These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
150 related articles for article (PubMed ID: 37922907)
21. Systematic misclassification of missense variants in BRCA1 and BRCA2 "coldspots". Dines JN; Shirts BH; Slavin TP; Walsh T; King MC; Fowler DM; Pritchard CC Genet Med; 2020 May; 22(5):825-830. PubMed ID: 31911673 [TBL] [Abstract][Full Text] [Related]
22. Twenty Years of BRCA1 and BRCA2 Molecular Analysis at MMCI - Current Developments for the Classification of Variants. Machackova E; Claes K; Mikova M; Házová J; Sťahlová EH; Vasickova P; Trbusek M; Navrátilová M; Svoboda M; Foretová L Klin Onkol; 2019; 32(Supplementum2):51-71. PubMed ID: 31409081 [TBL] [Abstract][Full Text] [Related]
23. Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2. Kuznetsov SG; Liu P; Sharan SK Nat Med; 2008 Aug; 14(8):875-81. PubMed ID: 18607349 [TBL] [Abstract][Full Text] [Related]
24. Reinterpretation of BRCA1 and BRCA2 variants of uncertain significance in patients with hereditary breast/ovarian cancer using the ACMG/AMP 2015 guidelines. So MK; Jeong TD; Lim W; Moon BI; Paik NS; Kim SC; Huh J Breast Cancer; 2019 Jul; 26(4):510-519. PubMed ID: 30725392 [TBL] [Abstract][Full Text] [Related]
25. Analysis of BRCA1/2 variants of unknown significance in the prospective Korean Hereditary Breast Cancer study. Kim JH; Park S; Park HS; Park JS; Lee ST; Kim SW; Lee JW; Lee MH; Park SK; Noh WC; Choi DH; Han W; Jung SH Sci Rep; 2021 Apr; 11(1):8485. PubMed ID: 33875706 [TBL] [Abstract][Full Text] [Related]
26. Germline mutations in BRCA1 and BRCA2 in epithelial ovarian cancer patients in Brazil. Maistro S; Teixeira N; Encinas G; Katayama ML; Niewiadonski VD; Cabral LG; Ribeiro RM; Gaburo Junior N; de Gouvêa AC; Carraro DM; Sabino EC; Diz MD; Chammas R; de Bock GH; Folgueira MA BMC Cancer; 2016 Dec; 16(1):934. PubMed ID: 27914478 [TBL] [Abstract][Full Text] [Related]
27. Comparative analysis of BRCA1 and BRCA2 variants of uncertain significance in patients with breast cancer: a multifactorial probability-based model versus ACMG standards and guidelines for interpreting sequence variants. Park KS; Cho EY; Nam SJ; Ki CS; Kim JW Genet Med; 2016 Dec; 18(12):1250-1257. PubMed ID: 27124784 [TBL] [Abstract][Full Text] [Related]
28. BRCA1 and BRCA2 unclassified variants and missense polymorphisms in Algerian breast/ovarian cancer families. Cherbal F; Salhi N; Bakour R; Adane S; Boualga K; Maillet P Dis Markers; 2012; 32(6):343-53. PubMed ID: 22684231 [TBL] [Abstract][Full Text] [Related]
30. A high-throughput functional complementation assay for classification of BRCA1 missense variants. Bouwman P; van der Gulden H; van der Heijden I; Drost R; Klijn CN; Prasetyanti P; Pieterse M; Wientjens E; Seibler J; Hogervorst FB; Jonkers J Cancer Discov; 2013 Oct; 3(10):1142-55. PubMed ID: 23867111 [TBL] [Abstract][Full Text] [Related]
31. Functional classification of DNA variants by hybrid minigenes: Identification of 30 spliceogenic variants of BRCA2 exons 17 and 18. Fraile-Bethencourt E; Díez-Gómez B; Velásquez-Zapata V; Acedo A; Sanz DJ; Velasco EA PLoS Genet; 2017 Mar; 13(3):e1006691. PubMed ID: 28339459 [TBL] [Abstract][Full Text] [Related]
32. Cosmic Whirl: Navigating the Comet Trail in DNA: H2AX Phosphorylation and the Enigma of Uncertain Significance Variants. Ustun Yilmaz S; Agaoglu NB; Manto K; Muftuoglu M; Özbek U Genes (Basel); 2024 Jun; 15(6):. PubMed ID: 38927659 [TBL] [Abstract][Full Text] [Related]
33. Prevalence of BRCA1, BRCA2, and PALB2 genomic alterations among 924 Taiwanese breast cancer assays with tumor-only targeted sequencing: extended data analysis from the VGH-TAYLOR study. Cheng HF; Tsai YF; Liu CY; Hsu CY; Lien PJ; Lin YS; Chao TC; Lai JI; Feng CJ; Chen YJ; Chen BF; Chiu JH; Tseng LM; Huang CC Breast Cancer Res; 2023 Dec; 25(1):152. PubMed ID: 38098088 [TBL] [Abstract][Full Text] [Related]
34. Next-generation sequencing of the BRCA1 and BRCA2 genes for the genetic diagnostics of hereditary breast and/or ovarian cancer. Trujillano D; Weiss ME; Schneider J; Köster J; Papachristos EB; Saviouk V; Zakharkina T; Nahavandi N; Kovacevic L; Rolfs A J Mol Diagn; 2015 Mar; 17(2):162-70. PubMed ID: 25556971 [TBL] [Abstract][Full Text] [Related]
35. Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain. Hu C; Huang H; Na J; Lumby C; Abozaid M; Holdren MA; Rao TJ; Karam R; Pesaran T; Weyandt JD; Csuy CM; Seelaus CA; Young CC; Fulk K; Heidari Z; Morais Lyra PC; Couch RE; Persons B; Polley EC; Gnanaolivu RD; Boddicker NJ; Monteiro ANA; Yadav S; Domchek SM; Richardson ME; Couch FJ Am J Hum Genet; 2024 Mar; 111(3):584-593. PubMed ID: 38417439 [TBL] [Abstract][Full Text] [Related]
36. Functional pre-therapeutic evaluation by genome editing of variants of uncertain significance of essential tumor suppressor genes. Billaud A; Chevalier LM; Augereau P; Frenel JS; Passot C; Campone M; Morel A Genome Med; 2021 Nov; 13(1):174. PubMed ID: 34749799 [TBL] [Abstract][Full Text] [Related]
37. Functional evaluation of BRCA1/2 variants of unknown significance with homologous recombination assay and integrative in silico prediction model. Guo Q; Ji S; Takeuchi K; Urasaki W; Suzuki A; Iwasaki Y; Saito H; Xu Z; Arai M; Nakamura S; Momozawa Y; Chiba N; Miki Y; Matsuura M; Sunada S J Hum Genet; 2023 Dec; 68(12):849-857. PubMed ID: 37731132 [TBL] [Abstract][Full Text] [Related]
38. Next step in molecular genetics of hereditary breast/ovarian cancer: Multigene panel testing in clinical actionably genes and prioritization algorithms in the study of variants of uncertain significance. Castillo-Guardiola V; Rosado-Jiménez L; Sarabia-Meseguer MD; Marín-Vera M; Macías-Cerrolaza JA; García-Hernández R; Zafra-Poves M; Sánchez-Henarejos P; Moreno-Locubiche MÁ; Cuevas-Tortosa E; Arnaldos-Carrillo M; Ayala de la Peña F; Alonso-Romero JL; Noguera-Velasco JA; Ruiz-Espejo F Eur J Med Genet; 2022 Apr; 65(4):104468. PubMed ID: 35245693 [TBL] [Abstract][Full Text] [Related]
39. Lourenço RA; Lança M; Monteiro Gil O; Cardoso J; Lourenço T; Pereira-Leal JB; Rodrigues AS; Rueff J; Nunes Silva S Mol Med Rep; 2023 Jul; 28(1):. PubMed ID: 37232349 [TBL] [Abstract][Full Text] [Related]
40. Detection of genomic variations in BRCA1 and BRCA2 genes by long-range PCR and next-generation sequencing. Hernan I; Borràs E; de Sousa Dias M; Gamundi MJ; Mañé B; Llort G; Agúndez JA; Blanca M; Carballo M J Mol Diagn; 2012; 14(3):286-93. PubMed ID: 22426013 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]