Publications:

Understanding and predicting the functional consequences of missense mutations in BRCA1 and BRCA2.

Scientific Reports

Aljarf, Raghad R; Shen, Mengyuan M; Pires, Douglas E V DEV; Ascher, David B DB

Publication Date: 2022-06-21

Variant appearance in text: BRCA1: V178A

PubMed Link: 35729312

Variant Present in the following documents:

• 41598_2022_13508_MOESM2_ESM.xlsx, sheet 1

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Prediction of the functional impact of missense variants in BRCA1 and BRCA2 with BRCA-ML.

Npj Breast Cancer

Hart, Steven N SN; Polley, Eric C EC; Shimelis, Hermella H; Yadav, Siddhartha S; Couch, Fergus J FJ

Publication Date: 2020

Variant appearance in text: BRCA1: 533T>C; Val178Ala

PubMed Link: 32377563

Variant Present in the following documents:

• 41523_2020_159_MOESM3_ESM.xlsx, sheet 1

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Prevalence of BRCA1 and BRCA2 pathogenic and likely pathogenic variants in non-selected ovarian carcinoma patients in Brazil.

Bmc Cancer

Cotrim, Deborah Porto DP; Ribeiro, Adriana Regina Gonçalves ARG; Paixão, Daniele D; de Queiroz Soares, Diogo Cordeiro DC; Jbili, Rima R; Pandolfi, Natasha Carvalho NC; Cezana, Camila C; de Cássia Mauro, Carine C; Mantoan, Henrique H; Bovolim, Graziele G; de Brot, Louise L; Torrezan, Giovana Tardin GT; Carraro, Dirce Maria DM; Baiocchi, Glauco G; da Cruz Formiga, Maria Nirvana MN; da Costa, Alexandre A B A AABA

Publication Date: 2019-01-03

Variant appearance in text: BRCA1: 533T>C; Val178Ala

PubMed Link: 30606148

Variant Present in the following documents:

• Main text
• 12885_2018_Article_5235.pdf

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Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models.

Genetics In Medicine : Official Journal Of The American College Of Medical Genetics

Hart, Steven N SN; Hoskin, Tanya T; Shimelis, Hermela H; Moore, Raymond M RM; Feng, Bingjian B; Thomas, Abigail A; Lindor, Noralane M NM; Polley, Eric C EC; Goldgar, David E DE; Iversen, Edwin E; Monteiro, Alvaro N A ANA; Suman, Vera J VJ; Couch, Fergus J FJ

Publication Date: 2019-01

Variant appearance in text: BRCA1: V178A

PubMed Link: 29884841

Variant Present in the following documents:

• NIHMS953431-supplement-Table_S2.xls, sheet 1

View BVdb publication page