A. David

1.7k citations

42 papers · 579 indexed · h-index 13

Impact in

Developmental Biology top 5%
- Congenital limb and hand anomalies
Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases

Papers in ⓘ

Genetics 17
- Genetic and rare skin diseases. 5
- Genomic variations and chromosomal abnormalities 4
- Genetic Syndromes and Imprinting 3
- Connective tissue disorders research 2
Molecular Biology 15
- Hedgehog Signaling Pathway Studies 3

Co-authors: Didier Lacombe (3 shared papers)Alain Verloès (2 shared papers)Bertrand Isidor (5 shared papers)Jacqueline Vigneron (1 shared paper)Dominique Bonneau (2 shared papers)Pierre Bitoun (1 shared paper)Cédric Le Caignec (6 shared papers)A Nivelon (1 shared paper)
Journals: Clinical Genetics (6 papers)Prenatal Diagnosis (3 papers)Journal of Medical Genetics (3 papers)Diagnostic and Interventional Imaging (2 papers)International Archives of Occupational and Environmental Health (1 paper)
Partner nations: France United States Switzerland

In The Last Decade

A. David

39 papers receiving 554 citations

Peers

Countries citing papers authored by A. David

Since Specialization

Citations

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

Fields of papers citing papers by A. David

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside A. David, 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 A. David Line = papers co-authored together A. David 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 42 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes Journal of Medical Genetics ·A. David, Pierre Bitoun, Didier Lacombe, Julien Lambert, A Nivelon, Jacqueline Vigneron, Alain Verloès	1999	72
2	Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype. Journal of Medical Genetics ·Michel Longy, Vincent Coulon, B. Duboué, A. David, M Larrègue, Charis Eng, Patrizia Amati, J.L. Kraimps, Armand Bottani, Didier Lacombe, Dominique Bonneau	1998	62
3	Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus. Journal of Medical Genetics ·Patrick Edery, Anna Pelet, Lois M. Mulligan, Laurent Abel, (unknown), Eleanor Dow, Dominique Bonneau, A. David, Wayne F. Flintoff, D Jan	1994	47
4	Identification of two novel mutations in Shh long-range regulator associated with familial pre-axial polydactyly Clinical Genetics ·Juliette Albuisson, Bertrand Isidor, Marion Giraud, Olivier Pichon, T. Marsaud, A. David, Cédric Le Caignec, Stéphane Bezieau	2010	44
5	Paramyotonia congenita with an SCN4A mutation affecting cardiac repolarization Neurology ·Yann Péréon, Gilles Lande, Sophie Demolombe, Sylvie Nguyen The Tich, Damien Sternberg, Hervé Le Marec, A. David	2003	35
6	Coffin‐Lowry syndrome: a multicenter study Clinical Genetics ·S Gilgenkrantz, Paula Mujica, Philippe Gruet, P Tridon, F. A. W. SCHWEITZER, A Nivelon‐Chevallier, J L Nivelon, Gérard Couillault, A. David, Alain Verloès, C Lambotte, C Piussan, M Mathieu	1988	29
7	Phenotype and genotype in females with POU3F4 mutations Clinical Genetics ·Sandrine Marlin, MP Moizard, A. David, N Chaissang, Martine Raynaud, Laurence Jonard, D Feldmann, N. Loundon, Françoise Denoyelle, Annick Toutain	2009	28
8	Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2 PubMed ·Valérie Biancalana, Marie‐Louise Briard, A. David, S Gilgenkrantz, Josseline Kaplan, M Mathieu, C Piussan, Jacques Poncin, Albert Schinzel, C Oudet	1992	24
9	Costello syndrome: report of six patients including one with an embryonal rhabdomyosarcoma European Journal of Pediatrics ·Sabine Sigaudy, G. Vittu, A. David, J. Vigneron, Didier Lacombe, A. Moncla, Elisabeth Flori, N. Philip	2000	23
10	Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families Clinical Genetics ·Florence Petit, A.‐S. Jourdain, Joris Andrieux, Geneviève Baujat, Clarisse Baumann, Claire Bénéteau, A. David, Laurence Faivre, Dominique Gaillard, Brigitte Gilbert‐Dussardier, Pierre‐Simon Jouk, Cédric Le Caignec, Philippe Loget, Laurent Pasquier, Nicole Porchet, Muriel Holder‐Espinasse, Sylvie Manouvrier‐Hanu, Fabienne Escande	2013	17
11	Autosomal dominant spondylocarpotarsal synostosis syndrome: Phenotypic homogeneity and genetic heterogeneity American Journal of Medical Genetics Part A ·Bertrand Isidor, Valérie Cormier‐Daire, M. Le Merrer, Thierry Lefrançois, Antoine Hamel, C. Le Caignec, A. David, Sébastien Jacquemont	2008	17
12	Asymptomatic carrier of two CFTR mutations: Consequences for prenatal diagnosis? Prenatal Diagnosis ·C. Verlingue, A. David, Marie‐Pierre Audrézet, M. G. Le Roux, Bernard Mercier, Jean‐Paul Moisan, Claude Férec	1993	14
13	Isolated and syndromic brachydactylies: Diagnostic value of hand X-rays Diagnostic and Interventional Imaging ·(unknown), (unknown), Marie Vincent, M.P. Quéré, T. Lefrançois, Éric Frampas, (unknown), A. David	2015	13
14	Extreme oral manifestations in a Marfan-type syndrome International Journal of Oral and Maxillofacial Surgery ·Roman Hossein Khonsari, Pierre Corre, Z. Boukerma-Vernex, J. Schmidt, Karine Renaudin, C Frayssé, M. Gayet-Delacroix, Philippe Khau Van Kien, A. David	2010	12
15	Arrêt circulatoire lors d'une anesthésie générale chez un enfant porteur d'une myopathie de Duchenne méconnue Annales Françaises d Anesthésie et de Réanimation ·J.F. Arnould, André Bigot, L. Steenbeke, A. David, J.M. Mussini	1986	12
16	Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis Clinical Genetics ·Damini Jawaheer, S‐HH Juo, Cédric Le Caignec, A. David, Christine Petit, PK Gregersen, S Dowbak, Aarti Damle, Ken McElreavey, Harry Ostrer	2003	11
17	A quantitative and semi-automatic measurement of transverse sinus stenosis improves idiopathic intracranial hypertension diagnostic accuracy Journal of Neuroradiology ·A. Pellerin, J. Aguilar Garcia, A. David, Jérémy Meyer, Béatrice Delasalle, Solène de Gaalon, E. Auffray Calvier, Hubert Desal, Romain Bourcier	2018	11
18	Currarino syndrome as an etiology of a neonatal Escherichia coli meningitis Journal of Perinatology ·J. Fleury, G. Picherot, Célia Cretolle, Guillaume Podevin, A. David, Julie Caillon, Jean‐Christophe Rozé, Christèle Gras‐Le Guen	2007	10
19	Congenital skin pedicles with or without amniotic band sequence: Extending the human phenotype resembling mouse disorganization American Journal of Medical Genetics Part A ·Bertrand Isidor, Geneviève Baujat, C. Le Caignec, Olivier Pichon, Dominique Martin‐Coignard, Annick Toutain, A. David	2009	10
20	Radiographic presentation of musculoskeletal involvement in Werner syndrome (adult progeria) Diagnostic and Interventional Imaging ·A. David, Marie Vincent, Pierre-Paul Arrigoni, S. Barbarot, M.-A. Pistorius, Bertrand Isidor, Éric Frampas	2016	9

About A. David

A. David is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 42 papers that have together received 579 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Congenital limb and hand anomalies (5 papers), Genetic and rare skin diseases. (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic Syndromes and Imprinting (3 papers), Hedgehog Signaling Pathway Studies (3 papers), Congenital gastrointestinal and neural anomalies (2 papers) and Connective tissue disorders research (2 papers). The work is most often cited by research in Developmental Biology (59 citations), Genetics (230 citations), Sensory Systems (31 citations), Molecular Biology (326 citations) and Genetics (41 citations). A. David has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Didier Lacombe, Alain Verloès, Bertrand Isidor, Jacqueline Vigneron, Dominique Bonneau, Pierre Bitoun, Cédric Le Caignec, A Nivelon, Olivier Pichon and M Larrègue. Their work appears in journals such as Clinical Genetics, Prenatal Diagnosis, Journal of Medical Genetics, Diagnostic and Interventional Imaging and International Archives of Occupational and Environmental Health.

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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