A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands
about
The genetics of autistic disorders and its clinical relevance: a review of the literatureNo association between oxytocin receptor (OXTR) gene polymorphisms and experimentally elicited social preferencesGenome-wide linkage analyses of quantitative and categorical autism subphenotypesMosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorderGestational exposure to low dose bisphenol A alters social behavior in juvenile mice.Morphological and behavioral characterization of adult mice deficient for SrGAP3.Serum Oxytocin Levels and an Oxytocin Receptor Gene Polymorphism (rs2254298) Indicate Social Deficits in Children and Adolescents with Autism Spectrum DisordersThe challenge of translation in social neuroscience: a review of oxytocin, vasopressin, and affiliative behavior.Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.Plasma oxytocin concentrations and OXTR polymorphisms predict social impairments in children with and without autism spectrum disorder.Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach.The oxytocin receptor gene (OXTR) is associated with autism spectrum disorder: a meta-analysis.The effects of birth order and birth interval on the phenotypic expression of autism spectrum disorder.The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han populationEvidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.High-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disordersA genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene.A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Imaging-genetics in autism spectrum disorder: advances, translational impact, and future directions.Links between genetics and pathophysiology in the autism spectrum disorders.Comparative two-dimensional polyacrylamide gel electrophoresis of the salivary proteome of children with autism spectrum disorder.The oxytocin system in drug discovery for autism: animal models and novel therapeutic strategiesBrain region-specific altered expression and association of mitochondria-related genes in autism.Genome-wide identification of transcriptional targets of RORA reveals direct regulation of multiple genes associated with autism spectrum disorder.Genetic and environmental factors in complex neurodevelopmental disorders.Shedding heat on oxytocin.A genome-wide screen for acrophobia susceptibility loci in a Finnish isolate.The contribution of oxytocin and vasopressin to mammalian social behavior: potential role in autism spectrum disorder.Are retinoids potential therapeutic agents in disorders of social cognition including autism?Glutamatergic candidate genes in autism spectrum disorder: an overview.Oxytocin system social function impacts in children with attention-deficit/hyperactivity disorder.Variants of the CNTNAP2 5' promoter as risk factors for autism spectrum disorders: a genetic and functional approach.The Plasma Membrane Calcium ATPases and Their Role as Major New Players in Human Disease.2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.Heterogeneous dysregulation of microRNAs across the autism spectrum.Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36.Redefining autism spectrum disorder using DSM-5: the implications of the proposed DSM-5 criteria for autism spectrum disorders.Association between the oxytocin receptor (OXTR) gene and autism: relationship to Vineland Adaptive Behavior Scales and cognition.Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.
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P2860
A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
A genome-wide search for allel ...... disorders on the Faroe Islands
@ast
A genome-wide search for allel ...... disorders on the Faroe Islands
@en
A genome-wide search for allel ...... disorders on the Faroe Islands
@nl
type
label
A genome-wide search for allel ...... disorders on the Faroe Islands
@ast
A genome-wide search for allel ...... disorders on the Faroe Islands
@en
A genome-wide search for allel ...... disorders on the Faroe Islands
@nl
prefLabel
A genome-wide search for allel ...... disorders on the Faroe Islands
@ast
A genome-wide search for allel ...... disorders on the Faroe Islands
@en
A genome-wide search for allel ...... disorders on the Faroe Islands
@nl
P2093
P2860
P356
P1433
P1476
A genome-wide search for allel ...... disorders on the Faroe Islands
@en
P2093
M B Lauritsen
P2860
P2888
P356
10.1038/SJ.MP.4001754
P407
P50
P577
2006-01-01T00:00:00Z