Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.
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Missense mutation in DISC1 C-terminal coiled-coil has GSK3β signaling and sex-dependent behavioral effects in miceDiscovering implicit entity relation with the gene-citation-gene networkGenome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia lociSchizophrenia and Depression Co-Morbidity: What We have Learned from Animal Models.Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia.708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits.Alterations in dendrite and spine morphology of cortical pyramidal neurons in DISC1-binding zinc finger protein (DBZ) knockout mice.Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects Neurotransmitter and Ion Channel Gene Sets.Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.DISC1 genetics, biology and psychiatric illnessFrontal cortical synaptic communication is abnormal in Disc1 genetic mouse models of schizophreniaGenetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia.14-3-3s are potential biomarkers for HIV-related neurodegeneration.Disturbance of oligodendrocyte function plays a key role in the pathogenesis of schizophrenia and major depressive disorder.Investigation of fasciculation and elongation protein ζ-1 (FEZ1) in peripheral blood reveals differences in gene expression in patients with schizophreniaAssociation between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma.No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association dataset.DBZ, a CNS-specific DISC1 binding protein, positively regulates oligodendrocyte differentiation.Rare disruptive variants in the DISC1 Interactome and Regulome: association with cognitive ability and schizophrenia.Investigation of the role of TCF4 rare sequence variants in schizophrenia.Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan.Autism Spectrum Disorder, Developmental and Psychiatric Features in 16p11.2 Duplication.Rare variants in TMEM132D in a case-control sample for panic disorder.Additive sex-specific influence of common non-synonymous DISC1 variants on amygdala, basal ganglia, and white cortical surface area in healthy young adults.
P2860
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P2860
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.
description
2011 nî lūn-bûn
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2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Sequencing of DISC1 pathway ge ...... a northern Swedish population.
@ast
Sequencing of DISC1 pathway ge ...... a northern Swedish population.
@en
type
label
Sequencing of DISC1 pathway ge ...... a northern Swedish population.
@ast
Sequencing of DISC1 pathway ge ...... a northern Swedish population.
@en
prefLabel
Sequencing of DISC1 pathway ge ...... a northern Swedish population.
@ast
Sequencing of DISC1 pathway ge ...... a northern Swedish population.
@en
P2093
P2860
P50
P1433
P1476
Sequencing of DISC1 pathway ge ...... a northern Swedish population
@en
P2093
An-Sofie Lenaerts
Annelie Nordin
Ignacio Medina Castello
Karl-Fredrik Norrback
Lars-Göran Nilsson
Lotte N Moens
Sonia De Zutter
Wim Glassee
P2860
P304
P356
10.1371/JOURNAL.PONE.0023450
P407
P50
P577
2011-08-11T00:00:00Z