Analysis of copy number variations at 15 schizophrenia-associated loci.
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Early interventions in risk groups for schizophrenia: what are we waiting for?Diametrical diseases reflect evolutionary-genetic tradeoffs: Evidence from psychiatry, neurology, rheumatology, oncology and immunologyGenetic disruption of voltage-gated calcium channels in psychiatric and neurological disordersNeuronal migration abnormalities and its possible implications for schizophreniaGenome-scale neurogenetics: methodology and meaningThe 15q11.2 BP1-BP2 microdeletion syndrome: a reviewCNVs in neuropsychiatric disordersNovel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in SchizophreniaOpposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile SeizuresWhole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.[Neurobiology of schizophrenia: new findings from the structure to the molecules].Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.Consensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.Copy number variations play important roles in heredity of common diseases: a novel method to calculate heritability of a polymorphism.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Genetically-Informed Patient Selection for iPSC Studies of Complex Diseases May Aid in Reducing Cellular Heterogeneity.Association of dopamine D1 receptor gene polymorphism with schizophrenia: a meta-analysisSchizophrenia genetics: emerging themes for a complex disorder.The genetics of early-onset bipolar disorder: A systematic review.High-resolution copy number variation analysis of schizophrenia in Japan.De novo CNVs in bipolar affective disorder and schizophrenia.No Evidence for Enrichment in Schizophrenia for Common Allelic Associations at Imprinted Loci.Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders.Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion SyndromeIdentification and functional characterization of rare SHANK2 variants in schizophrenia.Exome arrays capture polygenic rare variant contributions to schizophrenia.Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophreniaEvidence of Common Genetic Overlap Between Schizophrenia and Cognition.Gender differences in CNV burden do not confound schizophrenia CNV associations.Increased abundance of translation machinery in stem cell-derived neural progenitor cells from four schizophrenia patients.Common alleles contribute to schizophrenia in CNV carriers.Copy number variation in bipolar disorder.Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.Evidence that duplications of 22q11.2 protect against schizophreniaChromosomal microarray testing in adults with intellectual disability presenting with comorbid psychiatric disorders.SZGR 2.0: a one-stop shop of schizophrenia candidate genes.
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Analysis of copy number variations at 15 schizophrenia-associated loci.
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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 05 December 2013
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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
Analysis of copy number variations at 15 schizophrenia-associated loci.
@en
Analysis of copy number variations at 15 schizophrenia-associated loci.
@nl
type
label
Analysis of copy number variations at 15 schizophrenia-associated loci.
@en
Analysis of copy number variations at 15 schizophrenia-associated loci.
@nl
prefLabel
Analysis of copy number variations at 15 schizophrenia-associated loci.
@en
Analysis of copy number variations at 15 schizophrenia-associated loci.
@nl
P2093
P2860
P50
P1476
Analysis of copy number variations at 15 schizophrenia-associated loci
@en
P2093
Alexander L Richards
Gerwyn Mahoney-Davies
Kimberly D Chambert
Lyudmila Georgieva
Michael J Owen
Steven A McCarroll
P2860
P304
P356
10.1192/BJP.BP.113.131052
P407
P50
P577
2013-12-05T00:00:00Z