Albert David - Concepedia

Author

Albert David

Also Known As

A. David, A.Shub David, ALBERT DAVID, Albert David, Christina Fagerberg, Courtney J Haycraft, David, Albert, Grange, Dorothy K., Haycraft, Courtney, Marion Gérard

204

Publications

10.3K

Citations

H-Index

141

Concepts

All Affiliations

Inserm Centre Hospitalier Universitaire de Nantes Génétique Médicale & Génomique Fonctionelle Assistance Publique – Hôpitaux de Paris Hôpital Necker-Enfants Malades

About

Albert David is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	36	56	5.6K
2	Public Health	5	5	365
3	Natural Sciences	4	4	413
4	Arts	2	2	346
5	Health Sciences	1	1	51

Albert David

115

Publications

Citations

H-Index

Page 1

	Year	Citations
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family Frédéric Laumonnier, Frédérique Bonnet‐Brilhault, Marie Gomot, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologyMendelian DisorderSyndromic AutismGenetic Disorder	2004	756
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Nature Gene DosageGeneticsHuman PolymorphismMolecular GeneticsChromosome 16P11.2	2011	474
High cumulative risks of cancer in patients with <i>PTEN</i> hamartoma tumour syndrome Virginie Bubien, Françoise Bonnet, Véronique Brouste, Journal of Medical Genetics	2013	358
Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities Debra D’Angelo, Sébastien Lebon, Qixuan Chen, JAMA Psychiatry	2015	290
Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsGenetic Epidemiology	2005	276
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations Sébastien Albert, Hélène Blons, Laurence Jonard, European Journal of Human Genetics Developmental BiologyMedicineGeneticsAudiologyGenetic Epidemiology	2006	240
A Major Determinant for Binding and Aminoacylation of tRNAAla in Cytoplasmic Alanyl-tRNA Synthetase Is Mutated in Dominant Axonal Charcot-Marie-Tooth Disease Philippe Latour, Christel Thauvin‐Robinet, Chantal Baudelet-Méry, The American Journal of Human Genetics BiologyNatural SciencesGeneticsProtein BiosynthesisMolecular Genetics	2010	225
Mutations in MAP3K1 Cause 46,XY Disorders of Sex Development and Implicate a Common Signal Transduction Pathway in Human Testis Determination Alexander Pearlman, Johnny Loke, Cédric Le Caignec, The American Journal of Human Genetics SpermatogenesisHuman Testis DeterminationDevelopmental BiologySex DeterminationGenetic Disorder	2010	220
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis Zandra A. Jenkins, Margriet van Kogelenberg, Tim Morgan, Nature Genetics Somatic VariantCancer PathologyMendelian DisorderGenetic DisorderGenetics	2008	195
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis Bertrand Isidor, Pierre Lindenbaum, Olivier Pichon, Nature Genetics Bone DiseaseLast ExonRare Skeletal DisorderMendelian DisorderBone Morphogenic Protein	2011	193

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