Albert David

10.2k citations

151 papers · 7.9k · 1 hit paper · h-index 50

Impact in

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Genetic and Kidney Cyst Diseases
Developmental Biology top 1%

Papers in

Genetics 99
- Genomic variations and chromosomal abnormalities 36
- Genomics and Rare Diseases 27
- Connective tissue disorders research 21
- Genetics and Neurodevelopmental Disorders 14
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
- Genetic and rare skin diseases. 8
- Craniofacial Disorders and Treatments 7
Developmental Biology 15
- Congenital limb and hand anomalies 15

Co-authors: Cédric Le Caignec (32 shared papers)Bertrand Isidor (30 shared papers)Olivier Pichon (12 shared papers)Alain Verloès (12 shared papers)Martine Raynaud (4 shared papers)Jean‐Marie Rival (10 shared papers)Sébastien Jacquemont (5 shared papers)Sylvain Briault (2 shared papers)
Journals: Human Mutation (12 papers)European Journal of Human Genetics (12 papers)The American Journal of Human Genetics (9 papers)European Journal of Medical Genetics (9 papers)Journal of Medical Genetics (6 papers)
Partner nations: France United Kingdom Belgium

In The Last Decade

Albert David

150 papers receiving 7.5k citations

Albert David's Hit Papers

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X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family 2004 · 636 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2004 The American Journal of Human Genetics

Peers

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-authors

The 25 scholars most cited alongside Albert 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 Albert David Line = papers co-authored together Albert 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 151 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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 ·Frédéric Laumonnier, Frédérique Bonnet‐Brilhault, Marie Gomot, R. Blanc, Albert David, Marie‐Pierre Moizard, Martine Raynaud, Nathalie Ronce Hit paper breakdown →	2004	636
2	Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Nature ·Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G. Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen	2011	371
3	High cumulative risks of cancer in patients with PTEN hamartoma tumour syndrome Journal of Medical Genetics ·Virginie Bubien, Françoise Bonnet, Véronique Brouste, Stéphanie Hoppe, Emmanuelle Barouk-Simonet, Albert David, Patrick Edery, Armand Bottani	2013	268
4	Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations The American Journal of Human Genetics ·Jennifer J. Johnston, Isabelle M. Olivos-Glander, Christina Killoran, Emma M. Clement, Joyce Tannenbaum Turner, Kathryn F. Peters, Margaret H. Abbott, David J. Aughton	2005	223
5	SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations European Journal of Human Genetics ·Sébastien Albert, Hélène Blons, Laurence Jonard, D Feldmann, Pierre Chauvin, Nathalie Loundon, Annie Sergent-Allaoui, Muriel Houang	2006	197
6	Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities JAMA Psychiatry ·Debra D’Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin‐Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen M. Hanson, Anne Manuela Maillard	2015	190
7	A Major Determinant for Binding and Aminoacylation of tRNAAla in Cytoplasmic Alanyl-tRNA Synthetase Is Mutated in Dominant Axonal Charcot-Marie-Tooth Disease The American Journal of Human Genetics ·Philippe Latour, Christel Thauvin‐Robinet, Chantal Baudelet-Méry, Pierre Soichot, Véronica Cusin, Laurence Olivier Faivre, Marie-Claire Locatelli, Martine Mayençon	2010	189
8	Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis Nature Genetics ·Bertrand Isidor, Pierre Lindenbaum, Olivier Pichon, Stéphane Bezieau, Christian Dina C, Sébastien Jacquemont, Dominique Martin‐Coignard, Christel Thauvin‐Robinet	2011	161
9	Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination The American Journal of Human Genetics ·Alexander W. Pearlman, Johnny C. Loke, Cédric Le Caignec, Stefan J. White, Andrew Friedman, Nick Warr, John Willan, David G. Brauer	2010	159
10	Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis Nature Genetics ·Zandra A. Jenkins, Margriet van Kogelenberg, Tim Morgan, Aaron R. Jeffs, Ryuji Fukuzawa, Esther J. Pearl, Christina Thaller B, Anne V Hing	2008	155
11	Postnatal Changes of T, LH, and FSH in 46,XY Infants with Mutations in the AR Gene The Journal of Clinical Endocrinology & Metabolism ·Claire Morel Bouvattier, Jean‐Claude Carel, Claudine Lecointre, Albert David, Charles Sultan, Yves Morel, Jean‐Louis Chaussain +1 other	2002	149
12	Baraitser–Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases European Journal of Human Genetics ·Alain Verloès, Nataliya Di Donato, Julien Masliah‐Planchon, Marjolijn C.J. Jongmans, Omar A Abdul-Rahman, Beate Albrecht, Judith E Allanson, Han G. Brunner	2014	124
13	Treacher Collins syndrome: a clinical and molecular study based on a large series of patients Genetics in Medicine ·Marie Vincent, David Geneviève, Agnès Ostertag, Sandrine Marlin, Didier Lacombe, Dominique Martin‐Coignard, Christine Coubes, Albert David	2015	120
14	Characterization of large rearrangements in autosomal dominant polycystic kidney disease and the PKD1/TSC2 contiguous gene syndrome Kidney International ·Mark B. Consugar, Patrick A. Lundquist, Sandro Rossetti, Vickie J. Kubly, Denise L. Walker, Laureano J. Rangel, Richard Aspinwall, W. Patrick Niaudet	2008	116
15	Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia The American Journal of Human Genetics ·Sascha Vermeer, Alexander Hoischen, Rowdy P. P. Meijer, Christian Gilissen, Kornelia Neveling, Nienke Wieskamp, Arjan P.M. de Brouwer, Michel Koenig	2010	114
16	Molecular and clinical analysis ofRAF1in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation Human Mutation ·Tomoko Kobayashi, Yoko Aoki, Tetsuya Niihori, Hélène Cavé, Alain Verloès, Nobuhiko Okamoto, Hiroshi Kawame, Ikuma Fujiwara	2010	105
17	TCTN3 Mutations Cause Mohr-Majewski Syndrome The American Journal of Human Genetics ·Sophie Thomas, Marine Legendre, Sophie Saunier, Bettina Bessières, Caroline Alby, Maryse Bonnière, Annick Toutain, Laurence Lœuillet	2012	105
18	Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders Human Molecular Genetics ·Julie Demars, Mansur Ennuri Shmela, Sylvie Rossignol, Jun Okabe, Irène Netchine, Salah Azzi, Sylvie Cabrol, Cédric Le Caignec	2009	103
19	DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies European Journal of Human Genetics ·Jianling Ji, Hane Lee, Bob Argiropoulos, Naghmeh Dorrani, Julián A. Martínez-Agosto, Natalia Gomez‐Ospina, Natalie M. Gallant, Jonathan Bernstein	2015	103
20	A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies Brain ·Marie Coutelier, Giulia Coarelli, Marie‐Lorraine Monin, Juliette Konop, Claire-Sophie Davoine, Christelle Tesson, Rémi Valter, Mathieu Anheim	2017	94

About Albert David

Albert David is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Molecular Biology and Sensory Systems, having authored 151 papers that have together received 7.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (36 papers), Genomics and Rare Diseases (27 papers), Connective tissue disorders research (21 papers), Congenital limb and hand anomalies (15 papers), Genetics and Neurodevelopmental Disorders (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Genetic and rare skin diseases. (8 papers) and Craniofacial Disorders and Treatments (7 papers). The work is most often cited by research in Genetics (3.9k citations), Developmental Biology (239 citations), Sensory Systems (435 citations), Cellular and Molecular Neuroscience (492 citations) and Pediatrics, Perinatology and Child Health (370 citations). Albert David has collaborated with scholars based in France, United Kingdom and Belgium. Frequent co-authors include Cédric Le Caignec, Bertrand Isidor, Olivier Pichon, Alain Verloès, Martine Raynaud, Jean‐Marie Rival, Sébastien Jacquemont, Sylvain Briault, Patrick Calvas and Jamel Chelly. Their work appears in journals such as Human Mutation, European Journal of Human Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics and Journal of Medical Genetics.

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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Albert David's Hit Papers

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All Works

About Albert David

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