Albert David

10.3k total citations · 1 hit paper
92 papers, 3.1k citations indexed

About

Albert David is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Albert David has authored 92 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 44 papers in Genetics and 15 papers in Surgery. Recurrent topics in Albert David's work include Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (9 papers) and RNA modifications and cancer (8 papers). Albert David is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (9 papers) and RNA modifications and cancer (8 papers). Albert David collaborates with scholars based in France, Belgium and United Kingdom. Albert David's co-authors include Cédric Le Caignec, Bertrand Isidor, Olivier Pichon, Martine Raynaud, Patrick Calvas, Sylvain Briault, Sébastien Jacquemont, Alain Verloès, Jamel Chelly and Claude Moraine and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Blood.

In The Last Decade

Albert David

91 papers receiving 3.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family

2004 553 citations Frédéric Laumonnier, Frédérique Bonnet‐Brilhault et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Albert David France	30	1.8k	1.4k	340	298	292	92	3.1k
Christiane Zweier Germany	30	2.3k 1.3×	1.9k 1.3×	308 0.9×	270 0.9×	162 0.6×	82	4.0k
Lina Basel‐Vanagaite Israel	32	1.9k 1.0×	1.4k 1.0×	245 0.7×	468 1.6×	427 1.5×	111	3.6k
Ann C. M. Smith United States	32	1.8k 1.0×	2.1k 1.5×	423 1.2×	222 0.7×	197 0.7×	95	3.9k
Tayfun Özçelık Türkiye	30	1.5k 0.8×	859 0.6×	172 0.5×	541 1.8×	317 1.1×	59	3.1k
Donna M. Martin United States	38	2.2k 1.2×	1.1k 0.7×	261 0.8×	304 1.0×	167 0.6×	113	4.0k
Angelo Selicorni Italy	29	2.5k 1.4×	1.8k 1.3×	237 0.7×	191 0.6×	168 0.6×	176	3.8k
Tatsuya Kishino Japan	27	2.4k 1.3×	1.9k 1.3×	192 0.6×	164 0.6×	234 0.8×	64	3.3k
Heather E. McDermid Canada	29	2.1k 1.2×	2.0k 1.4×	333 1.0×	177 0.6×	119 0.4×	64	3.3k
Patrick Calvas France	31	2.1k 1.2×	1.4k 1.0×	338 1.0×	346 1.2×	348 1.2×	104	3.9k
Susan H. Blanton United States	43	2.8k 1.6×	2.3k 1.6×	245 0.7×	289 1.0×	542 1.9×	189	6.2k

Countries citing papers authored by Albert David

Since Specialization

Citations

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

Fields of papers citing papers by Albert David

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Albert David

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

Isidor, Bertrand & Albert David. (2014). Two girls with short stature, short neck, vertebral anomalies, Sprengel deformity and intellectual disability. European Journal of Medical Genetics. 58(1). 47–50. 10 indexed citations

Marlin, Sandrine, Sandra Chantot‐Bastaraud, Albert David, et al.. (2013). Discovery of a Large Deletion of KAL1 in 2 Deaf Brothers. Otology & Neurotology. 34(9). 1590–1594. 8 indexed citations

Khonsari, Roman Hossein, Maisa Seppala, Alan Pradel, et al.. (2013). The buccohypophyseal canal is an ancestral vertebrate trait maintained by modulation in sonic hedgehog signaling. BMC Biology. 11(1). 27–27. 32 indexed citations

Isidor, Bertrand, Sylvaine Poignant, G. Picherot, et al.. (2012). Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia?. American Journal of Medical Genetics Part A. 158A(7). 1754–1758. 2 indexed citations

Besnard, Thomas, Christel Vaché, David Baux, et al.. (2011). Non-USH2A mutations in USH2 patients. Human Mutation. 33(3). 504–510. 51 indexed citations

Isidor, Bertrand, Olivier Pichon, Richard Redon, et al.. (2010). Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13. The American Journal of Human Genetics. 87(1). 95–100. 31 indexed citations

Schmitt, Françoise, Hugues Piloquet, Marc‐David Leclair, et al.. (2009). Hereditary pancreatitis in children: surgical implications with special regard to genetic background. Journal of Pediatric Surgery. 44(11). 2078–2082. 14 indexed citations

Gloan, Laurianne Le, Olivier Pichon, Bertrand Isidor, et al.. (2008). A 8.26 Mb deletion in 6q16 and a 4.95 Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff–Parkinson–White syndrome. European Journal of Medical Genetics. 51(6). 651–657. 16 indexed citations

Isidor, Bertrand, Norbert Winer, Madeleine Joubert, et al.. (2008). Inherited 18q23 duplication in a fetus with multiple congenital anomalies. European Journal of Medical Genetics. 51(3). 231–238. 4 indexed citations

10.

Isidor, Bertrand, et al.. (2007). Genochondromatosis type II: Report of a new patient and further delineation of the phenotype. American Journal of Medical Genetics Part A. 143A(16). 1919–1921. 4 indexed citations

11.

Verloès, Alain, Dominique Brémond‐Gignac, Bertrand Isidor, et al.. (2006). Blepharophimosis‐mental retardation (BMR) syndromes: A proposed clinical classification of the so‐called Ohdo syndrome, and delineation of two new BMR syndromes, one X‐linked and one autosomal recessive. American Journal of Medical Genetics Part A. 140A(12). 1285–1296. 52 indexed citations

12.

Laumonnier, Frédéric, Frédérique Bonnet‐Brilhault, Marie Gomot, et al.. (2004). X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family. The American Journal of Human Genetics. 74(3). 552–557. 553 indexed citations breakdown →

13.

Sznajer, Yves, Clarisse Baumann, Albert David, et al.. (2003). Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome). European Journal of Pediatrics. 162(12). 863–867. 51 indexed citations

14.

Smith, Frances J.D., et al.. (2001). Novel Keratin 17 Mutations in Pachyonychia Congenita Type 2. Journal of Investigative Dermatology. 116(5). 806–808. 14 indexed citations

15.

Terrinoni, Alessandro, Frances J.D. Smith, Biagio Didona, et al.. (2001). Novel and Recurrent Mutations in the Genes Encoding Keratins K6a, K16 and K17 in 13 Cases of Pachyonychia Congenita. Journal of Investigative Dermatology. 117(6). 1391–1396. 45 indexed citations

16.

David, Albert, et al.. (2000). Les nouvelles fondations des sciences de gestion. 69 indexed citations

17.

Saugier-Véber, Pascale, Cosette Martin, Nathalie Le Meur, et al.. (1998). Identification of novelL1CAM mutations using fluorescence-assisted mismatch analysis. Human Mutation. 12(4). 259–266. 22 indexed citations

18.

Dahan, Karin, Laurence Heidet, Jing Zhou, et al.. (1995). Smooth muscle tumors associated with X-linked Alport syndrome: Carrier detection in females. Kidney International. 48(6). 1900–1906. 29 indexed citations

19.

Larget‐Piet, Dominique, S. Gerber, Dominique Bonneau, et al.. (1994). Genetic Heterogeneity of Usher Syndrome Type 1 in French Families. Genomics. 21(1). 138–143. 27 indexed citations

20.

David, Albert, et al.. (1991). Macrostomia, ectropion, atrophic skin, hypertrichosis: Another observation. American Journal of Medical Genetics. 39(1). 112–115. 22 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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