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Carolle Samson

Laval University

10

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1240

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

2008 The Journal of Steroid Biochemistry and Molecular Biology
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Erratum: 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 (Journal of Medical Genetics (2007) 44, (107-121))

2007 Journal of Medical Genetics
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No Evidence of BRCA1/2 Genomic Rearrangements in High-Risk French-Canadian Breast/Ovarian Cancer Families

2006 Genetic Testing
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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

2006 Journal of Medical Genetics
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No evidence of recurent BRCA1/2 genomic rearrangement in high risk French-Canadian breast/ovarian cancer families

2003 American Journal of Human Genetics
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Molecular epidemiology of BRCA1 and BRCA2 mutations in high risk French Canadian breast/ovarian cancer families

2001
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The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds.

1996 Nature Genetics
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Generation of an Integrated Transcription Map of the BRCA2 Region on Chromosome 13q12–q13

1996 Genomics
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Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21

1995 Genomics
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Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

1994 Nature Genetics
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Citations (292)