abstract
- Comment
- Free Full Text
Podcast: The Use of Gene Panels in Diagnostic Next Generation Sequencing. (Genetics in Medicine GenePod)
-
- Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients.
- LaDuca H, Stuenkel AJ, Dolinsky JS, Keiles S, Tandy S, Pesaran T, Chen E, Gau CL, Palmaer E, Shoaepour K, Shah D, Speare V, Gandomi S, Chao E.
- Genet Med. 2014 Nov;16(11):830-837. doi: 10.1038/gim.2014.40. Epub 2014 Apr 24.
- PMID: 24763289
- PubMed abstract
- Source abstract
Commentary:
Panel testing for inherited susceptibility to breast, ovarian, and colorectal cancer.
- PMID: 24991876
- PubMed abstract
- Free Full Text
Podcast: The Use of Gene Panels in Diagnostic Next Generation Sequencing. (Genetics in Medicine GenePod)
-
- Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer.
- Kiiski JI, Pelttari LM, Khan S, Freysteinsdottir ES, Reynisdottir I, Hart SN, Shimelis H, Vilske S, Kallioniemi A, Schleutker J, Leminen A, Bützow R, Blomqvist C, Barkardottir RB, Couch FJ, Aittomäki K, Nevanlinna H.
- Proc Natl Acad Sci U S A. 2014 Oct 21;111(42):15172-7. doi: 10.1073/pnas.1407909111. Epub 2014 Oct 6.
- PMID: 25288723
- PubMed abstract
- Source abstract
-
- gDNA enrichment by a transposase-based technology for NGS analysis of the whole sequence of BRCA1, BRCA2, and 9 genes involved in DNA damage repair.
- Chevrier S, Boidot R.
- J Vis Exp. 2014 Oct 6;(92):e51902. doi: 10.3791/51902.
- PMID: 25350069
- PubMed abstract
-
- Genetic testing today.
- Euhus D.
- Ann Surg Oncol. 2014 Oct;21(10):3209-15. doi: 10.1245/s10434-014-3906-0. Epub 2014 Jul 17.
- PMID: 25029991
- PubMed abstract
- Source abstract
-
- Benefits, Beneficence, and Bending Ethics: Questionable Billing Practices for Multigene Panels?
- Robert Resta.
- The DNA Exchange, 2014 Sep 28.
- Blog post
- Free Full Text
-
- Breast cancer genetic screening offers vital information, uncertainty.
- Judy Peres.
- Chicago Tribune, 2014 Sep 25.
Comments on NSGC Discussion Forum Cancer SIG
-
- Cancer risk assessment using genetic panel testing: considerations for clinical application.
- Hiraki S, Rinella ES, Schnabel F, Oratz R, Ostrer H.
- J Genet Couns. 2014 Aug;23(4):604-17. doi: 10.1007/s10897-014-9695-6. Epub 2014 Mar 7.
- PMID: 24599651
- PubMed abstract
- Source abstract
-
- An investigation of genetic counselors' testing recommendations: pedigree analysis and the use of multiplex breast cancer panel testing.
- Lundy MG, Forman A, Valverde K, Kessler L.
- J Genet Couns. 2014 Aug;23(4):618-32. doi: 10.1007/s10897-014-9692-9. Epub 2014 Feb 27.
- PMID: 24569857
- PubMed abstract
- Source abstract
-
- Genetic testing and familial implications in breast-ovarian cancer families.
- Oosterwijk JC, de Vries J, Mourits MJ, de Bock GH.
- Maturitas. 2014 Aug;78(4):252-257. doi: 10.1016/j.maturitas.2014.05.002. Epub 2014 May 9.
- PMID: 24894332
- PubMed abstract
- Source abstract
-
- Multigene panel testing: planning the next generation of research studies in clinical cancer genetics.
- Robson M.
- J Clin Oncol. 2014 Jul 1;32(19):1987-9. doi: 10.1200/JCO.2014.56.0474. Epub 2014 May 27.
- PMID: 24868020
- PubMed abstract
- Editorial / Commentary
- Free Full Text
Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
- PMID: 24733792
- PubMed abstract
- Source abstract
-
- Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
- Kurian AW, Hare EE, Mills MA, Kingham KE, McPherson L, Whittemore AS, McGuire V, Ladabaum U, Kobayashi Y, Lincoln SE, Cargill M, Ford JM.
- J Clin Oncol. 2014 Jul 1;32(19):2001-9. doi: 10.1200/JCO.2013.53.6607. Epub 2014 Apr 14.
- PMID: 24733792
- PubMed abstract
- Source abstract
Comment, Editorial:
Multigene panel testing: planning the next generation of research studies in clinical cancer genetics.
- PMID: 24868020
- PubMed abstract
- Free Full Text
Press: Multiple-Gene Sequencing Panel Assesses Hereditary Cancer Risk. (Medscape/Reuters)
Press: Study Supports Clinical Utility of Gene Panel Sequencing Approach. (GenomeWeb)
Blog post: Gene panel screens dozens of genes for cancer-associated mutations. (ScienceBlog)
-
- Opportunities and challenges of next-generation DNA sequencing for breast units.
- Pilgrim SM, Pain SJ, Tischkowitz MD.
- Br J Surg. 2014 Jul;101(8):889-98. doi: 10.1002/bjs.9458. Epub 2014 Mar 27.
- PMID: 24676784
- PubMed abstract
- Source abstract
- Review
- Free Full Text
News
Transforming Breast Cancer Care with NGS
-
- Personalized therapy for breast cancer.
- De Abreu FB, Schwartz GN, Wells WA, Tsongalis GJ.
- Clin Genet. 2014 Jul;86(1):62-7. doi: 10.1111/cge.12381. Epub 2014 Apr 9.
- PMID: 24635704
- PubMed abstract
- Source abstract
- Review
- Free Full Text
-
- Family-specific, novel, deleterious germline variants provide a rich resource to identify genetic predispositions for BRCAx familial breast cancer.
- Wen H, Kim YC, Snyder C, Xiao F, Fleissner EA, Becirovic D, Luo J, Downs B, Sherman S, Cowan KH, Lynch HT, Wang SM.
- BMC Cancer. 2014 Jun 26;14:470. doi: 10.1186/1471-2407-14-470.
- PMID: 24969172
- PubMed abstract
-
- Screening an Asymptomatic Person for Genetic Risk.
- [No authors listed]
- N Engl J Med. 2014 Jun 19;370(25):2442-2445.
- PMID: 24941182
- PubMed abstract
- Case vignette
- Free Full Text
Comments on NSGC Discussion Forum Cancer SIG
-
- The Validation and Clinical Implementation of BRCAplus: A Comprehensive High-Risk Breast Cancer Diagnostic Assay.
- Chong HK, Wang T, Lu HM, Seidler S, Lu H, Keiles S, Chao EC, Stuenkel AJ, Li X, Elliott AM.
- PLoS One. 2014 May 15;9(5):e97408. doi: 10.1371/journal.pone.0097408. eCollection 2014.
- PMID: 24830819
- PubMed abstract
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- Large panel genetic testing produces more questions than answers in breast cancer.
- [No author given]
- Medical Express, 2014 May 14.
- News
- Free Full Text
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- Next-generation sequencing for inherited breast cancer risk: counseling through the complexity.
- Rainville IR, Rana HQ.
- Curr Oncol Rep. 2014 Mar;16(3):371. doi: 10.1007/s11912-013-0371-z.
- PMID: 24488544
- PubMed abstract
- Source abstract
Comments on NSGC Discussion Forum Cancer SIG
Subject: Article request multigene panels
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- Genetic testing in hereditary breast and ovarian cancer using massive parallel sequencing.
- Ruiz A, Llort G, Yagüe C, Baena N, Viñas M, Torra M, Brunet A, Seguí MA, Saigí E, Guitart M.
- Biomed Res Int. 2014;2014:542541. doi: 10.1155/2014/542541. Epub 2014 Jun 26.
- PMID: 25136594
- PubMed abstract
- Source abstract
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- Multiplex genetic cancer testing identifies pathogenic mutations in TP53 and CDH1 in a patient with bilateral breast and endometrial adenocarcinoma.
- Heitzer E, Lax S, Lafer I, Müller SM, Pristauz G, Ulz P, Jahn S, Högenauer C, Petru E, Speicher MR, Geigl JB.
- BMC Med Genet. 2013 Dec 29;14:129. doi: 10.1186/1471-2350-14-129.
- PMID: 24373500
- PubMed abstract
- Case report
- Free PMC article
- Free Full Text
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- Supreme Court Ruling Broadens BRCA Testing Options.
- Azvolinsky A.
- J Natl Cancer Inst. 2013 Nov 20;105(22):1671-2. doi: 10.1093/jnci/djt342. Epub 2013 Nov 6.
- PMID: 24198329
- PubMed abstract
- Source abstract
- News
- Free Full Text
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- The "New" Genetic Testing: What You Need to Know.
- Rebecca Sutphen.
- FORCE. Be Empowered Webinars. 2013 Nov 18.
- Webinar
- Free video
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- Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2.
- Nguyen-Dumont T, Teo ZL, Pope BJ, Hammet F, Mahmoodi M, Tsimiklis H, Sabbaghian N, Tischkowitz M, Foulkes WD; Kathleen Cuningham Foundation Consortium for research into Familial Breast cancer (kConFab), Giles GG, Hopper JL; Australian Breast Cancer Family Registry, Southey MC, Park DJ.
- BMC Med Genomics. 2013 Nov 8;6:48. doi: 10.1186/1755-8794-6-48.
- PMID: 24206657
- PubMed abstract
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- The impact of next generation sequencing on the analysis of breast cancer susceptibility: a role for extremely rare genetic variation?
- Hilbers F, Vreeswijk M, van Asperen C, Devilee P.
- Clin Genet. 2013 Nov;84(5):407-14. doi: 10.1111/cge.12256. Epub 2013 Sep 12.
- PMID: 24025038
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Gene Panel Spots Mutations Other Breast Cancer Test Misses.
- Neil Osterweil.
- Medscape Medical News. Conference News. American Society of Human Genetics (ASHG) 63rd Annual Meeting. 2013 Oct 25.
- Conference report
- Free Full Text
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- Researchers Spar Over Tests for Breast Cancer Risks.
- Jocelyn Kaiser.
- ScienceInsider. 2013 Oct 24.
- News
- Free Full Text
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- Questions For The Panel.
- Robert Resta.
- The DNA Exchange. 2013 Sep 29.
- Blog post
- Free Full Text
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- Has Myriad Learned Their Lesson?
- Niki Lovick, Michelle Ernst.
- Yale Cancer Genetic Counseling. 2013 Sep 11.
- Blog post
- Free Full Text
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- Can Unknown Predisposition in Familial Breast Cancer be Family-Specific?
- Lynch H, Wen H, Kim YC, Snyder C, Kinarsky Y, Chen PX, Xiao F, Goldgar D, Cowan KH, Wang SM.
- Breast J. 2013 Sep;19(5):520-8. doi: 10.1111/tbj.12145. Epub 2013 Jun 26.
- PMID: 23800003
- PubMed abstract
- Source abstract
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- Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes.
- Feliubadaló L, Lopez-Doriga A, Castellsagué E, Del Valle J, Menéndez M, Tornero E, Montes E, Cuesta R, Gómez C, Campos O, Pineda M, González S, Moreno V, Brunet J, Blanco I, Serra E, Capellá G, Lázaro C.
- Eur J Hum Genet. 2013 Aug;21(8):864-70. doi: 10.1038/ejhg.2012.270. Epub 2012 Dec 19.
- PMID: 23249957
- PubMed abstract
- Source abstract
Press: The Future of BRCA1/BRCA2 Testing. (OncLive)
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- Myriad BRCA Patents Nixed: What Happens Next?
- Roxanne Nelson.
- Medscape Medical News. Oncology. 2013 Jun 21.
- News
- Free Full Text
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- Breast Cancer Gene Mutations More Common in Black Women.
- Johnson K.
- Medscape Medical News. Conference News. 2013 Jun 6.
- Conference report
- Free Full Text
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- Genetic breast cancer risk among black populations.
- Philippa Brice.
- PHG Foundation. 2013 Jun 4.
- News
- Free Full Text
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- Mutations in susceptibility genes common in younger African American women with breast cancer.
- John Easton.
- EurekAlert!. 2013 Jun 3.
- News
- Free Full Text
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- Breast cancer genes: beyond BRCA1 and BRCA2.
- Filippini SE, Vega A.
- Front Biosci (Landmark Ed). 2013 Jun 1;18:1358-72.
- PMID: 23747889
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Myriad to Replace BRACAnalysis, Other Hereditary Cancer Tests with MyRisk Panel.
- [No author given]
- GenomeWeb. 2013 May 9.
- News
- Free Full Text
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- Whole Exome Sequencing Suggests Much of Non-BRCA1/BRCA2 Familial Breast Cancer Is Due to Moderate and Low Penetrance Susceptibility Alleles.
- Gracia-Aznarez FJ, Fernandez V, Pita G, Peterlongo P, Dominguez O, de la Hoya M, Duran M, Osorio A, Moreno L, Gonzalez-Neira A, Rosa-Rosa JM, Sinilnikova O, Mazoyer S, Hopper J, Lazaro C, Southey M, Odefrey F, Manoukian S, Catucci I, Caldes T, Lynch HT, Hilbers FS, van Asperen CJ, Vasen HF, Goldgar D, Radice P, Devilee P, Benitez J.
- PLoS One. 2013;8(2):e55681. doi: 10.1371/journal.pone.0055681. Epub 2013 Feb 8.
- PMID: 23409019
- PubMed abstract
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- Inherited mutations in breast cancer genes in African American breast cancer patients revealed by targeted genomic capture and next-generation sequencing.
- Jane E. Churpek, Tom Walsh, Yonglan Zheng, Silvia Casadei, Anne M. Thornton, Ming K. Lee, Matthew Churpek, Dezheng Huo, Cecilia Zvosec, Fang Liu, Qun Niu, Jing Zhang, James Fackenthal, Mary-Claire King, Olufunmilayo I. Olopade.
- J Clin Oncol. 2013;31(Suppl): abstr CRA1501. 2013 ASCO Annual Meeting.
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- Personal genomic testing as part of the complete breast cancer risk assessment: a case report.
- Riordan S, Rodriguez DF, Kieran S.
- J Genet Couns. 2012 Oct;21(5):638-44. Epub 2012 May 19.
- PMID: 22610652
- PubMed abstract
- Source abstract
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- Exome Sequencing Identifies Rare Deleterious Mutations in DNA Repair Genes FANCC and BLM as Potential Breast Cancer Susceptibility Alleles.
- Thompson ER, Doyle MA, Ryland GL, Rowley SM, Choong DY, Tothill RW, Thorne H; kConFab, Barnes DR, Li J, Ellul J, Philip GK, Antill YC, James PA, Trainer AH, Mitchell G, Campbell IG.
- PLoS Genet. 2012 Sep;8(9):e1002894. doi: 10.1371/journal.pgen.1002894. Epub 2012 Sep 27.
- PMID: 23028338
- PubMed abstract
Comment:
Heterozygous mutations in DNA repair genes and hereditary breast cancer: a question of power.
- PMID: 23028381
- PubMed abstract
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- Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
- Johnston JJ, Rubinstein WS, Facio FM, Ng D, Singh LN, Teer JK, Mullikin JC, Biesecker LG.
- Am J Hum Genet. 2012 Jul 13;91(1):97-108. doi: 10.1016/j.ajhg.2012.05.021. Epub 2012 Jun 14.
- PMID: 22703879
- PubMed abstract
- Source abstract
Comments from NSGC Discussion Forum Cancer SIG
Subject: articles needed
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- BRCA1 and BRCA2 mutations among ovarian cancer patients from Colombia.
- Rodríguez AO, Llacuachaqui M, Pardo GG, Royer R, Larson G, Weitzel JN, Narod SA.
- Gynecol Oncol. 2012 Feb;124(2):236-43. doi: 10.1016/j.ygyno.2011.10.027. Epub 2011 Oct 29.
- PMID: 22044689
- PubMed abstract
- Source abstract