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Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders

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Year: 2013
Type: article
Study design: Observational Study
Source: European Journal of Human Genetics
DOI: 10.1038/ejhg.2013.88
Authors: Caroline Nava, Boris Keren, Cyril Mignot, Agnès Rastetter, Sandra Chantot-Bastaraud, Anne Faudet, Eric Fonteneau, Claire Amiet, Claudine Laurent, Aurélia Jacquette, Sandra Whalen, Alexandra Afenjar, Didier Périsse, Diane Doummar, Nathalie Dorison, Marion Leboyer, Jean-Pierre Siffroi, David Cohen, Alexis Brice, Delphine Héron, Christel Depienne
Institutions: Centre National de la Recherche Scientifique, Inserm, Assistance Publique – Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Institut du Cerveau, Université Pierre-et-Marie-Curie, Hôpital Armand-Trousseau, Université Paris-Est Créteil, Fondation FondaMental, Hôpital Albert-Chenevier, Institut Systèmes Intelligents et de Robotique
Language: English

Topic: Genomic variations and chromosomal abnormalities
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: Institut National de la Santé et de la Recherche Médicale, Fondation de France, Direction de l’hospitalisation et de l’offre de Soins
OpenAlex ID: W2101402077
FWCI: 6.176
Cites: 49
Cited by: 73
Related to: 10
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