Véronique David

4.5k total citations
70 papers, 2.2k citations indexed

About

Véronique David is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Véronique David has authored 70 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 27 papers in Hematology and 21 papers in Genetics. Recurrent topics in Véronique David's work include Iron Metabolism and Disorders (27 papers), Hedgehog Signaling Pathway Studies (24 papers) and Trace Elements in Health (17 papers). Véronique David is often cited by papers focused on Iron Metabolism and Disorders (27 papers), Hedgehog Signaling Pathway Studies (24 papers) and Trace Elements in Health (17 papers). Véronique David collaborates with scholars based in France, United States and Canada. Véronique David's co-authors include Sylvie Odent, Christèle Dubourg, Yves Deugnier, Pierre Brissot, Romain Moirand, Anne‐Marie Jouanolle, Jean‐Yves Le Gall, Laurent Pasquier, Dominique Guyader and Isabelle Gicquel and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Gastroenterology.

In The Last Decade

Véronique David

67 papers receiving 2.2k 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 29 1.1k 816 761 749 586 70 2.2k
Marco De Gobbi Italy 24 1.6k 1.6× 1.4k 1.7× 1.3k 1.7× 376 0.5× 971 1.7× 67 3.2k
Nursel Elçioğlu Türkiye 19 1.2k 1.2× 57 0.1× 85 0.1× 1.3k 1.7× 120 0.2× 70 2.0k
Solaf M. Elsayed Egypt 15 548 0.5× 100 0.1× 85 0.1× 471 0.6× 96 0.2× 63 1.1k
Beate Albrecht Germany 23 862 0.8× 39 0.0× 126 0.2× 1.0k 1.4× 88 0.2× 45 1.7k
J. J. Pointon United Kingdom 15 525 0.5× 758 0.9× 606 0.8× 437 0.6× 537 0.9× 27 1.6k
David J. Bunyan United Kingdom 23 991 0.9× 54 0.1× 216 0.3× 979 1.3× 26 0.0× 60 2.0k
Martine Blayau France 18 649 0.6× 79 0.1× 116 0.2× 404 0.5× 49 0.1× 44 1.1k
Philip G. Hollingshead United States 13 964 0.9× 555 0.7× 229 0.3× 426 0.6× 20 0.0× 16 1.9k
Katta M. Girisha India 24 977 0.9× 37 0.0× 159 0.2× 866 1.2× 40 0.1× 196 1.9k
Emilio Donti Italy 21 836 0.8× 608 0.7× 267 0.4× 404 0.5× 9 0.0× 96 1.6k

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.
Bouvet, Régis, et al.. (2020). PharmFrag: An Easy and Fast Multiplex Pharmacogenetics Assay to Simultaneously Analyze 9 Genetic Polymorphisms Involved in Response Variability of Anticancer Drugs. International Journal of Molecular Sciences. 21(24). 9650–9650. 1 indexed citations
2.
Vézain, Myriam, Marina Rubio, Valérie Dupé, et al.. (2018). A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis. Acta Neuropathologica Communications. 6(1). 109–109. 16 indexed citations
3.
Dupé, Valérie, Christèle Dubourg, Marie de Tayrac, & Véronique David. (2017). Du cyclope à la réalité. médecine/sciences. 33(11). 924–926. 1 indexed citations
4.
Hamdi‐Rozé, Houda, et al.. (2016). Regulation of downstream neuronal genes by proneural transcription factors during initial neurogenesis in the vertebrate brain. Neural Development. 11(1). 22–22. 14 indexed citations
5.
Chassaing, Nicolas, Erica E. Davis, Véronique David, et al.. (2016). Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network. Genome Research. 26(4). 474–485. 36 indexed citations
6.
Lan, Caroline Le, Annick Mosser, Martine Ropert, et al.. (2011). Sex and Acquired Cofactors Determine Phenotypes of Ferroportin Disease. Gastroenterology. 140(4). 1199–1207.e2. 46 indexed citations
7.
Dubourg, Christèle, Véronique David, Andrea Gropman, et al.. (2010). Clinical utility gene card for: Holoprosencephaly. European Journal of Human Genetics. 19(1). 3–3. 11 indexed citations
8.
Bendavid, Claude, Lucie Rochard, Jonathan Séguin, et al.. (2009). Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci. Human Mutation. 30(8). 1175–1182. 35 indexed citations
9.
Loréal, Olivier, Martine Ropert, Annick Mosser, et al.. (2007). Physiopathologie et génétique de l'hémochromatose HFE de type 1. La Presse Médicale. 36(9). 1271–1277. 2 indexed citations
10.
Gall, Jean‐Yves Le, Anne‐Marie Jouanolle, Jean Mosser, & Véronique David. (2005). Le métabolisme du fer chez l’homme. Bulletin de l Académie Nationale de Médecine. 189(8). 1635–1647. 1 indexed citations
11.
Gall, Jean‐Yves Le, Anne‐Marie Jouanolle, Patricia Fergelot, Jean Mosser, & Véronique David. (2004). Génétique des surcharges martiales primitives. Bulletin de l Académie Nationale de Médecine. 188(2). 247–263.
12.
Traiffort, Élisabeth, Christèle Dubourg, Hélène Faure, et al.. (2004). Functional Characterization of Sonic Hedgehog Mutations Associated with Holoprosencephaly. Journal of Biological Chemistry. 279(41). 42889–42897. 60 indexed citations
13.
Moirand, Romain, Dominique Guyader, Michel Mendler, et al.. (2002). HFE based re‐evaluation of heterozygous hemochromatosis. American Journal of Medical Genetics. 111(4). 356–361. 28 indexed citations
14.
Guillygomarc’h, Anne, Romain Moirand, Fabrice Lainé, et al.. (2001). Venesection therapy of insulin resistance-associated hepatic iron overload. Journal of Hepatology. 35(3). 344–349. 75 indexed citations
15.
Toutain, Bertrand, et al.. (2000). Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseases. Cytogenetic and Genome Research. 88(1-2). 82–86. 7 indexed citations
16.
Gicquel, Isabelle, et al.. (2000). The HFE Gene Undergoes Alternate Splicing Processes. Blood Cells Molecules and Diseases. 26(2). 155–162. 13 indexed citations
17.
Guyader, Dominique, Christian Jacquelinet, Romain Moirand, et al.. (1998). Noninvasive prediction of fibrosis in C282Y homozygous hemochromatosis. Gastroenterology. 115(4). 929–936. 224 indexed citations
18.
Pichon, Laurent, et al.. (1996). A new non-HLA multigene family associated with thePERB11 family within theMHC class I region. Immunogenetics. 44(4). 259–267. 12 indexed citations
19.
Boretto, Joëlle, Anne‐Marie Jouanolle, Jacqueline Yaouanq, et al.. (1992). Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis. Human Genetics. 89(1). 33–36. 22 indexed citations
20.
Jouanolle, Anne‐Marie, Jacqueline Yaouanq, Martine Blayau, et al.. (1990). HLA class I gene polymorphism in genetic hemochromatosis. Human Genetics. 85(3). 279–282. 9 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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