A. David

1.7k total citations
42 papers, 579 citations indexed

About

A. David is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, A. David has authored 42 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Molecular Biology and 8 papers in Surgery. Recurrent topics in A. David's work include Prenatal Screening and Diagnostics (6 papers), Genetic and rare skin diseases. (5 papers) and Congenital limb and hand anomalies (5 papers). A. David is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genetic and rare skin diseases. (5 papers) and Congenital limb and hand anomalies (5 papers). A. David collaborates with scholars based in France, United States and Switzerland. A. David's co-authors include Didier Lacombe, Alain Verloès, Bertrand Isidor, Pierre Bitoun, Dominique Bonneau, A Nivelon, Jacqueline Vigneron, Cédric Le Caignec, Olivier Pichon and Patrizia Amati and has published in prestigious journals such as The Lancet, Neurology and Journal of Medical Genetics.

In The Last Decade

A. David

39 papers receiving 554 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. David France	13	326	230	115	64	59	42	579
María‐Luisa Martínez‐Frías Spain	16	251 0.8×	327 1.4×	267 2.3×	155 2.4×	55 0.9×	22	801
Sylvie Manouvrier‐Hanu France	18	504 1.5×	395 1.7×	117 1.0×	99 1.5×	80 1.4×	57	846
J.H.A.M. Tuerlings Netherlands	18	440 1.3×	453 2.0×	83 0.7×	145 2.3×	42 0.7×	49	880
M D Crawfurd United Kingdom	18	250 0.8×	290 1.3×	80 0.7×	129 2.0×	28 0.5×	33	705
Odile Boute France	13	162 0.5×	222 1.0×	129 1.1×	89 1.4×	35 0.6×	31	471
Alicia Delicado Spain	16	340 1.0×	459 2.0×	129 1.1×	201 3.1×	37 0.6×	47	706
Robert Wallerstein United States	17	410 1.3×	399 1.7×	140 1.2×	180 2.8×	45 0.8×	66	924
Boris Utsch Germany	20	596 1.8×	391 1.7×	136 1.2×	224 3.5×	29 0.5×	32	951
M. Gonzalés France	16	244 0.7×	131 0.6×	100 0.9×	91 1.4×	17 0.3×	38	617
Anita Wischmeijer Italy	16	260 0.8×	333 1.4×	71 0.6×	96 1.5×	27 0.5×	29	622

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-authorship network of co-authors of A. David

This figure shows the co-authorship network connecting the top 25 collaborators of A. David. A scholar is included among the top collaborators of A. 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 A. David. A. David 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

David, A., et al.. (2023). Evaluation of local control after percutaneous microwave ablation versus partial nephrectomy: A propensity score matched study. PubMed. 34(1). 102534–102534. 4 indexed citations

David, A., et al.. (2023). Epidemiological profile of cancer at the laboratory of anatomy and pathological cytology of mungbere in the Democratic Republic of Congo. Journal of Cancer Policy. 37. 100434–100434.

David, A., Jérémy Meyer, Béatrice Delasalle, et al.. (2018). A quantitative and semi-automatic measurement of transverse sinus stenosis improves idiopathic intracranial hypertension diagnostic accuracy. Journal of Neuroradiology. 45(5). 329–332. 11 indexed citations

David, A., et al.. (2016). Radiographic presentation of musculoskeletal involvement in Werner syndrome (adult progeria). Diagnostic and Interventional Imaging. 98(5). 373–378. 9 indexed citations

Vincent, Marie, et al.. (2015). Isolated and syndromic brachydactylies: Diagnostic value of hand X-rays. Diagnostic and Interventional Imaging. 96(5). 443–448. 13 indexed citations

Petit, Florence, Joris Andrieux, Geneviève Baujat, et al.. (2013). Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families. Clinical Genetics. 85(5). 464–469. 17 indexed citations

Khonsari, Roman Hossein, Pierre Corre, Karine Renaudin, et al.. (2010). Extreme oral manifestations in a Marfan-type syndrome. International Journal of Oral and Maxillofacial Surgery. 39(6). 622–625. 12 indexed citations

Alessandri, J.L., A. David, Dominique Martin‐Coignard, et al.. (2010). Tibial developmental field defect in valproic acid embryopathy: Report on three cases. American Journal of Medical Genetics Part A. 152A(11). 2805–2809. 8 indexed citations

Albuisson, Juliette, Bertrand Isidor, Marion Giraud, et al.. (2010). Identification of two novel mutations in Shh long-range regulator associated with familial pre-axial polydactyly. Clinical Genetics. 79(4). 371–377. 44 indexed citations

10.

David, A., et al.. (2009). Syndrome de Conradi-Hünermann-Happle de disposition unilatérale. Annales de Dermatologie et de Vénéréologie. 137(1). 44–47. 3 indexed citations

11.

Winer, Norbert, Florence Kyndt, A. Paumier, et al.. (2008). Prenatal diagnosis of Larsen syndrome caused by a mutation in the filamin B gene. Prenatal Diagnosis. 29(2). 172–174. 6 indexed citations

12.

Fleury, J., G. Picherot, Célia Cretolle, et al.. (2007). Currarino syndrome as an etiology of a neonatal Escherichia coli meningitis. Journal of Perinatology. 27(9). 589–591. 10 indexed citations

13.

David, A., et al.. (2004). Posters. 3(4). 191–200. 4 indexed citations

14.

Caignec, C. Le, Christine Gicquel, Marie-Claire Gübler, et al.. (2004). Sonographic findings in Beckwith–Wiedemann syndrome related to H19 hypermethylation. Prenatal Diagnosis. 24(3). 165–168. 6 indexed citations

15.

Jawaheer, Damini, Cédric Le Caignec, A. David, et al.. (2003). Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis. Clinical Genetics. 63(6). 530–535. 11 indexed citations

16.

Maugard, Thierry, et al.. (1997). La sclérose hépatoportale: à propos d'un cas familial. Archives de Pédiatrie. 4(3). 251–254. 2 indexed citations

17.

Verlingue, C., A. David, Marie‐Pierre Audrézet, et al.. (1993). Asymptomatic carrier of two CFTR mutations: Consequences for prenatal diagnosis?. Prenatal Diagnosis. 13(12). 1143–1148. 14 indexed citations

18.

Merrer, M. Le, A. David, Françoise Goutières, & Marie‐Louise Briard. (1992). Digito‐reno‐cerebral syndrome: confirmation of Eronen syndrome. Clinical Genetics. 42(4). 196–198. 7 indexed citations

19.

Gilgenkrantz, S, Philippe Gruet, A Nivelon‐Chevallier, et al.. (1988). Coffin‐Lowry syndrome: a multicenter study. Clinical Genetics. 34(4). 230–245. 29 indexed citations

20.

David, A., et al.. (1986). Arrêt circulatoire lors d'une anesthésie générale chez un enfant porteur d'une myopathie de Duchenne méconnue. Annales Françaises d Anesthésie et de Réanimation. 5(6). 612–614. 12 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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