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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- Australasian Genetic Counselors’ Perceptions of Their Role in Supporting Clients’ Behavior Change.
- Jacobs C, Turbitt E, McEwen A, Atkins L.
- J Pers Med. 2022 Dec 23;13(1):30. doi: 10.3390/jpm13010030.
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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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- Investigating the presentation of uncertainty in an icon array: A randomized trial.
- Recchia G, Lawrence ACE, Freeman ALJ.
- PEC Innov. 2022 Dec;1:None. doi: 10.1016/j.pecinn.2021.100003.
- PMID: 36518604
- PubMed 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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- 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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- Use of a chatbot to increase uptake of cascade genetic testing.
- Schmidlen T, Jones CL, Campbell-Salome G, McCormick CZ, Vanenkevort E, Sturm AC.
- J Genet Couns. 2022 Oct;31(5):1219-1230. doi: 10.1002/jgc4.1592. Epub 2022 May 26.
- PMID: 35616645
- PubMed abstract
- Source abstract
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- Validation of the Knowledge of Genome Sequencing (KOGS) scale in cancer patients.
- Butow P, Napier C, Campbell R, Bartley N, Best M, Ballinger ML.
- Patient Educ Couns. 2022 Oct;105(10):3110-3115. doi: 10.1016/j.pec.2022.06.009. Epub 2022 Jun 16.
- PMID: 35738962
- PubMed abstract
- Source abstract
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- Patient Understanding of Tumor Genomic Testing: A Quality Improvement Effort.
- Senter L, Veney D, Surplus T, Haynam M, Adams EJ, Hampel H, Toland AE, Presley CJ, Padamsee TJ, Lee CN, Hovick SR, Stover DG.
- JCO Oncol Pract. 2022 Sep 21:OP2200316. doi: 10.1200/OP.22.00316. Epub ahead of print.
- PMID: 36130146
- 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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- 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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- How do women who are informed that they are at increased risk of breast cancer appraise their risk? A systematic review of qualitative research.
- Woof VG, Howell A, McWilliams L, Gareth Evans D, French DP.
- Br J Cancer. 2022 Aug 24. doi: 10.1038/s41416-022-01944-x. Epub ahead of print.
- PMID: 36002751
- PubMed abstract
- Review
- Free Full Text
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- Further validation of the Perceptions of Uncertainties in Genome Sequencing scale among patients with cancer undergoing tumor sequencing.
- Umstead KL, Campbell R, Napier CE, Bartley N, Best MC, Butow PN, Biesecker BB.
- Clin Genet. 2022 Aug;102(2):110-116. doi: 10.1111/cge.14169. Epub 2022 Jun 10.
- PMID: 35615816
- PubMed abstract
- Source 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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- Cancer patients' understandings of genetic variants of uncertain significance in clinical care.
- Amano Y, Raz A, Timmermans S, Shkedi-Rafid S.
- J Community Genet. 2022 Aug;13(4):381-388. doi: 10.1007/s12687-022-00594-z. Epub 2022 May 26.
- PMID: 35616809
- PubMed abstract
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- Comparing the attitudes of physicians and non-physicians toward communicating a patient's BRCA1 mutation to a first-degree relative against a patient's wishes.
- Zebrack JE, Yang W, Milone M, Coppes MJ.
- J Community Genet. 2022 Aug;13(4):403-410. doi: 10.1007/s12687-022-00591-2. Epub 2022 May 21.
- PMID: 35596048
- PubMed abstract
- Source abstract
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- Toward a better understanding of the experience of patients with moderate penetrance breast cancer gene pathogenic/likely pathogenic variants: A focus on ATM and CHEK2.
- McCormick S, Hicks S, Wooters M, Grant C.
- J Genet Couns. 2022 Aug;31(4):956-964. doi: 10.1002/jgc4.1568. Epub 2022 Mar 4.
- PMID: 35246915
- PubMed abstract
- Source abstract
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- The Communication Chain of Genetic Risk: Analyses of Narrative Data Exploring Proband–Provider and Proband–Family Communication in Hereditary Breast and Ovarian Cancer.
- Pedrazzani C, Aceti M, Schweighoffer R, Kaiser-Grolimund A, Bürki N, Chappuis PO, Graffeo R, Monnerat C, Pagani O, Rabaglio M, Katapodi MC, Caiata-Zufferey M.
- J Pers Med. 2022 Jul 29;12(8):1249. doi: 10.3390/jpm12081249.
- PMID: 36013197
- PubMed abstract
- Source abstract
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- A qualitative study of unaffected ATM and CHEK2 carriers: How participants make meaning of 'moderate risk' genetic results in a population breast cancer screening trial.
- James JE, Riddle L, Caruncho M, Koenig BA, Joseph G.
- J Genet Couns. 2022 Jul 25. doi: 10.1002/jgc4.1617. Epub ahead of print.
- PMID: 35877161
- PubMed abstract
- Source 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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- 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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- Genetic clinicians' confidence in BOADICEA comprehensive breast cancer risk estimates and counselees' psychosocial outcomes: a prospective study.
- Brédart A, De Pauw A, Tüchler A, Lakeman IMM, Anota A, Rhiem K, Schmutzler R, van Asperen CJ, Devilee P, Stoppa-Lyonnet D, Kop JL, Dolbeault S.
- Clin Genet. 2022 Jul;102(1):30-39. doi: 10.1111/cge.14147. Epub 2022 May 16.
- PMID: 35508697
- PubMed abstract
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- Validation of the Knowledge of Genome Sequencing (KOGS) scale in cancer patients.
- Butow P, Napier C, Campbell R, Bartley N, Best M, Ballinger ML.
- Patient Educ Couns. 2022 Jun 16:S0738-3991(22)00287-7. doi: 10.1016/j.pec.2022.06.009. Epub ahead of print.
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- Healthcare Predictors of Information Dissemination About Genetic Risks.
- Henderson V, Strayhorn SM, Bergeron NQ, Strahan DC, Ganschow PS, Khanna AS, Watson K, Hoskins K, Molina Y.
- Cancer Control. 2022 Jan-Dec [First Published 2022 Jun 6];29:10732748221104666. doi: 10.1177/10732748221104666.
- PMID: 35658635
- PubMed abstract
- Source abstract
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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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- Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access.
- Amendola LM, Shuster E, Leo MC, Dorschner MO, Rolf BA, Shirts BH, Gilmore MJ, Okuyama S, Zepp JM, Kauffman TL, Mittendorf KF, Bellcross C, Jenkins CL, Joseph G, Riddle L, Syngal S, Ukaegbu C, Goddard KAB, Wilfond BS, Jarvik GP; CHARM Study.
- Genet Med. 2022 Jun;24(6):1196-1205. doi: 10.1016/j.gim.2022.02.006. Epub 2022 Mar 16.
- PMID: 35305866
- PubMed abstract
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- Medical knowledge and information needs among women with pathogenic variants in moderate-risk genes for hereditary breast cancer attending genetic counseling at an academic hospital in Germany-A qualitative approach.
- Stracke C, Lemmen C, Rhiem K, Schmutzler R, Kautz-Freimuth S, Stock S.
- J Genet Couns. 2022 Jun;31(3):698-712. doi: 10.1002/jgc4.1536. Epub 2021 Nov 26.
- PMID: 34837291
- PubMed abstract
- Source abstract
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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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- Testing a best practices risk result format to communicate genetic risks.
- Davis KW, Roter DL, Schmidlen T, Scheinfeldt LB, Klein WMP.
- Patient Educ Couns. 2021 May;104(5):936-943. doi: 10.1016/j.pec.2020.10.021. Epub 2020 Oct 19.
- PMID: 33131927
- PubMed abstract
- Source abstract
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- How patients deal with an ambiguous medical test: Decision-making after genetic testing.
- Scherr CL, Ramesh S, Getachew-Smith H, Kalke K, Ramsey K, Fischhoff B, Vadaparampil ST.
- Patient Educ Couns. 2021 May;104(5):953-959. doi: 10.1016/j.pec.2020.10.020. Epub 2020 Oct 18.
- PMID: 33214013
- 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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- Incomplete Penetrance of Population-Based Genetic Screening Results in Electronic Health Record.
- Elhanan G, Kiser D, Neveux I, Dabe S, Bolze A, Metcalf WJ, Lu JT, Grzymski JJ.
- Front Genet. 2022 Apr 27;13:866169. doi: 10.3389/fgene.2022.866169.
- PMID: 35571025
- PubMed 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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- "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. 2022 Apr;21(2):143-155. doi: 10.1007/s10689-021-00251-3. Epub 2021 Apr 15.
- PMID: 33855648
- 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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- Psychosocial outcome and health behaviour intent of breast cancer patients with BRCA1/2 and PALB2 pathogenic variants unselected by a priori risk.
- Padmanabhan H, Hassan NT, Wong SW, Lee YQ, Lim J, Hasan SN, Yip CH, Teo SH, Thong MK, Mohd Taib NA, Yoon SY.
- PLoS One. 2022 Feb 15;17(2):e0263675. doi: 10.1371/journal.pone.0263675.
- PMID: 35167615
- PubMed abstract
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- Characteristics and experiences of patients from a community-based and consumer-directed hereditary cancer population screening initiative.
- Greve V, Odom K, Pudner S, Lamb NE, Cooper SJ, East K.
- HGG Adv. 2021 Aug 24 [eCollection 2022 Jan 13];3(1):100055. doi: 10.1016/j.xhgg.2021.100055.
- PMID: 35047846
- PubMed abstract
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- Genetic Literacy and Communication of Genetic Information in Families Concerned with Hereditary Breast and Ovarian Cancer: A Cross-Study Comparison in Two Countries and within a Timeframe of More Than 10 Years.
- Pedrazzani C, Ming C, Bürki N, Caiata-Zufferey M, Chappuis PO, Duquette D, Heinimann K, Heinzelmann-Schwarz V, Graffeo-Galbiati R, Merajver SD, Milliron KJ, Monnerat C, Pagani O, Rabaglio M, Katapodi MC.
- Cancers (Basel). 2021 Dec 13;13(24):6254. doi: 10.3390/cancers13246254.
- PMID: 34944873
- PubMed abstract
- Source abstract
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- Information needs on breast cancer genetic and non-genetic risk factors in relatives of women with a BRCA1/2 or PALB2 pathogenic variant.
- Brédart A, De Pauw A, Anota A, Tüchler A, Dick J, Müller A, Kop JL, Rhiem K, Schmutzler R, Devilee P, Stoppa-Lyonnet D, Dolbeault S.
- Breast. 2021 Dec;60:38-44. doi: 10.1016/j.breast.2021.08.011. Epub 2021 Aug 23.
- PMID: 34455229
- 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.
- Cancer Res Treat. 2021 Nov 17. doi: 10.4143/crt.2021.978. Epub ahead of print.
- PMID: 34793666
- PubMed abstract
- Source abstract
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- Telephone versus in-person genetic counseling for hereditary cancer risk: Patient predictors of differential outcomes.
- Binion S, Sorgen LJ, Peshkin BN, Valdimarsdottir H, Isaacs C, Nusbaum R, Graves KD, DeMarco T, Wood M, McKinnon W, Garber J, McCormick S, Ladd MK, Schwartz MD.
- J Telemed Telecare. 2021 Nov 15:1357633X211052220. doi: 10.1177/1357633X211052220. Epub ahead of print.
- PMID: 34779303
- PubMed abstract
- Source abstract
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- Challenges and Errors in Genetic Testing: The Fifth Case Series.
- Farmer MB, Bonadies DC, Pederson HJ, Mraz KA, Whatley JW, Darnes DR, Denton JJ, De Rosa D, Heatherly A, Kenney J, Lane K, Paul D, Pelletier RC, Shannon K, Williams D, Matloff ET.
- Cancer J. 2021 Nov-Dec 01;27(6):417-422. doi: 10.1097/PPO.0000000000000553.
- PMID: 34904802
- PubMed abstract
- Source abstract
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- Disparities between Uptake of Germline BRCA1/2 Gene Tests and Implementation of Post-test Management Strategies in Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer Patients.
- Hur YM, Mun J, Kim MK, Lee M, Kim YH, Kim SC.
- J Korean Med Sci. 2021 Oct 4;36(38):e241. doi: 10.3346/jkms.2021.36.e241.
- PMID: 34609091
- PubMed abstract
- Source abstract
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- Genetic counseling clinical documentation: Practice Resource of the National Society of Genetic Counselors.
- Hunt Brendish K, Patel D, Yu K, Alexander CK, Lemons J, Gunter A, Carmany EP.
- J Genet Couns. 2021 Oct;30(5):1336-1353. doi: 10.1002/jgc4.1491. Epub 2021 Aug 14.
- PMID: 34390070
- PubMed abstract
- Source abstract
- Guideline
- Free Full Text
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- Alternative Genetic Counseling Approach Leads to Higher Patient Satisfaction, Study Suggests.
- Curtin C.
- GenomeWeb. Research & Discovery. 2021 Sep 27.
- Conference report
- Free Full Text
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- Pretest Genetic Education Video Versus Genetic Counseling for Men Considering Prostate Cancer Germline Testing: A Patient-Choice Study to Address Urgent Practice Needs.
- Russo J, McDougall C, Bowler N, Shimada A, Gross L, Hyatt C, Kelly WK, Calvaresi A, Handley NR, Hirsch IH, Izes JK, Lallas CD, Mann M, Mark JR, Mille PJ, Preate D Jr, Trabulsi EJ, Tsang M, Chandrasekar T, Weiner PR, Gomella LG, Giri VN.
- JCO Precis Oncol. 2021 Sep 1;5:PO.21.00238. doi: 10.1200/PO.21.00238.
- PMID: 34589662
- PubMed abstract
- Source abstract
Research news: Men Give Thumbs Up to Video on Genetic Testing in Prostate Cancer. (Medscape Oncology)
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- Frequency of Contralateral Prophylactic Mastectomy in Breast Cancer Patients with a Negative BRCA1 and BRCA2 Rapid Genetic Test Result.
- Metcalfe KA, Eisen A, Poll A, Candib A, McCready D, Cil T, Wright F, Demsky R, Mancuso T, Sun P, Narod SA.
- Ann Surg Oncol. 2021 Sep;28(9):4967-4973. doi: 10.1245/s10434-021-09855-6. Epub 2021 Mar 24.
- PMID: 33761021
- PubMed abstract
- Source abstract
Commentary:
Genetic Testing and De-escalation of Contralateral Prophylactic Mastectomy.
- PMID: 33796999
- PubMed abstract
- Free Full Text
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- Patient-Reported Outcomes following Genetic Testing for Familial Hypercholesterolemia, Breast and Ovarian Cancer Syndrome, and Lynch Syndrome: A Systematic Review.
- Hendricks-Sturrup RM, Joseph L, Lu CY.
- J Pers Med. 2021 Aug 27;11(9):850. doi: 10.3390/jpm11090850.
- PMID: 34575627
- PubMed abstract
- Source abstract
- Review
- Free PMC article
- Free Full Text
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- Community research collaboration to develop a promotores-based hereditary breast cancer education program for Spanish-speaking Latinas.
- Almeida R, Lopez-Macha A, Dugatkin T, Joseph G, Duron Y, Hurtado de Mendoza A, D Graves K, Fejerman L.
- Health Educ Res. 2021 Jun 11:cyab011. doi: 10.1093/her/cyab011. Epub ahead of print.
- PMID: 34113985
- 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.
- Milo Rasouly H, 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. 2021 Jun;30(3):742-754. doi: 10.1002/jgc4.1364. Epub 2020 Dec 26.
- PMID: 33368851
- PubMed abstract
- Source abstract
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- A Collaborative Model to Implement Flexible, Accessible and Efficient Oncogenetic Services for Hereditary Breast and Ovarian Cancer: The C-MOnGene Study.
- Lapointe J, Dorval M, Chiquette J, Joly Y, Guertin JR, Laberge M, Gekas J, Hébert J, Pomey MP, Cruz-Marino T, Touhami O, Blanchet Saint-Pierre A, Gagnon S, Bouchard K, Rhéaume J, Boisvert K, Brousseau C, Castonguay L, Fortier S, Gosselin I, Lachapelle P, Lavoie S, Poirier B, Renaud MC, Ruizmangas MG, Sebastianelli A, Roy S, Côté M, Racine MM, Roy MC, Côté N, Brisson C, Charette N, Faucher V, Leblanc J, Dubeau MÈ, Plante M, Desbiens C, Beaumont M, Simard J, Nabi H.
- Cancers (Basel). 2021 May 31;13(11):2729. doi: 10.3390/cancers13112729.
- PMID: 34072979
- PubMed abstract
- Source abstract
- Study protocol
- Free PMC article
- Free Full Text
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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 May;161(2):516-520. doi: 10.1016/j.ygyno.2021.02.013. Epub 2021 Feb 19.
- PMID: 33618842
- PubMed abstract
- Source abstract
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- A Comparison of Patient-Reported Outcomes Following Consent for Genetic Testing Using an Oncologist- or Genetic Counselor-Mediated Model of Care.
- McCuaig JM, Thain E, Malcolmson J, Keshavarzi S, Armel SR, Kim RH.
- Curr Oncol. 2021 Apr 8;28(2):1459-1471. doi: 10.3390/curroncol28020138.
- PMID: 33917963
- 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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- Psychosocial Interventions for Women with a BRCA1 or BRCA2 Mutation: A Scoping Review.
- Boghosian T, McCuaig JM, Carlsson L, Metcalfe KA.
- Cancers (Basel). 2021 Mar 24;13(7):1486. doi: 10.3390/cancers13071486.
- PMID: 33804884
- PubMed abstract
- Source abstract
- Review
- Free PMC article
- Free Full Text
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- Variations in breast cancer surgical treatment and timing: determinants and disparities.
- Dankwa-Mullan I, George J, Roebuck MC, Tkacz J, Willis VC, Reyes F, Arriaga YE.
- Breast Cancer Res Treat. 2021 Mar 10. doi: 10.1007/s10549-021-06155-1. Epub ahead of print.
- PMID: 33689057
- PubMed abstract
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- 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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- 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. 2021 Jan 19;5:PO.20.00199. doi: 10.1200/PO.20.00199.
- PMID: 34250392
- PubMed abstract
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Press: Survey: Genetic Counseling Leads Some Patients to Cheaper BRCA Tests. (GenomeWeb)
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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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- Cognitive and Psychological Impact of BRCA Genetic Counseling in Before and After Definitive Surgery Breast Cancer Patients.
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News:
Pretest genetic counseling informs patients with BRCA mutation.
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Press Release: Pre-Test Genetic Counseling Increases Cancer Knowledge for BRCA Patients (Moffitt Cancer Center)
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- French women's breast self-examination practices with time after undergoing BRCA1/2 genetic testing.
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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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- Retraction Note
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- Permanence of the information given during oncogenetic counseling to persons at familial risk of breast/ovarian and/or colon cancer.
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- Exploring the short-term impact of DNA-testing in breast cancer patients: the counselees' perception matters, but the actual BRCA1/2 result does not.
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