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- Unexpected Findings in Hereditary Breast and Ovarian Cancer Syndrome: Low-Level Constitutional Mosaicism in BRCA2.
- Mayoral I, Almeida Santiago A, Sánchez-Zapardiel JM, Hidalgo Calero B, de la Hoya M, Gómez-Sanz A, de Miguel Reyes M, Robles L.
- Genes (Basel). 2023 Feb 15;14(2):502. doi: 10.3390/genes14020502.
- Case report
- Free Full Text
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- Patient uptake of updated genetic testing following uninformative BRCA1 and BRCA2 results.
- Macklin-Mantia SK, Clift KE, Maimone S, Hodge DO, Riegert-Johnson D, Hines SL.
- J Genet Couns. 2022 Dec 7. doi: 10.1002/jgc4.1665. Epub ahead of print.
- PMID: 36478495
- PubMed abstract
- Source abstract
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- Testing a deliberative democracy method with citizens of African ancestry to weigh pros and cons of targeted screening for hereditary breast and ovarian cancer risk.
- Guan Y, Pathak S, Ballard D, Veluswamy JK, McCullough LE, McBride CM, Gornick MC.
- Front Public Health. 2022 Nov 8;10:984926. doi: 10.3389/fpubh.2022.984926.
- PMID: 36424974
- PubMed abstract
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- Genetic Testing Challenges in Oncology: Missed Variant Update Delays Li-Fraumeni Diagnosis.
- Ray T.
- Precision Oncology News. 2022 Oct 12.
- Case report
- Free Full Text
Special article:
Is there a duty to reinterpret genetic data? The ethical dimensions.
- PMID: 31616070
- PubMed abstract
- Free Full Text
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- Integrating hereditary breast and ovarian cancer genetic counselling and testing into mainstream clinical practice: Legal and ethical challenges.
- Charron M, Kaiser B, Dauge A, Gallois H, Lapointe J, Dorval M, Nabi H, Joly Y.
- Crit Rev Oncol Hematol. 2022 Oct;178:103797. doi: 10.1016/j.critrevonc.2022.103797. Epub 2022 Aug 27.
- PMID: 36031172
- PubMed abstract
- Source abstract
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- Investigating factors that influence genetic counselors' decisions to refer patients to mental health providers.
- Hayes T, Cunningham M, Trepanier A.
- J Genet Couns. 2022 Oct;31(5):1113-1124. doi: 10.1002/jgc4.1582. Epub 2022 Apr 23.
- PMID: 35460529
- PubMed abstract
- Source abstract
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- Effects of diet education on empowerment for individuals who have an increased risk of developing breast or colon cancer: A pilot study.
- Tlusty K, Jackson M, Riley B, Blase T.
- J Genet Couns. 2022 Oct;31(5):1138-1147. doi: 10.1002/jgc4.1584. Epub 2022 May 3.
- PMID: 35502599
- PubMed abstract
- Source abstract
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- Cross-sectional clinical cancer genomics community of practice survey analysis of provider attitudes and beliefs regarding the use of deceased family member tissue to guide living family member genetic cancer risk assessment.
- Nehoray B, Slavin TP, Sun CL, Hurley K, King E, Tsang KK, Cervantes A, Mokhnatkin JV, Sand S, Mejia R, Reb A, Samimi G, Gray S, Blazer KR, Weitzel JN.
- J Genet Couns. 2022 Oct;31(5):1164-1172. doi: 10.1002/jgc4.1587. Epub 2022 May 26.
- PMID: 35617031
- PubMed abstract
- Source abstract
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- Perspectives on Spanish language concordant cancer genetic counseling sessions from the Spanish-speaking population.
- Jimenez S, Matthews A, Darrah R, Schreiber A, Ricker C, Wolfe Schneider K.
- J Genet Couns. 2022 Sep 19. doi: 10.1002/jgc4.1628. Epub ahead of print.
- PMID: 36117419
- PubMed abstract
- Source abstract
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- Implementation and outcome evaluations of a multi-site improvement program in cancer genetics.
- Bednar EM, Harper B, Walsh MT Jr, Rechis R, Bilbao M, Carr RL, Eppolito AL, Goedde T, Levin B, Mattie K, Morman NA, Rath K, Russ P, Siettmann JM, Warshal D, Wise E, Yobbi C, Lu KH.
- J Genet Couns. 2022 Sep 19. doi: 10.1002/jgc4.1633. Epub ahead of print.
- PMID: 36117454
- PubMed abstract
- Source abstract
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- Constitutional Mosaicism: A Critical Issue in the Definition of BRCA-Inherited Cancer Risk.
- Tenedini E, Piana S, Toss A, Marino M, Barbieri E, Artuso L, Venturelli M, Gasparini E, Mandato VD, Marchi I, Castellano S, Luppi M, Trenti T, Cortesi L, Tagliafico E.
- JCO Precis Oncol. 2022 Aug [2022 Sep 8];6:e2200138. doi: 10.1200/PO.22.00138.
- PMID: 36075010
- PubMed abstract
- Source abstract
- Case report
- Free Full Text
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- Reclassification of clinically-detected sequence variants: Framework for genetic clinicians and clinical scientists by CanVIG-UK (Cancer Variant Interpretation Group UK).
- Loong L, Garrett A, Allen S, Choi S, Durkie M, Callaway A, Drummond J, Burghel GJ, Robinson R, Torr B, Berry IR, Wallace AJ, Eccles DM, Ellard S, Baple E, Evans DG, Woodward ER, Kulkarni A, Lalloo F, Tischkowitz M, Lucassen A, Hanson H, Turnbull C; CanVIG-UK.
- Genet Med. 2022 Sep;24(9):1867-1877. doi: 10.1016/j.gim.2022.05.002. Epub 2022 Jun 3.
- PMID: 35657381
- PubMed abstract
- Guideline
- Free Full Text
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- BRCA testing on buccal swab to improve access to healthcare and cancer prevention: a performance evaluation.
- De Paolis E, Perrucci A, Marchetti C, Pietragalla A, Scambia G, Urbani A, Fagotti A, Minucci A.
- Int J Gynecol Cancer. 2022 Aug 26:ijgc-2022-003718. doi: 10.1136/ijgc-2022-003718. Epub ahead of print.
- PMID: 36028233
- PubMed abstract
- Source abstract
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- Nijmegen Breakage Syndrome.
- Varon R, Demuth I, Chrzanowska KH.
- 1999 May 17 [updated 2022 Aug 18]. In: GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors.
- PMID: 20301355
- PubMed abstract
- Review
- Free Full Text
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- Dual BRCA1 and BRCA2 pathogenic variants in an adolescent with syndromic intellectual disability.
- Algouneh A, Caudle M, Balci T, Andrade A, Penava D, Saleh M.
- Clin Case Rep. 2022 Aug 8;10(8):e6202. doi: 10.1002/ccr3.6202.
- PMID: 35957765
- PubMed abstract
- Source abstract
- Case Report
- Free PMC article
- Free Full Text
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- Making BRCA1 genetic test reports easier to understand through user-centered design: A randomized trial.
- Recchia G, Lawrence ACE, Capacchione L, Freeman ALJ.
- Genet Med. 2022 Aug;24(8):1684-1696. doi: 10.1016/j.gim.2022.04.016. Epub 2022 May 6.
- PMID: 35522238
- PubMed abstract
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- Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients.
- Levin Fridman A, Raz A, Timmermans S, Shkedi-Rafid S.
- J Genet Couns. 2022 Aug;31(4):912-921. doi: 10.1002/jgc4.1560. Epub 2022 Feb 4.
- PMID: 35122362
- PubMed abstract
- Source abstract
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- Genetic counselors' experience with reimbursement and patient out-of-pocket cost for multi-cancer gene panel testing for hereditary cancer syndromes.
- Weldon CB, Trosman JR, Liang SY, Douglas MP, Scheuner MT, Kurian A, Schaa KL, Roscow B, Erwin D, Phillips KA.
- J Genet Couns. 2022 Jul 28. doi: 10.1002/jgc4.1614. Epub ahead of print.
- PMID: 35900261
- PubMed abstract
- Source abstract
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- Outcomes of retesting in patients with previously uninformative cancer genetics evaluations.
- Dettwyler SA, Koeppe ES, Jacobs MF, Stoffel EM.
- Fam Cancer. 2022 Jul;21(3):375-385. doi: 10.1007/s10689-021-00276-8. Epub 2021 Sep 21. Erratum in: Fam Cancer. 2021 Oct 28.
- PMID: 34545504
- PubMed abstract
- Source abstract
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- Evaluating Costs Associated With Genetic Counseling Among Commercially Insured US Patients With Cancer From 2013 to 2019.
- Roberson ML, Padi-Adjirackor NA, Hooker G, Pal T.
- JAMA Health Forum. 2022 Jul 29 [eCollection 2022 Jul];3(7):e222260. doi: 10.1001/jamahealthforum.2022.2260.
- PMID: 35983580
- PubMed abstract
- Source abstract
Research news: Genetic Counseling for Cancer Often Costs Patients Nothing. (Medscape Oncology)
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- Characterization of variant reclassification and patient re-contact in a cancer genetics clinic.
- Muir SM, Reagle R.
- J Genet Couns. 2022 Jun 28. doi: 10.1002/jgc4.1600. Epub ahead of print.
- PMID: 35763673
- PubMed abstract
- Source abstract
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- What Chris Evert’s Story Can Teach the World about Genetic Testing.
- Matloff ET.
- FORCE. Blog. 2022 Jun 22.
- Blog post
- Free Full Text
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- Advocating for equitable management of hereditary cancer syndromes.
- Caffrey RG.
- J Genet Couns. 2022 Jun;31(3):584-589. doi: 10.1002/jgc4.1548. Epub 2022 Jan 14.
- PMID: 35032082
- PubMed abstract
- Source abstract
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- Ethical, legal, and sociocultural challenges of genomic research in Jordan: a mixed methods study in patients with breast cancer with Jordanian-Palestinian heritage.
- Al-Omari A, Al-Hussaini M, Zahran F, Abdel-Razeq H.
- Lancet. 2022 Jun;399 Suppl 1:S26. doi: 10.1016/S0140-6736(22)01161-8.
- PMID: 35786261
- PubMed abstract
- Source abstract
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- Cancer Causative Mutations Occurring in Early Embryogenesis.
- Pareja F, Ptashkin RN, Brown DN, Derakhshan F, Selenica P, da Silva EM, Gazzo AM, Da Cruz Paula A, Breen K, Shen R, Marra A, Zehir A, Benayed R, Berger MF, Ceyhan-Birsoy O, Jairam S, Sheehan M, Patel U, Kemel Y, Casanova-Murphy J, Schwartz CJ, Vahdatinia M, Comen E, Borsu L, Pei X, Riaz N, Abramson DH, Weigelt B, Walsh MF, Hadjantonakis AK, Ladanyi M, Offit K, Stadler ZK, Robson ME, Reis-Filho JS, Mandelker D.
- Cancer Discov. 2022 Apr 1;12(4):949-957. doi: 10.1158/2159-8290.CD-21-1110.
- PMID: 34949653
- PubMed abstract
- Source abstract
Commentary:
Patchwork Cancer Predisposition.
- PMID: 35373283
- PubMed abstract
- Source abstract
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- Opinions and experiences of recontacting patients: a survey of Australasian genetic health professionals.
- Vora BB, Mountain H, Nichols C, Schofield L.
- J Community Genet. 2022 Apr;13(2):193-199. doi: 10.1007/s12687-021-00570-z. Epub 2022 Jan 11.
- PMID: 35013911
- PubMed abstract
- Source abstract
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- Uptake of genetic counseling and multi-gene panel testing among women in the Intermountain West with previous negative BRCA1 and BRCA2 results contacted for updated testing.
- Mooney R, Espinel W, Elrick A, Kehoe K, Kohlmann W, Kaphingst KA.
- J Genet Couns. 2022 Apr;31(2):470-478. doi: 10.1002/jgc4.1513. Epub 2021 Sep 27.
- PMID: 34570943
- PubMed abstract
- Source abstract
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- Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study.
- Richardson B, Fitzgerald-Butt SM, Spoonamore KG, Wetherill L, Helm BM, Breman AM.
- J Genet Couns. 2022 Apr;31(2):479-488. doi: 10.1002/jgc4.1514. Epub 2021 Sep 27.
- PMID: 34570930
- PubMed abstract
- Source abstract
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- Japanese women's reasons for accompaniment status to hereditary breast and ovarian cancer-focused genetic counseling.
- Matsukawa M, Torishima M, Satoh C, Honda S, Kosugi S.
- J Genet Couns. 2022 Apr;31(2):497-509. doi: 10.1002/jgc4.1519. Epub 2021 Oct 18.
- PMID: 34661949
- PubMed abstract
- Source abstract
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- Transforming the 2-week wait (2WW) pathway: management of breast pain in primary care.
- Jahan M, Bartholomeuz T, Milburn N, Rogers V, Sibbering M, Robertson J.
- BMJ Open Qual. 2022 Mar;11(1):e001634. doi: 10.1136/bmjoq-2021-001634.
- PMID: 35289304
- PubMed abstract
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- BRCA1/2 testing for genetic susceptibility to cancer after 25 years: A scoping review and a primer on ethical implications.
- Petrova D, Cruz M, Sánchez MJ.
- Breast. 2022 Feb;61:66-76. doi: 10.1016/j.breast.2021.12.005. Epub 2021 Dec 11.
- PMID: 34920368
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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- Polygenic risk in familial breast cancer: Changing the dynamics of communicating genetic risk.
- Gregory G, Das Gupta K, Meiser B, Barlow-Stewart K, Geelan-Small P, Kaur R, Scheepers-Joynt M, McInerny S, Taylor S, Antill Y, Salmon L, Smyth C, Young MA, James PA, Yanes T.
- J Genet Couns. 2022 Feb;31(1):120-129. doi: 10.1002/jgc4.1458. Epub 2021 Jul 5.
- PMID: 34223688
- PubMed abstract
- Source abstract
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- Tennis Star Chris Evert Teaches Us That Genetic Testing Is A Lifetime Match.
- Matloff E.
- Forbes. Healthcare. 2022 Jan 17.
- Commentary
- Free Full Text
News: Tennis Star Chris Evert Teaches Us That Genetic Testing Is a Lifetime Match. (My Gene Counsel)
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- Remote AI Supported E-Multidisciplinary Oncology Conference in Breast Cancer as a Technology and Method to Optimize Outcomes in the Peripheries.
- Mammas CS, Mamma AS, Papaxoinis G, Georgiou I.
- Stud Health Technol Inform. 2022 Jan 14;289:309-312. doi: 10.3233/SHTI210921.
- PMID: 35062154
- PubMed abstract
- Source abstract
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- A dangerous breast cancer gene mutation changed my life. As a health reporter, I want you to know about it. The PALB2 mutation is lesser-known than BRCA. It’s time to change that.
- Berger S.
- The Lily. (Washington Post). 2021 Dec 27.
- Press
- Free Full Text
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- Unselected Women's Experiences of Receiving Genetic Research Results for Hereditary Breast and Ovarian Cancer: A Qualitative Study.
- Forbes Shepherd R, Forrest LE, Tutty E, Pearce A, Devereux L, James PA, Campbell IG, Trainer A, Young MA.
- Genet Test Mol Biomarkers. 2021 Dec;25(12):741-748. doi: 10.1089/gtmb.2021.0115.
- PMID: 34918982
- PubMed abstract
- Source abstract
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- Fragmented responsibility: views of Israeli HCPs regarding patient recontact following variant reclassification.
- Fridman AL, Raz A, Timmermans S, Shkedi-Rafid S.
- J Community Genet. 2021 Oct 5:1–6. doi: 10.1007/s12687-021-00556-x. Epub ahead of print.
- PMID: 34609721
- PubMed abstract
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- Genetic counseling clinical documentation: Practice Resource of the National Society of Genetic Counselors.
- Hunt Brendish K, Patel D, Yu K, Alexander CK, Lemons J, Gunter A, Carmany EP.
- J Genet Couns. 2021 Oct;30(5):1336-1353. doi: 10.1002/jgc4.1491. Epub 2021 Aug 14.
- PMID: 34390070
- PubMed abstract
- Source abstract
- Guideline
- Free Full Text
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- Out-of-pocket and private pay in clinical genetic testing: a scoping review.
- Grant P, Langlois S, Lynd LD; GenCOUNSEL Study, Austin JC, Elliott AM.
- Clin Genet. 2021 Jun 3. doi: 10.1111/cge.14006. Epub ahead of print.
- PMID: 34080181
- PubMed abstract
- Source abstract
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- State of recent literature on communication about cancer genetic testing among Latinx populations.
- Chavez-Yenter D, Chou WS, Kaphingst KA.
- J Genet Couns. 2021 Jun;30(3):911-918. doi: 10.1002/jgc4.1351. Epub 2020 Nov 3.
- PMID: 33142015
- PubMed abstract
- Source abstract
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- Genetic Testing Challenges in Oncology: BRCA1-Positive Breast Cancer Patient Told She's Negative.
- Ray T.
- Precision Oncology News. Biomarkers. BRCA. 2021 Mar 26.
- Press, Case report
- Free Full Text
Blog post: Genetic Testing Challenges in Oncology: BRCA1-Positive Breast Cancer Patient Told She’s Negative. (My Gene Counsel)
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- Variations in breast cancer surgical treatment and timing: determinants and disparities.
- Dankwa-Mullan I, George J, Roebuck MC, Tkacz J, Willis VC, Reyes F, Arriaga YE.
- Breast Cancer Res Treat. 2021 Mar 10. doi: 10.1007/s10549-021-06155-1. Epub ahead of print.
- PMID: 33689057
- PubMed abstract
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- BRCA1/2 genes mutations, ovarian reserve and female reproductive outcomes: a systematic literature review.
- Merlino L, Chiné A, Galli C, Piccioni MG.
- Minerva Ginecol. 2020 Aug 3. doi: 10.23736/S0026-4784.20.04624-9. Epub ahead of print.
- PMID: 32744451
- PubMed abstract
- Source abstract
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- Genetic Testing Challenges in Oncology: False Positive After Testing at Pop-Up Booth.
- Ray T.
- Precision Oncology News. 2019 Dec 2.
- Case report, Press
- Free Full Text
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- Genetic counselors' comfort and knowledge of cancer risk assessment for transgender patients.
- Berro T, Zayhowski K, Field T, Channaoui N, Sotelo J.
- J Genet Couns. 2019 Sep 27. doi: 10.1002/jgc4.1172. [Epub ahead of print]
- PMID: 31562693
- PubMed abstract
- Source abstract
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- A family pedigree of malignancies associated with BRCA1 pathogenic variants: a reflection of the state of art in China.
- Li W, Li L, Wu M.
- Hered Cancer Clin Pract. 2019 Sep 10;17:26. doi: 10.1186/s13053-019-0126-4. eCollection 2019.
- PMID: 31516641
- PubMed abstract
- Case report
- Free PMC article
- Free Full Text
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- Familial disclosure by genetic healthcare professionals: a useful but sparingly used legal provision in France.
- Derbez B, de Pauw A, Stoppa-Lyonnet D, Galactéros F, de Montgolfier S.
- J Med Ethics. 2019 Aug 28. pii: medethics-2018-105212. doi: 10.1136/medethics-2018-105212. [Epub ahead of print]
- PMID: 31462451
- PubMed abstract
- Source abstract
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- Who's on third? Regulation of third-party genetic interpretation services.
- Guerrini CJ, Wagner JK, Nelson SC, Javitt GH, McGuire AL.
- Genet Med. 2019 Aug 12. doi: 10.1038/s41436-019-0627-6. [Epub ahead of print]
- PMID: 31402353
- PubMed abstract
- Source abstract
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- CancerIQ, GeneMatters Integrate Technology to Widen Access to Genetic Counselors.
- [No author given]
- GenomeWeb. 2019 Jun 27.
- News
- Free Full Text
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- Cancer genetic counselors' experiences with transgender patients: A qualitative study.
- Zayhowski K, Park J, Boehmer U, Gabriel C, Berro T, Campion M.
- J Genet Couns. 2019 Jun;28(3):641-653. doi: 10.1002/jgc4.1092. Epub 2019 Feb 5.
- PMID: 30720922
- PubMed abstract
- Source abstract
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- Trans-counseling: A case series of transgender individuals at high risk for BRCA1 pathogenic variants.
- Sacca RE, Koeller DR, Rana HQ, Garber JE, Morganstern DE.
- J Genet Couns. 2019 Jun;28(3):708-716. doi: 10.1002/jgc4.1046. Epub 2019 Jan 24.
- PMID: 30680866
- PubMed abstract
- Source abstract
- Case report
- Free Full Text
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- Hospital apologises to woman given wrong test result for breast cancer gene.
- [No author given]
- The Irish Times. 2019 May 29.
- Press
- Free Full Text
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- BRCA Exchange Launches.
- [No authors listed]
- Cancer Discov. 2019 Mar;9(3):311-312. doi: 10.1158/2159-8290.CD-NB2019-008. Epub 2019 Jan 24.
- PMID: 30679172
- PubMed abstract
- Source abstract
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- A comparison of cancer risk assessment and testing outcomes in patients from underserved vs. tertiary care settings.
- Rana HQ, Cochrane SR, Hiller E, Akindele RN, Nibecker CM, Svoboda LA, Cronin AM, Garber JE, Lathan CS.
- J Community Genet. 2018 Jul;9(3):233-241. doi: 10.1007/s12687-017-0347-z. Epub 2017 Nov 18.
- PMID: 29151150
- PubMed abstract
- Source abstract
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- A Trans-Feminine Youth with a BRCA1 Mutation: Case Study.
- Wolf-Gould CS, Riley MR, Carswell JM.
- LGBT Health. 2018 May/Jun;5(4):270-272. doi: 10.1089/lgbt.2017.0148. Epub 2018 May 11.
- PMID: 29750596
- PubMed abstract
- Source abstract
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- Racial/Ethnic Disparities in BRCA Counseling and Testing: a Narrative Review.
- Williams CD, Bullard AJ, O'Leary M, Thomas R, Redding TS 4th, Goldstein K.
- J Racial Ethn Health Disparities. 2019 Apr 8. doi: 10.1007/s40615-018-00556-7. [Epub ahead of print]
- PMID: 30963508
- PubMed abstract
- Source abstract
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- The Right Not to Know: When Ignorance Is Bliss but Deadly.
- Clausen AM.
- Global Health NOW. 2018 Mar 20.
Commentary: The right not to know when not knowing is dangerous. (FORCE. XRAYS.)
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- Medical Strategy or Marketing Strategy?
- Resta R.
- The DNA Exchange. 2018 Mar 18.
- Blog post
- Free Full Text
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- Impact of a genetic counseling requirement prior to genetic testing.
- Stenehjem DD, Au T, Sainski AM, Bauer H, Brown K, Lancaster J, Stevens V, Brixner DI.
- BMC Health Serv Res. 2018 Mar 7;18(1):165. doi: 10.1186/s12913-018-2957-5.
- PMID: 29514700
- PubMed abstract
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- Assessment of Current Genetic Counselor Practices in Post-Visit Written Communications to Patients.
- VandenBoom E, Trepanier AM,Carmany EP.
- J Genet Couns. 2017 Oct 12. doi: 10.100/s10897-017-0163-y. [Epub ahead of print]
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- The Impact of Mental Illness on Uptake of Genetic Counseling for Hereditary Breast Cancer and Ovarian Cancer in a Multiethnic Cohort of Breast Cancer Patients.
- Ackerman MG, Shapiro PA, Coe A, Trivedi MS, Crew KD.
- Breast J. 2017 Sep;23(5):519-524. doi: 10.1111/tbj.12791. Epub 2017 Mar 21.
- PMID: 28323373
- PubMed abstract
- Source abstract
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- Large, Prospective Analysis of the Reasons Patients Do Not Pursue BRCA Genetic Testing Following Genetic Counseling.
- Hayden S, Mange S, Duquette D, Petrucelli N, Raymond VM; BRCA Clinical Network Partners.
- J Genet Couns. 2017 Aug;26(4):859-865. doi: 10.1007/s10897-016-0064-5. Epub 2017 Jan 16.
- PMID: 28093663
- PubMed abstract
- Source abstract
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- Impact of Payer Constraints on Access to Genetic Testing.
- Whitworth P, Beitsch P, Arnell C, Cox HC, Brown K, Kidd J, Lancaster JM.
- J Oncol Pract. 2017 Jan;13(1):e47-e56. doi: 10.1200/JOP.2016.013581. Epub 2016 Oct 23.
- PMID: 28084878
- PubMed abstract
- Source abstract
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- Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?
- Cragun D, Scherr C, Camperlengo L, Vadaparampil ST, Pal T.
- Genet Test Mol Biomarkers. 2016 Oct;20(10):569-578. Epub 2016 Aug 15.
- PMID: 27525501
- PubMed abstract
- Source abstract
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- Methods to identify BRCA testing in claims data.
- Lynch J, Berse B.
- Am J Obstet Gynecol. 2016 Jul;215(1):133-4. doi: 10.1016/j.ajog.2016.03.049. Epub 2016 Apr 12.
- PMID: 27083760
- PubMed abstract
- Source abstract
- Letter
- Free Full Text
Letter / Reply:
Reply.
- PMID: 27060422
- PubMed abstract
- Source abstract
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- Evolution of cancer risk assessment and counseling related to psychological, financial and legal implications.
- Snyder C.
- Fam Cancer. 2016 Jul;15(3):493-6. doi: 10.1007/s10689-016-9890-8.
- PMID: 26920353
- PubMed abstract
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- Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital.
- Palmero EI, Galvão HC, Fernandes GC, Paula AE, Oliveira JC, Souza CP, Andrade CE, Romagnolo LG, Volc S, C Neto M, Sabato C, Grasel R, Mauad E, Reis RM, Michelli RA.
- Genet Mol Biol. 2016 May 13;39(2):168-177. doi: 10.1590/1678-4685-GMB-2014-0364.
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- More People Seek Genetic Testing, But There Aren't Enough Counselors.
- Todd Bookman.
- NPR. Morning Edition. 2016 Apr 18.
- News, Audio/Transcript
- Free Full Text
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- DAKOTACARE Update: Genetic Counseling Requirement for BRCA 1/2 Testing.
- Amundson EP, Jamison S.
- S D Med. 2016 Jan;69(1):36.
- PMID: 26882582
- PubMed abstract
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- Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing.
- Scherr CL, Lindor NM, Malo TL, Couch FJ, Vadaparampil ST.
- Clin Genet. 2015 Dec;88(6):523-9. doi: 10.1111/cge.12563. Epub 2015 Feb 26.
- PMID: 25640009
- PubMed abstract
- Source abstract
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- Genetics and Cancer Risk: More options, more tests, more prevention, more survivors.
- Billie J. Marek.
- The Monitor. 2015 Jun 25.
- Press article
- Free Full Text
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- Genetic counseling for fanconi anemia: crosslinking disciplines.
- Zierhut HA, Tryon R, Sanborn EM.
- J Genet Couns. 2014 Dec;23(6):910-21. doi: 10.1007/s10897-014-9754-z. Epub 2014 Sep 20.
- PMID: 25236480
- PubMed abstract
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Research news: Fanconi Anemia: Genetic Counseling Research (Perspectives in Genetic Counseling)
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- Identifying hereditary cancer: genetic counseling and cancer risk assessment.
- Lewis KM.
- Curr Probl Cancer. 2014 Nov-Dec;38(6):216-25. doi: 10.1016/j.currproblcancer.2014.10.002. Epub 2014 Oct 29.
- PMID: 25432528
- PubMed abstract
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- Medical genetic counseling for breast cancer in primary care: a synthesis of major determinants of physicians' practices in primary care settings.
- Jbilou J, Halilem N, Blouin-Bougie J, Amara N, Landry R, Simard J.
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- Fanconi anaemia, BRCA2 mutations and childhood cancer: a developmental perspective from clinical and epidemiological observations with implications for genetic counselling.
- Meyer S, Tischkowitz M, Chandler K, Gillespie A, Birch JM, Evans DG.
- J Med Genet. 2014 Feb;51(2):71-5. doi: 10.1136/jmedgenet-2013-101642. Epub 2013 Nov 20.
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- U.S. Preventive Services Task Force Finds Benefit in Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer for Small Group of High-Risk Women.
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- Yale Cancer Genetic Counseling. 2014 Jan 2.
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- A Myriad of Choices: How the Supreme Court’s Decision Has Affected Clinical Practice.
- Kristen Hanson.
- Perspectives in Genetic Counseling. 35(4):6-7. 2013 Qtr 4.
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- Star Power.
- Robert Resta.
- The DNA Exchange. 2013 Jun 16.
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- Using core public health functions to promote BRCA best practices among health plans.
- Duquette D, Lewis K, McLosky J, Bach J.
- Public Health Genomics. [2012 Jan;]15(2):92-7. doi: 10.1159/000334267. Epub 2011 Dec 20.
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