about
The Kraepelinian dichotomy - going, going... but still not goneCNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personalityDistinct circuit-dependent functions of presynaptic neurexin-3 at GABAergic and glutamatergic synapses.LRRTM2 functions as a neurexin ligand in promoting excitatory synapse formationHeterozygous deletion of α-neurexin I or α-neurexin II results in behaviors relevant to autism and schizophrenia.Gene × Environment Interactions in Schizophrenia: Evidence from Genetic Mouse ModelsMutations in NRXN1 in a family multiply affected with brain disorders: NRXN1 mutations and brain disordersCopy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplicationsLRRTM1-deficient mice show a rare phenotype of avoiding small enclosures--a tentative mouse model for claustrophobia-like behaviour.Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disordersE Proteins and ID Proteins: Helix-Loop-Helix Partners in Development and DiseaseConsensus paper of the WFSBP Task Force on Biological Markers: Criteria for biomarkers and endophenotypes of schizophrenia part II: Cognition, neuroimaging and genetics.Genomic structural variation in psychiatric disorders.De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.Neurexin in embryonic Drosophila neuromuscular junctions.Neurodevelopmental disorders: mechanisms and boundary definitions from genomes, interactomes and proteomes.An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis.Neurexins.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Potential Value of Genomic Copy Number Variations in Schizophrenia.RETRACTED: Identification of gene ontologies linked to prefrontal-hippocampal functional coupling in the human brain.Identification of candidate single-nucleotide polymorphisms in NRXN1 related to antipsychotic treatment response in patients with schizophrenia.Microdeletions of 3q29 confer high risk for schizophrenia.Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.A population-based longitudinal study of childhood neurodevelopmental disorders, IQ and subsequent risk of psychotic experiences in adolescence.Systematic prioritization and integrative analysis of copy number variations in schizophrenia reveal key schizophrenia susceptibility genes.The penetrance of copy number variations for schizophrenia and developmental delay.A pilot study on collective effects of 22q13.31 deletions on gray matter concentration in schizophreniaMicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion SyndromeIdentification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.Functional impacts of NRXN1 knockdown on neurodevelopment in stem cell modelsMethylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophreniaMeCP2 regulates the synaptic expression of a Dysbindin-BLOC-1 network component in mouse brain and human induced pluripotent stem cell-derived neurons.Copy number variants in German patients with schizophreniaA case-control association study of NRXN1 polymorphisms with schizophrenia in Chinese Han population.Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sample.Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis.Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumThe genetics of Tourette disorder
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Neurexin 1 (NRXN1) deletions in schizophrenia
@ast
Neurexin 1 (NRXN1) deletions in schizophrenia
@en
Neurexin 1 (NRXN1) deletions in schizophrenia
@nl
type
label
Neurexin 1 (NRXN1) deletions in schizophrenia
@ast
Neurexin 1 (NRXN1) deletions in schizophrenia
@en
Neurexin 1 (NRXN1) deletions in schizophrenia
@nl
prefLabel
Neurexin 1 (NRXN1) deletions in schizophrenia
@ast
Neurexin 1 (NRXN1) deletions in schizophrenia
@en
Neurexin 1 (NRXN1) deletions in schizophrenia
@nl
P2093
P2860
P50
P3181
P356
P1476
Neurexin 1 (NRXN1) deletions in schizophrenia
@en
P2093
Andres Ingason
David A Collier
Michael J Owen
P2860
P3181
P356
10.1093/SCHBUL/SBP079
P407
P577
2009-09-01T00:00:00Z