Gene-network analysis identifies susceptibility genes related to glycobiology in autism - Wikidata - awgldk - TriplyDB

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

http://www.wikidata.org/entity/Q33459263

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Neuroscience in the era of functional genomics and systems biology Genetics of autistic disorders: review and clinical implications Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder Characterization of the deleted in autism 1 protein family: implications for studying cognitive disorders.Linking genes to diseases: it's all in the data.Differential expression of six genes and correlation with fatness traits in a unique broiler population Serum glycopattern and Maackia amurensis lectin-II binding glycoproteins in autism spectrum disorder Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS MIRA: mutual information-based reporter algorithm for metabolic networks The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.Rai1 frees mice from the repression of active wake behaviors by light.DIA1R is an X-linked gene related to Deleted In Autism-1.Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice.Heterozygous deletion at the RLN1 locus in a family with testicular germ cell cancer identified by integrating copy number variation data with phenome and interactome information.A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder.Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior δ ENaC: a novel divergent amiloride-inhibitable sodium channel RAI1 transcription factor activity is impaired in mutants associated with Smith-Magenis Syndrome.Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autism A phylogenetic study of SPBP and RAI1: evolutionary conservation of chromatin binding modules.Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia).Scan-statistic approach identifies clusters of rare disease variants in LRP2, a gene linked and associated with autism spectrum disorders, in three datasets.The molecular genetics of autism spectrum disorders: genomic mechanisms, neuroimmunopathology, and clinical implications The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.Perspectives on zebrafish models of hallucinogenic drugs and related psychotropic compounds.Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.Protein signatures of oxidative stress response in a patient specific cell line model for autism.LW-AFC Effects on N-glycan Profile in Senescence-Accelerated Mouse Prone 8 Strain, a Mouse Model of Alzheimer's Disease.Altered brain gene expression but not steroid biochemistry in a genetic mouse model of neurodevelopmental disorder.Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: a systematic review and meta-analysis.Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.Genetic risk in autism: new associations and clinical testing.Autism spectrum disorders: the quest for genetic syndromes.SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders.Biomarkers in autism spectrum disorder: the old and the new.Glutamatergic candidate genes in autism spectrum disorder: an overview.Functional annotation of genes overlapping copy number variants in autistic patients: focus on axon pathfinding.Glycan susceptibility factors in autism spectrum disorders.

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Gene-network analysis identifies susceptibility genes related to glycobiology in autism

http://www.wikidata.org/entity/Q33459263

description

2009 nî lūn-bûn

@nan

2009 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի մայիսին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

@ast

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

@en

type

label

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

@ast

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

@en

prefLabel

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

@ast

Gene-network analysis identifies susceptibility genes related to glycobiology in autism

@en

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Gene-network analysis identifies susceptibility genes related to glycobiology in autism

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Bert van der Zwaag

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Emma van Daalen

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Eva H Brilstra

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Frits A Beemer

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Hans Kristian Ploos van Amstel

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Henk A Spierenburg

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Hylke M Blauw

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J Peter H Burbach

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Jacob A S Vorstman

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Jacobine E Buizer-Voskamp

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P2860

The genetics of autistic disorders and its clinical relevance: a review of the literature

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

Strong association of de novo copy number mutations with autism

Identifying autism loci and genes by tracing recent shared ancestry

Structural variation of chromosomes in autism spectrum disorder

Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase

A unified genetic theory for sporadic and inherited autism

Genome-wide atlas of gene expression in the adult mouse brain

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Primer3 on the WWW for general users and for biologist programmers

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Herman van Engeland

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