David Geneviève

9.3k total citations
80 papers, 2.3k citations indexed

About

David Geneviève is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, David Geneviève has authored 80 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Genetics, 35 papers in Molecular Biology and 10 papers in Surgery. Recurrent topics in David Geneviève's work include Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (13 papers) and Genetics and Neurodevelopmental Disorders (9 papers). David Geneviève is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Genomics and Rare Diseases (13 papers) and Genetics and Neurodevelopmental Disorders (9 papers). David Geneviève collaborates with scholars based in France, United States and United Kingdom. David Geneviève's co-authors include Valérie Cormier‐Daire, Jeanne Amiel, Arnold Münnich, Stanislas Lyonnet, Vincent Gâtinois, Damien Sanlaville, Michel Vekemans, Loïc de Pontual, Jean‐Pierre Fryns and Willy M. Nillesen and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Blood.

In The Last Decade

David Geneviève

73 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David Geneviève France	24	1.3k	1.1k	285	235	233	80	2.3k
Rika Kosaki Japan	25	1.3k 0.9×	846 0.8×	297 1.0×	125 0.5×	379 1.6×	113	2.3k
Mohnish Suri United Kingdom	24	1.2k 0.9×	736 0.7×	200 0.7×	160 0.7×	260 1.1×	82	2.2k
Yasemin Alanay Türkiye	26	994 0.7×	1.0k 0.9×	370 1.3×	130 0.6×	162 0.7×	108	2.1k
Vincent El Ghouzzi France	27	1.1k 0.8×	1.0k 0.9×	204 0.7×	180 0.8×	233 1.0×	44	2.1k
Małgorzata Krajewska‐Walasek Poland	23	1.4k 1.0×	1.0k 0.9×	298 1.0×	172 0.7×	149 0.6×	110	2.2k
Beyhan Tüysüz Türkiye	24	1.4k 1.0×	988 0.9×	231 0.8×	122 0.5×	469 2.0×	139	2.5k
Andreas Winterpacht Germany	33	2.5k 1.8×	1.4k 1.3×	232 0.8×	218 0.9×	252 1.1×	85	3.7k
Israela Lerer Israel	29	1.2k 0.9×	972 0.9×	238 0.8×	210 0.9×	108 0.5×	77	2.5k
Muriel Holder‐Espinasse France	26	1.1k 0.8×	1.0k 0.9×	358 1.3×	138 0.6×	114 0.5×	74	2.0k
Eissa Faqeih Saudi Arabia	28	1.5k 1.1×	920 0.8×	151 0.5×	159 0.7×	238 1.0×	80	2.2k

Countries citing papers authored by David Geneviève

Since Specialization

Citations

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

Fields of papers citing papers by David Geneviève

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Geneviève

This figure shows the co-authorship network connecting the top 25 collaborators of David Geneviève. A scholar is included among the top collaborators of David Geneviève 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 David Geneviève. David Geneviève is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Apparailly, Florence, et al.. (2024). Abnormal Immune Profile in Individuals with Kabuki Syndrome. Journal of Clinical Immunology. 45(1). 7–7. 1 indexed citations

Goel, Himanshu, Pauline Burger, Jean‐Louis Mandel, et al.. (2024). Speech and language in DDX3X‐neurodevelopmental disorder: A call for early augmentative and alternative communication intervention. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 195(6). e32971–e32971. 5 indexed citations

Mandel, Jean‐Louis, Bernard Baertschi, Damien Sanlaville, et al.. (2020). Réflexions éthiques sur le dépistage génétique préconceptionnel en population générale : le débat français et l’avis de la Société Française de Médecine Prédictive et Personnalisée. Ethics Medicine and Public Health. 12. 100439–100439.

Michot, Caroline, Geneviève Baujat, S. Baron, et al.. (2019). Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review. Clinical Genetics. 96(4). 309–316. 31 indexed citations

Thévenon, Julien, Yannis Duffourd, Sophie Nambot, et al.. (2018). TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutation. American Journal of Medical Genetics Part A. 176(12). 2813–2818. 12 indexed citations

Mau‐Them, Frédéric Tran, Julien Thévenon, Thomas Guignard, et al.. (2018). LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters. European Journal of Medical Genetics. 62(3). 161–166. 19 indexed citations

Subsol, Gérard, Marie-José Perez, David Geneviève, et al.. (2018). Three-dimensional computer-assisted dissection of pancreatic lymphatic anatomy on human fetuses: a step toward automatic image alignment. Surgical and Radiologic Anatomy. 40(5). 587–597. 3 indexed citations

Balandraud, Nathalie, Nathalie Lambert, Isabelle Auger, et al.. (2017). TMEM187-IRAK1Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic Origin. Journal of Immunology Research. 2017. 1–12. 9 indexed citations

Yauy, Kévin, Frédéric Tran Mau‐Them, Marjolaine Willems, et al.. (2017). B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation. Genetics in Medicine. 20(2). 269–274. 21 indexed citations

10.

Chassaing, Nicolas, Nicola Ragge, Julie Plaisancié, et al.. (2016). Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia. American Journal of Medical Genetics Part A. 170(7). 1895–1898. 25 indexed citations

11.

Schneider, Anouck, Jacques Puechberty, Bee Ling Ng, et al.. (2015). Identification of disrupted AUTS2 and EPHA6 genes by array painting in a patient carrying a de novo balanced translocation t(3;7) with intellectual disability and neurodevelopment disorder. American Journal of Medical Genetics Part A. 167(12). 3031–3037. 8 indexed citations

12.

Pellestor, Franck, Vincent Gâtinois, Jacques Puechberty, David Geneviève, & Geneviève Lefort. (2014). Chromothripsis: potential origin in gametogenesis and preimplantation cell divisions. A review. Fertility and Sterility. 102(6). 1785–1796. 49 indexed citations

13.

Pinson, Lucile, Linda Mannini, Marjolaine Willems, et al.. (2013). CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome. American Journal of Medical Genetics Part A. 164(1). 177–181. 20 indexed citations

14.

Kleefstra, Tjitske, Han G. Brunner, Jeanne Amiel, et al.. (2006). Loss-of-Function Mutations in Euchromatin Histone Methyl Transferase 1 (EHMT1) Cause the 9q34 Subtelomeric Deletion Syndrome. The American Journal of Human Genetics. 79(2). 370–377. 276 indexed citations

15.

Geneviève, David, R. Walter, Philippe Gorry, et al.. (2005). Gorlin syndrome presenting as prenatal chylothorax in a girl. Prenatal Diagnosis. 25(11). 997–999. 8 indexed citations

16.

Geneviève, David, Damien Sanlaville, Laurence Faivre, et al.. (2005). Paternal deletion of the GNAS imprinted locus (including Gnasxl) in two girls presenting with severe pre- and post-natal growth retardation and intractable feeding difficulties. European Journal of Human Genetics. 13(9). 1033–1039. 61 indexed citations

17.

Cazeneuve, Cécile, David Geneviève, Hasmik Hayrapetyan, et al.. (2003). Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations. Arthritis & Rheumatism. 48(8). 2324–2331. 36 indexed citations

18.

Sanlaville, Damien, Serge Romana, Jeanne Amiel, et al.. (2002). A CGH study of 27 patients with CHARGE association. Clinical Genetics. 61(2). 135–138. 21 indexed citations

19.

Geneviève, David, Valérie Cormier‐Daire, Damien Sanlaville, et al.. (2002). Mild phenotype in a 15‐year‐old boy with Pallister–Killian syndrome. American Journal of Medical Genetics Part A. 116A(1). 90–93. 30 indexed citations

20.

Cazeneuve, Cécile, Stéphanie Papin, Françoise Roudot‐Thoraval, et al.. (2000). Identification of MEFV-Independent Modifying Genetic Factors for Familial Mediterranean Fever. The American Journal of Human Genetics. 67(5). 1136–1143. 155 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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