Singleton deletions throughout the genome increase risk of bipolar disorder
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The Kraepelinian dichotomy - going, going... but still not goneThe genetics of bipolar disorderRare deletions at the neurexin 3 locus in autism spectrum disorderA novel balanced chromosomal translocation found in subjects with schizophrenia and schizotypal personality disorder: altered l-serine level associated with disruption of PSAT1 gene expressionMicroRNA dysregulation in psychiatric diseaseCNVs: harbingers of a rare variant revolution in psychiatric geneticsGenome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanicsGenome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorderA 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 ODZ4Synaptic proteins and receptors defects in autism spectrum disordersInheritance model introduces differential bias in CNV calls between parents and offspringSimultaneous copy number losses within multiple subtelomeric regions in early-onset type 2 diabetes mellitusGenomic 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 intelligenceComparative 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 disorderDe 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 psychosesCopy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorderLarge 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 disordersDuplications 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
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
@pt
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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Singleton deletions throughout the genome increase risk of bipolar disorder
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C Nievergelt
E A Nwulia
E S Gershon
H J Edenberg
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P2888
P304
P356
10.1038/MP.2008.144
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P577
2008-12-30T00:00:00Z
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P6179
1022003103