Methods, tools, sessions beyond the traditional approach to HBOC genetic counseling and testing; includes test result disclosure alternatives, telegenetics, group counseling, video-teleconferencing, online counseling, etc. Also includes papers covering situations in which there may be little, no, or insufficient provision of genetic counseling, as in some circumstances of direct-to-consumer genetic testing, provision of testing by unqualified providers, etc.
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- Improving Uptake of Cancer Genetic Risk Assessment in a Remote Tailored Risk Communication and Navigation Intervention: Large Effect Size but Room to Grow.
- Kinney AY, Walters ST, Lin Y, Lu SE, Kim A, Ani J, Heidt E, Le Compte CJG, O'Malley D, Stroup A, Paddock LE, Grumet S, Boyce TW, Toppmeyer DL, McDougall JA.
- J Clin Oncol. 2023 Feb 14:JCO2200751. doi: 10.1200/JCO.22.00751. Epub ahead of print.
- PMID: 36787512
- PubMed abstract
•• Identifier: NCT03326713: Genetic Risk Assessment for Cancer Education and Empowerment (GRACE) Project (GRACE). (ClinicalTrials.gov . Accessed 2023 Feb 14.)
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- Mainstream genetic testing for high-grade ovarian, tubal and peritoneal cancers: A tertiary referral centre experience.
- Srinivasa S, Bowman M, Titterton L, Harnett P, Brand A, Kirk J, Ragunathan A.
- Aust N Z J Obstet Gynaecol. 2023 Feb 13. doi: 10.1111/ajo.13650. Epub ahead of print.
- PMID: 36785489
- PubMed abstract
- Source abstract
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- Implementing digital systems to facilitate genetic testing for hereditary cancer syndromes: An observational study of four clinical workflows.
- Wang C, Lu H, Bowen DJ, Xuan Z.
- Genet Med. 2023 Feb 10:S1098-3600(23)00815-8. doi: 10.1016/j.gim.2023.100802. Epub ahead of print.
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- Socioeconomic Factors Are Associated With Disparities in Germline Testing in Pancreatic Cancer.
- King D, Scott R.
- OncLive. 2023 Feb 5.
- Conference report, Interview
- Free Full Text
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- Proactive breast cancer risk assessment in primary care: a review based on the principles of screening.
- Usher-Smith JA, Hindmarch S, French DP, Tischkowitz M, Moorthie S, Walter FM, Dennison RA, Stutzin Donoso F, Archer S, Taylor L, Emery J, Morris S, Easton DF, Antoniou AC.
- Br J Cancer. 2023 Feb 3:1–11. doi: 10.1038/s41416-023-02145-w. Epub ahead of print.
- PMID: 36737659
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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- Cultural adaptations to a telephone genetic counseling protocol and booklet for Latina breast cancer survivors at risk for hereditary breast and ovarian cancer.
- Gómez-Trillos S, Graves KD, Fiallos K, Schwartz MD, Peshkin BN, Hamilton H, Sheppard VB, Vadaparampil ST, Campos C, Cupertino AP, Alzamora MC, Lynce F, Hurtado-de-Mendoza A.
- Transl Behav Med. 2023 Jan 24:ibac106. doi: 10.1093/tbm/ibac106. Epub ahead of print.
- PMID: 36694918
- PubMed abstract
- Source abstract
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- Innovative approaches to expanding cancer genetic testing in Michigan (project might). [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Stoffel EM, Austin S, Koeppe E, Hanson EN, Delacroix E, Rizzo E, Griggs JJ, Resnicow K.
- Fam Cancer. [P-17: Research Categories» Delivery of Care and Alternative Models.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Performance of INHERET® risk assessment tool for identifying pathogenic germline variants among individuals referred for cancer genetics evaluation. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Henry ML, Pialtos K, Fry S, Koeppe E, Osborne J, Cook A, Hulswitt B, Milliron KJ, Merajver S, Stoffel E.
- Fam Cancer. [P-21: Research Categories» Delivery of Care and Alternative Models.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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- Genetic Testing Challenges in Oncology: Patient With Pending Bill Has BRCA1 Result Withheld.
- Ray T.
- Precision Oncology News. 2023 Jan 23.
- Case report
- Free Full Text
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- Racial Differences in Germline Genetic Testing for Prostate Cancer: A Systematic Review.
- Briggs LG, Steele GL, Qian ZJ, Subbana S, Alkhatib KY, Labban M, Langbein BJ, Nguyen DD, Cellini J, Kilbridge K, Kibel AS, Trinh QD, Rana HQ, Cole AP.
- JCO Oncol Pract. 2023 Jan 12:OP2200634. doi: 10.1200/OP.22.00634. Epub ahead of print.
- PMID: 36649495
- PubMed abstract
- Source abstract
•• Commentary:
Germline Testing in Prostate Cancer: Implementation and Disparities of Care.
- PMID: 36720077
- PubMed abstract
- Free Full Text
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- Implementation of a Telehealth Genetic Testing Station to Deliver Germline Testing for Men With Prostate Cancer.
- Kwon DH, Gordon KM, Tong B, Borno HT, Beigh M, Fattah D, Schleicher A, Aggarwal RR, Blanco AM, Small EJ, Dhawan M.
- JCO Oncol Pract. 2023 Jan 12:OP2200638. doi: 10.1200/OP.22.00638. Epub ahead of print.
- PMID: 36649492
- PubMed abstract
- Source abstract
•• Commentary:
Germline Testing in Prostate Cancer: Implementation and Disparities of Care.
- PMID: 36720077
- PubMed abstract
- Free Full Text
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- High-dose chemotherapy with stem cell rescue to treat stage III homologous deficient breast cancer: factors influencing clinical implementation.
- Verbeek JGE, de Jong VMT, Wijnja HM, Jager A, Linn SC, Retèl VP, van Harten WH.
- BMC Cancer. 2023 Jan 7;23(1):26. doi: 10.1186/s12885-022-10412-x.
- PMID: 36611165
- PubMed abstract
- Guideline
- Free Full Text
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- Internet-Based Germline Genetic Testing for Men With Metastatic Prostate Cancer.
- Cheng HH, Sokolova AO, Gulati R, Bowen D, Knerr SA, Klemfuss N, Grivas P, Hsieh A, Lee JK, Schweizer MT, Yezefski T, Zhou A, Yu EY, Nelson PS, Montgomery B.
- JCO Precis Oncol. 2023 Jan;7:e2200104. doi: 10.1200/PO.22.00104.
- PMID: 36623239
- PubMed abstract
- Source abstract
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- Outcomes of Universal Point-of-Care Genetic Testing in Diverse Patients With Pancreatic Ductal Adenocarcinoma.
- Drogan CM, Kindler HL, Gao G, Kupfer SS.
- JCO Precis Oncol. 2023 Jan;7:e2200196. doi: 10.1200/PO.22.00196.
- PMID: 36689696
- PubMed abstract
- Source abstract
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- Clinical Cancer and Direct-to-Consumer Genetic Test Result-Sharing Behavior: Findings from HINTS 2020.
- Makhnoon S, Yu R, Peterson SK, Shete S.
- J Pers Med. 2022 Dec 22;13(1):18. doi: 10.3390/jpm13010018.
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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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- Does mainstream BRCA testing affect surgical decision-making in newly-diagnosed breast cancer patients?
- Ain Q, Richardson C, Mutebi M, George A, Kemp Z, Rusby JE.
- Breast. 2022 Dec 6:S0960-9776(22)00193-X. doi: 10.1016/j.breast.2022.12.001. Epub ahead of print.
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- A digital pathway for genetic testing in UK NHS patients with cancer: BRCA-DIRECT randomised study internal pilot.
- Torr B, Jones C, Choi S, Allen S, Kavanaugh G, Hamill M, Garrett A, MacMahon S, Loong L, Reay A, Yuan L, Valganon Petrizan M, Monson K, Perry N, Fallowfield L, Jenkins V, Gold R, Taylor A, Gabe R, Wiggins J, Lucassen A, Manchanda R, Gandhi A, George A, Hubank M, Kemp Z, Evans DG, Bremner S, Turnbull C.
- J Med Genet. 2022 Dec;59(12):1179-1188. doi: 10.1136/jmg-2022-108655. Epub 2022 Jul 22.
- PMID: 35868849
- PubMed abstract
•• Trial registration number: ISRCTN87845055: BRCA-DIRECT- Is digitally delivered information about genetic testing feasible, effective and acceptable to women with breast cancer?. (ISRCTN registry)
•• Press: UK Pilot Study Suggests Digital Pathway May Expand BRCA Testing in Breast Cancer. (GenomeWeb)
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- Halo Diagnostics, Ikonopedia Partner to Provide Genetic Testing for Breast Cancer.
- [No author given]
- Precision Oncology News. 2022 Nov 28.
- News
- Free Full Text
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- UK Pilot Study Suggests Digital Pathway May Expand BRCA Testing in Breast Cancer.
- [No author given]
- GenomeWeb. The Scan. 2022 Nov 23.
- News
- Free Full Text
•• Original research:
A digital pathway for genetic testing in UK NHS patients with cancer: BRCA-DIRECT randomised study internal pilot.
- PMID: 35868849
- PubMed abstract
- Free Full Text
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- Development of a web-based, theory-guided narrative intervention for women at elevated risk for breast cancer.
- Katz ML, Senter L, Reiter PL, Emerson B, Ennis AC, Shane-Carson KP, Aeilts A, Cassingham HR, Schnell PM, Agnese DM, Toland AE, Sweet K.
- Patient Educ Couns. 2022 Oct 29:S0738-3991(22)00820-5. doi: 10.1016/j.pec.2022.10.348. Epub ahead of print.
- PMID: 36333195
- PubMed abstract
- Source abstract
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- Nest Genomics Building EHR-Integrated Clinical Decision Support for Genetics-Informed Care.
- Cohen JK.
- GenomeWeb. Disease Areas. Cancer. 2022 Oct 25.
- News
- Source abstract
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- Germline Genetic Testing in Breast Cancer: Systemic Therapy Implications.
- Bhardwaj PV, Abdou YG.
- Curr Oncol Rep. 2022 Oct 18. doi: 10.1007/s11912-022-01340-x. Epub ahead of print.
- PMID: 36255604
- PubMed abstract
- Source abstract
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- An Accessible Communication System for Population-Based Genetic Testing: Development and Usability Study.
- Coffin T, Bowen D, Swisher E, Lu K, Rayes N, Norquist B, Blank S, Levine D, Bakkum-Gamez J, Fleming G, Olopade O, D'Andrea A, Nebgen D, Peterson C, Munsell M, Gavin K, Lechner R, Crase J, Polinsky D, Romero I.
- JMIR Form Res. 2022 Oct 17;6(10):e34055. doi: 10.2196/34055.
- PMID: 36251350
- PubMed abstract
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- Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome?
- Kahn RM, Ahsan MD, Chapman-Davis E, Holcomb K, Nitecki R, Rauh-Hain JA, Fowlkes RK, Tubito F, Pires M, Christos PJ, Tkachuk K, Krinsky H, Sharaf RN, Offit K, Lipkin S, Frey MK.
- Fam Cancer. 2022 Oct 8. doi: 10.1007/s10689-022-00316-x. Epub ahead of print.
- PMID: 36207653
- PubMed abstract
- Source abstract
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- Genetic testing for patients at risk of hereditary breast and ovarian cancer.
- DeTroye A, Gabbett K, Yi C, Judice M, Luu V, Nelson B, Gregory T.
- JAAPA. 2022 Oct 1;35(10):48-52. doi: 10.1097/01.JAA.0000873796.81961.da.
- PMID: 36165549
- PubMed abstract
- Source abstract
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- Evaluation of a mainstream genetic testing program for women with ovarian or breast cancer.
- Ip E, Young AL, Scheinberg T, Harrison M, Beale P, Goodwin A.
- Asia Pac J Clin Oncol. 2022 Oct;18(5):e414-e419. doi: 10.1111/ajco.13741. Epub 2022 Jan 30.
- PMID: 35098668
- PubMed abstract
- Source abstract
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- Talking about Risk, UncertaintieS of Testing IN Genetics (TRUSTING): development and evaluation of an educational programme for healthcare professionals about BRCA1 & BRCA2 testing.
- Fallowfield L, Solis-Trapala I, Starkings R, May S, Matthews L, Eccles D, Evans DG, Turnbull C, Crawford G, Jenkins V.
- Br J Cancer. 2022 Oct;127(6):1116-1122. doi: 10.1038/s41416-022-01871-x. Epub 2022 Jun 17.
- PMID: 35715636
- PubMed abstract
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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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- Mainstream germline genetic testing for patients with epithelial ovarian cancer leads to higher testing rates and a reduction in genetics-related healthcare costs from a healthcare payer perspective.
- Bokkers K, Frederix GWJ, Velthuizen ME, van der Aa M, Gerestein CG, van Dorst EBL, Lange JG, Louwers JA, Koole W, Zweemer RP, Ausems MGEM.
- Gynecol Oncol. 2022 Oct;167(1):115-122. doi: 10.1016/j.ygyno.2022.08.011. Epub 2022 Aug 26.
- PMID: 36031452
- PubMed abstract
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- Attitudes and training needs of oncologists and surgeons in mainstreaming breast cancer genetic counseling in a low-to-middle income Asian country.
- Lee YQ, Yoon SY, Hassan T, Padmanabhan H, Yip CH, Keng WT, Thong MK, Ahmad Annuar MA, Mohd Taib NA, Teo SH.
- J Genet Couns. 2022 Oct;31(5):1080-1089. doi: 10.1002/jgc4.1579. Epub 2022 Apr 28.
- PMID: 35481858
- 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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- Low BRCA1 and BRCA2 Germline Mutation Rates in a French-Canadian Population with a Diagnosis of Epithelial Tubo-Ovarian Carcinoma.
- Bernard J, Mehros W, Gregoire J, Douville P, Renaud MC, Sebastianelli A, Langlais EL, Plante M.
- J Obstet Gynaecol Can. 2022 Oct;44(10):1047-1053. doi: 10.1016/j.jogc.2022.06.005. Epub 2022 Jun 30.
- PMID: 35779836
- PubMed abstract
- Source abstract
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- Returning individual genomic results to population-based cohort study participants with BRCA1/2 pathogenic variants.
- Ohneda K, Hamanaka Y, Kawame H, Fuse N, Nagami F, Suzuki Y, Yamaguchi-Kabata Y, Shimada M, Masamune A, Aoki Y, Ishida T, Yamamoto M.
- Breast Cancer. 2022 Sep 26. doi: 10.1007/s12282-022-01404-7. Epub ahead of print.
- PMID: 36161580
- PubMed abstract
- Source abstract
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- Patient-facing digital tools for delivering genetic services: a systematic review.
- Lee W, Shickh S, Assamad D, Luca S, Clausen M, Somerville C, Tafler A, Shaw A, Hayeems R, Bombard Y, Genetics Navigator Study Team.
- J Med Genet. 2022 Sep 22:jmedgenet-2022-108653. doi: 10.1136/jmg-2022-108653. Epub ahead of print.
- PMID: 36137613
- 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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- Universal Germline Genetic Testing for Hereditary Cancer Syndromes in Patients With Solid Tumor Cancer.
- Esplin ED, Nielsen SM, Bristow SL, Garber JE, Hampel H, Rana HQ, Samadder NJ, Shore ND, Nussbaum RL.
- JCO Precis Oncol. 2022 Sep [2022 Sep 15];6:e2100516. doi: 10.1200/PO.21.00516.
- PMID: 36108258
- PubMed abstract
- Source abstract
- Commentary
- Free Full Text
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- Mainstream genetic testing for women with ovarian cancer provides a solid basis for patients to make a well-informed decision about genetic testing.
- Bokkers K, Bleiker EMA, Hoogendam JP, Velthuizen ME, Schreuder HWR, Gerestein CG, Lange JG, Louwers JA, Koudijs MJ, Ausems MGEM, Zweemer RP.
- Hered Cancer Clin Pract. 2022 Sep 8;20(1):33. doi: 10.1186/s13053-022-00238-w.
- PMID: 36076240
- PubMed abstract
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- Current status of hereditary breast and ovarian cancer practice among gynecologic oncologists in Japan: a nationwide survey by the Japan Society of Gynecologic Oncology (JSGO).
- Kobayashi Y, Masuda K, Hiraswa A, Takehara K, Tsuda H, Watanabe Y, Oda K, Nagase S, Mandai M, Okamoto A, Yaegashi N, Mikami M, Enomoto T, Aoki D, Katabuchi H; Working Group on Clinical Practice for Cancer Genomic Medicine and HBOC, Japan Society of Gynecologic Oncology.
- J Gynecol Oncol. 2022 Sep;33(5):e61. doi: 10.3802/jgo.2022.33.e61. Epub 2022 Jul 18.
- PMID: 35882604
- PubMed abstract
- Source abstract
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- Disparities in germline testing among racial minorities with prostate cancer.
- Weise N, Shaya J, Javier-Desloges J, Cheng HH, Madlensky L, McKay RR.
- Prostate Cancer Prostatic Dis. 2022 Sep;25(3):403-410. doi: 10.1038/s41391-021-00469-3. Epub 2021 Nov 13.
- PMID: 34775478
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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- An evidence-based practice guideline of the National Society of Genetic Counselors for telehealth genetic counseling.
- Green S, Hartzfeld D, Terry AB, Fissell K, Friedman S, Paolino N, Principe K, Sandbach J, Trzupek K, Winheld S, Malinowski J.
- J Genet Couns. 2022 Aug 30. doi: 10.1002/jgc4.1627. Epub ahead of print.
- PMID: 36054686
- PubMed abstract
- Source abstract
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- Experience with a nurse-driven genetic counseling pathway of Italian women with uninformative BRCA test result.
- Blondeaux E, Lambertini M, Buzzatti G, Bruzzone C, Baraga M, Pisani R, Del Mastro L, Pronzato P, Varesco L, Bonelli L.
- J Genet Couns. 2022 Aug 29. doi: 10.1002/jgc4.1630. Epub ahead of print.
- PMID: 36036895
- PubMed abstract
- Source abstract
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- A pilot study investigating feasibility of mainstreaming germline BRCA1 and BRCA2 testing in high-risk patients with breast and/or ovarian cancer in three tertiary Cancer Centres in Ireland.
- McVeigh TP, Sweeney KJ, Brennan DJ, McVeigh UM, Ward S, Strydom A, Seal S, Astbury K, Donnellan P, Higgins J, Keane M, Kerin MJ, Malone C, McGough P, McLaughlin R, O'Leary M, Rushe M, Barry MK, MacGregor G, Sugrue M, Yousif A, Al-Azawi D, Berkeley E, Boyle TJ, Connolly EM, Nolan C, Richardson E, Giffney C, Doyle SB, Broderick S, Boyd W, McVey R, Walsh T, Farrell M, Gallagher DJ, Rahman N, George AJ.
- Fam Cancer. 2022 Aug 27. doi: 10.1007/s10689-022-00313-0. Epub ahead of print.
- PMID: 36029389
- PubMed abstract
- Source abstract
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- GeneHome - a Novel Model to Deliver Care to Individuals with Genetic Predisposition to Cancer.
- Nocera Zachariah N, Lee MC, Chang MD, Moore C, Wang X.
- Cancer Control. 2022 Jan-Dec [First published 2022 Aug 17];29:10732748221109951. doi: 10.1177/10732748221109951.
- PMID: 35976772
- PubMed abstract
- Source abstract
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- JSCREEN and K.I.C.K Partner to Kick Cancer with Genetic Testing.
- Kickel Hernandez K.
- FORCE. Blog. 2022 Aug 16.
- Blog post
- Free Full Text
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- Cascade Testing for Hereditary Cancer Syndromes: Should We Move Toward Direct Relative Contact? A Systematic Review and Meta-Analysis.
- Frey MK, Ahsan MD, Bergeron H, Lin J, Li X, Fowlkes RK, Narayan P, Nitecki R, Rauh-Hain JA, Moss HA, Baltich Nelson B, Thomas C, Christos PJ, Hamilton JG, Chapman-Davis E, Cantillo E, Holcomb K, Kurian AW, Lipkin S, Offit K, Sharaf RN.
- J Clin Oncol. 2022 Aug 12:JCO2200303. doi: 10.1200/JCO.22.00303. Epub ahead of print.
- PMID: 35960887
- PubMed abstract
- Source abstract
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- Evaluating the Effectiveness of a Telehealth Cancer Genetics Program: A BRCA Pilot Study.
- Rose E, Hardy MW, Gates R, Stanislaw C, Meisel J, Grinzaid KA.
- Public Health Genomics. 2022 Aug 9:1-14. doi: 10.1159/000525658. Epub ahead of print.
- PMID: 35944511
- PubMed abstract
- Source abstract
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- Training promotores to lead virtual hereditary breast cancer education sessions for Spanish-speaking individuals of Latin American heritage in California.
- Reyna M, Almeida R, Lopez-Macha A, Fuller S, Duron Y, Fejerman L.
- BMC Womens Health. 2022 Aug 8;22(1):336. doi: 10.1186/s12905-022-01902-y.
- PMID: 35941639
- PubMed abstract
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- A Woman Needs to Know She Is a BRCA Carrier Before She Develops Breast Cancer.
- Hughes KS, Yin K.
- Ann Surg Oncol. 2022 Aug;29(8):4667-4669. doi: 10.1245/s10434-022-11860-2. Epub 2022 May 12.
- PMID: 35552928
- PubMed abstract
- Commentary
- Free Full Text
Original research:
Comparison of Outcomes Between BRCA Pathogenic Variant Carriers Undergoing Breast-Conserving Surgery Versus Mastectomy.
- PMID: 35585432
- PubMed abstract
- Source abstract
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- Relatively Speaking: COVID-19’s Impact on Cancer Screenings and Genetic Counseling Services.
- Haidle JL.
- Inside Precision Medicine. 2022 Aug 16 [2022 Aug];9(4).
- Commentary
- Free Full Text
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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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- Germline genetics of prostate cancer.
- Khan HM, Cheng HH.
- Prostate. 2022 Aug;82 Suppl 1:S3-S12. doi: 10.1002/pros.24340.
- PMID: 35657157
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Impact of comprehensive family history and genetic analysis in the multidisciplinary pancreatic tumor clinic setting.
- Everett JN, Dettwyler SA, Jing X, Stender C, Schmitter M, Baptiste A, Chun J, Kawaler EA, Khanna LG, Gross SA, Gonda TA, Beri N, Oberstein PE, Simeone DM.
- Cancer Med. 2022 Jul 30. doi: 10.1002/cam4.5059. Epub ahead of print.
- PMID: 35906821
- PubMed abstract
- Source abstract
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- Survey on implementation of molecular testing in ovarian cancer and PARP inhibitor: a national North-Eastern German Society of Gynecologic Oncology/Young Academy of Gynecologic Oncology/Arbeitsgemeinschaft Gynäkologische Onkologie intergroup analysis.
- Nguyen-Sträuli BD, Baum J, Meyer-Wilmes P, Kreklau A, Buschmann C, El Ouardi N, Fotopoulou C, Hummel M, Chekerov R, Braicu E, Sehouli J, Pietzner K.
- Int J Gynecol Cancer. 2022 Jul 27:ijgc-2022-003637. doi: 10.1136/ijgc-2022-003637. Epub ahead of print.
- PMID: 35896275
- PubMed abstract
- Source abstract
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- An Electronic Health Record Tool Increases Genetic Counseling Referral of Individuals at Hereditary Cancer Risk: An Intervention Study.
- Wurtmann EJ, Baldinger S, Olet S, Daley A, Swenson KK.
- Public Health Genomics. 2022 Jul 27:1-7. doi: 10.1159/000525447. Epub ahead of print.
- PMID: 35896061
- PubMed abstract
- Source abstract
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- Remote vs in-person BRCA1/2 non-carriers test disclosure: patients' choice during Covid-19 pandemic restriction.
- Costanzo S, De Summa S, Maurmo L, Digennaro M, Patruno M, Paradiso A.
- Fam Cancer. 2022 Jul 22. doi: 10.1007/s10689-022-00307-y. Epub ahead of print.
- PMID: 35867288
- PubMed abstract
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- Precise, Genotype-First Breast Cancer Prevention: Experience With Transferring Monogenic Findings From a Population Biobank to the Clinical Setting.
- Jürgens H, Roht L, Leitsalu L, Nõukas M, Palover M, Nikopensius T, Reigo A, Kals M, Kallak K, Kütner R, Budrikas K, Kuusk S, Valvere V, Laidre P, Toome K, Rekker K, Tooming M, Ülle Murumets, Kahre T, Kruuv-Käo K, Õunap K, Padrik P, Metspalu A, Esko T, Fischer K, Tõnisson N.
- Front Genet. 2022 Jul 22;13:881100. doi: 10.3389/fgene.2022.881100.
- PMID: 35938029
- PubMed abstract
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- The Clinical and Psychosocial Outcomes for Women Who Received Unexpected Clinically Actionable Germline Information Identified through Research: An Exploratory Sequential Mixed-Methods Comparative Study.
- Forrest LE, Forbes Shepherd R, Tutty E, Pearce A, Campbell I, Devereux L, Trainer AH, James PA, Young MA.
- J Pers Med. 2022 Jul 7;12(7):1112. doi: 10.3390/jpm12071112.
- PMID: 35887609
- PubMed abstract
- Source abstract
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- Positive experiences of healthcare professionals with a mainstreaming approach of germline genetic testing for women with ovarian cancer.
- Bokkers K, Zweemer RP, Koudijs MJ, Stehouwer S, Velthuizen ME, Bleiker EMA, Ausems MGEM.
- Fam Cancer. 2022 Jul;21(3):295-304. doi: 10.1007/s10689-021-00277-7. Epub 2021 Oct 7.
- PMID: 34617209
- PubMed abstract
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- TRACEBACK: Testing of Historical Tubo-Ovarian Cancer Patients for Hereditary Risk Genes as a Cancer Prevention Strategy in Family Members.
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- BRCA1/2 germline testing in non-mucinous epithelial ovarian carcinoma: changing international practice and implications for service provision.
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- Identifying Needs: a Qualitative Study of women's Experiences Regarding Rapid Genetic Testing for Hereditary Breast and Ovarian Cancer in the DNA BONus Study.
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Webinar: June 2016 Webinar: Spreading the word: a review of two family communication intervention studies. (NSGC. Cancer SIG. Webinar Recordings. 2016 Jun 29.)
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- When knowledge of a heritable gene mutation comes out of the blue: treatment-focused genetic testing in women newly diagnosed with breast cancer.
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- Eur J Hum Genet. 2016 Nov;24(11):1517-1523. doi: 10.1038/ejhg.2016.69. Epub 2016 Jun 22.
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- BRACAVENIR - impact of a psychoeducational intervention on expectations and coping in young women (aged 18-30 years) exposed to a high familial breast/ovarian cancer risk: study protocol for a randomized controlled trial.
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Comments from NSGC Discussion Forum Cancer SIG
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- Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer.
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Comments on NSGC Discussion Forum Cancer SIG
Subject: Register for June Journal Club; Reminder, webinar this Friday
Webinar: June 2016 Webinar: Spreading the word: a review of two family communication intervention studies (NSGC Cancer SIG: Webinar Recordings)
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- Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?
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- Want A BRCA Test? Some Insurers Require Genetic Counseling First.
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- Insurers May Insist On Counseling Before Genetic Tests For Breast Cancer.
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- Waiting for Cancer
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- Finding all BRCA pathogenic mutation carriers: best practice models.
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- Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.
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- Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients.
- George A, Riddell D, Seal S, Talukdar S, Mahamdallie S, Ruark E, Cloke V, Slade I, Kemp Z, Gore M, Strydom A, Banerjee S, Hanson H, Rahman N.
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Comments on NSGC Discussion Forum Cancer SIG
News:
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Press: Simplified the Process. (GenomeWeb)
Press: All women with ovarian cancer should be offered genetic testing – so why aren’t they? (Science Blog)
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- Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations.
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- J Med Genet. 2016 Jul;53(7):472-80. doi: 10.1136/jmedgenet-2015-103740. Epub 2016 Mar 18.
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- The Unbearably Slow Adoption of Genetic Cancer Tests
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- The Atlantic. 2016 Jul.
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Comments on NSGC Discussion Forum Cancer SIG
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- June 2016 Webinar: Spreading the word: a review of two family communication intervention studies.
- Ilana Solomon.
- NSGC. Cancer SIG. Webinar Recordings. 2016 Jun 29.
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Communicating genetic test results within the family: Is it lost in translation? A survey of relatives in the randomized six-step study.
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- The integration of BRCA testing into oncology clinics.
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- The Quality of Genetic Counseling and Connected Factors as Evaluated by Male BRCA1/2 Mutation Carriers in Finland.
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- Predictive Genetic Testing and Alternatives to Face to Face Results Disclosure: A Retrospective Review of Patients Preference for Alternative Modes of BRCA 1 and 2 Results Disclosure in the Republic of Ireland.
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- Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling.
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- High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling.
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- Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
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- Front Oncol. 2016 May 13;6:120. doi: 10.3389/fonc.2016.00120. eCollection 2016.
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- The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety.
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- A new paradigm of genetic testing for hereditary breast/ovarian cancers.
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- Reaching high-risk underserved individuals for cancer genetic counseling by video-teleconferencing.
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- A targeted approach to genetic counseling in breast cancer patients: the experience of an Italian local project.
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- Tumori. 2016 Feb 4;102(1):45-50. doi: 10.5301/tj.5000407. Epub 2015 Sep 10.
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- Utilizing Remote Real-Time Videoconferencing to Expand Access to Cancer Genetic Services in Community Practices: A Multicenter Feasibility Study.
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- Does rapid genetic counseling and testing in newly diagnosed breast cancer patients cause additional psychosocial distress? results from a randomized clinical trial.
- Wevers MR, Ausems MG, Verhoef S, Bleiker EM, Hahn DE, Brouwer T, Hogervorst FB, van der Luijt RB, van Dalen T, Theunissen EB, van Ooijen B, de Roos MA, Borgstein PJ, Vrouenraets BC, Vriens E, Bouma WH, Rijna H, Vente JP, Kieffer JM, Valdimarsdottir HB, Rutgers EJ, Witkamp AJ, Aaronson NK.
- Genet Med. 2016 Feb;18(2):137-144. doi: 10.1038/gim.2015.50. Epub 2015 Apr 23.
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- Sweeping Up after the Kardashians: What We Wish had been Covered in Their Genetic Testing Episode.
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- My Gene Counsel. 2016 Jan 22.
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- Genetic screening for gynecological cancer: where are we heading?
- Manchanda R, Jacobs I.
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- ReCAP: Economic Evaluation Alongside a Clinical Trial of Telephone Versus In-Person Genetic Counseling for BRCA1/2 Mutations in Geographically Underserved Areas.
- Chang Y, Near AM, Butler KM, Hoeffken A, Edwards SL, Stroup AM, Kohlmann W, Gammon A, Buys SS, Schwartz MD, Peshkin BN, Kinney AY, Mandelblatt JS, Chang Y, Near AM, Butler KM, Hoeffken A, Edwards SL, Stroup AM, Kohlmann W, Gammon A, Buys SS, Schwartz MD, Peshkin BN, Kinney AY, Mandelblatt JS.
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- Genetic Testing for BRCA Mutations Today and Tomorrow-About the ABOUT Study.
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- JAMA Oncol. 2015 Dec 1;1(9):1225-1226. doi: 10.1001/jamaoncol.2015.3269.
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Comments on NSGC Discussion Forum Cancer SIG
Subject: Dr. Narod's commentary on pre-test genetic counseling
Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
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- Strategies for recruitment of relatives of BRCA mutation carriers to a genetic testing program in the Bahamas.
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- Clin Genet. 2015 Aug;88(2):182-6. doi: 10.1111/cge.12468. Epub 2014 Sep 6.
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- Aligning policy to promote cascade genetic screening for prevention and early diagnosis of heritable diseases.
- George R, Kovak K, Cox SL.
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- Pre-test genetic counseling services for hereditary breast and ovarian cancer delivered by non-genetics professionals in the state of Florida.
- Vadaparampil ST, Scherr CL, Cragun D, Malo TL, Pal T.
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- Pilot Testing of a Psycho-educational Telephone Intervention for Women Receiving Uninformative BRCA1/2 Genetic Test Results.
- Maheu C, Meschino WS, Hu W, Honeyford J, Ambus I, Kidd M, Benea A, Gao X, Azadbakhsh M, Rochefort C, Esplen MJ.
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- Accuracy of recall of information about a cancer-predisposing BRCA1/2 gene mutation among patients and relatives.
- Jacobs C, Dancyger C, Smith JA, Michie S.
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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.
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Research news: Fanconi Anemia: Genetic Counseling Research (Perspectives in Genetic Counseling)
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- Expanding Access to BRCA1/2 Genetic Counseling with Telephone Delivery: A Cluster Randomized Trial.
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- J Natl Cancer Inst. 2014 Nov 5;106(12). pii: dju328. doi: 10.1093/jnci/dju328. Print 2014 Dec.
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Press: Phone Counseling for BRCA1/2 Gene Tests 'Non-inferior' to In-Person. (Healthy Living/Reuters)
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- Development of a communication protocol for telephone disclosure of genetic test results for cancer predisposition.
- Patrick-Miller LJ, Egleston BL, Fetzer D, Forman A, Bealin L, Rybak C, Peterson C, Corbman M, Albarracin J, Stevens E, Daly MB, Bradbury AR.
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- Breast cancer risk counseling: a teachable moment?
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Comments on NSGC Discussion Forum Cancer SIG
Subject: Article request
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- Active approach for breast cancer genetic counseling during radiotherapy: long-term psychosocial and medical impact.
- Baars JE, Bleiker EM, van Riel E, Rodenhuis CC, Velthuizen ME, Schlich KJ, Ausems MG.
- Clin Genet. 2014 Jun;85(6):524-31. doi: 10.1111/cge.12335. Epub 2014 Feb 4.
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- More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling.
- Sie AS, van Zelst-Stams WA, Spruijt L, Mensenkamp AR, Ligtenberg MJ, Brunner HG, Prins JB, Hoogerbrugge N.
- Fam Cancer. 2014 Jun;13(2):143-51. doi: 10.1007/s10689-013-9686-z.
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- Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.
- Schwartz MD, Valdimarsdottir HB, Peshkin BN, Mandelblatt J, Nusbaum R, Huang AT, Chang Y, Graves K, Isaacs C, Wood M, McKinnon W, Garber J, McCormick S, Kinney AY, Luta G, Kelleher S, Leventhal KG, Vegella P, Tong A, King L.
- J Clin Oncol. 2014 Mar 1;32(7):618-26. doi: 10.1200/JCO.2013.51.3226. Epub 2014 Jan 21.
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Editorial:
Is it time to embrace telephone genetic counseling in the oncology setting?
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- Impact of rapid genetic counselling and testing on the decision to undergo immediate or delayed prophylactic mastectomy in newly diagnosed breast cancer patients: findings from a randomised controlled trial.
- Wevers MR, Aaronson NK, Verhoef S, Bleiker EM, Hahn DE, Kuenen MA, van der Sanden-Melis J, Brouwer T, Hogervorst FB, van der Luijt RB, Valdimarsdottir HB, van Dalen T, Theunissen EB, van Ooijen B, de Roos MA, Borgstein PJ, Vrouenraets BC, Vriens E, Bouma WH, Rijna H, Vente JP, Witkamp AJ, Rutgers EJ, Ausems MG.
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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.
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- London hospital widens access to genetic tests for ovarian cancer.
- Arie S.
- BMJ. 2014 Jan 28;348:g1179. doi: 10.1136/bmj.g1179.
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- New genetic testing pathway for cancer patients.
- Philippa Brice.
- PHG Foundation, 2014 Jan 24.
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- A rapid genetic counselling and testing in newly diagnosed breast cancer is associated with high rate of risk-reducing mastectomy in BRCA1/2-positive Italian women.
- Cortesi L, Razzaboni E, Toss A, De Matteis E, Marchi I, Medici V, Tazzioli G, Andreotti A, De Santis G, Pignatti M, Federico M.
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Viewpoint: Rapid BRCA Testing Informs Choice of Mastectomy. (Medscape Oncology)
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- Self administered screening for hereditary cancers in conjunction with mammography and ultrasound.
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- Fam Cancer. 2013 Dec;12(4):651-6. doi: 10.1007/s10689-013-9641-z.
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- Implementation and outcomes of telephone disclosure of clinical BRCA1/2 test results.
- Patrick-Miller L, Egleston BL, Daly M, Stevens E, Fetzer D, Forman A, Bealin L, Rybak C, Peterson C, Corbman M, Bradbury AR.
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- Variants of uncertain significance in BRCA testing: evaluation of surgical decisions, risk perception, and cancer distress.
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- Clin Genet. 2013 Nov;84(5):464-472. doi: 10.1111/cge.12097. Epub 2013 Feb 20.
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- Has Myriad Learned Their Lesson?
- Niki Lovick, Michelle Ernst.
- Yale Cancer Genetic Counseling. 2013 Sep 11.
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- A focus group study on breast cancer risk presentation: one format does not fit all.
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- Timing of referral for genetic counseling and genetic testing in patients with ovarian, fallopian tube, or primary peritoneal carcinoma.
- Novetsky AP, Smith K, Babb SA, Jeffe DB, Hagemann AR, Thaker PH, Powell MA, Mutch DG, Massad LS, Zighelboim I.
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Comments on NSGC Discussion Forum Cancer SIG
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- Implementation of a breast cancer genetic service in South Africa - lessons learned.
- Schoeman M, Apffelstaedt JP, Baatjes K, Urban M.
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- Star Power.
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- The DNA Exchange. 2013 Jun 16.
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- Dealing with the unexpected: consumer responses to direct-access BRCA mutation testing.
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Comments on NSGC Discussion Forum
Subject: Current thoughts on 23andme?
Press: Consumers have few negative reactions to the results of genetic testing for cancer mutations. (EurekAlert!)
Press: Get ready for the risks of genetic testing. (CNN)
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- How should we discuss genetic testing with women newly diagnosed with breast cancer? Design and implementation of a randomized controlled trial of two models of delivering education about treatment-focused genetic testing to younger women newly diagnosed with breast cancer.
- Watts KJ, Meiser B, Mitchell G, Kirk J, Saunders C, Peate M, Duffy J, Kelly PJ, Gleeson M, Barlow-Stewart K, Rahman B, Friedlander M, Tucker K; TFGT Collaborative Group.
- BMC Cancer. 2012 Jul 28;12:320. doi: 10.1186/1471-2407-12-320.
- PMID: 22838957
- PubMed abstract
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- Grace Rock's consent.
- Ross TS.
- Endocr Relat Cancer. 2012 Jul 22;19(4):C29-31. doi: 10.1530/ERC-12-0186. Print 2012 Aug.
- PMID: 22691626
- PubMed abstract
- Source abstract
- Case Report, Commentary
- Free Full Text
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- Psychological Distress with Direct-to-Consumer Genetic Testing: A Case Report of an Unexpected BRCA Positive Test Result.
- Dohany L, Gustafson S, Ducaine W, Zakalik D.
- J Genet Couns. 2012 Jun;21(3):399-401. Epub 2012 Jan 21.
- PMID: 22271377
- PubMed abstract
- Source abstract
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- DNA-testing for BRCA1/2 prior to genetic counselling in patients with breast cancer: design of an intervention study, DNA-direct.
- Sie AS, Spruijt L, van Zelst-Stams WA, Mensenkamp AR, Ligtenberg MJ, Brunner HG, Prins JB, Hoogerbrugge N.
- BMC Womens Health. 2012 May 8;12:12. doi: 10.1186/1472-6874-12-12.
- PMID: 22569005
- PubMed abstract
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- The introduction of a choice to learn pre-symptomatic DNA test results for BRCA or Lynch syndrome either face-to-face or by letter.
- Voorwinden JS, Jaspers JP, ter Beest JG, Kievit Y, Sijmons RH, Oosterwijk JC.
- Clin Genet. 2012 May;81(5):421-9. doi: 10.1111/j.1399-0004.2011.01811.x. Epub 2011 Dec 13.
- PMID: 22091929
- PubMed abstract
- Source abstract
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- A pre-visit website with question prompt sheet for counselees facilitates communication in the first consultation for breast cancer genetic counseling: findings from a randomized controlled trial.
- Albada A, van Dulmen S, Ausems MG, Bensing JM.
- Genet Med. 2012 May;14(5):535-42. doi: 10.1038/gim.2011.42. Epub 2012 Jan 12.
- PMID: 22241101
- PubMed abstract
- Source abstract
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- Effects of a pre-visit educational website on information recall and needs fulfilment in breast cancer genetic counselling, a randomized controlled trial.
- Albada A, van Dulmen S, Bensing JM, Ausems MG.
- Breast Cancer Res. 2012 Mar 6;14(2):R37.
- PMID: 22394647
- PubMed abstract
Retraction:
Retraction: Effects of a pre-visit educational website on information recall and needs fulfilment in breast cancer genetic counselling, a randomized controlled trial.
- PMID: 23130551
- PubMed abstract
- Retraction Note
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- A pre-visit tailored website enhances counselees' realistic expectations and knowledge and fulfils information needs for breast cancer genetic counselling.
- Albada A, van Dulmen S, Lindhout D, Bensing JM, Ausems MG.
- Fam Cancer. 2012 Mar;11(1):85-95. doi: 10.1007/s10689-011-9479-1.
- PMID: 21901499
- PubMed abstract
- Source abstract
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- Patient outcomes associated with group and individual genetic counseling formats.
- Rothwell E, Kohlmann W, Jasperson K, Gammon A, Wong B, Kinney A.
- Fam Cancer. 2012 Mar;11(1):97-106. doi: 10.1007/s10689-011-9486-2.
- PMID: 22057473
- PubMed abstract
- Source abstract
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- Using tumour pathology to identify people at high genetic risk of breast and colorectal cancers.
- Hopper JL, Jenkins MA, Dowty JG, Dite GS, Apicella C, Keogh L, Win AK, Young JP, Buchanan D, Walsh MD, Rosty C, Baglietto L, Severi G, Phillips KA, Wong EM, Dobrovic A, Waring P, Winship I, Ramus SJ, Giles GG, Southey MC.
- Pathology. 2012 Feb;44(2):89-98. doi: 10.1097/PAT.0b013e32834e8e5b.
- PMID: 22198256
- PubMed abstract
- Source abstract