Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies - Wikidata - thesis-toulmin - TriplyDB

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies

http://www.wikidata.org/entity/Q28751388

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Evaluating genetic markers and neurobiochemical analytes for fluoxetine response using a panel of mouse inbred strains Neurogenetics of depression: a focus on reward processing and stress sensitivity The genetics of major depression Toward an integration of cognitive and genetic models of risk for depression Genetic risk prediction in complex disease Genetic determinants of depression: recent findings and future directions Restoration of Sp4 in Forebrain GABAergic Neurons Rescues Hypersensitivity to Ketamine in Sp4 Hypomorphic Mice.Phasic and Tonic mGlu7 Receptor Activity Modulates the Thalamocortical Network Genome-wide linkage on chromosome 10q26 for a dimensional scale of major depression Altered functional protein networks in the prefrontal cortex and amygdala of victims of suicide The adhesion protein IgSF9b is coupled to neuroligin 2 via S-SCAM to promote inhibitory synapse development The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects Biological pathways, candidate genes, and molecular markers associated with quality-of-life domains: an update MK4MDD: a multi-level knowledge base and analysis platform for major depressive disorder Genome-wide association study of comorbid depressive syndrome and alcohol dependence Genome-wide association scan of trait depression A genome-wide association study of depressive symptoms A mega-analysis of genome-wide association studies for major depressive disorder Prolonged Ketamine Effects in Sp4 Hypomorphic Mice: Mimicking Phenotypes of Schizophrenia.Reduced NMDAR1 expression in the Sp4 hypomorphic mouse may contribute to endophenotypes of human psychiatric disorders Convergent functional genomic studies of ω-3 fatty acids in stress reactivity, bipolar disorder and alcoholism.Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia.Dopamine genetic risk score predicts depressive symptoms in healthy adults and adults with depression.The genetics of major depression: moving beyond the monoamine hypothesis.GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia The effect of COMT Val158Met and DRD2 C957T polymorphisms on executive function and the impact of early life stress.Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders.NMDA receptor hypofunction induces dysfunctions of energy metabolism and semaphorin signaling in rats: a synaptic proteome study.The BDNF Val66Met polymorphism does not moderate the effect of self-reported physical activity on depressive symptoms in midlife Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder.Prioritization and evaluation of depression candidate genes by combining multidimensional data resources.Overview of the genetics of major depressive disorder Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.Genome-wide DNA methylation scan in major depressive disorder.The genetic interacting landscape of 63 candidate genes in Major Depressive Disorder: an explorative study.A fine-mapping study of 7 top scoring genes from a GWAS for major depressive disorder.Blood transcriptomic biomarkers in adult primary care patients with major depressive disorder undergoing cognitive behavioral therapy.Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder.A recessive genetic model and runs of homozygosity in major depressive disorder.

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Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies

http://www.wikidata.org/entity/Q28751388

description

2011 nî lūn-bûn

@nan

2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

Novel loci for major depressio ...... meta-analysis of three studies

@ast

Novel loci for major depressio ...... meta-analysis of three studies

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Novel loci for major depressio ...... meta-analysis of three studies

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type

label

Novel loci for major depressio ...... meta-analysis of three studies

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Novel loci for major depressio ...... meta-analysis of three studies

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Novel loci for major depressio ...... meta-analysis of three studies

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prefLabel

Novel loci for major depressio ...... meta-analysis of three studies

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Novel loci for major depressio ...... meta-analysis of three studies

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Novel loci for major depressio ...... meta-analysis of three studies

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Molecular Psychiatry

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Novel loci for major depressio ...... meta-analysis of three studies

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A R Sanders

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D F Levinson

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D Jancic

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E J Peters

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H A Garriock

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J B Kraft

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J S Yokoyama

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J Shi

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A Swedish National Twin Study of Lifetime Major Depression

Estimation of significance thresholds for genomewide association scans

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

The NCBI dbGaP database of genotypes and phenotypes

Common variants at 30 loci contribute to polygenic dyslipidemia

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Common variants conferring risk of schizophrenia

Variations in the vesicular monoamine transporter 1 gene (VMAT1/SLC18A1) are associated with bipolar i disorder

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

WGAViewer: software for genomic annotation of whole genome association studies

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202-15

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scholarly article

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2104333

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10.1038/MP.2009.125

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2

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16

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Myrna M. Weissman

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40805892

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1030423071

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20038947

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genome-wide association study

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2888856

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