171 related articles for article (PubMed ID: 29124491)
1. From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals.
Augusto BM; Lake P; Scherr CL; Couch FJ; Lindor NM; Vadaparampil ST
J Community Genet; 2018 Jul; 9(3):209-215. PubMed ID: 29124491
[TBL] [Abstract][Full Text] [Related]
2. Genetic counselors' practices and confidence regarding variant of uncertain significance results and reclassification from BRCA testing.
Scherr CL; Lindor NM; Malo TL; Couch FJ; Vadaparampil ST
Clin Genet; 2015 Dec; 88(6):523-9. PubMed ID: 25640009
[TBL] [Abstract][Full Text] [Related]
3. A preliminary investigation of genetic counselors' information needs when receiving a variant of uncertain significance result: a mixed methods study.
Scherr CL; Lindor NM; Malo TL; Couch FJ; Vadaparampil ST
Genet Med; 2015 Sep; 17(9):739-46. PubMed ID: 25569439
[TBL] [Abstract][Full Text] [Related]
4. Experiences of patients seeking to participate in variant of uncertain significance reclassification research.
Makhnoon S; Garrett LT; Burke W; Bowen DJ; Shirts BH
J Community Genet; 2019 Apr; 10(2):189-196. PubMed ID: 30027524
[TBL] [Abstract][Full Text] [Related]
5. Patient goals, motivations, and attitudes in a patient-driven variant reclassification study.
Tsai GJ; Garrett LT; Makhnoon S; Bowen DJ; Burke W; Shirts BH
J Genet Couns; 2019 Jun; 28(3):558-569. PubMed ID: 31163102
[TBL] [Abstract][Full Text] [Related]
6. Assessing parental understanding of variant reclassification in pediatric neurology and developmental pediatrics clinics.
Margolin A; Helm BM; Treat K; Prucka SK; Halverson CME
J Community Genet; 2021 Oct; 12(4):663-670. PubMed ID: 34558037
[TBL] [Abstract][Full Text] [Related]
7. Next-Generation Sequencing in Order to Better Characterize a BRCA Variant of Uncertain Significance.
Sorscher S; Ramkissoon S
Case Rep Oncol; 2017; 10(2):634-637. PubMed ID: 28868023
[TBL] [Abstract][Full Text] [Related]
8. Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance.
Tsai GJ; RaƱola JMO; Smith C; Garrett LT; Bergquist T; Casadei S; Bowen DJ; Shirts BH
Genet Med; 2019 Jun; 21(6):1435-1442. PubMed ID: 30374176
[TBL] [Abstract][Full Text] [Related]
9. Assessing management practices for variants of uncertain significance among genetic counselors in pediatrics.
Cheung C; Berger SM; Ross M; Kramer T; Li Y; Andrews C; Dergham KR; Spitz E; Florido ME; Ahimaz P
J Genet Couns; 2024 Jan; ():. PubMed ID: 38217320
[TBL] [Abstract][Full Text] [Related]
10. Variants of unknown significance in BRCA testing: impact on risk perception, worry, prevention and counseling.
Richter S; Haroun I; Graham TC; Eisen A; Kiss A; Warner E
Ann Oncol; 2013 Nov; 24 Suppl 8():viii69-viii74. PubMed ID: 24131974
[TBL] [Abstract][Full Text] [Related]
11. Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance.
Solomon I; Harrington E; Hooker G; Erby L; Axilbund J; Hampel H; Semotiuk K; Blanco A; Klein WMP; Giardiello F; Leonard L
J Genet Couns; 2017 Aug; 26(4):866-877. PubMed ID: 28127677
[TBL] [Abstract][Full Text] [Related]
12. Factors predicting reclassification of variants of unknown significance.
Wright M; Menon V; Taylor L; Shashidharan M; Westercamp T; Ternent CA
Am J Surg; 2018 Dec; 216(6):1148-1154. PubMed ID: 30217367
[TBL] [Abstract][Full Text] [Related]
13. A multicenter study of clinical impact of variant of uncertain significance reclassification in breast, ovarian and colorectal cancer susceptibility genes.
Makhnoon S; Levin B; Ensinger M; Mattie K; Volk RJ; Zhao Z; Mendoza T; Shete S; Samiian L; Grana G; Grainger A; Arun B; Shirts BH; Peterson SK
Cancer Med; 2023 Feb; 12(3):2875-2884. PubMed ID: 36426404
[TBL] [Abstract][Full Text] [Related]
14. Clinical interpretation and recommendations for patients with a variant of uncertain significance in BRCA1 or BRCA2: a survey of genetic counseling practice.
Petrucelli N; Lazebnik N; Huelsman KM; Lazebnik RS
Genet Test; 2002; 6(2):107-13. PubMed ID: 12215249
[TBL] [Abstract][Full Text] [Related]
15. Evolution of Hereditary Breast Cancer Genetic Services: Are Changes Reflected in the Knowledge and Clinical Practices of Florida Providers?
Cragun D; Scherr C; Camperlengo L; Vadaparampil ST; Pal T
Genet Test Mol Biomarkers; 2016 Oct; 20(10):569-578. PubMed ID: 27525501
[TBL] [Abstract][Full Text] [Related]
16. Characterization of variant reclassification and patient re-contact in a cancer genetics clinic.
Muir SM; Reagle R
J Genet Couns; 2022 Dec; 31(6):1261-1272. PubMed ID: 35763673
[TBL] [Abstract][Full Text] [Related]
17. Cancer patients' experience of receiving variant of uncertain significance results: An Asian perspective.
Ishak ND; Shaw T; Li ST; Yuen J; Goh HX; Chua ZY; Suresh P; Que FVF; Zhang Z; Chiang J; Ngeow J
J Genet Couns; 2023 Oct; ():. PubMed ID: 37864575
[TBL] [Abstract][Full Text] [Related]
18. Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors.
Bennett JS; Bernhardt M; McBride KL; Reshmi SC; Zmuda E; Kertesz NJ; Garg V; Fitzgerald-Butt S; Kamp AN
Pediatr Cardiol; 2019 Dec; 40(8):1679-1687. PubMed ID: 31535183
[TBL] [Abstract][Full Text] [Related]
19. Clinical Decision-Making in Patients with Variant of Uncertain Significance in BRCA1 or BRCA2 Genes.
Welsh JL; Hoskin TL; Day CN; Thomas AS; Cogswell JA; Couch FJ; Boughey JC
Ann Surg Oncol; 2017 Oct; 24(10):3067-3072. PubMed ID: 28766224
[TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 35616809
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]