Search details
1.
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Nature
; 459(7246): 528-33, 2009 May 28.
Article
in English
| MEDLINE | ID: mdl-19404256
2.
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Nature
; 459(7246): 569-73, 2009 May 28.
Article
in English
| MEDLINE | ID: mdl-19404257
3.
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Am J Hum Genet
; 82(1): 160-4, 2008 Jan.
Article
in English
| MEDLINE | ID: mdl-18179894
4.
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.
J Med Genet
; 47(2): 81-90, 2010 Feb.
Article
in English
| MEDLINE | ID: mdl-19546099
5.
Parent-of-origin effects of the serotonin transporter gene associated with autism.
Am J Med Genet B Neuropsychiatr Genet
; 156(2): 139-44, 2011 Mar.
Article
in English
| MEDLINE | ID: mdl-21302342
6.
Transmission disequilibrium testing of the chromosome 15q11-q13 region in autism.
Am J Med Genet B Neuropsychiatr Genet
; 147B(7): 1116-25, 2008 Oct 05.
Article
in English
| MEDLINE | ID: mdl-18361419
7.
Heterogeneous association between engrailed-2 and autism in the CPEA network.
Am J Med Genet B Neuropsychiatr Genet
; 147B(2): 187-93, 2008 Mar 05.
Article
in English
| MEDLINE | ID: mdl-17948868
8.
Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism.
Neurosci Lett
; 417(1): 6-9, 2007 Apr 24.
Article
in English
| MEDLINE | ID: mdl-17383819
9.
5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism.
Am J Psychiatry
; 163(12): 2148-56, 2006 Dec.
Article
in English
| MEDLINE | ID: mdl-17151167
10.
A pharmacogenetic study of escitalopram in autism spectrum disorders.
Autism Res
; 3(1): 1-7, 2010 Feb.
Article
in English
| MEDLINE | ID: mdl-20020537
11.
Association and mutation analyses of 16p11.2 autism candidate genes.
PLoS One
; 4(2): e4582, 2009.
Article
in English
| MEDLINE | ID: mdl-19242545
12.
Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample.
Autism Res
; 1(2): 108-13, 2008 Apr.
Article
in English
| MEDLINE | ID: mdl-19360657
13.
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Biol Psychiatry
; 63(12): 1111-7, 2008 Jun 15.
Article
in English
| MEDLINE | ID: mdl-18374305
14.
Family-based association testing of glutamate transporter genes in autism.
Psychiatr Genet
; 21(4): 212-3, 2011 Aug.
Article
in English
| MEDLINE | ID: mdl-21085054
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