Violaine Bourdon

2.3k total citations
27 papers, 955 citations indexed

About

Violaine Bourdon is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Violaine Bourdon has authored 27 papers receiving a total of 955 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Genetics. Recurrent topics in Violaine Bourdon's work include Genetic factors in colorectal cancer (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Cancer Genomics and Diagnostics (6 papers). Violaine Bourdon is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Cancer Genomics and Diagnostics (6 papers). Violaine Bourdon collaborates with scholars based in France, Tunisia and Switzerland. Violaine Bourdon's co-authors include Philippe Jonveaux, Christophe Philippe, Cécile Arnould, Hagay Sobol, M. J. Grégoire, Ruud Berger, Sylviane Olschwang, Philippe Mourrain, Jean‐Christophe Palauqui and Hervé Vaucheret and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and The Plant Cell.

In The Last Decade

Violaine Bourdon

26 papers receiving 940 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Violaine Bourdon France 12 607 309 267 203 102 27 955
James Tepperberg United States 15 362 0.6× 532 1.7× 86 0.3× 149 0.7× 67 0.7× 28 889
Tanya Rozovskaia Israel 11 1.5k 2.5× 195 0.6× 366 1.4× 74 0.4× 61 0.6× 11 1.7k
G.C. Beverstock Netherlands 14 318 0.5× 259 0.8× 198 0.7× 67 0.3× 96 0.9× 30 634
Anne W. Higgins United States 11 529 0.9× 360 1.2× 101 0.4× 409 2.0× 70 0.7× 17 885
Jacob L. Glass United States 14 980 1.6× 301 1.0× 293 1.1× 111 0.5× 65 0.6× 26 1.2k
Yair S. Manor Israel 5 800 1.3× 280 0.9× 83 0.3× 97 0.5× 54 0.5× 6 1.0k
Fiorella Shabtai Israel 17 229 0.4× 314 1.0× 116 0.4× 109 0.5× 71 0.7× 47 601
Helen Impey Australia 9 815 1.3× 256 0.8× 286 1.1× 124 0.6× 42 0.4× 12 1.1k
John Bernat United States 11 582 1.0× 205 0.7× 94 0.4× 82 0.4× 52 0.5× 28 951
Kevin Clark United Kingdom 11 913 1.5× 781 2.5× 96 0.4× 128 0.6× 145 1.4× 16 1.3k

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-authorship network of co-authors of Violaine Bourdon

This figure shows the co-authorship network connecting the top 25 collaborators of Violaine Bourdon. A scholar is included among the top collaborators of Violaine Bourdon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Violaine Bourdon. Violaine Bourdon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Hamadou, Walid Sabri, Nouha Bouali, Violaine Bourdon, et al.. (2021). Mutational analysis of apoptotic genes in familial aggregation of hematological malignancies. Bulletin du Cancer. 108(9). 798–805.
2.
Hamadou, Walid Sabri, Violaine Bourdon, Yosra Ben Youssef, et al.. (2017). GATA2 gene analysis in several forms of hematological malignancies including familial aggregations. Annals of Hematology. 96(10). 1635–1639. 6 indexed citations
3.
Hamadou, Walid Sabri, Violaine Bourdon, Yosra Ben Youssef, et al.. (2016). Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases. Familial Cancer. 16(1). 153–157. 6 indexed citations
4.
Hamadou, Walid Sabri, Violaine Bourdon, Yosra Ben Youssef, et al.. (2016). ARLTS1, potential candidate gene in familial aggregation of hematological malignancies. Bulletin du Cancer. 104(2). 123–127. 9 indexed citations
5.
Hamadou, Walid Sabri, Souhail Besbes, Violaine Bourdon, et al.. (2015). Familial hematological malignancies: ASXL1 gene investigation. Clinical & Translational Oncology. 18(4). 385–390. 11 indexed citations
6.
Noguchi, Tetsuro, Violaine Bourdon, & Hagay Sobol. (2014). About Sequence Quality: Impact on Clinical Applications. Genetic Testing and Molecular Biomarkers. 18(5). 299–305. 1 indexed citations
7.
Hassanein, Mohamed, Laëtitia Huiart, Violaine Bourdon, et al.. (2013). Prediction of BRCA1 Germ-Line Mutation Status in Patients with Breast Cancer Using Histoprognosis Grade, MS110, Lys27H3, Vimentin, and KI67. Pathobiology. 80(5). 219–227. 10 indexed citations
8.
Rouleau, Étienne, Hélène Zattara, Cédrick Lefol, et al.. (2011). First large rearrangement in the MUTYH gene and attenuated familial adenomatous polyposis syndrome. Clinical Genetics. 80(3). 301–303. 12 indexed citations
9.
Rousseau, Guillaume, Tetsuro Noguchi, Violaine Bourdon, Hagay Sobol, & Sylviane Olschwang. (2011). SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis. BMC Neurology. 11(1). 9–9. 52 indexed citations
10.
Bourdon, Violaine, Laëtitia Huiart, François Eisinger, et al.. (2009). Molecular study of CEPBA in familial hematological malignancies. Familial Cancer. 8(4). 581–584. 4 indexed citations
11.
12.
Tournier, Isabelle, Brigitte Bressac–de Paillerets, H. Sobol, et al.. (2004). Significant contribution of germline BRCA2 rearrangements in male breast cancer families. HAL (Le Centre pour la Communication Scientifique Directe). 7 indexed citations
13.
Tournier, Isabelle, Brigitte Bressac–de Paillerets, Dominique Stoppa-Lyonnet, et al.. (2004). Significant Contribution of Germline BRCA2 Rearrangements in Male Breast Cancer Families. Cancer Research. 64(22). 8143–8147. 81 indexed citations
14.
Bourdon, Violaine, et al.. (2003). Chromosome imbalances in oligodendroglial tumors detected by comparative genomic hybridization. Annales de Génétique. 47(2). 105–111. 10 indexed citations
15.
Bourdon, Violaine, et al.. (2003). MECP2 Mutations or Polymorphisms in Mentally Retarded Boys. Molecular Diagnosis. 7(1). 3–7. 26 indexed citations
16.
Bienvenu, Thierry, Laurent Villard, Nicolás de Roux, et al.. (2002). Spectrum of MECP2 Mutations in Rett Syndrome. Genetic Testing. 6(1). 1–6. 14 indexed citations
17.
Bensoussan, Danièle, Françoise Le Deist, Véronique Latger‐Cannard, et al.. (2002). T‐cell immune constitution after peripheral blood mononuclear cell transplantation in complete DiGeorge syndrome. British Journal of Haematology. 117(4). 899–906. 18 indexed citations
18.
Bourdon, Violaine, et al.. (2001). Deletion screening by fluorescence in situ hybridization in Rett syndrome patients. Annales de Génétique. 44(4). 191–194. 11 indexed citations
19.
Bourdon, Violaine, et al.. (2001). A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients. Human Genetics. 108(1). 43–50. 63 indexed citations
20.
Arnould, Cécile, Christophe Philippe, Violaine Bourdon, et al.. (1999). 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. 8(9). 1741–1749. 186 indexed citations

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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