A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

Author:

Ma Deqiong,Salyakina Daria,Jaworski James M.,Konidari Ioanna,Whitehead Patrice L.,Andersen Ashley N.,Hoffman Joshua D.,Slifer Susan H.,Hedges Dale J.,Cukier Holly N.,Griswold Anthony J.,McCauley Jacob L.,Beecham Gary W.,Wright Harry H.,Abramson Ruth K.,Martin Eden R.,Hussman John P.,Gilbert John R.,Cuccaro Michael L.,Haines Jonathan L.,Pericak-Vance Margaret A.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference34 articles.

1. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene;Alarcón;Am J Hum Genet,2008

2. A high-density SNP genome-wide linkage scan in a large autism extended pedigree;Allen-Brady;Mol Psychiatry,2008

3. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism;Arking;Am J of Hum Genet,2008

4. Autism Genetics Resource Exchange. (2008) 2008-last update, AGRE[Homepage of Autism Speaks], [Online]. Available: http://www.agre.org/ [2008, July].

5. Autism as a strongly genetic disorder: evidence from a British twin study;Bailey;Psychol Med,1995

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