Clients' assessment of, satisfaction with, preferences for, reflections on, criticism/advice on genetic counseling and testing for HBOC
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- Exploring the role of a multidisciplinary hereditary gynecologic oncology clinic in epithelial ovarian cancer risk-reducing surgical decision-making practices: A mixed-methods study.
- Casalino S, Bruce S, Serfas K, Altman AD, Kean S, Lambert P, McManus KJ, Hartley JN, Nachtigal MW.
- J Genet Couns. 2023 Feb 20. doi: 10.1002/jgc4.1684. Epub ahead of print.
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- Measuring high-risk parents' opinions about direct-to-consumer genetic testing for adult-onset inherited cancer syndromes in their adolescent and young adult children.
- Hasser E, Peshkin BN, Hamilton JG, Brower J, Ovadia H, Friedman Ross L, Sacca R, Tarini B, Domchek SM, Vittone S, Sleiman M Jr, Isaacs C, Knerr S, Wilfond BS, Tercyak KP.
- J Genet Couns. 2023 Feb 7. doi: 10.1002/jgc4.1685. Epub ahead of print.
- PMID: 36748334
- PubMed abstract
- Source abstract
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- Predicting Openness of Communication in Families With Hereditary Breast and Ovarian Cancer Syndrome: Natural Language Processing Analysis.
- Baroutsou V, Cerqueira Gonzalez Pena R, Schweighoffer R, Caiata-Zufferey M, Kim S, Hesse-Biber S, Ciorba FM, Lauer G, Katapodi M; CASCADE Consortium.
- JMIR Form Res. 2023 Jan 19;7:e38399. doi: 10.2196/38399.
- PMID: 36656633
- PubMed abstract
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- Adding a genetic counseling assistant improves efficiency of hereditary cancer genetic counseling without impacting patient experience.
- Cohen SA, Nixon DM, Lichtenberg E.
- J Genet Couns. 2023 Jan 8. doi: 10.1002/jgc4.1671. Epub ahead of print.
- PMID: 36617522
- PubMed abstract
- Source abstract
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- Genetic Testing in the Latinx community: Impact of acculturation and provider relationships.
- Ioffe YJ, Hong L, Joachim-Célestin M, Soret C, Montgomery S, Unternaehrer JJ.
- Gynecol Oncol. 2022 Dec 26;169:125-130. doi: 10.1016/j.ygyno.2022.12.001. Epub ahead of print.
- PMID: 36577267
- PubMed abstract
- Source abstract
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- Informational needs of individuals from BRCA-harboring families: a systematic review and content analysis.
- Park SY, Kim Y, Kim S, Katapodi MC.
- Genet Med. 2022 Dec 18:S1098-3600(22)01068-1. doi: 10.1016/j.gim.2022.100001. Epub ahead of print.
- Review
- Free Full Text
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- Patient-reported outcomes associated with reflex BRCA1/2 tumor and subsequent germline panel genetic testing for high-grade serous ovarian cancer.
- McCuaig JM, Stockley TL, Ferguson SE, Vicus D, Brennenstuhl S, Ott K, Kim RH, Metcalfe KA.
- J Genet Couns. 2022 Dec 7. doi: 10.1002/jgc4.1661. Epub ahead of print.
- PMID: 36478486
- PubMed abstract
- Source abstract
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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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- BRCAShare-Assessment of an animated digital message for intrafamilial communication of pathogenic variant positive test results: A feasibility study.
- Aeilts AM, Carpenter KM, Hovick SR, Byrne L, Shoben AB, Senter L.
- J Genet Couns. 2022 Nov 25. doi: 10.1002/jgc4.1656. Epub ahead of print.
- PMID: 36426678
- PubMed abstract
- Source abstract
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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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- Testing a deliberative democracy method with citizens of African ancestry to weigh pros and cons of targeted screening for hereditary breast and ovarian cancer risk.
- Guan Y, Pathak S, Ballard D, Veluswamy JK, McCullough LE, McBride CM, Gornick MC.
- Front Public Health. 2022 Nov 8;10:984926. doi: 10.3389/fpubh.2022.984926.
- PMID: 36424974
- PubMed abstract
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- 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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- From the patient to the population: Use of genomics for population screening.
- Mighton C, Shickh S, Aguda V, Krishnapillai S, Adi-Wauran E, Bombard Y.
- Front Genet. 2022 Oct 24;13:893832. doi: 10.3389/fgene.2022.893832.
- PMID: 36353115
- PubMed abstract
- Review
- Free PMC article
- Free Full Text
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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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- 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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- 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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- Assessment of psychosocial difficulties by genetic clinicians and distress in women at high risk of breast cancer: a prospective study.
- Brédart A, Kop JL, Tüchler A, De Pauw A, Cano A, Dick J, Rhiem K, Devilee P, Schmutzler R, Stoppa-Lyonnet D, Dolbeault S.
- Eur J Hum Genet. 2022 Sep;30(9):1067-1075. doi: 10.1038/s41431-022-01096-9. Epub 2022 Apr 11.
- PMID: 35399119
- PubMed 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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- Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single-institute exploratory study.
- Mochiki I, Okugawa Y, Hashizume R, Imai H, Ikejiri M, Ogura T, Nakatani K, Hori H.
- J Genet Couns. 2022 Aug 25. doi: 10.1002/jgc4.1629. Epub ahead of print.
- PMID: 36007133
- PubMed abstract
- Source abstract
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- I know things now: The challenges for genetic counseling of adolescents with a family history of hereditary breast cancer.
- Wilfond BS.
- J Pediatr. 2022 Aug 16:S0022-3476(22)00728-4. doi: 10.1016/j.jpeds.2022.08.019. Epub ahead of print.
- PMID: 35985537
- PubMed abstract
- Source abstract
Original research:
Mother and Daughter Perspectives on Genetic Counseling and Testing of Adolescents for Hereditary Breast Cancer Risk.
- PMID: 35777474
- 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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- Motivation and family communication in hereditary prostate cancer genetic testing: Survey of patients from a US tertiary medical center.
- Finn CM, McCormick S, Peterson D, Niendorf KB, Rodgers LH.
- J Genet Couns. 2022 Aug 8. doi: 10.1002/jgc4.1624. Epub ahead of print.
- PMID: 35941805
- PubMed abstract
- Source abstract
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- A qualitative reflexive thematic analysis into the experiences of being identified with a BRCA1/2 gene alteration: "So many little, little traumas could have been avoided".
- Warner NZ, Groarke A.
- BMC Health Serv Res. 2022 Aug 6;22(1):1007. doi: 10.1186/s12913-022-08372-w.
- PMID: 35933387
- PubMed abstract
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- Making BRCA1 genetic test reports easier to understand through user-centered design: A randomized trial.
- Recchia G, Lawrence ACE, Capacchione L, Freeman ALJ.
- Genet Med. 2022 Aug;24(8):1684-1696. doi: 10.1016/j.gim.2022.04.016. Epub 2022 May 6.
- PMID: 35522238
- PubMed abstract
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- Experiences of individuals with a variant of uncertain significance on genetic testing for hereditary cancer risks: a mixed method systematic review.
- Gould D, Walker R, Makari-Judson G, Seven M.
- J Community Genet. 2022 Aug;13(4):371-379. doi: 10.1007/s12687-022-00600-4. Epub 2022 Jul 12.
- PMID: 35819584
- PubMed abstract
- Source abstract
- Review
- Free PMC article
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- Adapting a Theoretically-Based intervention for underserved clinical populations at increased risk for hereditary Cancer: Lessons learned from the BRCA-Gist experience.
- Hurtado-de-Mendoza A, Reyna VF, Wolfe CR, Gómez-Trillos S, Sutton AL, Brennan A, Sheppard VB.
- Prev Med Rep. 2022 Jul 5 [eCollection 2022 Aug];28:101887. doi: 10.1016/j.pmedr.2022.101887.
- PMID: 35855922
- PubMed abstract
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- Genetic counselors' experience with reimbursement and patient out-of-pocket cost for multi-cancer gene panel testing for hereditary cancer syndromes.
- Weldon CB, Trosman JR, Liang SY, Douglas MP, Scheuner MT, Kurian A, Schaa KL, Roscow B, Erwin D, Phillips KA.
- J Genet Couns. 2022 Jul 28. doi: 10.1002/jgc4.1614. Epub ahead of print.
- PMID: 35900261
- PubMed abstract
- Source abstract
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- 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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- Insight into how patients with prostate cancer interpret and communicate genetic test results: implications for families.
- Leader AE, Mercado J, Klein A, Hyatt C, Gross L, Brandt R, Giri VN.
- J Community Genet. 2022 Jul 22. doi: 10.1007/s12687-022-00603-1. Epub ahead of print.
- PMID: 35869324
- 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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- Contraception and Hormone Replacement Therapy in Healthy Carriers of Germline BRCA1/2 Genes Pathogenic Variants: Results from an Italian Survey.
- Massarotti C, Buonomo B, Dellino M, Campanella M, De Stefano C, Ferrari A, Anserini P, Lambertini M, Peccatori FA.
- Cancers (Basel). 2022 Jul 15;14(14):3457. doi: 10.3390/cancers14143457.
- PMID: 35884518
- PubMed abstract
- Source 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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- Women's thoughts on receiving and sharing genetic information: Considerations for genetic counseling.
- Pfledderer CD, Gren LH, Frost CJ, Andrulis IL, Chung WK, Genkinger J, Glendon G, Hopper JL, John EM, Southey M, Terry MB, Daly MB.
- J Genet Couns. 2022 Jul 6. doi: 10.1002/jgc4.1599. Epub ahead of print.
- PMID:35794807
- PubMed abstract
- Source abstract
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- Hereditary ovarian cancer risk reduction: a retrospective evaluation of patient perspectives and service provision at a regional hereditary gynaecologic cancer clinic 2006-2016.
- Adolph L, Warias A, Stairs J, Collins-McNeil K, Penney L, Kieser K.
- BMC Womens Health. 2022 Jun 29;22(1):263. doi: 10.1186/s12905-022-01844-5.
- PMID: 35768821
- PubMed abstract
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- Mother and Daughter Perspectives on Genetic Counseling and Testing of Adolescents for Hereditary Breast Cancer Risk.
- Jennings C, Wynn J, Miguel C, Levinson E, Florido ME, White M, Sands CB, Schwartz LA, Daly M, O'Toole K, Buys SS, Glendon G, Hanna D, Andrulis IL, Terry MB, Chung WK, Bradbury A.
- J Pediatr. 2022 Jun 28:S0022-3476(22)00601-1. doi: 10.1016/j.jpeds.2022.06.027. Epub ahead of print.
- PMID: 35777474
- PubMed abstract
- Source abstract
Commentary:
I know things now: The challenges for genetic counseling of adolescents with a family history of hereditary breast cancer.
- PMID: 35985537
- PubMed abstract
- Source abstract
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- Pilot study of a culturally sensitive intervention to promote genetic counseling for breast cancer risk.
- Henderson V, Madrigal JM, Kendall LC, Parekh P, Newsome J, Chukwudozie IB, Comer-Hagans L, Coffey V, Grumbach G, Spencer S, Rodgers C, Kaur R, Balay L, Maga T, Ramamonjiarivelo Z, Balthazar C, Winn R, Watson K, Odoms-Young A, Hoskins KF.
- BMC Health Serv Res. 2022 Jun 25;22(1):826. doi: 10.1186/s12913-022-08193-x.
- PMID: 35752812
- PubMed abstract
Identifier: NCT04082117: Uptake of Genetic Counseling Among African American Women. (ClinicalTrials.gov)
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- Population-based BRCA1/2 testing programmes are highly acceptable in the Jewish community: results of the JeneScreen Study.
- Tiller JM, Cousens NE, Kaur R, Rowley S, Ko YA, Mahale S, Bankier A, Meiser B, Barlow-Stewart K, Burnett L, Jacobs C, James P, Trainer A, Neil S, Campbell IG, Andrews L, Delatycki M.
- J Med Genet. 2022 Jun 3:jmedgenet-2022-108519. doi: 10.1136/jmedgenet-2022-108519. Epub ahead of print.
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- Perceptions and care Recommendations from Previvors: Qualitative analysis of female BRCA1/2 mutation Carriers' experience with genetic testing and counseling.
- Dibble KE, Donorfio LKM, Britner PA, Bellizzi KM.
- Gynecol Oncol Rep. 2022 May 2 [eCollection 2022 Jun];41:100989. doi: 10.1016/j.gore.2022.100989.
- PMID: 35540028
- PubMed abstract
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- Attitudes and interest in incorporating BRCA1/2 cancer susceptibility testing into reproductive carrier screening for Ashkenazi Jewish men and women.
- Hardy MW, Peshkin BN, Rose E, Ladd MK, Binion S, Tynan M, McBride CM, Grinzaid KA, Schwartz MD.
- J Community Genet. 2022 Jun;13(3):281-292. doi: 10.1007/s12687-022-00590-3. Epub 2022 Apr 29.
- PMID: 35486291
- PubMed abstract
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- Assessing the acceptability, feasibility, and usefulness of a psychosocial screening tool to patients and clinicians in a clinical genetics service in Australia.
- Monohan K, Purvis R, Sexton A, Kentwell M, Thet M, Stafford L, Forrest L.
- J Genet Couns. 2022 Jun;31(3):653-662. doi: 10.1002/jgc4.1532. Epub 2021 Nov 17.
- PMID: 34788484
- PubMed abstract
- Source abstract
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- Transgender patients' perspectives on their cancer genetic counseling experiences.
- Rolle L, Zayhowski K, Koeller D, Chiluiza D, Carmichael N.
- J Genet Couns. 2022 Jun;31(3):781-791. doi: 10.1002/jgc4.1544. Epub 2021 Dec 28.
- PMID: 34964220
- PubMed abstract
- Source abstract
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- Personalised Risk Prediction in Hereditary Breast and Ovarian Cancer: A Protocol for a Multi-Centre Randomised Controlled Trial.
- Archer S, Fennell N, Colvin E, Laquindanum R, Mills M, Dennis R, Stutzin Donoso F, Gold R, Fan A, Downes K, Ford J, Antoniou AC, Kurian AW, Evans DG, Tischkowitz M.
- Cancers (Basel). 2022 May 31;14(11):2716. doi: 10.3390/cancers14112716.
- PMID: 35681696
- PubMed abstract
- Source abstract
- Study protocol
- Free PMC article
- Free Full Text
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- Patient Experience with a Gynecologic Oncology-Initiated Genetic Testing Model for Women with Tubo-Ovarian Cancer.
- Sadinsky MB, Power J, Ambrosio E, Palma L, Zeng X, Foulkes WD, Weber E.
- Curr Oncol. 2022 May 15;29(5):3565-3575. doi: 10.3390/curroncol29050288.
- PMID: 35621678
- PubMed abstract
- Source abstract
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- Psychosocial impact of proactive rapid genetic counseling following breast cancer diagnosis.
- Kritzik R, Usoro E, Peshkin BN, Isaacs C, Valdimarsdottir HB, Willey S, O'Neill S, DeMarco T, Nusbaum R, Jandorf L, Kelleher S, Schwartz MD.
- Psychooncology. 2022 May;31(5):788-797. doi: 10.1002/pon.5863. Epub 2021 Dec 18.
- PMID: 34921700
- PubMed abstract
- Source abstract
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- Unselected Population Genetic Testing for Personalised Ovarian Cancer Risk Prediction: A Qualitative Study Using Semi-Structured Interviews.
- Gaba F, Oxley S, Liu X, Yang X, Chandrasekaran D, Kalsi J, Antoniou A, Side L, Sanderson S, Waller J, Ahmed M, Wallace A, Wallis Y, Menon U, Jacobs I, Legood R, Marks D, Manchanda R.
- Diagnostics (Basel). 2022 Apr 19;12(5):1028. doi: 10.3390/diagnostics12051028.
- PMID: 35626184
- PubMed abstract
- Source abstract
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- Reflex BRCA1 and BRCA2 tumour genetic testing for high-grade serous ovarian cancer: streamlined for clinicians but what do patients think?
- McCuaig JM, Ferguson SE, Vicus D, Ott K, Stockley TL, Kim RH, Metcalfe KA.
- Hered Cancer Clin Pract. 2022 Apr 13;20(1):15. doi: 10.1186/s13053-022-00221-5.
- PMID: 35418215
- PubMed abstract
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- Psychological Determinants of Men's Adherence to Cascade Screening for BRCA1/2.
- Ongaro G, Petrocchi S, Calvello M, Bonanni B, Feroce I, Pravettoni G.
- Curr Oncol. 2022 Apr 2;29(4):2490-2503. doi: 10.3390/curroncol29040203.
- PMID: 35448177
- PubMed abstract
- Source abstract
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- Large-scale group genetic counseling: Evaluation of a novel service delivery model in a Canadian hereditary cancer clinic.
- Lohn Z, Fok A, Richardson M, Derocher H, Mung SW, Nuk J, Yuson J, Jevon M, A Schrader K, Sun S.
- J Genet Couns. 2022 Apr;31(2):459-469. doi: 10.1002/jgc4.1512. Epub 2021 Oct 1.
- PMID: 34596310
- PubMed abstract
- Source abstract
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- Japanese women's reasons for accompaniment status to hereditary breast and ovarian cancer-focused genetic counseling.
- Matsukawa M, Torishima M, Satoh C, Honda S, Kosugi S.
- J Genet Couns. 2022 Apr;31(2):497-509. doi: 10.1002/jgc4.1519. Epub 2021 Oct 18.
- PMID: 34661949
- PubMed abstract
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- Assessing the relationship between patient preferences for recontact after BRCA1 or BRCA2 genetic testing and their monitoring coping style in a Norwegian sample.
- Dahle Ommundsen RM, Strømsvik N, Hamang A.
- J Genet Couns. 2022 Apr;31(2):554-564. doi: 10.1002/jgc4.1526. Epub 2021 Oct 30.
- PMID: 34716741
- PubMed abstract
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- Attitude towards hereditary cancer risk management among women with cancer in Taiwan.
- Fang SY, Hsieh LL, Hung CF, Hung FH, Peng HP, Yang AS, Wang YA.
- Support Care Cancer. 2022 Apr;30(4):3625-3632. doi: 10.1007/s00520-021-06742-4. Epub 2022 Jan 14.
- PMID: 35028717
- PubMed abstract
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- Intention to Inform Relatives, Rates of Cascade Testing, and Preference for Patient-Mediated Communication in Families Concerned with Hereditary Breast and Ovarian Cancer and Lynch Syndrome: The Swiss CASCADE Cohort.
- Sarki M, Ming C, Aissaoui S, Bürki N, Caiata-Zufferey M, Erlanger TE, Graffeo-Galbiati R, Heinimann K, Heinzelmann-Schwarz V, Monnerat C, Probst-Hensch N, Rabaglio M, Zürrer-Härdi U, Chappuis PO, Katapodi MC, On Behalf Of The Cascade Consortium.
- Cancers (Basel). 2022 Mar 23;14(7):1636. doi: 10.3390/cancers14071636.
- PMID: 35406409
- PubMed abstract
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- Hospital-based ovarian cancer patient traceback program results in minimal genetic testing uptake.
- Weinmann S, Phillips S, Sweet K, Cosgrove CM, Senter L.
- Gynecol Oncol. 2022 Mar;164(3):615-621. doi: 10.1016/j.ygyno.2021.12.027. Epub 2022 Jan 5.
- PMID: 34998598
- PubMed abstract
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- "It was an important part of my treatment": a qualitative study of Norwegian breast Cancer patients' experiences with mainstreamed genetic testing.
- Strømsvik N, Olsson P, Gravdehaug B, Lurås H, Schlichting E, Jørgensen K, Wangensteen T, Vamre T, Heramb C, Mæhle L, Grindedal EM.
- Hered Cancer Clin Pract. 2022 Feb 5;20(1):6. doi: 10.1186/s13053-022-00212-6.
- PMID: 35123550
- PubMed abstract
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- Stakeholder attitudes towards establishing a national genomics registry of inherited cancer predisposition: a qualitative study.
- Meiser B, Monnik M, Austin R, Nichols C, Cops E, Salmon L, Spurdle AB, Macrae F, Taylor N, Pachter N, James P, Kaur R.
- J Community Genet. 2022 Feb;13(1):59-73. doi: 10.1007/s12687-021-00559-8. Epub 2021 Nov 2.
- PMID: 34727336
- PubMed abstract
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- Heterogeneity in how women value risk-stratified breast screening.
- Wheeler JCW, Keogh L, Sierra MA, Devereux L, Jones K, IJzerman MJ, Trainer AH.
- Genet Med. 2022 Jan;24(1):146-156. doi: 10.1016/j.gim.2021.09.002. Epub 2021 Nov 30.
- PMID: 34906505
- PubMed abstract
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- Unselected Women's Experiences of Receiving Genetic Research Results for Hereditary Breast and Ovarian Cancer: A Qualitative Study.
- Forbes Shepherd R, Forrest LE, Tutty E, Pearce A, Devereux L, James PA, Campbell IG, Trainer A, Young MA.
- Genet Test Mol Biomarkers. 2021 Dec;25(12):741-748. doi: 10.1089/gtmb.2021.0115.
- PMID: 34918982
- PubMed abstract
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- Understanding patients' views and willingness toward the use of telehealth in a cancer genetics service in Asia.
- Sim J, Shaw T, Li ST, Courtney E, Yuen J, Chiang J, Nazir M, Tan R, Ngeow J.
- J Genet Couns. 2021 Dec;30(6):1658-1670. doi: 10.1002/jgc4.1432. Epub 2021 May 1.
- PMID: 33934420
- PubMed abstract
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- The role of psychosocial factors in Black women's self-efficacy in receiving genetic counseling and testing.
- Ding H, Sutton AL, Hurtado-de-Mendoza A, Sheppard VB.
- J Genet Couns. 2021 Dec;30(6):1719-1726. doi: 10.1002/jgc4.1439. Epub 2021 Jun 4.
- PMID: 34085362
- PubMed abstract
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- Implication and Influence of Multigene Panel Testing with Genetic Counseling in Korean Patients with BRCA1/2 Mutation-Negative Breast Cancer.
- Park JS, Shin S, Lee YJ, Lee ST, Nam EJ, Han JW, Lee SH, Kim TI, Park HS.
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Press: Shortage of Genetic Counselors in Face of Growing Need. (Medscape Conference News)
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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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