Albert David

10.3k citations

92 papers · 3.1k indexed · 1 hit paper · h-index 30

Impact in

Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Molecular Biology top 5%
- Congenital heart defects research
- Sexual Differentiation and Disorders
- RNA and protein synthesis mechanisms

Papers in ⓘ

Genetics 44
- Genomic variations and chromosomal abnormalities 10
- Connective tissue disorders research 9
- Genetics and Neurodevelopmental Disorders 7
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
Developmental Biology 2

Co-authors: Cédric Le Caignec (31 shared papers)Bertrand Isidor (29 shared papers)Olivier Pichon (12 shared papers)Patrick Calvas (2 shared papers)Martine Raynaud (3 shared papers)Jamel Chelly (2 shared papers)Claude Moraine (2 shared papers)Sylvain Briault (2 shared papers)
Journals: Human Mutation (8 papers)European Journal of Medical Genetics (7 papers)The American Journal of Human Genetics (4 papers)European Journal of Human Genetics (3 papers)American Journal of Medical Genetics Part A (23 papers)
Partner nations: France Belgium United Kingdom

In The Last Decade

Albert David

91 papers receiving 3.0k citations

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 · 553 citations

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 92 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, Romuald Blanc, Albert David, Marie‐Pierre Moizard, Martine Raynaud, Nathalie Ronce, Éric Lemonnier, Patrick Calvas, Béatrice Laudier, Jamel Chelly, Jean‐Pierre Fryns, Hans‐Hilger Ropers, Ben C.J. Hamel, Christian Andrés, Catherine Barthélémy, Claude Moraine, Sylvain Briault Hit paper breakdown →	2004	553
2	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, Valérie Layet, Olivier Caron, Brigitte Gilbert‐Dussardier, Capucine Delnatte, Catherine Dugast, Jean‐Pierre Fricker, Dominique Bonneau, Nicolas Sévenet, Michel Longy, F. Caux, (unknown)	2013	225
3	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, P Soichot, Véronica Cusin, Laurence Faivre, Marie-Claire Locatelli, Martine Mayençon, Annie Sarcey, Emmanuel Broussolle, William Camu, Albert David, Robert Rousson	2010	171
4	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, Sébastien Jacquemont, Dominique Martin‐Coignard, Christel Thauvin‐Robinet, Martine Le Merrer, Jean‐Louis Mandel, Albert David, Laurence Faivre, Valérie Cormier‐Daire, Richard Redon, Cédric Le Caignec	2011	148
5	Postnatal Changes of T, LH, and FSH in 46,XY Infants with Mutations in the AR Gene The Journal of Clinical Endocrinology & Metabolism ·Claire Bouvattier, Jean‐Claude Carel, C Lecointre, Albert David, Charles Sultan, Anne‐Marie Bertrand, Yves Morel, Jean‐Louis Chaussain	2002	104
6	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 E Shmela, Sylvie Rossignol, Jun Okabe, Irène Netchine, Salah Azzi, Sylvie Cabrol, Cédric Le Caignec, Albert David, Yves Le Bouc, Assam El‐Osta, Christine Gicquel	2009	92
7	Les nouvelles fondations des sciences de gestion Albert David, Armand Hatchuel, Romain Laufer	2000	69
8	Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28 The American Journal of Human Genetics ·Florence Kyndt, Jean‐Jacques Schott, Jean‐Noël Trochu, Florence Baranger, O. Herbert, Valerie E. Scott, Édith Fressinaud, Albert David, Jean‐Paul Moisan, Jean-Brieuc Bouhour, Hervé Le Marec, Bernard Bénichou	1998	66
9	A de novoADCY5 mutation causes early‐onset autosomal dominant chorea and dystonia Movement Disorders ·Raphaël Carapito, Nicodème Paul, Meiggie Untrau, Marion Le Gentil, Louise Ott, Ghada Alsaleh, Pierre Jochem, Mirjana Radosavljevic, Cédric Le Caignec, Albert David, Philippe Damier, Bertrand Isidor, Seiamak Bahram	2014	59
10	High risk of malignancy in mosaic variegated aneuploidy syndrome American Journal of Medical Genetics ·Sébastien Jacquemont, M. Boceno, Jean Marie Rival, Françoise Méchinaud, Albert David	2002	54
11	GermlineLEMD3 mutations are rare in sporadic patients with isolated melorheostosis Human Mutation ·Jan Hellemans, Philippe Debeer, Michael Wright, Andreas Janecke, Klaus Kjaer, Peter Verdonk, Ravi Savarirayan, Lina Basel, Celia Moss, Johannes Roth, Albert David, Anne De Paepe, Paul Coucke, Geert Mortier	2006	53
12	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 ·Alain Verloès, Dominique Brémond‐Gignac, Bertrand Isidor, Albert David, Clarisse Baumann, M Leroy, René Stevens, Y. Gillerot, Delphine Héron, Bénédicte Héron, Brigitte Benzacken, Didier Lacombe, Han G. Brunner, Pierre Bitoun	2006	52
13	Further delineation of the congenital form of X-linked dyskeratosis congenita (Hoyeraal-Hreidarsson syndrome) European Journal of Pediatrics ·Yves Sznajer, Clarisse Baumann, Albert David, Hubert Journel, Didier Lacombe, Yves Pérel, Pascale Blouin, J. Segura, Jean‐Pierre Cézard, Michel Peuchmaur, Tomy Vulliamy, Inderjeet Dokal, Alain Verloès	2003	51
14	Non-USH2A mutations in USH2 patients Human Mutation ·Thomas Besnard, Christel Vaché, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Sylvie Odent, Patricia Blanchet, Patrick Calvas, Christian Hamel, Hélène Dollfus, Geneviève Lina‐Granade, James Lespinasse, Albert David, Bertrand Isidor, G Morin, Sue Malcolm, Sylvie Tuffery‐Giraud, Mireille Claustres, Anne‐Françoise Roux	2011	51
15	Familial acampomelic form of campomelic dysplasia caused by a 960 kb deletion upstream of SOX9 American Journal of Medical Genetics Part A ·Claire Lecointre, Olivier Pichon, Antoine Hamel, Yves Héloury, Laurence Michel‐Calemard, Yves Morel, Albert David, Cédric Le Caignec	2009	50
16	The DNA polymerase genes of several HMU-bacteriophages have similar group I introns with highly divergent open reading frames Nucleic Acids Research ·Heidi Goodrich‐Blair, Albert David	1994	46
17	Molecular apocrine differentiation is a common feature of breast cancer in patients with germline PTEN mutations Breast Cancer Research ·Guillaume Banneau, Mickaël Guedj, Gaëtan MacGrogan, Isabelle de Mascarel, Valérie Velasco, Renaud Schiappa, Valérie Bonadona, Albert David, Catherine Dugast, Brigitte Gilbert‐Dussardier, Olivier Ingster, P. Vabres, F. Caux, Aurélien de Reyniès, Richard Iggo, Nicolas Sévenet, Françoise Bonnet, Michel Longy	2010	46
18	Novel and Recurrent Mutations in the Genes Encoding Keratins K6a, K16 and K17 in 13 Cases of Pachyonychia Congenita Journal of Investigative Dermatology ·Alessandro Terrinoni, Frances J.D. Smith, Biagio Didona, Flora Canzona, Mauro Paradisi, Marcel Huber, Daniel Hohl, Albert David, Alain Verloès, Irene M. Leigh, Colin S. Munro, Gerry Melino, W.H. Irwin McLean	2001	45
19	Four-Year Follow-up of Diagnostic Service in USH1 Patients Investigative Ophthalmology & Visual Science ·Anne‐Françoise Roux, Valérie Faugère, Christel Vaché, David Baux, Thomas Besnard, Susana Léonard, Catherine Blanchet, Christian Hamel, Michel Mondain, Brigitte Gilbert‐Dussardier, Patrick Edery, Didier Lacombe, Dominique Bonneau, Muriel Holder‐Espinasse, Umberto Ambrosetti, Hubert Journel, Albert David, Geneviève Lina‐Granade, Sue Malcolm, Mireille Claustres	2011	42
20	Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxia American Journal of Medical Genetics Part A ·Bertrand Isidor, Olivier Pichon, S. Baron, Albert David, Cédric Le Caignec	2009	39

About Albert David

Albert David is a scholar working on Genetics, Developmental Biology, Genetics, Molecular Biology and Cell Biology, having authored 92 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Connective tissue disorders research (9 papers), RNA modifications and cancer (8 papers), Congenital heart defects research (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Skin and Cellular Biology Research (6 papers). The work is most often cited by research in Genetics (1.4k citations), Molecular Biology (1.8k citations), Sensory Systems (99 citations), Cell Biology (292 citations) and Cognitive Neuroscience (340 citations). Albert David has collaborated with scholars based in France, Belgium and United Kingdom. Frequent co-authors include Cédric Le Caignec, Bertrand Isidor, Olivier Pichon, Patrick Calvas, Martine Raynaud, Jamel Chelly, Claude Moraine, Sylvain Briault, Marie Gomot and Alain Verloès. Their work appears in journals such as Human Mutation, European Journal of Medical Genetics, The American Journal of Human Genetics, European Journal of Human Genetics and American Journal of Medical Genetics Part A.

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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