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- 2017
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Mark
Gender differences in autism spectrum disorders: Divergence among specific core symptoms
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- Contribution to journal › Article
- 2014
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Mark
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.
(
- Contribution to journal › Article
- 2013
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Mark
Heterozygous FA2H mutations in autism spectrum disorders
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- Contribution to journal › Article
- 2012
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Mark
SHANK1 Deletions in Males with Autism Spectrum Disorder
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- Contribution to journal › Article
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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
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- 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
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- Contribution to journal › Article
- 2009
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Mark
An investigation of ribosomal protein L10 gene in autism spectrum disorders
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- Contribution to journal › Article
- 2008
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Mark
Abnormal melatonin synthesis in autism spectrum disorders
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- Contribution to journal › Article
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Mark
Analysis of X chromosome inactivation in autism spectrum disorders
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- Contribution to journal › Article
- 2006
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Mark
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders
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- 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
- 2003
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Mark
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
(
- Contribution to journal › Article