Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic BRCA1...

por Alenezi, Wejdan M., Fierheller, Caitlin T., Revil, Timothée, Serruya, Corinne, Mes-Masson, Anne-Marie, Foulkes, William D., Provencher, Diane, El Haffaf, Zaki, Ragoussis, Jiannis, Tonin, Patricia N.
Publicado 2022

Genetic analyses of DNA repair pathway associated genes implicate new candidate cancer predisposing genes in ancestrally defined ovarian cancer cases

por Alenezi, Wejdan M., Fierheller, Caitlin T., Serruya, Corinne, Revil, Timothée, Oros, Kathleen K., Subramanian, Deepak N., Bruce, Jeffrey, Spiegelman, Dan, Pugh, Trevor, Campbell, Ian G., Mes-Masson, Anne-Marie, Provencher, Diane, Foulkes, William D., Haffaf, Zaki El, Rouleau, Guy, Bouchard, Luigi, Greenwood, Celia M. T., Ragoussis, Jiannis, Tonin, Patricia N.
Publicado 2023

The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population

por Alenezi, Wejdan M., Milano, Larissa, Fierheller, Caitlin T., Serruya, Corinne, Revil, Timothée, Oros, Kathleen K., Behl, Supriya, Arcand, Suzanna L., Nayar, Porangana, Spiegelman, Dan, Gravel, Simon, Mes-Masson, Anne-Marie, Provencher, Diane, Foulkes, William D., El Haffaf, Zaki, Rouleau, Guy, Bouchard, Luigi, Greenwood, Celia M. T., Masson, Jean-Yves, Ragoussis, Jiannis, Tonin, Patricia N.
Publicado 2022

Molecular Genetic Characteristics of FANCI, a Proposed New Ovarian Cancer Predisposing Gene

por Fierheller, Caitlin T., Alenezi, Wejdan M., Serruya, Corinne, Revil, Timothée, Amuzu, Setor, Bedard, Karine, Subramanian, Deepak N., Fewings, Eleanor, Bruce, Jeffrey P., Prokopec, Stephenie, Bouchard, Luigi, Provencher, Diane, Foulkes, William D., El Haffaf, Zaki, Mes-Masson, Anne-Marie, Tischkowitz, Marc, Campbell, Ian G., Pugh, Trevor J., Greenwood, Celia M. T., Ragoussis, Jiannis, Tonin, Patricia N.
Publicado 2023

A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene

por Fierheller, Caitlin T., Guitton-Sert, Laure, Alenezi, Wejdan M., Revil, Timothée, Oros, Kathleen K., Gao, Yuandi, Bedard, Karine, Arcand, Suzanna L., Serruya, Corinne, Behl, Supriya, Meunier, Liliane, Fleury, Hubert, Fewings, Eleanor, Subramanian, Deepak N., Nadaf, Javad, Bruce, Jeffrey P., Bell, Rachel, Provencher, Diane, Foulkes, William D., El Haffaf, Zaki, Mes-Masson, Anne-Marie, Majewski, Jacek, Pugh, Trevor J., Tischkowitz, Marc, James, Paul A., Campbell, Ian G., Greenwood, Celia M. T., Ragoussis, Jiannis, Masson, Jean-Yves, Tonin, Patricia N.
Publicado 2021