Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia - Wikidata - awgldk - TriplyDB

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

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Genome-wide copy number analysis uncovers a new HSCR gene: NRG3 Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder DISC1: a key lead in studying cortical development and associated brain disorders Neuregulin 3 Mediates Cortical Plate Invasion and Laminar Allocation of GABAergic Interneurons Natural Selection in the Great Apes Association study of neuregulin-1 gene polymorphisms in a North Indian schizophrenia sample.Relationship of the Brief UCSD Performance-based Skills Assessment (UPSA-B) to multiple indicators of functioning in people with schizophrenia and bipolar disorder Gene expression patterns of chicken neuregulin 3 in association with copy number variation and frameshift deletion.Common genetic variation in Neuregulin 3 (NRG3) influences risk for schizophrenia and impacts NRG3 expression in human brain.The neuregulin signaling pathway and schizophrenia: from genes to synapses and neural circuits.Genetic insights into the functional elements of language.The phenotype of recurrent 10q22q23 deletions and duplications.Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling Genetic neuropathology of schizophrenia: new approaches to an old question and new uses for postmortem human brains Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation Transient overexposure of neuregulin 3 during early postnatal development impacts selective behaviors in adulthood.Sensitivity and specificity of the UCSD Performance-based Skills Assessment (UPSA-B) for identifying functional milestones in schizophrenia.Identification and functional studies of regulatory variants responsible for the association of NRG3 with a delusion phenotype in schizophrenia.Improving the understanding of the link between cognition and functional capacity in schizophrenia and bipolar disorder.Factor structure of cognition and functional capacity in two studies of schizophrenia and bipolar disorder: Implications for genomic studies.Neurological dysfunctions associated with altered BACE1-dependent Neuregulin-1 signaling.Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients.Modeling neurodevelopmental cognitive deficits in tasks with cross-species translational validity Neuregulin 3 Knockout Mice Exhibit Behaviors Consistent with Psychotic Disorders.Linkage analysis of schizophrenia in African-American families Neuregulin 1-erbB4 pathway in schizophrenia: From genes to an interactome Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans.Role of the Neuregulin Signaling Pathway in Nicotine Dependence and Co-morbid Disorders.Evidence from mouse and man for a role of neuregulin 3 in nicotine dependence.Effects of neuregulin 3 genotype on human prefrontal cortex physiology.Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.Genetics and smoking.Genomics and pharmacogenomics of schizophrenia.Neuregulin-ERBB signaling in the nervous system and neuropsychiatric diseases Constitutive loss and acute pharmacological manipulation of ErbB4 signaling do not affect attention and inhibitory control in mice.Neuregulin 3 and its roles in schizophrenia risk and presentation.A New Case of the Rare 10q22.3q23.2 Microdeletion Flanked by Low-Copy Repeats 3/4.Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia.Self-domestication in Homo sapiens: Insights from comparative genomics.Temporal, Diagnostic, and Tissue-Specific Regulation of NRG3 Isoform Expression in Human Brain Development and Affective Disorders.

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Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

http://www.wikidata.org/entity/Q24643955

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2009 nî lūn-bûn

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2009 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@ast

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@en

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@nl

type

label

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@ast

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@en

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@nl

prefLabel

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@ast

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

@en

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

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J.AJHG.2008.12.005

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American Journal of Human Genetics

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Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

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Andrew S Cutting

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Ann E Pulver

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David Valle

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Dimitrios Avramopoulos

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Gary Steel

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Gerald Nestadt

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Kung-Yee Liang

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M Daniele Fallin

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Ningping Feng

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Paula Wolyniec

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P2860

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

Interactions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophrenia

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Neuregulin-3 (NRG3): a novel neural tissue-enriched protein that binds and activates ErbB4

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

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Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease

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