Violaine Bourdon

Biochemistry, Genetics and Molecular Biology · Life Sciences

22h-index2.3kcitations65works0.02yr avg
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Research Topics

BRCA gene mutations in cancer(12), RNA and protein synthesis mechanisms(10), CRISPR and Genetic Engineering(10), Cancer Genomics and Diagnostics(10), Genomics and Rare Diseases(10)

Publications63 total

Supplementary Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Supplementary Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Supplementary Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Supplementary Data from Skipping Nonsense to Maintain Function: The Paradigm of <i>BRCA2</i> Exon 12
2023Open Access
Data from Skipping Nonsense to Maintain Function: The Paradigm of <i>BRCA2</i> Exon 12
2023Open Access
Supplementary Tables from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Supplementary Data Tables S1-S4 from Skipping Nonsense to Maintain Function: The Paradigm of <i>BRCA2</i> Exon 12
2023Open Access
Supplementary Data Tables S1-S4 from Skipping Nonsense to Maintain Function: The Paradigm of <i>BRCA2</i> Exon 12
2023Open Access
Supplementary Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Supplementary Tables from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Supplementary Data from Skipping Nonsense to Maintain Function: The Paradigm of <i>BRCA2</i> Exon 12
2023Open Access
Supplementary Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Data from Skipping Nonsense to Maintain Function: The Paradigm of <i>BRCA2</i> Exon 12
2023Open Access
Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Supplementary Data from Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using <i>BRCA2</i> Exon 3 as a Model System
2023Open Access
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach
The American Journal of Human Genetics·2021· 29 citedOpen Access
A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers
BMC Medical Research Methodology·2021· 7 citedOpen Access
5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints
Cancers·2021· 12 citedOpen Access
Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies
Bulletin du Cancer·2021
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Frequent Co-authors

Hagay Sobol(22), Capucine Delnatte(15), Dominique Stoppa‐Lyonnet(14), Pascaline Gaildrat(13), Mélanie Léoné(13), Sandrine M. Caputo(13), Sophie Krieger(12), Florence Coulet(12), Nadia Boutry‐Kryza(12), Hélène Dreyfus(12), Valérie Bonadona(12), Paul Gesta(12), François Eisinger(11), Virginie Caux‐Moncoutier(11), Françoise Bonnet‐Dorion(10), Alexandra Martins(10), Brigitte Bressac–de Paillerets(9), Philippe Jonveaux(9), Rosette Lidereau(9), T Noguchi(9)