Singleton deletions throughout the genome increase risk of bipolar disorder - Wikidata - awgldk - TriplyDB

Singleton deletions throughout the genome increase risk of bipolar disorder

Singleton deletions throughout the genome increase risk of bipolar disorder

http://www.wikidata.org/entity/Q37326513

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The Kraepelinian dichotomy - going, going... but still not gone The genetics of bipolar disorder Rare deletions at the neurexin 3 locus in autism spectrum disorder A novel balanced chromosomal translocation found in subjects with schizophrenia and schizotypal personality disorder: altered l-serine level associated with disruption of PSAT1 gene expression MicroRNA dysregulation in psychiatric disease CNVs: harbingers of a rare variant revolution in psychiatric genetics Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Synaptic proteins and receptors defects in autism spectrum disorders Inheritance model introduces differential bias in CNV calls between parents and offspring Simultaneous copy number losses within multiple subtelomeric regions in early-onset type 2 diabetes mellitus Genomic structural variation in psychiatric disorders.Genetic research into bipolar disorder: the need for a research framework that integrates sophisticated molecular biology and clinically informed phenotype characterization.Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Accuracy of CNV Detection from GWAS Data.Rare copy number deletions predict individual variation in intelligence Comparative linkage meta-analysis reveals regionally-distinct, disparate genetic architectures: application to bipolar disorder and schizophrenia.Genetic architectures of psychiatric disorders: the emerging picture and its implications.Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disorders.Genomic hypomethylation in the human germline associates with selective structural mutability in the human genome.A multilevel model to address batch effects in copy number estimation using SNP arrays.Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder.Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder De novo CNVs in bipolar affective disorder and schizophrenia.Detection of copy number variants reveals association of cilia genes with neural tube defects.Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample.Cross-disorder analysis of bipolar risk genes: further evidence of DGKH as a risk gene for bipolar disorder, but also unipolar depression and adult ADHD.Rare copy number deletions predict individual variation in human brain metabolite concentrations in individuals with alcohol use disorders.New findings in the genetics of major psychoses Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder Large common deletions associate with mortality at old age.Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms.Expanding the range of ZNF804A variants conferring risk of psychosis.Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.A genotype resource for postmortem brain samples from the Autism Tissue Program.

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Singleton deletions throughout the genome increase risk of bipolar disorder

http://www.wikidata.org/entity/Q37326513

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 December 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Singleton deletions throughout the genome increase risk of bipolar disorder

@en

Singleton deletions throughout the genome increase risk of bipolar disorder.

@nl

type

label

Singleton deletions throughout the genome increase risk of bipolar disorder

@en

Singleton deletions throughout the genome increase risk of bipolar disorder.

@nl

prefLabel

Singleton deletions throughout the genome increase risk of bipolar disorder

@en

Singleton deletions throughout the genome increase risk of bipolar disorder.

@nl

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Molecular Psychiatry

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Singleton deletions throughout the genome increase risk of bipolar disorder

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C Bloss

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C Nievergelt

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D Craig

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D Koller

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D Zhang

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E A Nwulia

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E N Smith

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E S Gershon

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F McMahon

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H J Edenberg

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P2860

Rare chromosomal deletions and duplications increase risk of schizophrenia

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Genome-wide association study of bipolar disorder in European American and African American individuals

Strong association of de novo copy number mutations with autism

Large recurrent microdeletions associated with schizophrenia

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

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

Mapping autism risk loci using genetic linkage and chromosomal rearrangements.

Association between microdeletion and microduplication at 16p11.2 and autism

Whole-genome association study of bipolar disorder

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376-380

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10.1038/MP.2008.144

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John I. Nurnberger

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2008-12-30T00:00:00Z

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bipolar disorder

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