Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
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The Human Phenotype Ontology in 2017New insights into the generation and role of de novo mutations in health and diseaseGenome-Wide Meta-Analysis of Sciatica in Finnish PopulationPublicly Available Data Provide Evidence against NR1H3 R415Q Causing Multiple Sclerosis.Neuroinflammation - using big data to inform clinical practice.The impact of rare and low-frequency genetic variants in common diseaseRethinking the Epigenetic Framework to Unravel the Molecular Pathology of Schizophrenia.Non-Coding Loss-of-Function Variation in Human Genomes.Neuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translation.Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.Stress and the Emerging Roles of Chromatin Remodeling in Signal Integration and Stable Transmission of Reversible Phenotypes.Rare PDCD11 variations are not associated with risk of schizophrenia in Japan.Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.Histone chaperone HIRA regulates neural progenitor cell proliferation and neurogenesis via β-catenin.Neuroscience-informed computer-assisted cognitive training in schizophrenia.The schizophrenia risk gene ZNF804A: clinical associations, biological mechanisms and neuronal functions.Endophenotype best practices.Toward development of epigenetic drugs for central nervous system disorders: Modulating neuroplasticity via H3K4 methylation.The road to precision psychiatry: translating genetics into disease mechanisms.Molecular mechanisms underlying noncoding risk variations in psychiatric genetic studiesEpigenetic Mistakes in Neurodevelopmental Disorders.Histone Lysine Methylation and Neurodevelopmental Disorders.The epigenomics of schizophrenia, in the mouse.Genetics of Schizophrenia: Ready to Translate?Shifting the focus toward rare variants in schizophrenia to close the gap from genotype to phenotype.Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.Schizophrenia and the neurodevelopmental continuum:evidence from genomicsExploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7.Construction of an Exome-Wide Risk Score for Schizophrenia Based on a Weighted Burden Test.Whole genome sequencing in psychiatric disorders: the WGSPD consortium.Rare genetic variants and schizophrenia.Psychiatric Genomics: An Update and an Agenda.Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.Progress in Genetic Studies of Tourette's Syndrome.XPAT: a toolkit to conduct cross-platform association studies with heterogeneous sequencing datasets.Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability.Neuronal Deletion of Kmt2a/Mll1 Histone Methyltransferase in Ventral Striatum is Associated with Defective Spike-Timing-Dependent Striatal Synaptic Plasticity, Altered Response to Dopaminergic Drugs, and Increased Anxiety.
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P2860
Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Rare loss-of-function variants ...... a and developmental disorders.
@en
Rare loss-of-function variants ...... a and developmental disorders.
@nl
type
label
Rare loss-of-function variants ...... a and developmental disorders.
@en
Rare loss-of-function variants ...... a and developmental disorders.
@nl
prefLabel
Rare loss-of-function variants ...... a and developmental disorders.
@en
Rare loss-of-function variants ...... a and developmental disorders.
@nl
P2093
P2860
P50
P356
P1433
P1476
Rare loss-of-function variants ...... ia and developmental disorders
@en
P2093
Aarno Palotie
Alison Foster
Carmel Moore
Christina M Hultman
Conrad Iyegbe
Daniel Geschwind
David Roberts
David St Clair
Elena Prigmore
P2860
P2888
P304
P356
10.1038/NN.4267
P407
P50
P577
2016-03-14T00:00:00Z