Molecular and clinical characterization of 25 individuals with exonic deletions ofNRXN1and comprehensive review of the literature-Reference-Cited by-同舟云学术

Molecular and clinical characterization of 25 individuals with exonic deletions ofNRXN1and comprehensive review of the literature

Published:2013-03-26 Issue:4 Volume:162 Page:388-403
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Béna Frédérique,Bruno Damien L.,Eriksson Mats,van Ravenswaaij-Arts Conny,Stark Zornitza,Dijkhuizen Trijnie,Gerkes Erica,Gimelli Stefania,Ganesamoorthy Devika,Thuresson Ann Charlotte,Labalme Audrey,Till Marianne,Bilan Frédéric,Pasquier Laurent,Kitzis Alain,Dubourgm Christele,Rossi Massimiliano,Bottani Armand,Gagnebin Maryline,Sanlaville Damien,Gilbert-Dussardier Brigitte,Guipponi Michel,van Haeringen Arie,Kriek Marjolein,Ruivenkamp Claudia,Antonarakis Stylianos E.,Anderlid Britt Marie,Slater Howard R.,Schoumans Jacqueline

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Reference48 articles.

1. Direct measure of the de novo mutation rate in autism and schizophrenia cohorts;Awadalla;Am J Hum Genet,2010

2. Hotspots of large rare deletions in the human genome;Bradley;PLoS ONE,2010

3. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes;Bucan;PLoS Genet,2009

4. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders;Ching;Am J Med Genet B Neuropsychiatr Genet,2010

5. Rare chromosomal deletions and duplications increase risk of schizophrenia;Consortium IS;Nature,2008

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