Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database
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Non-muscle myosin II in disease: mechanisms and therapeutic opportunitiesGenetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical LandscapeRare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery.Whole-exome sequencing identifies a novel de novo mutation in DYNC1H1 in epileptic encephalopathiesAutism spectrum disorder and epileptic encephalopathy: common causes, many questions.Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter geneA pharmacological mouse model suggests a novel risk pathway for postpartum psychosis.denovo-db: a compendium of human de novo variants.Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability.Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration.LoFtool: a gene intolerance score based on loss-of-function variants in 60 706 individuals.Open Chromatin Profiling in hiPSC-Derived Neurons Prioritizes Functional Noncoding Psychiatric Risk Variants and Highlights Neurodevelopmental Loci.High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.Targeted sequencing and functional analysis reveal brain-size-related genes and their networks in autism spectrum disorders.Quantitative mapping of genetic similarity in human heritable diseases by shared mutations.Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.Progress in Genetic Studies of Tourette's Syndrome.Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.Lack of replication of previous autism spectrum disorder GWAS hits in European populations.Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing.Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.Searching for ancient balanced polymorphisms shared between Neanderthals and Modern Humans.Rare gene deletions in genetic generalized and Rolandic epilepsies
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P2860
Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database
description
2015 nî lūn-bûn
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2015年の論文
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2015年論文
@yue
2015年論文
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2015年論文
@zh-hk
2015年論文
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2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
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2015年论文
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name
Genes with de novo mutations a ...... covered from NPdenovo database
@ast
Genes with de novo mutations a ...... covered from NPdenovo database
@en
type
label
Genes with de novo mutations a ...... covered from NPdenovo database
@ast
Genes with de novo mutations a ...... covered from NPdenovo database
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prefLabel
Genes with de novo mutations a ...... covered from NPdenovo database
@ast
Genes with de novo mutations a ...... covered from NPdenovo database
@en
P2093
P2860
P50
P356
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Genes with de novo mutations a ...... covered from NPdenovo database
@en
P2093
Huiqian Chen
Jinchen Li
Qianzhi Shao
Xianfeng Li
P2860
P2888
P304
P356
10.1038/MP.2015.40
P407
P577
2015-04-07T00:00:00Z