Design considerations for massively parallel sequencing studies of common familial cancers

por Feng, BJ, Tavtigian, SV, Southey, MC, Goldgar, DE
Publicado 2012

Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing

por Blanc, R, Jammot, A, Nguyen-Dumont, T, Teo, ZL, Odefrey, FA, Hammet, F, Goldgar, DE, Park, DJ, Southey, MC
Publicado 2012

Expanded genetic analysis of a PALB2 c.3113G>A mutation carrying multiple-case breast cancer family via exome sequencing

por Teo, ZL, Park, DJ, Odefrey, F, Hammet, F, Nguyen-Dumont, T, Tsimiklis, H, Pope, BJ, Lonie, A, Winship, I, Giles, GG, Hopper, JL, Southey, MC
Publicado 2012

Identification of a novel disease-associated variant in the BRCA1 3’UTR that introduces a functional miR-103 target site

por Brewster, BL, Rossiello, F, French, JD, Edwards, SL, Wong, EM, Whiley, P, Waddell, N, Chen, X, Bove, B, Spurdle, AB, Radice, P, Godwin, AK, Southey, MC, Brown, MA, Peterlongo, P
Publicado 2012

Identification of new breast cancer predisposition genes via whole exome sequencing

por Southey, MC, Park, DJ, Lesueur, F, Odefrey, F, Nguyen-Dumont, T, Hammet, F, Neuhausen, SL, John, EM, Andrulis, IL, Chenevix-Trench, G, Baglietto, L, Le Calvez-Kelm, F, Pertesi, M, Lonie, A, Pope, B, Sinilnikova, O, Tsimiklis, H, Giles, GG, Hopper, JL, Tavtigian, SV, Goldgar, DE
Publicado 2012