Found: 18
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The Role of Causal and Intentional Judgments in Moral Reasoning in Individuals with High Functioning Autism.
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- Journal of Autism & Developmental Disorders, 2013, v. 43, n. 2, p. 458, doi. 10.1007/s10803-012-1588-7
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- Article
Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q11.2, Specifically Breakpoints 1 to 2.
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- Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 3, p. 355, doi. 10.1002/aur.1378
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- Article
Gene x environment interactions in autism spectrum disorders: role of epigenetic mechanisms.
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- Frontiers in Psychiatry, 2014, v. 5, p. 1, doi. 10.3389/fpsyt.2014.00053
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- Article
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
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- Journal of Pineal Research, 2011, v. 51, n. 4, p. 394, doi. 10.1111/j.1600-079X.2011.00902.x
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- Article
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
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- Nature Genetics, 2007, v. 39, n. 1, p. 25, doi. 10.1038/ng1933
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- Article
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders.
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- PLoS Genetics, 2012, v. 8, n. 2, p. 1, doi. 10.1371/journal.pgen.1002521
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- Article
Individuals with Autism Spectrum Disorders Do Not Use Social Stereotypes in Irony Comprehension.
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- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0095568
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- Article
Variations of the Candidate SEZ6L2 Gene on Chromosome 16p11.2 in Patients with Autism Spectrum Disorders and in Human Populations.
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- PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0017289
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- Article
Memory for Self-Performed Actions in Individuals with Asperger Syndrome.
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- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013370
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- Article
Identification of Pathway-Biased and Deleterious Melatonin Receptor Mutants in Autism Spectrum Disorders and in the General Population.
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- PLoS ONE, 2010, v. 5, n. 7, p. 1, doi. 10.1371/journal.pone.0011495
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- Article
Telepsychiatry for Children and Adolescents: A Review of the PROMETTED Project.
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- Telemedicine & e-Health, 2018, v. 24, n. 1, p. 3, doi. 10.1089/tmj.2017.0041
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- Article
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.
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- BMC Medical Genetics, 2010, v. 11, p. 108, doi. 10.1186/1471-2350-11-108
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- Article
Search for copy number variants in chromosomes15q11-q13 and 22q11.2 in obsessive compulsivedisorder.
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- BMC Medical Genetics, 2010, v. 11, p. 100, doi. 10.1186/1471-2350-11-100
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- Article
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
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- BMC Medical Genetics, 2009, v. 10, p. 1, doi. 10.1186/1471-2350-10-7
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- Article
Mutation analysis of the NSD1 gene in patients with autismspectrum disorders and macrocephaly.
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- BMC Medical Genetics, 2007, v. 8, p. 68, doi. 10.1186/1471-2350-8-68
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- Article
Common genetic variants, acting additively, are a major source of risk for autism.
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- Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-9
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- Article
High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.
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- Molecular Autism, 2012, v. 3, n. 1, p. 5, doi. 10.1186/2040-2392-3-5
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- Article
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation.
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- Human Mutation, 2015, v. 36, n. 9, p. 842, doi. 10.1002/humu.22816
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- Article