Violaine Bourdon

2.4k citations

50 papers · 2k · h-index 20

Impact in

Genetics top 2%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
Hematology top 5%
- Acute Myeloid Leukemia Research

Papers in

Genetics 32
- BRCA gene mutations in cancer 19
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 5
Hematology 7
- Acute Myeloid Leukemia Research 6

Co-authors: Philippe Jonveaux (8 shared papers)Christophe Philippe (5 shared papers)Hagay Sobol (16 shared papers)Roland Berger (1 shared paper)M. J. Grégoire (1 shared paper)Tetsuro Noguchi (9 shared papers)Sylviane Olschwang (5 shared papers)Hervé Vaucheret (2 shared papers)
Journals: Journal of Medical Genetics (3 papers)Annals of Hematology (3 papers)Cancer Research (3 papers)Nucleic Acids Research (3 papers)The Plant Cell (2 papers)
Partner nations: France Tunisia United Kingdom

In The Last Decade

Violaine Bourdon

48 papers receiving 1.9k citations

Peers

Countries citing papers authored by Violaine Bourdon

Since Specialization

Citations

This map shows the geographic impact of Violaine Bourdon's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Violaine Bourdon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Violaine Bourdon more than expected).

Fields of papers citing papers by Violaine Bourdon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Violaine Bourdon. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Violaine Bourdon. The network helps show where Violaine Bourdon may publish in the future.

Co-authors

The 25 scholars most cited alongside Violaine Bourdon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Violaine Bourdon Line = papers co-authored together Violaine Bourdon links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers The American Journal of Human Genetics ·Antonis C. Antoniou, Amanda B. Spurdle, Olga M. Sinilnikova, Sue C. Healey, Karen A. Pooley, Rita Katharina Schmutzler, Beatrix Versmold, Christoph Engel	2008	228
2	Arabidopsis Mutants Impaired in Cosuppression The Plant Cell ·Taline Elmayan, Sandrine Balzergue, Fabrice Béon, Violaine Bourdon, Jeremy Daubremet, Yvette Guenet, Philippe Mourrain, Jean‐Christophe Palauqui	1998	219
3	The Signal Transducer and Activator of Transcription STAT5b Gene Is a New Partner of Retinoic Acid Receptor in Acute Promyelocytic-Like Leukaemia Human Molecular Genetics ·Christophe Philippe, Violaine Bourdon, M. J. Grégoire, Roland Berger, Philippe Jonveaux +1 other	1999	219
4	Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants Human Mutation ·Claude Houdayer, Virginie Caux‐Moncoutier, Sophie Krieger, Michel Barrois, Françoise Bonnet, Violaine Bourdon, Myriam Bronner, Monique Buisson	2012	199
5	High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder Blood ·Claude Preudhomme, Aline Renneville, Violaine Bourdon, Nathalie Philippe, Catherine Roche‐Lestienne, Nicolas Boissel, Nathalie Dhédin, Pascale Cornillet‐Lefèbvre	2009	152
6	Significant Contribution of Germline BRCA2 Rearrangements in Male Breast Cancer Families Cancer Research ·Isabelle Tournier, Brigitte Bressac–de Paillerets, Hagay Sobol, Dominique Stoppa‐Lyonnet, Rosette Lidereau, Michel Barrois, Sylvie Mazoyer, Florence Coulet	2004	86
7	Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort Nucleic Acids Research ·Raphaël Leman, Pascaline Gaildrat, Gérald Le Gac, Chandran Ka, Yann Fichou, Marie‐Pierre Audrézet, Virginie Caux‐Moncoutier, Sandrine M. Caputo	2018	80
8	A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients Human Genetics ·Violaine Bourdon, Christophe Philippe, Orianne Labrune, Daniel Amsallem, Philippe Jonveaux +1 other	2001	76
9	SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis BMC Neurology ·Tetsuro Noguchi, Violaine Bourdon, Hagay Sobol, Sylviane Olschwang +1 other	2011	69
10	Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus Nature Communications ·Kate Lawrenson, Siddhartha Kar, Karen McCue, Karoline B. Kuchenbaecker, K Kyriaki Michailidou, Jonathan P. Tyrer, Jonathan Beesley, Susan J. Ramus	2016	69
11	Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application toMLH1germline mutations in Lynch syndrome Human Mutation ·Étienne Rouleau, Cédrick Lefol, Violaine Bourdon, Florence Coulet, Tetsuro Noguchi, Florent Soubrier, Ivan Bièche, Sylviane Olschwang	2009	53
12	The contribution of germline rearrangements to the spectrum of BRCA2 mutations Journal of Medical Genetics ·Francesco Casilli, Isabelle Tournier, Olga M. Sinilnikova, Florence Coulet, Florent Soubrier, Claude Houdayer, Hagay Sobol, Violaine Bourdon	2006	49
13	Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP: Figure 1 Journal of Medical Genetics ·Arnaud Lagarde, Étienne Rouleau, Anthony Ferrari, Tetsuro Noguchi, Adrien Briaux, Violaine Bourdon, Virginie Rémy, Pascaline Gaildrat	2010	37
14	The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer npj Breast Cancer ·Gisella Figlioli, Massimo Bogliolo, Irene Catucci, Laura Caleca, Sandra Viz-Lasheras, Roser M. Pujol, Johanna I. Kiiski, Taru Muranen	2019	35
15	A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers Nature Communications ·Juliette Coignard, Michael J. Lush, Jonathan Beesley, Tracy A. O’Mara, Joe Dennis, Jonathan P. Tyrer, Daniel R. Barnes, Lesley McGuffog	2021	29
16	Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers Human Molecular Genetics ·David G. Cox, Jacques Simard, Daniel Sinnett, Yosr Hamdi, Penny Soucy, Manon Ouimet, Laure Barjhoux, Carole Verny-Pierre	2011	28
17	MECP2 Mutations or Polymorphisms in Mentally Retarded Boys Molecular Diagnosis ·Violaine Bourdon, Christophe Philippe, Dominique Martin, Alain Verloès, Agnès Grandemenge, Philippe Jonveaux	2003	27
18	Skipping Nonsense to Maintain Function: The Paradigm of BRCA2 Exon 12 Cancer Research ·Laëtitia Meulemans, Romy L.S. Mesman, Sandrine M. Caputo, Sophie Krieger, Marine Guillaud-Bataille, Virginie Caux‐Moncoutier, Mélanie Léoné, Nadia Boutry‐Kryza	2020	27
19	Calibration of Pathogenicity Due to Variant-Induced Leaky Splicing Defects by Using BRCA2 Exon 3 as a Model System Cancer Research ·Hélène Tubeuf, Sandrine M. Caputo, Teresa L. Sullivan, Julie Rondeaux, Sophie Krieger, Virginie Caux‐Moncoutier, Julie Hauchard, Alice Fiévet	2020	22
20	Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach The American Journal of Human Genetics ·Sandrine M. Caputo, Lisa Golmard, Mélanie Léoné, Francesca Damiola, Marine Guillaud-Bataille, Françoise Révillion-Carette, Étienne Rouleau, Nicolas Derive	2021	22

About Violaine Bourdon

Violaine Bourdon is a scholar working on Genetics, Hematology, Pathology and Forensic Medicine, Molecular Biology and Oncology, having authored 50 papers that have together received 2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (19 papers), Acute Myeloid Leukemia Research (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (5 papers), Genetic factors in colorectal cancer (4 papers), RNA Research and Splicing (3 papers), Cancer-related Molecular Pathways (3 papers) and Plant Molecular Biology Research (2 papers). The work is most often cited by research in Genetics (933 citations), Hematology (206 citations), Molecular Biology (468 citations), Pathology and Forensic Medicine (107 citations) and Plant Science (196 citations). Violaine Bourdon has collaborated with scholars based in France, Tunisia and United Kingdom. Frequent co-authors include Philippe Jonveaux, Christophe Philippe, Hagay Sobol, Roland Berger, M. J. Grégoire, Tetsuro Noguchi, Sylviane Olschwang, Hervé Vaucheret, Katia Wostrikoff and Philippe Mourrain. Their work appears in journals such as Journal of Medical Genetics, Annals of Hematology, Cancer Research, Nucleic Acids Research and The Plant Cell.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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