Intellectual disability is associated with increased runs of homozygosity in simplex autism - Test2 - elhamkhani - TriplyDB

Intellectual disability is associated with increased runs of homozygosity in simplex autism

Intellectual disability is associated with increased runs of homozygosity in simplex autism

http://www.wikidata.org/entity/Q37010426

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Sex and gender differences in autism spectrum disorder: summarizing evidence gaps and identifying emerging areas of priority Advances in understanding - genetic basis of intellectual disability Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms Genetics of consanguinity and inbreeding in health and disease.A novel relationship for schizophrenia, bipolar and major depressive disorder Part 5: a hint from chromosome 5 high density association screen.Bio-collections in autism research.Evolutionary behavioral genetics.Evidence of Inbreeding in Hodgkin Lymphoma.Long contiguous stretches of homozygosity spanning shortly the imprinted loci are associated with intellectual disability, autism and/or epilepsy.Genome-wide Survey of Runs of Homozygosity Identifies Recessive Loci for Bone Mineral Density in Caucasian and Chinese Populations.Inbreeding and homozygosity in breast cancer survival.Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate.Autism Spectrum Disorder, Intellectual Disability, and Delayed Walking.Structural and genomic variation in preterm birth.Genetic diagnosis of autism spectrum disorders: the opportunity and challenge in the genomics era.Heterozygosity Ratio, a Robust Global Genomic Measure of Autozygosity and Its Association with Height and Disease Risk A novel test for recessive contributions to complex diseases implicates Bardet-Biedl syndrome gene BBS10 in idiopathic type 2 diabetes and obesity Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population.Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Runs of homozygosity: windows into population history and trait architecture.Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred.Excess of runs of homozygosity is associated with severe cognitive impairment in intellectual disability.Whole genome sequencing of a dizygotic twin suggests a role for the serotonin receptor HTR7 in autism spectrum disorder.Assessing runs of Homozygosity: a comparison of SNP Array and whole genome sequence low coverage data.Genetic variation in the oxytocin receptor gene is associated with a social phenotype in autism spectrum disorders.Strong correlation of downregulated genes related to synaptic transmission and mitochondria in post-mortem autism cerebral cortex.Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland Runs of homozygosity associate with decreased risks of lung cancer in never-smoking East Asian females

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Intellectual disability is associated with increased runs of homozygosity in simplex autism

http://www.wikidata.org/entity/Q37010426

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 03 July 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Intellectual disability is ass ...... homozygosity in simplex autism

@en

Intellectual disability is ass ...... omozygosity in simplex autism.

@nl

type

label

Intellectual disability is ass ...... homozygosity in simplex autism

@en

Intellectual disability is ass ...... omozygosity in simplex autism.

@nl

prefLabel

Intellectual disability is ass ...... homozygosity in simplex autism

@en

Intellectual disability is ass ...... omozygosity in simplex autism.

@nl

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J.AJHG.2013.06.004

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American Journal of Human Genetics

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Intellectual disability is ass ...... homozygosity in simplex autism

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Abbie M Frederick

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Bernie Devlin

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Elizabeth W Triche

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Emma W Viscidi

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Matthew W State

http://www.w3.org/2001/XMLSchema#string

Michael Schmidt

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Michael T Murtha

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Shailender Nagpal

http://www.w3.org/2001/XMLSchema#string

Simons Simplex Collection Genetics Consortium

http://www.w3.org/2001/XMLSchema#string

Sorin Istrail

http://www.w3.org/2001/XMLSchema#string

P2860

Epidemiology of Pervasive Developmental Disorders

Identifying autism loci and genes by tracing recent shared ancestry

PLINK: a tool set for whole-genome association and population-based linkage analyses

A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly

Mutations in BCKD-kinase lead to a potentially treatable form of autism with epilepsy

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

De Novo Gene Disruptions in Children on the Autistic Spectrum

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

Genetic mapping in human disease

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scholarly article

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10.1016/J.AJHG.2013.06.004

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1

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Daniel Geschwind

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2013-07-03T00:00:00Z

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262043937

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23830515

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