Provider practices concerning family history collection, ascertainment, and utilization, and approaches to enhance these.
Patient knowledge and accuracy in providing family history; tools to assist patient provision of family history information.
List was last updated on
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- Importance of timely genetics services and critical evaluation of diagnosis and reported family history when assessing for hereditary cancer syndromes. [2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022.]
- Malca S.
- Fam Cancer. [P-08: Case Reports» Case Series on any topic.] 2023 Jan 23. doi: 10.1007/s10689-022-00324-x. Epub ahead of print.
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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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- Factors that influence the management recommendations breast surgeons provide to women with pathogenic variants in moderate penetrance breast cancer susceptibility genes.
- Vanderwal A, Lewis J, Basil J, Atzinger C, Widmeyer K.
- J Genet Couns. 2023 Jan 15. doi: 10.1002/jgc4.1674. Epub ahead of print.
- PMID: 36642783
- PubMed abstract
- Source abstract
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- January 2023: Awareness of genetic testing – results and analysis from the 2020 Health Information National Trends Survey.
- Mechanic L, Helzlsouer K.
- Genet Med. GenePOD. 2023 Jan 9.
- Podcast
- Free Audio
•• Original research:
Awareness and use of genetic testing: An analysis of the Health Information National Trends Survey 2020.
- PMID: 36136089
- PubMed abstract
- Free Full Texts
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- Awareness and use of genetic testing: An analysis of the Health Information National Trends Survey 2020.
- Tiner JC, Mechanic LE, Gallicchio L, Gillanders EM, Helzlsouer KJ.
- Genet Med. 2022 Dec;24(12):2526-2534. doi: 10.1016/j.gim.2022.08.023. Epub 2022 Sep 22.
- PMID: 36136089
- PubMed abstract
•• Podcast: January 2023: Awareness of genetic testing – results and analysis from the 2020 Health Information National Trends Survey. (Genetics in Medicine GenePOD)
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- Prenatal genetic counseling practices regarding recommendations for cancer genetic counseling: A retrospective chart review from two academic institutions.
- Saba LF, Sullivan CM, Solomon T, Huguenard S, Nassef SA.
- J Genet Couns. 2022 Oct;31(5):1062-1070. doi: 10.1002/jgc4.1577. Epub 2022 Apr 18.
- PMID: 35434961
- PubMed abstract
- Source abstract
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- Cancer screening and breast cancer family history in Spanish-speaking Hispanic/Latina women in California.
- Tamayo LI, Perez F, Perez A, Hernandez M, Martinez A, Huang X, Zavala V, Ziv E, Neuhausen S, Carvajal-Carmona LG, Duron Y, Fejerman L.
- Front Oncol. 2022 Sep 28;12:940162. doi: 10.3389/fonc.2022.940162.
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- Survey: 30 Percent of Women Don’t Know Family Cancer History
- [No author given]
- Inside Precision Medicine. Topics. Oncology. 2022 Sep 28.
- News
- Free Full Text
Press Release: Family Cancer History Still a Mystery to Many Women, Myriad Genetics Survey Finds. (GlobeNewswire)
Media Deck: Myriad Women’s Health Survey Infographics (Myriad Genetics)
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- Primary care physician referral practices regarding BRCA1/2 genetic counseling in a major health system.
- Linfield DT, Rothberg MB, Pfoh ER, Noss R, Cassard L, Powers JC, Lipold L, Martinez KA.
- Breast Cancer Res Treat. 2022 Sep;195(2):153-160. doi: 10.1007/s10549-022-06523-5. Epub 2022 Jul 16.
- PMID: 35842521
- PubMed abstract
- Source abstract
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- Environmental scan of family chart linking for genetic cascade screening in a U.S. integrated health system.
- Haas CB, Ralston J, Fullerton SM, Scrol A, Henrikson NB.
- Front Genet. 2022 Aug 11;13:886650. doi: 10.3389/fgene.2022.886650.
- PMID: 36035175
- PubMed 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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- Patient and Clinician Decision Support to Increase Genetic Counseling for Hereditary Breast and Ovarian Cancer Syndrome in Primary Care: A Cluster Randomized Clinical Trial.
- Kukafka R, Pan S, Silverman T, Zhang T, Chung WK, Terry MB, Fleck E, Younge RG, Trivedi MS, McGuinness JE, He T, Dimond J, Crew KD.
- JAMA Netw Open. 2022 Jul 18;5(7):e2222092. doi: 10.1001/jamanetworkopen.2022.22092.
- PMID: 35849397
- PubMed abstract
Identifier: NCT03470402: Decision Support for BRCA Testing in Ethnically Diverse Women. (ClinicalTrials.gov)
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- Genetic testing in prostate cancer management: Considerations informing primary care.
- Giri VN, Morgan TM, Morris DS, Berchuck JE, Hyatt C, Taplin ME.
- CA Cancer J Clin. 2022 Jul;72(4):360-371. doi: 10.3322/caac.21720. Epub 2022 Feb 24.
- PMID: 35201622
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Identification of women at risk of hereditary breast-ovarian cancer among participants in a population-based breast cancer screening.
- Bonelli L, Valle I, Rebora I, Ricci P, Biocchi L, Bruschi G, Parodi S, Bruzzone C, Varesco L.
- Fam Cancer. 2022 Jul;21(3):309-318. doi: 10.1007/s10689-021-00281-x. Epub 2021 Oct 20.
- PMID: 34669096
- PubMed abstract
- Source abstract
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- Can Automated Alerts in the Electronic Health Record Encourage Referrals for Genetic Counseling and Testing Among Patients at High Risk for Hereditary Cancer Syndromes?
- Zorn KK, Simonson ME, Faulkner JL, Carr CL, Acuna J, Hall TL, Jenkins JF, Drummond KL, Curran GM.
- JCO Oncol Pract. 2022 Jul;18(7):e1219-e1224. doi: 10.1200/OP.21.00641. Epub 2022 Mar 22.
- PMID: 35316088
- PubMed abstract
- Source abstract
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- Worldwide review with meta-analysis of women's awareness about breast cancer.
- Wang YJ, Wang F, Yu LX, Xiang YJ, Zhou F, Huang SY, Zheng C, Fu QY, Li L, Gao DZ, Zhang Q, Ma ZB, Yu ZG, Liu LY.
- Patient Educ Couns. 2022 Jul;105(7):1818-1827. doi: 10.1016/j.pec.2021.12.012. Epub 2021 Dec 18.
- PMID: 34952749
- PubMed abstract
- Review
- Free Full Text
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- Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews.
- Mittendorf KF, Lewis HS, Duenas DM, Eubanks DJ, Gilmore MJ, Goddard KAB, Joseph G, Kauffman TL, Kraft SA, Lindberg NM, Reyes AA, Shuster E, Syngal S, Ukaegbu C, Zepp JM, Wilfond BS, Porter KM.
- Hered Cancer Clin Pract. 2022 Jun 10;20(1):22. doi: 10.1186/s13053-022-00231-3.
- PMID: 35689290
- PubMed abstract
Identifier: NCT03426878: Cancer Health Assessments Reaching Many (CHARM). (ClinicalTrials.gov)
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- Increased family history documentation in internal medicine resident continuity clinic at a community hospital through resident-led structured genetic education program.
- Chenbhanich J, Riano I, Madhavaram S, Cristancho C, Poloju A, Zavala González VA, Kosaisawe N, Treadwell T.
- J Community Genet. 2022 Jun;13(3):347-354. doi: 10.1007/s12687-022-00581-4. Epub 2022 Mar 1.
- PMID: 35230657
- PubMed abstract
- Source abstract
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- Prevalence of Americans reporting a family history of cancer indicative of increased cancer risk: Estimates from the 2015 National Health Interview Survey.
- Kumerow MT, Rodriguez JL, Dai S, Kolor K, Rotunno M, Peipins LA.
- Prev Med. 2022 Jun;159:107062. doi: 10.1016/j.ypmed.2022.107062. Epub 2022 Apr 20.
- PMID: 35460723
- PubMed abstract
- Source abstract
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- UC Davis Looks to Expand Genetic Breast Cancer Risk Education, Outreach for Hispanic Women.
- Kanski A.
- Precision Oncology News. Technology. 2022 May 19.
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- Perceived risk and risk reduction behaviours of female first-degree relatives of breast cancer patients attending care at Uganda cancer institute.
- Ainembabazi P, Abila DB, Manyangwa G, Anguzu G, Musaazi J, Mutyaba I, Osingada CP, Mwaka AD.
- Psychooncology. 2022 May 18. doi: 10.1002/pon.5963. Epub ahead of print.
- PMID: 35584282
- PubMed abstract
- Source abstract
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- Helix: A Digital Tool to Address Provider Needs for Prostate Cancer Genetic Testing in Clinical Practice.
- Giri VN, Walker A, Gross L, Trabulsi EJ, Lallas CD, Kelly WK, Gomella LG, Fischer C, Loeb S.
- Clin Genitourin Cancer. 2022 Apr;20(2):e104-e113. doi: 10.1016/j.clgc.2021.11.009. Epub 2021 Nov 27.
- PMID: 35012874
- PubMed abstract
- Source abstract
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- Room for improvement in capturing cancer family history in a gynecologic oncology outpatient setting.
- Lin J, Wolfe I, Ahsan MD, Krinsky H, Lackner AI, Pelt J, Bolouvi K, Gamble C, Thomas C, Christos PJ, Cantillo E, Holcomb K, Chapman-Davis E, Sharaf R, Lipkin SM, Blank SV, Frey MK.
- Gynecol Oncol Rep. 2022 Feb 14 [eCollection 2022 Apr];40:100941. doi: 10.1016/j.gore.2022.100941.
- PMID: 35242980
- PubMed abstract
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- You Don’t Have a BRCA Mutation, But Could You Have Lynch Syndrome?
- [No author given]
- My Gene Counsel. Genetic Journal. 2022 Mar 22.
- Blog post
- Free Full Text
Original research:
Errors in delivery of cancer genetics services: implications for practice.
- PMID: 20806621
- PubMed abstract
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- Do current family history-based genetic testing guidelines contribute to breast cancer health inequities?
- Jakuboski SH, McDonald JA, Terry MB.
- NPJ Breast Cancer. 2022 Mar 22;8(1):36. doi: 10.1038/s41523-022-00391-4.
- PMID: 35319016
- PubMed abstract
- Commentary. Review.
- Free Full Text
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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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- Hereditary Breast and Ovarian Cancer: An Updated Primer for OB/GYNs.
- Bellcross CA.
- Obstet Gynecol Clin North Am. 2022 Mar;49(1):117-147. doi: 10.1016/j.ogc.2021.11.005.
- PMID: 35168766
- PubMed abstract
- Source abstract
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- Retrospective assessment of barriers and access to genetic services for hereditary cancer syndromes in an integrated health care delivery system.
- Muessig KR, Zepp JM, Keast E, Shuster EE, Reyes AA, Arnold B, Ingphakorn C, Gilmore MJ, Kauffman TL, Hunter JE, Knerr S, Feigelson HS, Goddard KAB.
- Hered Cancer Clin Pract. 2022 Feb 10;20(1):7. doi: 10.1186/s13053-022-00213-5.
- PMID: 35144679
- PubMed abstract
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- Genetic Testing Challenges in Oncology: Prior Retinoblastoma Not Considered in Test Ordering.
- Ray T.
- Precision Oncology News. Disease Areas. 2021 Dec 22.
- Case report
- Free Full Text
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- Comparison of a Cancer Family History Collection and Risk Assessment Tool - ItRunsInMyFamily - with Risk Assessment by Health-Care Professionals.
- Ritchie JB, Welch BM, Allen CG, Frey LJ, Morrison H, Schiffman JD, Alekseyenko AV, Dean B, Hughes Halbert C, Bellcross C.
- Public Health Genomics. 2021 Dec 6:1-9. doi: 10.1159/000520001. Epub ahead of print.
- PMID: 34872100
- PubMed abstract
- Source abstract
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- Hereditary Cancer Risk Using a Genetic Chatbot Before Routine Care Visits.
- Nazareth S, Hayward L, Simmons E, Snir M, Hatchell KE, Rojahn S, Slotnick RN, Nussbaum RL.
- Obstet Gynecol. 2021 Dec 1;138(6):860-870. doi: 10.1097/AOG.0000000000004596.
- PMID: 34735417
- PubMed abstract
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- Conference Session Highlight: I'm Not White, Can I Still Have a Mutation?
- Stallings E, Goldberg D.
- FORCE. Blog. 2021 Nov 19.
- Blog post
- Free Full Text
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- Cascade Genetic Testing for Hereditary Cancer Risk: An Underutilized Tool for Cancer Prevention.
- Whitaker KD, Obeid E, Daly MB, Hall MJ.
- JCO Precis Oncol. 2021 Nov;5:1387-1396. doi: 10.1200/PO.21.00163.
- PMID: 34994636
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Genetic Testing Challenges in Oncology: Same Multigene Cancer Risk Panel Not Right for All.
- Ray T.
- Precision Oncology News. Biomarkers. BRCA. 2021 Oct 28.
- Case report
- Free Full Text
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- Experience and Perceptions of a Family Health History Risk Assessment Tool among Multi-Ethnic Asian Breast Cancer Patients.
- Yoon S, Goh H, Fung SM, Tang S, Matchar D, Ginsburg GS, Orlando LA, Ngeow J, Wu RR.
- J Pers Med. 2021 Oct 19;11(10):1046. doi: 10.3390/jpm11101046.
- PMID: 34683187
- PubMed abstract
- Source abstract
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- Care of men with cancer-predisposing BRCA variants.
- Horton R, Pharoah P, Hayward J, Lucassen A.
- BMJ. 2021 Oct 14;375:n2376. doi: 10.1136/bmj.n2376.
- PMID: 34649841
- PubMed abstract
- Source abstract
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- Breast Cancer Risk Assessment and Primary Prevention Advice in Primary Care: A Systematic Review of Provider Attitudes and Routine Behaviours.
- Bellhouse S, Hawkes RE, Howell SJ, Gorman L, French DP.
- Cancers (Basel). 2021 Aug 18;13(16):4150. doi: 10.3390/cancers13164150.
- PMID: 34439302
- PubMed abstract
- Source abstract
- Review
- Free PMC article
- Free full text
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- Evaluation and comparison of hereditary Cancer guidelines in the population.
- Ritchie JB, Bellcross C, Allen CG, Frey L, Morrison H, Schiffman JD, Welch BM.
- Hered Cancer Clin Pract. 2021 Jul 17;19(1):31. doi: 10.1186/s13053-021-00188-9.
- PMID: 34274008
- PubMed abstract
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- Disclosure of familial implications of pathogenic variants in breast-cancer genes to patients: Opportunity for prompting family communication.
- Makhnoon S, Smith HS, Bednar EM, Bhatt A, Turner L, Arun B, Volk RJ, Peterson SK.
- J Community Genet. 2021 Jul;12(3):439-447. doi: 10.1007/s12687-021-00504-9. Epub 2021 Jan 22.
- PMID: 33481188
- PubMed abstract
- Source abstract
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- Genetic Testing Challenges in Oncology: Inaccurate Patient Claims Complicate Cancer Risk Management.
- Ray T.
- Precision Oncology News. Biomarkers. BRCA. 2021 Jun 30.
- Press, Case report
- Free Full Text
Blog post: Genetic Testing Challenges in Oncology: Inaccurate Patient Claims Complicate Cancer Risk Management. (My Gene Counsel)
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- A Retrospective 5-Year Single Center Study Highlighting the Risk of Cancer Predisposition in Adolescents and Young Adults.
- Jordan F, Huber S, Sommer S, Schenkirsch G, Frühwald MC, Trepel M, Claus R, Kuhlen M.
- Cancers (Basel). 2021 Jun 17;13(12):3033. doi: 10.3390/cancers13123033.
- PMID: 34204522
- PubMed abstract
- Source abstract
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- Training courses on hereditary breast and ovarian cancer to strengthen cross-sectoral care in underserved areas.
- Kühn F, Karsten MM, Kendel F, Feufel MA, Speiser D.
- Patient Educ Couns. 2021 Jun;104(6):1431-1437. doi: 10.1016/j.pec.2020.10.035. Epub 2020 Nov 1.
- PMID: 33162275
- PubMed abstract
- Source abstract
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- Modernizing family health history: achievable strategies to reduce implementation gaps.
- Wildin RS, Messersmith DJ, Houwink EJF.
- J Community Genet. 2021 May 24. doi: 10.1007/s12687-021-00531-6. Epub ahead of print.
- PMID: 34028705
- PubMed abstract
- Source abstract
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- A Case-Based Clinical Approach to the Investigation, Management and Screening of Families with BRCA2 Related Prostate Cancer.
- King B, McHugh J, Snape K.
- Appl Clin Genet. 2021 May 20;14:255-266. doi: 10.2147/TACG.S261737.
- PMID: 34295175
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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- Use of a Standardized Tool to Identify Women at Risk for Hereditary Breast and Ovarian Cancer.
- Nurs Womens Health. 2021 Apr 29:S1751-4851(21)00080-5. doi: 10.1016/j.nwh.2021.03.008. Epub ahead of print.
- PMID: 33933425
- PubMed abstract
- Source abstract
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- Genetic Testing Challenges in Oncology: BRCA1-Positive Patient Told Paternal Cancer Risk Unimportant.
- Ray T.
- Precision Oncology News. Biomarkers. BRCA. 2021 Apr 29.
- Press, Case report
- Free Full Text
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- Value of a genetics clinic evaluation in identifying women at risk for hereditary breast-ovarian cancer syndrome.
- Hinshaw JC, Zhao LP, Brimm JE, Payne TH, Hisama FM.
- J Genet Couns. 2021 Apr 21. doi: 10.1002/jgc4.1425. Epub ahead of print.
- PMID: 33881185
- PubMed abstract
- Source abstract
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- The Prevent Ovarian Cancer Program (POCP): Identification of women at risk for ovarian cancer using complementary recruitment approaches.
- Tone AA, McCuaig JM, Ricker N, Boghosian T, Romagnuolo T, Stickle N, Virtanen C, Zhang T, Kim RH, Ferguson SE, May T, Laframboise S, Armel S, Demsky R, Volenik A, Stuart-McEwan T, Shaw P, Oza A, Kamel-Reid S, Stockley T, Bernardini MQ.
- Gynecol Oncol. 2021 Apr 13:S0090-8258(21)00321-8. doi: 10.1016/j.ygyno.2021.04.011. Epub ahead of print.
- PMID: 33858678
- PubMed abstract
- Source abstract
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- Wer braucht eine genetische Beratung? [Who must be referred for genetic counseling?].
- Monnerat C, Dobbie M.
- Ther Umsch. 2021 Apr;78(3):145-148. German. doi: 10.1024/0040-5930/a001251.
- PMID: 33775137
- PubMed abstract
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- What’s Autism Got To Do With It?
- [No author given]
- My Gene Counsel. Genetic Journal. 2021 Mar 27.
- Blog post
- Free Full Text
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- Clinical implementation of an oncology-specific family health history risk assessment tool.
- Fung SM, Wu RR, Myers RA, Goh J, Ginsburg GS, Matchar D, Orlando LA, Ngeow J.
- Hered Cancer Clin Pract. 2021 Mar 20;19(1):20. doi: 10.1186/s13053-021-00177-y.
- PMID: 33743786
- PubMed abstract
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- Correspondence on "Assessing relatives' readiness for hereditary cancer cascade genetic testing" by Bednar et al.
- Carlson J.
- Genet Med. 2021 Mar 19. doi: 10.1038/s41436-020-01094-6. Epub ahead of print.
- PMID: 33742172
- PubMed abstract
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Original research:
Assessing relatives' readiness for hereditary cancer cascade genetic testing.
- PMID: 31857708
- PubMed abstract
- Source abstract
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- Genetic Testing Challenges in Oncology: Forged Genetic Test Report Leads to Incorrect Management.
- Ray T.
- Precision Oncology News. Diagnostics. 2021 Mar 1.
- Press
- Free Full Text
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- Tracing Our Family Mutation to an Unlikely Place.
- Eldridge C.
- FORCE. Blog. 2021 Jan 13.
- Blog post
- Free Full Text
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- Genetic Testing Challenges in Oncology: Woman Without High Breast Cancer Risk Recommended Surgery.
- Ray T.
- Precision Oncology News. 2020 Dec 22.
- Case report
- Free Full Text
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- CanRisk Tool - A web interface for the prediction of breast and ovarian cancer risk and the likelihood of carrying genetic pathogenic variants.
- Carver T, Hartley S, Lee A, Cunningham AP, Archer S, Babb de Villiers C, Roberts J, Ruston R, Walter FM, Tischkowitz M, Easton DF, Antoniou AC.
- Cancer Epidemiol Biomarkers Prev. 2020 Dec 17:cebp.1319.2020. doi: 10.1158/1055-9965.EPI-20-1319. Epub ahead of print.
- PMID: 33335023
- PubMed abstract
- Source abstract
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- Genetic Testing Challenges in Oncology: BRCA2-Positive Healthy Young Man Recommended Mastectomy.
- Ray T.
- Precision Oncology News. 2020 Nov 25.
- Press. Case report.
- Free Full Text
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- Finding Hope on the Other Side of Surgery After Learning of my ATM Mutation.
- Townsend C.
- FORCE. Blog. 2020 Nov 13.
- Blog post
- Free Full Text
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- Previvor at 25 - The Beginning has just Begun.
- Wilson L.
- FORCE. Blog. 2020 Nov 10.
- Blog post
- Free Full Text
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- Knowledge and practice regarding prostate cancer germline testing among urologists: Gaps to address for optimal implementation.
- Loeb S, Byrne N, Walter D, Makarov DV, Wise DR, Becker D, Giri VN.
- Cancer Treat Res Commun. 2020 Sep 28;25:100212. doi: 10.1016/j.ctarc.2020.100212. Epub ahead of print.
- PMID: 33091732
- PubMed abstract
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- Improving primary care identification of familial breast cancer risk using proactive invitation and decision support.
- Qureshi N, Dutton B, Weng S, Sheehan C, Chorley W, Robertson JFR, Kendrick D, Kai J.
- Fam Cancer. 2020 Jun 11. doi: 10.1007/s10689-020-00188-z. Epub ahead of print.
- PMID: 32524330
- PubMed abstract
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- Executive Summary of the Early-Onset Breast Cancer Evidence Review Conference.
- Chelmow D, Pearlman MD, Young A, Bozzuto L, Dayaratna S, Jeudy M, Kremer ME, Scott DM, O'Hara JS.
- Obstet Gynecol. 2020 Jun;135(6):1457-1478. doi: 10.1097/AOG.0000000000003889.
- PMID: 32459439
- PubMed abstract
- Executive Summary, Review
- Free Full Text
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- Utilization of health information technology among cancer genetic counselors.
- Ritchie JB, Allen CG, Morrison H, Nichols M, Lauzon SD, Schiffman JD, Hughes Halbert C, Welch BM.
- Mol Genet Genomic Med. 2020 May 28:e1315. doi: 10.1002/mgg3.1315. Epub ahead of print.
- PMID: 32468681
- PubMed abstract
- Source abstract
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- Use of telephone intake for family history taking at a cancer genetics service in Asia.
- Chin XW, Ang ZLT, Tan RYC, Courtney E, Shaw T, Chen Y, Li ST, Ngeow JYY.
- J Genet Couns. 2020 May 5. doi: 10.1002/jgc4.1286. [Epub ahead of print]
- PMID: 32368849
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- National Minority Cancer Awareness Month: Is the Cancer in Your Family Hereditary?
- Wu J.
- FORCE Blog. 2020 Apr 22.
Blog post: Luck Is More Than Just A Rainbow: A Previvor’s Story. (FORCE Blog)
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- Adventist Health, CancerIQ Collaboration Identifying More Patients for Guidelines-Supported Genetic Testing.
- Versel N.
- GenomeWeb. 2020 Apr 3.
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- Assessing relatives' readiness for hereditary cancer cascade genetic testing.
- Bednar EM, Sun CC, McCurdy S, Vernon SW.
- Genet Med. 2020 Apr;22(4):719-726. doi: 10.1038/s41436-019-0735-3. Epub 2019 Dec 20.
- PMID: 31857708
- PubMed abstract
- Source abstract
Letter:
Correspondence on "Assessing relatives' readiness for hereditary cancer cascade genetic testing" by Bednar et al.
- PMID: 33742172
- PubMed abstract
- Source abstract
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- What men want: Qualitative analysis of what men with prostate cancer (PCa) want to learn regarding genetic referral, counseling, and testing.
- Greenberg S, Slager S, Neil BO, Cooney K, Maughan B, Stopa N, Venne V, Zickmund S, Colonna S.
- Prostate. 2020 Apr;80(5):441-450. doi: 10.1002/pros.23959. Epub 2020 Feb 6.
- PMID: 32027768
- PubMed abstract
- Source abstract
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- Ethnic disparities in the frequency of cancer reported in family histories.
- Maves H, Flodman P, Nathan D, Smith M.
- J Genet Couns. 2020 Mar 28. doi: 10.1002/jgc4.1264. [Epub ahead of print]
- PMID: 32222057
- PubMed abstract
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- Familial risk of breast cancer by dynamic, accumulative, and static definitions of family history.
- Mukama T, Kharazmi E, Sundquist K, Sundquist J, Brenner H, Fallah M.
- Cancer. 2020 Mar 10. doi: 10.1002/cncr.32815. [Epub ahead of print]
- PMID: 32154920
- PubMed abstract
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- How genomic information is accessed in clinical practice: an electronic survey of UK general practitioners.
- Evans WRH, Tranter J, Rafi I, Hayward J, Qureshi N.
- J Community Genet. 2020 Mar 3. doi: 10.1007/s12687-020-00457-5. [Epub ahead of print]
- PMID: 32125658
- PubMed abstract
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- Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: Recommendation Statement.
- [No authors listed]
- Am Fam Physician. 2020 Feb 15;101(4):233-238.
- PMID: 32053325
- PubMed abstract
- Guidelines
- Free Full Text
CME Activity:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer.
- PMID: 32053324
- PubMed abstract
- Source abstract
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- Breast cancer suspected to originate from familial hereditary tumors: A case report.
- Yamamoto S, Chishima T, Sugae S, Shibata Y, Yamada A.
- Clin Case Rep. 2020 Feb 8;8(4):648-652. doi: 10.1002/ccr3.2698. eCollection 2020 Apr.
- PMID: 32274028
- PubMed abstract
- Source abstract
- Case report
- Free PMC article
- Free full text
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- Breast cancer screening implications of risk modeling among female relatives of ATM and CHEK2 carriers.
- Weidner AE, Liggin ME, Zuniga BI, Tezak AL, Wiesner GL, Pal T.
- Cancer. 2020 Jan 22. doi: 10.1002/cncr.32715. [Epub ahead of print]
- PMID: 31967672
- PubMed abstract
- Source abstract
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- Prospective Feasibility Trial of a Novel Strategy of Facilitated Cascade Genetic Testing Using Telephone Counseling.
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