1 – 16 of 16
- show: 20
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2016
-
Mark
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism
(
- Contribution to journal › Article
- 2014
-
Mark
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
(
- Contribution to journal › Article
- 2013
-
Mark
Heterozygous FA2H mutations in autism spectrum disorders
(
- Contribution to journal › Article
- 2012
-
Mark
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
(
- Contribution to journal › Article
- 2009
-
Mark
Possible association between the androgen receptor gene and autism spectrum disorder
(
- Contribution to journal › Article
-
Mark
An investigation of ribosomal protein L10 gene in autism spectrum disorders
(
- Contribution to journal › Article
-
Mark
Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
(
- Contribution to journal › Article
- 2008
-
Mark
Abnormal melatonin synthesis in autism spectrum disorders
(
- Contribution to journal › Article
-
Mark
Analysis of X chromosome inactivation in autism spectrum disorders
(
- Contribution to journal › Article
- 2007
-
Mark
Mutation screening of the ARX gene in patients with autism
(
- Contribution to journal › Article
-
Mark
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly
(
- Contribution to journal › Article
-
Mark
Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly
(
- Contribution to journal › Article
- 2006
-
Mark
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders
(
- Contribution to journal › Article
-
Mark
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders
(
- Contribution to journal › Article
- 2005
-
Mark
Support for the association between the rare functional variant 1425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder
(
- Contribution to journal › Article
- 2003
-
Mark
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
(
- Contribution to journal › Article