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Analysis of the RELN gene as a genetic risk factor for autism

Analysis of the RELN gene as a genetic risk factor for autism

http://www.wikidata.org/entity/Q28294614

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The neuropathology of autism: where do we stand?The genetics of autistic disorders and its clinical relevance: a review of the literature Genetics of autism spectrum disorder Advances in autism genetics: on the threshold of a new neurobiology The role of immune dysfunction in the pathophysiology of autism Genetics of autistic disorders: review and clinical implications The involvement of Reelin in neurodevelopmental disorders.Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders Genetics of Autism Spectrum Disorder: Current Status and Possible Clinical Applications Genomics and autism spectrum disorder Mice with Dab1 or Vldlr insufficiency exhibit abnormal neonatal vocalization patterns Reelin and Neuropsychiatric Disorders.Autism: the quest for the genes A heterogeneity-based genome search meta-analysis for autism-spectrum disorders A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands Neuronal connectivity as a convergent target of gene × environment interactions that confer risk for Autism Spectrum Disorders An evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autism A brain region-specific predictive gene map for autism derived by profiling a reference gene set Genomic Footprints in Selected and Unselected Beef Cattle Breeds in Korea.Differential monocyte responses to TLR ligands in children with autism spectrum disorders.Application of family-based association testing to assess the genotype-phenotype association involved in complex traits using single-nucleotide polymorphisms.[Genetic and brain structure anomalies in autism spectrum disorders. Towards an understanding of the aetiopathogenesis?].Genome-wide linkage in Utah autism pedigrees Bio-collections in autism research.Transcriptional dysregulation of neocortical circuit assembly in ASD Mapping pathological phenotypes in reelin mutant mice.The oxytocin receptor gene (OXTR) is associated with autism spectrum disorder: a meta-analysis.Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.Altered T cell responses in children with autism.A forward genetic screen in mice identifies mutants with abnormal cortical patterning.The neurobiology of autism.Characterization of neonatal vocal and motor repertoire of reelin mutant mice Altered posterior cingulate cortical cyctoarchitecture, but normal density of neurons and interneurons in the posterior cingulate cortex and fusiform gyrus in autism.Gender-specific effect of Mthfr genotype and neonatal vigabatrin interaction on synaptic proteins in mouse cortex Autism: a "critical period" disorder?Autism risk assessment in siblings of affected children using sex-specific genetic scores.Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility Links between genetics and pathophysiology in the autism spectrum disorders.

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Analysis of the RELN gene as a genetic risk factor for autism

http://www.wikidata.org/entity/Q28294614

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2005 nî lūn-bûn

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2005 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի հունիսին հրատարակված գիտական հոդված

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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name

Analysis of the RELN gene as a genetic risk factor for autism

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Analysis of the RELN gene as a genetic risk factor for autism

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Analysis of the RELN gene as a genetic risk factor for autism

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type

label

Analysis of the RELN gene as a genetic risk factor for autism

@ast

Analysis of the RELN gene as a genetic risk factor for autism

@en

Analysis of the RELN gene as a genetic risk factor for autism

@nl

prefLabel

Analysis of the RELN gene as a genetic risk factor for autism

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Analysis of the RELN gene as a genetic risk factor for autism

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Analysis of the RELN gene as a genetic risk factor for autism

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Molecular Psychiatry

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Analysis of the RELN gene as a genetic risk factor for autism

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A E Ashley-Koch

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D A Skaar

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E R Martin

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G R DeLong

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J E Stenger

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Synergistic contributions of cyclin-dependant kinase 5/p35 and Reelin/Dab1 to the positioning of cortical neurons in the developing mouse brain

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

Concordance for the syndrome of autism in 40 pairs of afflicted twins

Lack of evidence for an association between WNT2 and RELN polymorphisms and autism

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

Autism as a strongly genetic disorder: evidence from a British twin study

Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study

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10.1038/SJ.MP.4001614

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