| Literature Review of BARD1 as a Cancer Predisposing Gene with a Focus on Breast and Ovarian Cancers WM Alenezi, CT Fierheller, N Recio, PN Tonin Genes 11 (8), 856, 2020 | 42 | 2020 |
| The genetic analyses of French Canadians of Quebec facilitate the characterization of new cancer predisposing genes implicated in hereditary breast and/or ovarian cancer … CT Fierheller, WM Alenezi, PN Tonin Cancers 13 (14), 3406, 2021 | 15 | 2021 |
| A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene CT Fierheller, L Guitton-Sert, WM Alenezi, T Revil, KK Oros, Y Gao, ... Genome medicine 13 (1), 1-26, 2021 | 14 | 2021 |
| The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique … WM Alenezi, L Milano, CT Fierheller, C Serruya, T Revil, KK Oros, S Behl, ... Cancers 14 (9), 2251, 2022 | 8 | 2022 |
| Case Review: Whole-Exome Sequencing Analyses Identify Carriers of a Known Likely Pathogenic Intronic BRCA1 Variant in Ovarian Cancer Cases Clinically Negative for Pathogenic … WM Alenezi, CT Fierheller, T Revil, C Serruya, AM Mes-Masson, ... Genes 13 (4), 697, 2022 | 6 | 2022 |
| The Genetic and Molecular Analyses of RAD51C and RAD51D Identifies Rare Variants Implicated in Hereditary Ovarian Cancer from a Genetically Unique Population. Cancers 2022, 14 … WM Alenezi, L Milano, CT Fierheller, C Serruya, T Revil, KK Oros, S Behl, ... s Note: MDPI stays neutral with regard to jurisdictional claims in published …, 2022 | 2 | 2022 |
| The genetic analysis of a founder Northern American population of European descent identifies FANCI as a candidate familial ovarian cancer risk gene CT Fierheller, L Guitton-Sert, WM Alenezi, T Revil, KK Oros, K Bedard, ... medRxiv, 2020 | 2 | 2020 |
| The genomic landscape of carriers of rare variants in FANCI, a new candidate ovarian cancer predisposing gene C Fierheller, WM Alenezi, C Serruya, T Revil, J Nadaf, AM Mes-Masson, ... Cancer Research 81 (13_Supplement), 2056-2056, 2021 | 1 | 2021 |
| Abstract A25: Investigating the co-occurrence of potentially pathogenic DNA repair pathways alleles in BRCA1 or BRCA2 mutation carrier women with ovarian cancer. WM Alenezi, T Revil, D Badescu, SL Arcand, G Rouleau, I Ragoussis, ... Molecular Cancer Research 15 (4_Supplement), A25-A25, 2017 | | 2017 |
| Investigating the co-occurrence of potentially pathogenic DNA repair pathways alleles in BRCA1 or BRCA2 mutation carrier women with ovarian cancer WM Alenezi, T Revil, D Badescu, SL Arcand, G Rouleau, I Ragoussis, ... MOLECULAR CANCER RESEARCH 15, 2017 | | 2017 |
| Supplementary Method: The Genetic Analyses of French Cana-dians of Quebec Facilitate the Characterization of New Cancer Predisposing Genes Implicated in Hereditary Breast and … CT Fierheller, WM Alenezi, PN Tonin | | |
