C. Samson

Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21.

J. Rommens, P. Tonin, S. Narod, 1995, Genomics.

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

J. Rommens, M. Skolnick, P. Tonin, 1994, Nature Genetics.

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

J. Rommens, A. Thomas, M. Skolnick, 1996, Nature Genetics.

Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer

B. Knoppers, B. Godard, D. Easton, 2006, Journal of Medical Genetics.

Contaminating DNA in human saliva alters the detection of variants from whole genome sequencing

J. C. Jacobsen, R. Snell, W. Whitford, 2020, Scientific Reports.

No Evidence of BRCA 1 / 2 Genomic Rearrangements in High-Risk French-Canadian Breast / Ovarian Cancer Families

M. Dumont, J. Simard, D. Goldgar, 2009 .

No Evidence of BRCA1/2 genomic rearrangements in high-risk French-Canadian breast/ovarian cancer families.

M. Dumont, J. Simard, D. Goldgar, 2006, Genetic testing.

Characterization of HSD17B1 sequence variants in breast cancer cases from French Canadian families with high risk of breast and ovarian cancer

J. Simard, F. Durocher, C. Samson, 2008, The Journal of Steroid Biochemistry and Molecular Biology.

Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13.

J. Rommens, M. Skolnick, F. Couch, 1996, Genomics.