Information taken away, retained by patients/clients from Genetic Counseling/Testing; perceptions (risk perception, etc.) effected by counseling/testing
List was last updated on
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- "I wish that there was more info": characterizing the uncertainty experienced by carriers of pathogenic ATM and/or CHEK2 variants.
- Reyes KG, Clark C, Gerhart M, Newson AJ, Ormond KE.
- Fam Cancer. 2021 Apr 15. doi: 10.1007/s10689-021-00251-3. Epub ahead of print.
- PMID: 33855648
- PubMed abstract
- Source abstract
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- Videoconferencing to deliver genetics services: a systematic review of telegenetics in light of the COVID-19 pandemic.
- Brown EG, Watts I, Beales ER, Maudhoo A, Hayward J, Sheridan E, Rafi I.
- Genet Med. 2021 Apr 6. doi: 10.1038/s41436-021-01149-2. Epub ahead of print.
- PMID: 33824502
- PubMed abstract
- Review
- Free Full Text
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- The Knowledge and Attitude of Patients Diagnosed with Epithelial Ovarian Cancer towards Genetic Testing.
- Shin W, Jeong G, Son Y, Seo SS, Kang S, Park SY, Lim MC.
- Int J Environ Res Public Health. 2021 Feb 26;18(5):2312. doi: 10.3390/ijerph18052312.
- PMID: 33652933
- PubMed abstract
- Source abstract
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- The role of the genetic testing industry in patient education of hereditary cancer: An observational study assessing the quality of patient education videos.
- Greenberg DC, Kamara D, Tatsugawa Z, Mendoza M, Pineda E, Holschneider CH, Zakhour M.
- Gynecol Oncol. 2021 Feb 19:S0090-8258(21)00150-5. doi: 10.1016/j.ygyno.2021.02.013. Epub ahead of print.
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- Implications of Multigene Panel Testing on Psychosocial Outcomes: A Comparison of Patients With Pancreatic and Breast or Ovarian Cancer.
- Koptiuch C, Espinel WF, Kohlmann WK, Zhao J, Kaphingst KA.
- JCO Precis Oncol. 2020;5:235-244. doi: 10.1200/PO.20.00199. Epub 2021 Jan 19.
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- Influence of lived experience on risk perception among women who received a breast cancer polygenic risk score: 'Another piece of the pie'.
- Willis AM, Smith SK, Meiser B, James PA, Ballinger ML, Thomas DM, Yanes T, Young MA.
- J Genet Couns. 2021 Jan 19. doi: 10.1002/jgc4.1384. Epub ahead of print.
- PMID: 33470033
- PubMed abstract
- Source abstract
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- GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing.
- Rasouly HM, Cuneo N, Marasa M, DeMaria N, Chatterjee D, Thompson JJ, Fasel DA, Wynn J, Chung WK, Appelbaum P, Weng C, Bakken S, Gharavi AG.
- J Genet Couns. 2020 Dec 26. doi: 10.1002/jgc4.1364. Epub ahead of print.
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- Understanding of Inheritance and Genetic Variation Assessed through the Use of an Engaging Real-Life Survey.
- Ephrem E, Gleason E, Maurer K, Sullivan KE.
- Public Health Genomics. 2020 Dec 8:1-6. doi: 10.1159/000512086. Epub ahead of print.
- PMID: 33291115
- PubMed abstract
- Source abstract
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- Testing a Best Practices Risk Result Format to Communicate Genetic Risks.
- Davis K, Roter DL, Schmidlen T, Scheinfeldt LB, Klein WMP.
- Patient Educ Couns. 2020 Oct 19:S0738-3991(20)305589. doi: 10.1016/j.pec.2020.10.021. Epub ahead of print.
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- How Patients Deal with an Ambiguous Medical Test: Decision-Making after Genetic Testing.
- Scherra CL, Ramesh S, Getachew-Smith H, Kalke K, Ramsey K, Fischhoff B, Vadaparampil ST.
- Patient Educ Couns. 2020 Oct 18:S0738-3991(20)305577. doi: 10.1016/j.pec.2020.10.020. Epub ahead of print.
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- Experiences and attitudes of hereditary cancer screening patients in a consumer directed testing model.
- Greve V, Garner M, Odom K, Cooper SJ, East KM.
- Patient Educ Couns. 2020 Oct 11:S0738-3991(20)305498. doi: 10.1016/j.pec.2020.10.014. Epub ahead of print.
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- A pilot randomized trial of an educational intervention to increase genetic counseling and genetic testing among Latina breast cancer survivors.
- Conley CC, Castro-Figueroa EM, Moreno L, Dutil J, García JD, Burgos C, Ricker C, Kim J, Graves KD, Ashing KT, Quinn GP, Soliman H, Vadaparampil ST.
- J Genet Couns. 2020 Sep 16. doi: 10.1002/jgc4.1324. Epub ahead of print.
- PMID: 32936981
- PubMed abstract
- Source abstract
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- Informing models of cancer genetic care in the era of multigene panel testing with patient-led recommendations.
- Underhill-Blazey M, Blonquist T, Chittenden A, Pozzar R, Nayak M, Lansang K, Hong F, Garber J, Stopfer JE.
- J Genet Couns. 2020 Aug 26. doi: 10.1002/jgc4.1317. Epub ahead of print.
- PMID: 32851753
- PubMed abstract
- Source abstract
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- Using patient perspectives to inform communication training materials for health care professionals discussing BRCA mutation testing.
- Shilling V, Catt S, Jenkins V, Fallowfield L.
- Breast Cancer Res Treat. 2020 Aug 18. doi: 10.1007/s10549-020-05871-4. Epub ahead of print.
- PMID: 32812179
- PubMed abstract
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- Presymptomatic Awareness of Germline Pathogenic BRCA Variants and Associated Outcomes in Women With Breast Cancer.
- Hadar T, Mor P, Amit G, Lieberman S, Gekhtman D, Rabinovitch R, Levy-Lahad E.
- JAMA Oncol. 2020 Jul 9. doi: 10.1001/jamaoncol.2020.2059. Epub ahead of print.
- PMID: 32644100
- PubMed abstract
- Source abstract
Research news: Study Sees Survival Boost For BRCA1/2 Carriers Tested Before Breast Cancer Diagnosis. (GenomeWeb)
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- A Modern Dilemma: How Experts Grapple with Ambiguous Genetic Test Results.
- Scherr CL, Ross Arguedas AA, Getachew-Smith H, Marshall-Fricker C, Shrestha N, Brooks K, Fischhoff B, Vadaparampil ST.
- Med Decis Making. 2020 Jul;40(5):655-668. doi: 10.1177/0272989X20935864.
- PMID: 32734842
- PubMed abstract
- Source abstract
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- Women's responses and understanding of polygenic breast cancer risk information.
- Yanes T, Kaur R, Meiser B, Scheepers-Joynt M, McInerny S, Barlow-Stewart K, Antill Y, Salmon L, Smyth C, James PA, Young MA.
- Fam Cancer. 2020 May 20. doi: 10.1007/s10689-020-00185-2. Epub ahead of print.
- PMID: 32430685
- PubMed abstract
- Source abstract
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- Patient perspectives on variant reclassification after cancer susceptibility testing.
- Halverson CME, Connors LM, Wessinger BC, Clayton EW, Wiesner GL.
- Mol Genet Genomic Med. 2020 Apr 24:e1275. doi: 10.1002/mgg3.1275. [Epub ahead of print]
- PMID: 32329193
- PubMed abstract
- Source abstract
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- Mainstream consent programs for genetic counseling in cancer patients: A systematic review.
- Scheinberg T, Young A, Woo H, Goodwin A, Mahon KL, Horvath LG.
- Asia Pac J Clin Oncol. 2020 Apr 20. doi: 10.1111/ajco.13334. [Epub ahead of print]
- PMID: 32309911
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Longitudinal outcomes with cancer multigene panel testing in previously tested BRCA1/2 negative patients.
- Bradbury AR, Egleston BL, Patrick-Miller LJ, Rustgi N, Brandt A, Brower J, DiGiovanni L, Fetzer D, Berkelbach C, Long JM, Powers J, Stopfer JE, Domchek SM.
- Clin Genet. 2020 Apr;97(4):601-609. doi: 10.1111/cge.13716.
- PMID: 32022897
- PubMed abstract
- Source abstract
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- The impact of communicating uncertain test results in cancer genetic counseling: A systematic mixed studies review.
- Medendorp NM, van Maarschalkerweerd PEA, Murugesu L, Daams JG, Smets EMA, Hillen MA.
- Patient Educ Couns. 2020 Mar 19. pii: S0738-3991(20)30149-X. doi: 10.1016/j.pec.2020.03.015. [Epub ahead of print]
- PMID: 32278626
- PubMed abstract
- Review
- Free Full Text
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- Updated Guideline Moves Genetic Testing Beyond BRCA.
- Narozniak R.
- OncologyLive. 2020 Mar 13;21(6).
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
- PMID: 31429903
- PubMed abstract
- Free full text
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- Do Preferred Risk Formats Lead to Better Understanding? A Multicenter Controlled Trial on Communicating Familial Breast Cancer Risks Using Different Risk Formats.
- Henneman L, van Asperen CJ, Oosterwijk JC, Menko FH, Claassen L, Timmermans DR.
- Patient Prefer Adherence. 2020 Feb 19;14:333-342. doi: 10.2147/PPA.S232941. eCollection 2020.
- PMID: 32109999
- PubMed abstract
- Source abstract
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- Disparities in BRCA counseling across providers in a diverse population of young breast cancer survivors.
- Reid S, Cragun D, Tezak A, Weidner A, Moore J, Mayer IA, Shu XO, Ye F, Fan R, Vadaparampil S, Pal T.
- Genet Med. 2020 Feb 18. doi: 10.1038/s41436-020-0762-0. [Epub ahead of print]
- PMID: 32066870
- PubMed abstract
- Source abstract
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- Experts say more women should be tested for BRCA1 and BRCA2 genetic mutations.
- Printz C.
- Cancer. 2020 Feb 15;126(4):693. doi: 10.1002/cncr.32723.
- PMID: 31995244
- PubMed abstract
- News
- Free full text
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
- PMID: 31429903
- PubMed abstract
- Free full text
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- Referencing BRCA in hereditary cancer risk discussions: In search of an anchor in a sea of uncertainty.
- Waltz M, Prince AER, O'Daniel JM, Foreman AKM, Powell BC, Berg JS.
- J Genet Couns. 2020 Jan 22. doi: 10.1002/jgc4.1219. [Epub ahead of print]
- PMID: 31967382
- PubMed abstract
- Source abstract
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- Patients with pathogenic variants for breast cancer other than BRCA1 and BRCA2: qualitative interviews about health care experiences.
- Clift KE, Macklin SK, Hines SL.
- Hered Cancer Clin Pract. 2019 Dec 16;17:32. doi: 10.1186/s13053-019-0132-6. eCollection 2019.
- PMID: 31890060
- PubMed abstract
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- Clinical utility of hereditary cancer panel testing: Impact of PALB2, ATM, CHEK2, NBN, BRIP1, RAD51C, and RAD51D results on patient management and adherence to provider recommendations.
- Vysotskaia V, Kaseniit KE, Bucheit L, Ready K, Price K, Johansen Taber K.
- Cancer. 2019 Nov 4. doi: 10.1002/cncr.32572. [Epub ahead of print]
- PMID: 31682005
- PubMed abstract
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- Decision Making About Genetic Testing Among Women With a Personal and Family History of Breast Cancer.
- Scott D, Friedman S, Telli ML, Kurian AW.
- J Oncol Pract. 2019 Oct 15:JOP1900221. doi: 10.1200/JOP.19.00221. [Epub ahead of print]
- PMID: 31613719
- PubMed abstract
- Source abstract
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- Do Women who Receive a Negative BRCA1/2 Risk Result Understand the Implications for Breast Cancer Risk?
- Guan Y, Condit CM, Escoffery C, Bellcross CA, McBride CM.
- Public Health Genomics. 2019 Oct 9:1-8. doi: 10.1159/000503129. [Epub ahead of print]
- PMID: 31597139
- PubMed abstract
- Source abstract
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- Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
- US Preventive Services Task Force, Owens DK, Davidson KW, Krist AH, Barry MJ, Cabana M, Caughey AB, Doubeni CA, Epling JW Jr, Kubik M, Landefeld CS, Mangione CM, Pbert L, Silverstein M, Simon MA, Tseng CW, Wong JB.
- JAMA. 2019 Aug 20;322(7):652-665. doi: 10.1001/jama.2019.10987.
- PMID: 31429903
- PubMed abstract
- Guidelines
- Free Full Text
Evidence report, Review:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force.
- PMID: 31429902
- PubMed abstract
- Free Full Text
Guidelines [Internet]:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA1/2-Related Cancer in Women: A Systematic Review for the U.S. Preventive Services Task Force [Internet].
- PMID: 31479213
- PubMed abstract
- Free Full Text
Editorial:
Broadening Criteria for BRCA1/2 Evaluation: Placing the USPSTF Recommendation in Context.
- PMID: 31429878
- PubMed abstract
- Source abstract
Editorial:
USPSTF Recommendations for BRCA1 and BRCA2 Testing in the Context of a Transformative National Cancer Control Plan.
- PMID: 31429910
- PubMed abstract
- Free Full Text
Editorial:
Hereditary Cancer Evaluation in 2019-a Rapidly Evolving Landscape.
- PMID: 31429864
- PubMed abstract
- Source abstract
Editorial:
US Preventive Services Task Force Breast Cancer Recommendation Statement on Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer.
- PMID: 31429868
- PubMed abstract
- Source abstract
News:
USPSTF Calls for More BRCA Screening.
- PMID: 31527132
- PubMed abstract
- Source abstract
Patient Page:
Should I Be Tested for BRCA Mutations?
- PMID: 31429898
- PubMed abstract
- Free Full Text
Audio Interview, CME Activity: USPSTF Recommendation: Assessment, Counseling, and Testing for BRCA-Related Cancer. (JAMA)
Press: USPSTF Recommendations on BRCA Mutation Testing. (Medscape Oncology)
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- Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force.
- Nelson HD, Pappas M, Cantor A, Haney E, Holmes R.
- JAMA. 2019 Aug 20;322(7):666-685. doi: 10.1001/jama.2019.8430.
- PMID: 31429902
- PubMed abstract
- Guidelines
- Free Full Text
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
- PMID: 31429903
- PubMed abstract
- Free Full Text
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA1/2-Related Cancer in Women: A Systematic Review for the U.S. Preventive Services Task Force [Internet].
- PMID: 31479213
- PubMed abstract
- Free Full Text
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- Should I Be Tested for BRCA Mutations?
- Jin J.
- JAMA. 2019 Aug 20;322(7):702. doi: 10.1001/jama.2019.11251.
- PMID: 31429898
- PubMed abstract
- Patient Page
- Free Full Text
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
- PMID: 31429903
- PubMed abstract
- Free Full Text
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- USPSTF Recommendation: Assessment, Counseling, and Testing for BRCA-Related Cancer.
- Mangione CM.
- JAMA. 2019 Aug 20.
- Audio Interview, CME Activity
- Free Audio
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
- PMID: 31429903
- PubMed abstract
- Free Full Text
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- Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA1/2-Related Cancer in Women: A Systematic Review for the U.S. Preventive Services Task Force [Internet].
- Nelson HD, Pappas M, Cantor A, Haney E, Holmes R, Stillman L.
- Rockville (MD): Agency for Healthcare Research and Quality (US); 2019 Aug. Report No.: 19-05251-EF-1. U.S. Preventive Services Task Force Evidence Syntheses, formerly Systematic Evidence Reviews.
- PMID: 31479213
- PubMed abstract
- Source abstract
- Guidelines
- Free Full Text
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer: US Preventive Services Task Force Recommendation Statement.
- PMID: 31429903
- PubMed abstract
- Free Full Text
Guidelines:
Risk Assessment, Genetic Counseling, and Genetic Testing for BRCA-Related Cancer in Women: Updated Evidence Report and Systematic Review for the US Preventive Services Task Force.
- PMID: 31429902
- PubMed abstract
- Free Full Text
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- MAGENTA (Making Genetic testing accessible): a prospective randomized controlled trial comparing online genetic education and telephone genetic counseling for hereditary cancer genetic testing.
- Rayes N, Bowen DJ, Coffin T, Nebgen D, Peterson C, Munsell MF, Gavin K, Lechner R, Crase J, Polinsky D, Romero I, Blank SV, Levine DA, Norquist BM, Swisher EM, Lu KH.
- BMC Cancer. 2019 Jul 2;19(1):648. doi: 10.1186/s12885-019-5868-x.
- PMID: 31266460
- PubMed abstract
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- Accuracy in risk understanding among BRCA1/2-mutation carriers.
- Speiser D, Rebitschek FG, Feufel MA, Brand H, Besch L, Kendel F.
- Patient Educ Couns. 2019 May 5. pii: S0738-3991(18)30887-5. doi: 10.1016/j.pec.2019.05.007. [Epub ahead of print]
- PMID: 31079956
- PubMed abstract
- Source abstract
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- A narrative overview of the patients' outcomes after multigene cancer panel testing, and a thorough evaluation of its implications for genetic counselling.
- Esteban I, Lopez-Fernandez A, Balmaña J.
- Eur J Med Genet. 2019 May;62(5):342-349. doi: 10.1016/j.ejmg.2018.11.027. Epub 2018 Nov 23.
- PMID: 30476626
- PubMed abstract
- Source abstract
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- Development and testing of the KnowGene scale to assess general cancer genetic knowledge related to multigene panel testing.
- Underhill-Blazey M, Stopfer J, Chittenden A, Nayak MM, Lansang K, Lederman R, Garber J, Gundersen DA.
- Patient Educ Couns. 2019 Apr 13. pii: S0738-3991(19)30138-7. doi: 10.1016/j.pec.2019.04.014. [Epub ahead of print]
- PMID: 31010603
- PubMed abstract
- Source abstract
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- Communication about genetic testing with breast and ovarian cancer patients: a scoping review.
- Jacobs C, Patch C, Michie S.
- Eur J Hum Genet. 2019 Apr;27(4):511-524. doi: 10.1038/s41431-018-0310-4. Epub 2018 Dec 20.
- PMID: 30573802
- PubMed abstract
- Review
- Free Full Text
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- Uncertainty related to multigene panel testing for cancer: a qualitative study on counsellors' and counselees' views.
- Medendorp NM, Hillen MA, Murugesu L, Aalfs CM, Stiggelbout AM, Smets EMA.
- J Community Genet. 2019 Apr;10(2):303-312. doi: 10.1007/s12687-018-0393-1. Epub 2018 Nov 14.
- PMID: 30430454
- PubMed abstract
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- Experiences and interpretations of BRCA1/2 testing among women affected by breast or ovarian cancer who received a negative result.
- Stafford L, Flehr A, Judd F, Lindeman GJ, Gibson P, Komiti A, Mann GB, Kentwell M.
- J Community Genet. 2019 Mar 27. doi: 10.1007/s12687-019-00415-w. [Epub ahead of print]
- PMID: 30919324
- PubMed abstract
- Source abstract
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- Impact of Implementing B-RSTTM to Screen for Hereditary Breast and Ovarian Cancer on Risk Perception and Genetic Counseling Uptake Among Women in an Academic Safety Net Hospital.
- Wernke K, Bellcross C, Gabram S, Ali N, Stanislaw C.
- Clin Breast Cancer. 2019 Mar 11. pii: S1526-8209(18)30730-4. doi: 10.1016/j.clbc.2019.02.014. [Epub ahead of print]
- PMID: 31005475
- PubMed abstract
- Source abstract
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- Cancer communication research in the era of genomics and precision medicine: a scoping review.
- Kaphingst KA, Peterson E, Zhao J, Gaysynsky A, Elrick A, Hong SJ, Krakow M, Pokharel M, Ratcliff CL, Klein WMP, Khoury MJ, Chou WS.
- Genet Med. 2018 Dec 21. doi: 10.1038/s41436-018-0402-0. [Epub ahead of print]
- PMID: 30573799
- PubMed abstract
- Source abstract
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- Use and Patient-Reported Outcomes of Clinical Multigene Panel Testing for Cancer Susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study.
- Hall MJ, Patrick-Miller LJ, Egleston BL, Domchek SM, Daly MB, Ganschow P, Grana G, Olopade OI, Fetzer D, Brandt A, Chambers R, Clark DF, Forman A, Gaber R, Gulden C, Horte J, Long JM, Lucas T, Madaan S, Mattie K, McKenna D, Montgomery S, Nielsen S, Powers J, Rainey K, Rybak C, Savage M, Seelaus C, Stoll J, Stopfer JE, Yao XS, Bradbury AR.
- JCO Precis Oncol. 2018;2. doi: 10.1200/PO.18.00199. Epub 2018 Dec 18.
- PMID: 31819920
- PubMed abstract
- Source abstract
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- Black and Minority Ethnic women's decision-making for risk reduction strategies after BRCA testing: Use of context and knowledge.
- Machirori M, Patch C, Metcalfe A.
- Eur J Med Genet. 2018 Dec 12. pii: S1769-7212(18)30405-1. doi: 10.1016/j.ejmg.2018.12.006. [Epub ahead of print]
- PMID: 30550831
- PubMed abstract
- Source abstract
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- A narrative overview of the patients’ outcomes after multigene cancer panel testing: Thorough evaluation of its implications for genetic counselling.
- Estebana I, Lopez-Fernandez A, Balmaña J.
- Eur J Med Genet. 2018 Nov 23. pii: S1769-7212(18)30422-1. doi: 10.1016/j.ejmg.2018.11.027. [Epub ahead of print]
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- Next-Generation Service Delivery: A Scoping Review of Patient Outcomes Associated with Alternative Models of Genetic Counseling and Genetic Testing for Hereditary Cancer.
- McCuaig JM, Armel SR, Care M, Volenik A, Kim RH, Metcalfe KA.
- Cancers (Basel). 2018 Nov 13;10(11). pii: E435. doi: 10.3390/cancers10110435.
- PMID: 30428547
- PubMed abstract
- Source abstract
- Review
- Free Full Text
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- Predictors of risk-reducing surgery intentions following genetic counseling for hereditary breast and ovarian cancer.
- Ladd MK, Peshkin BN, Senter L, Baldinger S, Isaacs C, Segal H, Philip S, Phillips C, Shane K, Martin A, Weinstein V, Pilarski R, Jeter J, Sweet K, Hatten B, Wurtmann EJ, Phippen S, Bro D, Schwartz MD.
- Transl Behav Med. 2018 Nov 10. doi: 10.1093/tbm/iby101. [Epub ahead of print]
- PMID: 30418620
- PubMed abstract
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- Improving comprehension of genetic counseling for hereditary breast and ovarian cancer clients with a visual tool.
- Tea MM, Tan YY, Staudigl C, Eibl B, Renz R, Asseryanis E, Berger A, Pfeiler G, Singer CF.
- PLoS One. 2018 Jul 12;13(7):e0200559. doi: 10.1371/journal.pone.0200559. eCollection 2018.
- PMID: 30001421
- PubMed abstract
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- Patients' Views of Treatment-Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of BRCA1 and BRCA2 Testing.
- Wright S, Porteous M, Stirling D, Lawton J, Young O, Gourley C, Hallowell N.
- J Genet Couns. 2018 May 11. doi: 10.1007/s10897-018-0261-5. [Epub ahead of print]
- PMID: 29752676
- PubMed abstract
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- Communicating with Daughters About Familial Risk of Breast Cancer: Individual, Family, and Provider Influences on Women's Knowledge of Cancer Risk.
- Peipins LA, Rodriguez JL, Hawkins NA, Soman A, White MC, Hodgson ME, DeRoo LA, Sandler DP.
- J Womens Health (Larchmt). 2018 May;27(5):630-639. doi: 10.1089/jwh.2017.6528. Epub 2018 Jan 29.
- PMID: 29377785
- PubMed abstract
- Source abstract
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- Examination of the Patient-Focused Impact of Cancer Telegenetics Among a Rural Population: Comparison with Traditional In-Person Services.
- Solomons NM, Lamb AE, Lucas FL, McDonald EF, Miesfeldt S.
- Telemed J E Health. 2018 Feb;24(2):130-138. doi: 10.1089/tmj.2017.0073. Epub 2017 Jul 21.
- PMID: 28737998
- PubMed abstract
- Source abstract
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- Family Communication, Risk Perception and Cancer Knowledge of Young Adults from BRCA1/2 Families: a Systematic Review.
- Young AL, Butow PN, Vetsch J, Quinn VF, Patenaude AF, Tucker KM, Wakefield CE.
- J Genet Couns. 2017 Dec;26(6):1179-1196. doi: 10.1007/s10897-017-0125-4. Epub 2017 Jun 30.
- PMID: 28667568
- PubMed abstract
- Source 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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- Effect on perceived control and psychological distress of genetic knowledge in women with breast cancer receiving a BRCA1/2 test result.
- Brédart A, Kop JL, De Pauw A, Caron O, Fajac A, Noguès C, Stoppa-Lyonnet D, Dolbeault S.
- Breast. 2017 Feb;31:121-127. doi: 10.1016/j.breast.2016.10.024. Epub 2016 Nov 9.
- PMID: 27837705
- PubMed abstract
- Source abstract
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- Long-term experiences with genetic consultation in people with hereditary breast and ovarian cancer.
- Eismann S, Vetter L, Keller M, Bruckner T, Golatta M, Hennings A, Domschke C, Dikow N, Sohn C, Heil J, Schott S.
- Arch Gynecol Obstet. 2016 Nov;294(5):1011-1018. Epub 2016 Jun 10.
- PMID: 27282618
- PubMed abstract
- Source abstract
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- Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer.
- Jacobs AS, Schwartz MD, Valdimarsdottir H, Nusbaum RH, Hooker GW, DeMarco TA, Heinzmann JE, McKinnon W, McCormick SR, Davis C, Forman AD, Lebensohn AP, Dalton E, Tully DM, Graves KD, Similuk M, Kelly S, Peshkin BN.
- Fam Cancer. 2016 Oct;15(4):529-39. doi: 10.1007/s10689-016-9900-x.
- PMID: 26969308
- PubMed abstract
- Source abstract
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- Quality of Life and Psychological State in Chinese Breast Cancer Patients Who Received BRCA1/2 Genetic Testing.
- Qiu J, Guan J, Yang X, Wu J, Liu G, Di G, Chen C, Hou Y, Han Q, Shen Z, Shao Z, Hu Z.
- PLoS One. 2016 Jul 18;11(7):e0158531. doi: 10.1371/journal.pone.0158531. eCollection 2016.
- PMID: 27428375
- PubMed abstract
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- Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations.
- Manchanda R, Burnell M, Loggenberg K, Desai R, Wardle J, Sanderson SC, Gessler S, Side L, Balogun N, Kumar A, Dorkins H, Wallis Y, Chapman C, Tomlinson I, Taylor R, Jacobs C, Legood R, Raikou M, McGuire A, Beller U, Menon U, Jacobs I.
- J Med Genet. 2016 Jul;53(7):472-80. doi: 10.1136/jmedgenet-2015-103740. Epub 2016 Mar 18.
- PMID: 26993268
- PubMed abstract
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Comments on NSGC Discussion Forum
Subject: Current thoughts on 23andme?
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Retraction:
Retraction: Effects of a pre-visit educational website on information recall and needs fulfilment in breast cancer genetic counselling, a randomized controlled trial.
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