162 related articles for article (PubMed ID: 30217367)
1. 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]
2. 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]
3. 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]
4. 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]
5. Outcomes of 92 patient-driven family studies for reclassification of variants of uncertain significance.
Tsai GJ; Rañola 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]
6. Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing.
Mersch J; Brown N; Pirzadeh-Miller S; Mundt E; Cox HC; Brown K; Aston M; Esterling L; Manley S; Ross T
JAMA; 2018 Sep; 320(12):1266-1274. PubMed ID: 30264118
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Preconception carrier screening yield: effect of variants of unknown significance in partners of carriers with clinically significant variants.
Fridman H; Behar DM; Carmi S; Levy-Lahad E
Genet Med; 2020 Mar; 22(3):646-653. PubMed ID: 31624327
[TBL] [Abstract][Full Text] [Related]
11. Power of pedigree likelihood analysis in extended pedigrees to classify rare variants of uncertain significance in cancer risk genes.
Rosenthal EA; Ranola JMO; Shirts BH
Fam Cancer; 2017 Oct; 16(4):611-620. PubMed ID: 28534081
[TBL] [Abstract][Full Text] [Related]
12. Understanding variants of uncertain significance in the era of multigene panels: Through the eyes of the patient.
Reuter C; Chun N; Pariani M; Hanson-Kahn A
J Genet Couns; 2019 Aug; 28(4):878-886. PubMed ID: 31050105
[TBL] [Abstract][Full Text] [Related]
13. Reassessment of the NF1 variants of unknown significance found during the 20-year activity of a genetics diagnostic laboratory.
Martorana D; Barili V; Uliana V; Ambrosini E; Riva M; De Sensi E; Luppi E; Messina C; Caleffi E; Pisani F; Percesepe A
Eur J Med Genet; 2023 Nov; 66(11):104847. PubMed ID: 37751797
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Release of reclassified VUS results of now deceased patients to family members: Practices and opinions.
Lascurain S; Thull D; Durst A; Bear T; Mai PL
J Genet Couns; 2024 Jan; ():. PubMed ID: 38189571
[TBL] [Abstract][Full Text] [Related]
16. Classification and Clinical Management of Variants of Uncertain Significance in High Penetrance Cancer Predisposition Genes.
Moghadasi S; Eccles DM; Devilee P; Vreeswijk MP; van Asperen CJ
Hum Mutat; 2016 Apr; 37(4):331-6. PubMed ID: 26777316
[TBL] [Abstract][Full Text] [Related]
17. Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes.
Miller IM; Lewis KL; Lawal TA; Ng D; Johnston JJ; Biesecker BB; Biesecker LG
Genet Med; 2019 Mar; 21(3):748-752. PubMed ID: 29997389
[TBL] [Abstract][Full Text] [Related]
18. Impact of Multigene Panel Testing on Surgical Decision Making in Breast Cancer Patients.
Pederson HJ; Gopalakrishnan D; Noss R; Yanda C; Eng C; Grobmyer SR
J Am Coll Surg; 2018 Apr; 226(4):560-565. PubMed ID: 29360614
[TBL] [Abstract][Full Text] [Related]
19. The effects of genomic germline variant reclassification on clinical cancer care.
Slavin TP; Manjarrez S; Pritchard CC; Gray S; Weitzel JN
Oncotarget; 2019 Jan; 10(4):417-423. PubMed ID: 30728895
[TBL] [Abstract][Full Text] [Related]
20. The frequency of gene variant reclassification and its impact on clinical management in the inherited arrhythmia clinic.
Young WJ; Maung S; Ahmet S; Kirkby C; Ives C; Schilling RJ; Lowe M; Lambiase PD
Heart Rhythm; 2024 Jun; 21(6):903-910. PubMed ID: 38218330
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]