Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk. - Wikidata - awgldk - TriplyDB

Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.

Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.

http://www.wikidata.org/entity/Q34053455

about

HERVs expression in Autism Spectrum Disorders Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.Genome-wide copy number variation analysis in extended families and unrelated individuals characterized for musical aptitude and creativity in music.Towards identification of individual etiologies by resolving genomic and biological conundrums in patients with autism spectrum disorders.Inheritance model introduces differential bias in CNV calls between parents and offspring Support vector machine model of developmental brain gene expression data for prioritization of Autism risk gene candidates.A chromosomal microdeletion of 15q in a female patient with epilepsy, ID, and autism spectrum disorder: a case report.Novel H3K4me3 marks are enriched at human- and chimpanzee-specific cytogenetic structures.A candidate gene association study further corroborates involvement of contactin genes in autism Transcriptomics of maternal and fetal membranes can discriminate between gestational-age matched preterm neonates with and without cognitive impairment diagnosed at 18-24 months.Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease A discovery resource of rare copy number variations in individuals with autism spectrum disorder.The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.Evaluating mitochondrial DNA variation in autism spectrum disorders.Novel microduplication of CHL1 gene in a patient with autism spectrum disorder: a case report and a brief literature review.A molecular genetic study of autism and related phenotypes in extended pedigrees Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.Human iPSC Glial Mouse Chimeras Reveal Glial Contributions to Schizophrenia.Perturbed proteostasis in autism spectrum disorders.Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes.Homophilic binding of the neural cell adhesion molecule CHL1 regulates development of ventral midbrain dopaminergic pathways.Loss of ICA69 potentiates long-lasting hyperalgesia after subcutaneous formalin injection into the mouse hindpaw.Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.Differential microRNA expression in the prefrontal cortex of mouse offspring induced by glyphosate exposure during pregnancy and lactation.Cell Adhesion Molecule Close Homolog of L1 (CHL1) Guides the Regrowth of Regenerating Motor Axons and Regulates Synaptic Coverage of Motor Neurons.Synaptic Disorders

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Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.

http://www.wikidata.org/entity/Q34053455

description

2011 nî lūn-bûn

@nan

2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Copy number variants in extend ...... ially involved in autism risk.

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Deqiong Ma

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Harry H Wright

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Ioanna Konidari

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James M Jaworski

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John R Gilbert

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Laura D Nations

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Michael L Cuccaro

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Patrice L Whitehead

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Ramkumar Menon

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Ruth K Abramson

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Population structure and eigenanalysis

Epidemiology of Pervasive Developmental Disorders

Neurexophilins form a conserved family of neuropeptide-like glycoproteins

The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons

Functional impact of global rare copy number variation in autism spectrum disorders

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Rare structural variation of synapse and neurotransmission genes in autism

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Strong association of de novo copy number mutations with autism

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

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scholarly article

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10.1371/JOURNAL.PONE.0026049

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10

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Margaret A. Pericak-Vance

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2011-10-07T00:00:00Z

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51733508

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22016809

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Autism spectrum

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3189231

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