Véronique David

2.4k total citations
40 papers, 1.6k citations indexed

About

Véronique David is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Véronique David has authored 40 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 8 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Véronique David's work include Iron Metabolism and Disorders (6 papers), Hedgehog Signaling Pathway Studies (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Véronique David is often cited by papers focused on Iron Metabolism and Disorders (6 papers), Hedgehog Signaling Pathway Studies (5 papers) and Genomic variations and chromosomal abnormalities (5 papers). Véronique David collaborates with scholars based in France, United States and United Kingdom. Véronique David's co-authors include Yves Deugnier, Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Jean‐Yves Le Gall, Cathérine Henry, Sylvie Odent, Thierry Sapey, Michel-Henry Mendler and D. Guyader and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Gastroenterology.

In The Last Decade

Véronique David

39 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Véronique David France 19 523 408 406 348 265 40 1.6k
Neil A. Hanchard United States 20 401 0.8× 242 0.6× 354 0.9× 255 0.7× 65 0.2× 54 1.2k
MH Freedman Canada 27 582 1.1× 846 2.1× 457 1.1× 384 1.1× 58 0.2× 64 1.9k
Laura Breda United States 22 1.0k 2.0× 1.0k 2.5× 241 0.6× 1.2k 3.4× 257 1.0× 86 2.4k
Ki Wai Chik Hong Kong 19 613 1.2× 335 0.8× 228 0.6× 258 0.7× 30 0.1× 57 1.4k
D. J. Bowen United Kingdom 25 338 0.6× 1.1k 2.6× 190 0.5× 255 0.7× 125 0.5× 84 1.7k
Eyal Grunebaum Canada 25 612 1.2× 329 0.8× 517 1.3× 146 0.4× 27 0.1× 113 1.9k
Jacqueline Yaouanq France 20 188 0.4× 582 1.4× 175 0.4× 393 1.1× 327 1.2× 39 1.6k
Takeshi Taketani Japan 25 1.2k 2.2× 649 1.6× 184 0.5× 249 0.7× 35 0.1× 119 2.1k
Bruno Costes France 22 512 1.0× 123 0.3× 201 0.5× 344 1.0× 67 0.3× 40 1.9k
Rosanna Verardi Italy 18 318 0.6× 246 0.6× 77 0.2× 157 0.5× 83 0.3× 43 1.1k

Countries citing papers authored by Véronique David

Since Specialization
Citations

This map shows the geographic impact of Véronique David'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 Véronique David with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Véronique David more than expected).

Fields of papers citing papers by Véronique David

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Véronique David. 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 Véronique David. The network helps show where Véronique David may publish in the future.

Co-authorship network of co-authors of Véronique David

This figure shows the co-authorship network connecting the top 25 collaborators of Véronique David. A scholar is included among the top collaborators of Véronique David 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 Véronique David. Véronique David 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.
Morcel, Karine, Tanguy Watrin, Laurent Pasquier, et al.. (2011). Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci. Orphanet Journal of Rare Diseases. 6(1). 9–9. 42 indexed citations
2.
Jaillard, Sylvie, Philippe Loget, Josette Lucas, et al.. (2010). Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect. European Journal of Medical Genetics. 54(2). 186–188. 2 indexed citations
3.
Dupé, Valérie, Lucie Rochard, Sandra Mercier, et al.. (2010). NOTCH, a new signaling pathway implicated in holoprosencephaly. Human Molecular Genetics. 20(6). 1122–1131. 37 indexed citations
4.
Meur, Nathalie Le, Muriel Holder‐Espinasse, Sylvie Jaillard, et al.. (2009). MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. Journal of Medical Genetics. 47(1). 22–29. 150 indexed citations
5.
Bouguen, Guillaume, Sylvain Manfrédi, Martine Blayau, et al.. (2007). Colorectal Adenomatous Polyposis Associated with MYH Mutations: Genotype and Phenotype Characteristics. Diseases of the Colon & Rectum. 50(10). 1612–1617. 23 indexed citations
6.
Milet, Jacqueline, Catherine Bourgain, Anne Marie Jouanolle, et al.. (2007). Common Variants in the BMP2, BMP4, and HJV Genes of the Hepcidin Regulation Pathway Modulate HFE Hemochromatosis Penetrance. The American Journal of Human Genetics. 81(4). 799–807. 90 indexed citations
7.
Bendavid, Claude, Laurent Pasquier, Tanguy Watrin, et al.. (2006). Phenotypic variability of a 4q34 → qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother. European Journal of Medical Genetics. 50(1). 66–72. 27 indexed citations
8.
David, Véronique, Laurent Mély, Daniel Siret, & J.‐C. Dubus. (2002). Inhalation et nébulisation chez l'enfant. Archives de Pédiatrie. 9. 415–421. 3 indexed citations
9.
10.
David, Véronique. (2000). Mise en condition de l'enfant en détresse respiratoire. Archives de Pédiatrie. 7. 44s–47s. 1 indexed citations
11.
Fairfax, A J, Véronique David, & Gill Douce. (1999). Laryngeal aspergillosis following high dose inhaled fluticasone therapy for asthma. Thorax. 54(9). 860–861. 40 indexed citations
12.
Mezi, Silvia, et al.. (1999). 99m Tc MIBI prone scintimammography in breast Paget's disease: a case report.. Oncology Reports. 6(1). 45–8. 1 indexed citations
13.
Benson, Carol B., et al.. (1997). Early singleton pregnancy outcome: effects of maternal age and mode of conception.. Radiology. 203(2). 399–403. 9 indexed citations
14.
Mosser, Jean, et al.. (1997). A YAC contig and an STS map spanning at least 3.9 megabasepairs telomeric to HLA-A. Immunogenetics. 45(6). 447–451. 3 indexed citations
15.
Héloury, Yves, et al.. (1996). Pneumothorax bilatéral et rectocolite hémorragique. Archives de Pédiatrie. 3(9). 874–876. 2 indexed citations
16.
Pichon, Laurent, et al.. (1996). La région HLA de classe I du CMH : une des régions les plus complexes du génome humain ?. médecine/sciences. 12(11). 1209–1209. 2 indexed citations
17.
Brissot, Pierre, Christian Jacquelinet, Hervé Jouanolle, et al.. (1991). Short-term prednisolone followed by recombinant human α-interferon alone or combined with adenine-arabinoside in chronic hepatitis B. Journal of Hepatology. 12(2). 181–189. 5 indexed citations
18.
Zappone, Elisabetta, Kelly Theriault, Véronique David, et al.. (1991). Polymorphism in a ferritin H gene from chromosome 6p. Human Genetics. 86(6). 557–61. 5 indexed citations
19.
Jouanolle, Anne Marie, et al.. (1991). A Hindlll RFLP at the FTHP1 locus on chromosome 6. Nucleic Acids Research. 19(13). 3762–3762. 1 indexed citations
20.
David, Véronique, Jacqueline Yaouanq, Martine Blayau, et al.. (1989). Ferritin H gene polymorphism in idiopathic hemochromatosis. Human Genetics. 81(2). 123–126. 16 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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