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Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Estimation of significance thresholds for genomewide association scans
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MANIC DEPRESSIVE ILLNESS
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A framework for interpreting genome-wide association studies of psychiatric disorders
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
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A survey of genetic human cortical gene expression
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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
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Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits
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Tissue-Specific Genetic Control of Splicing: Implications for the Study of Complex Traits

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Genome-wide Association: From Confounded to Confident
inferred← citeshttps://doi.org/10.1186/1471-2350-15-2openalex-snapshot
Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1
inferred← citeshttps://doi.org/10.1186/1471-244x-10-59openalex-snapshot
The DAOA/G30 locus and affective disorders: haplotype based association study in a polydiagnostic approach
inferred← citeshttps://doi.org/10.1186/2193-9616-1-15openalex-snapshot
Comparison of gene expression profiles in the blood, hippocampus and prefrontal cortex of rats
inferred← citeshttps://doi.org/10.1186/s12863-015-0274-0openalex-snapshot
Comparative genome-wide association studies of a depressive symptom phenotype in a repeated measures setting by race/ethnicity in the multi-ethnic study of atherosclerosis
inferred← citeshttps://doi.org/10.1186/s12916-023-02931-6openalex-snapshot
Identification of a psychiatric risk gene NISCH at 3p21.1 GWAS locus mediating dendritic spine morphogenesis and cognitive function
inferred← citeshttps://doi.org/10.1186/s13073-016-0308-xopenalex-snapshot
Identification of the BRD1 interaction network and its impact on mental disorder risk
inferred← citeshttps://doi.org/10.1186/s40345-018-0132-xopenalex-snapshot
Detecting significant genotype–phenotype association rules in bipolar disorder: market research meets complex genetics
inferred← citeshttps://doi.org/10.1186/s40345-021-00228-2openalex-snapshot
Predicting the risk and timing of major mood disorder in offspring of bipolar parents: exploring the utility of a neural network approach
inferred← citeshttps://doi.org/10.1186/s41065-019-0095-7openalex-snapshot
Association of SYNE1 locus with bipolar disorder in Chinese population
inferred← citeshttps://doi.org/10.1192/bjp.bp.110.079665openalex-snapshot
From predisposition to illness: genetically sensitive intermediate pathways to mood disorders
inferred← citeshttps://doi.org/10.1192/bjp.bp.114.156976openalex-snapshot
Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance
inferred← citeshttps://doi.org/10.1192/j.eurpsy.2019.6openalex-snapshot
An atlas of genetic correlations between psychiatric disorders and human blood plasma proteome
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002134openalex-snapshot
Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004229openalex-snapshot
Genomic View of Bipolar Disorder Revealed by Whole Genome Sequencing in a Genetic Isolate
inferred← citeshttps://doi.org/10.1371/journal.pone.0009697openalex-snapshot
A New Statistic to Evaluate Imputation Reliability
inferred← citeshttps://doi.org/10.1371/journal.pone.0015463openalex-snapshot
Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder
inferred← citeshttps://doi.org/10.1371/journal.pone.0051504openalex-snapshot
Molecular Sex Differences in Human Serum
inferred← citeshttps://doi.org/10.1371/journal.pone.0064947openalex-snapshot
Possible Associations of NTRK2 Polymorphisms with Antidepressant Treatment Outcome: Findings from an Extended Tag SNP Approach
inferred← citeshttps://doi.org/10.1371/journal.pone.0070964openalex-snapshot
Genetic Variants on 3q21 and in the Sp8 Transcription Factor Gene (SP8) as Susceptibility Loci for Psychotic Disorders: A Genetic Association Study
inferred← citeshttps://doi.org/10.1371/journal.pone.0128605openalex-snapshot
Explore the Features of Brain-Derived Neurotrophic Factor in Mood Disorders
inferred← citeshttps://doi.org/10.1371/journal.pone.0157086openalex-snapshot
Functional Characterization of Schizophrenia-Associated Variation in CACNA1C
inferred← citeshttps://doi.org/10.1586/ecp.10.35openalex-snapshot
Imaging genetics: implications for research on variable antidepressant drug response
inferred← citeshttps://doi.org/10.2217/pgs-2020-0157openalex-snapshot
Therapy Response Prediction in Major Depressive Disorder: Current and Novel Genomic Markers Influencing Pharmacokinetics and Pharmacodynamics
inferred← citeshttps://doi.org/10.2217/pme.12.67openalex-snapshot
Research Highlights: Highlights from the Latest Articles in Psychiatric Genetics
inferred← citeshttps://doi.org/10.3109/15622975.2011.596220openalex-snapshot
The genetic blueprint of major depressive disorder: Contributions of imaging genetics studies
inferred← citeshttps://doi.org/10.3389/fgene.2013.00087openalex-snapshot
Converging evidence for epistasis between ANK3 and potassium channel gene KCNQ2 in bipolar disorder
inferred← citeshttps://doi.org/10.3389/fpsyt.2014.00098openalex-snapshot
Integrated Neurobiology of Bipolar Disorder
inferred← citeshttps://doi.org/10.3390/futurepharmacol4030032openalex-snapshot
Pharmacogenetics and the Blood–Brain Barrier: A Whirlwind Tour of Potential Clinical Utility
inferred← citeshttps://doi.org/10.37099/mtu.dc.etdr/436openalex-snapshot
Heterologous Expression and Purification of Full-Length Human Polybromo-1 Protein
inferred← citeshttps://doi.org/10.4018/978-1-4666-8559-8.ch009openalex-snapshot
Genomic Technologies and the Emergence of BRICS (Brazil, Russia, India, China, and South Africa)
inferred← citeshttps://doi.org/10.4018/978-1-4666-8559-8.ch012openalex-snapshot
Wealth Creation from the Commercialization of Genomics Science
inferred← citeshttps://doi.org/10.4061/2010/159761openalex-snapshot
Pharmacogenomics of Mood Stabilizers in the Treatment of Bipolar Disorder
inferred← citeshttps://doi.org/10.4236/ojpsych.2013.31008openalex-snapshot
Genomics of schizophrenia and pharmacogenomics of antipsychotic drugs
inferred← citeshttps://doi.org/10.47749/t/unicamp.2011.784055openalex-snapshot
Aplicação de modelos estatísticos e desenvolvimento de algoritmos para estudo genético de doenças neuro-psiquiátricas
inferred← citeshttps://doi.org/10.48496/9v1q-rb59openalex-snapshot
Genome-Scale Genetics: Lessons from Founder Populations
inferred← citeshttps://doi.org/10.5124/jkma.25.0143openalex-snapshot
Recent advances in the genetic architecture of bipolar disorder and its clinical implications: a narrative review
inferred← citeshttps://doi.org/10.5706/nph201212009openalex-snapshot
Beyond structural equation modeling: model properties and effect size from a Bayesian viewpoint. An example of complex phenotype-genotype associations in depression.
inferred← citeshttps://doi.org/10.6084/m9.figshare.14889673openalex-snapshot
Additional file 1 of Predicting the risk and timing of major mood disorder in offspring of bipolar parents: exploring the utility of a neural network approach
inferred← citeshttps://doi.org/10.6084/m9.figshare.26604079openalex-snapshot
Additional file 1 of Identification of a psychiatric risk gene NISCH at 3p21.1 GWAS locus mediating dendritic spine morphogenesis and cognitive function
inferred← citeshttps://doi.org/10.6084/m9.figshare.26604082openalex-snapshot
Additional file 2 of Identification of a psychiatric risk gene NISCH at 3p21.1 GWAS locus mediating dendritic spine morphogenesis and cognitive function
inferred← citeshttps://doi.org/10.7936/k7vt1qgmopenalex-snapshot
Gene Association Mapping in the Era of Next-Generation Sequencing and Systems Biology
inferred← citeshttps://doi.org/10.7936/k7wd3xkcopenalex-snapshot
New methods for discovering common and rare genetic variants in human disease
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