A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.
Bmc Medical Genomics
Mucaki, Eliseos J EJ; Caminsky, Natasha G NG; Perri, Ami M AM; Lu, Ruipeng R; Laederach, Alain A; Halvorsen, Matthew M; Knoll, Joan H M JH; Rogan, Peter K PK
BRCA2 variants and cardiovascular disease in a multi-ethnic study.
Bmc Medical Genetics
Zbuk, Kevin K; Xie, Changchun C; Young, Robin R; Heydarpour, Mahyar M; Pare, Guillaume G; Davis, A Darlene AD; Miller, Ruby R; Lanktree, Matthew B MB; Saleheen, Danish D; Danesh, John J; Yusuf, Salim S; Engert, James C JC; Hegele, Robert A RA; Anand, Sonia S SS
Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2: potential modifying effect of BRCA1/BRCA2 mutation carrier status.
Breast Cancer Research And Treatment
Figueiredo, Jane C JC; Brooks, Jennifer D JD; Conti, David V DV; Poynter, Jenny N JN; Teraoka, Sharon N SN; Malone, Kathleen E KE; Bernstein, Leslie L; Lee, Won D WD; Duggan, David J DJ; Siniard, Ashley A; Concannon, Patrick P; Capanu, Marinela M; Lynch, Charles F CF; Olsen, Jørgen H JH; Haile, Robert W RW; Bernstein, Jonine L JL