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- 2016
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Mark
Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism
(
- Contribution to journal › Article
- 2013
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Mark
Heterozygous FA2H mutations in autism spectrum disorders
(
- Contribution to journal › Article
- 2012
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Mark
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
(
- Contribution to journal › Article
- 2011
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Mark
Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations
(
- Contribution to journal › Article
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Mark
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
(
- Contribution to journal › Article
- 2010
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Mark
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls
(
- Contribution to journal › Article
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Mark
Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population
(
- Contribution to journal › Article
- 2009
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Mark
Possible association between the androgen receptor gene and autism spectrum disorder
(
- Contribution to journal › Article
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Mark
An investigation of ribosomal protein L10 gene in autism spectrum disorders
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- Contribution to journal › Article
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Mark
Screening for Genomic Rearrangements and Methylation Abnormalities of the 15q11-q13 Region in Autism Spectrum Disorders
(
- Contribution to journal › Article
- 2008
-
Mark
Analysis of X chromosome inactivation in autism spectrum disorders
(
- Contribution to journal › Article
- 2007
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Mark
Mutation screening of the ARX gene in patients with autism
(
- Contribution to journal › Article
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Mark
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly
(
- Contribution to journal › Article
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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
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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
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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