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Mendelian Randomization Study Using Dopaminergic Neuron‐Specific eQTL Nominates Potential Causal Genes for Parkinson's Disease

Movement disorders, 2022-12, Vol.37 (12), p.2451-2456

2022

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Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk

Nature communications, 2019-02, Vol.10 (1), p.670-19, Article 670

2019

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In vivo study sheds new light on the dendritic spine pathology hypothesis of schizophrenia

Molecular psychiatry, 2022-04, Vol.27 (4), p.1866-1868

2022

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Down-Regulation of SIRT1 Gene Expression in Major Depressive Disorder

The American journal of psychiatry, 2016-10, Vol.173 (10), p.1046-1046

2016

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SZDB: A Database for Schizophrenia Genetic Research

Schizophrenia bulletin, 2017-03, Vol.43 (2), p.459-471

2017

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SZDB2.0: an updated comprehensive resource for schizophrenia research

Human genetics, 2020-10, Vol.139 (10), p.1285-1297

2020

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Functional variants fine‐mapping and gene function characterization provide insights into the role of ZNF323 in schizophrenia pathogenesis

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2021-01, Vol.186 (1), p.28-39

2021

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Regulatory mechanisms of major depressive disorder risk variants

Molecular psychiatry, 2020-09, Vol.25 (9), p.1926-1945

2020

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The schizophrenia susceptibility gene NAGA regulates dendritic spine density: further evidence for the dendritic spine pathology of schizophrenia

Molecular psychiatry, 2021-12, Vol.26 (12), p.7102-7104

2021

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The integrated landscape of causal genes and pathways in schizophrenia

Translational psychiatry, 2018-03, Vol.8 (1), p.67-14, Article 67

2018

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Integration of GWAS and brain eQTL identifies FLOT1 as a risk gene for major depressive disorder

Neuropsychopharmacology (New York, N.Y.), 2019-08, Vol.44 (9), p.1542-1551

2019

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Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes

Nature communications, 2018-02, Vol.9 (1), p.838-16, Article 838

2018

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A missense variant in NDUFA6 confers schizophrenia risk by affecting YY1 binding and NAGA expression

Molecular psychiatry, 2021-11, Vol.26 (11), p.6896-6911

2021

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Proteome-wide Association Study Provides Insights Into the Genetic Component of Protein Abundance in Psychiatric Disorders

Biological psychiatry (1969), 2021-12, Vol.90 (11), p.781-789

2021

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Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder

Neuropsychopharmacology (New York, N.Y.), 2018-09, Vol.43 (10), p.2146-2153

2018

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Transcriptome-wide association study identifies new susceptibility genes and pathways for depression

Translational psychiatry, 2021-05, Vol.11 (1), p.306-13, Article 306

2021

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Genome wide association study identifies four loci for early onset schizophrenia

Translational psychiatry, 2021-04, Vol.11 (1), p.248-248, Article 248

2021

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Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia

BMC medicine, 2021-08, Vol.19 (1), p.177-15, Article 177

2021

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Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder

Neuropsychopharmacology (New York, N.Y.), 2019-08, Vol.44 (9), p.1552-1561

2019

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Functional genomic analysis delineates regulatory mechanisms of GWAS-identified bipolar disorder risk variants

Genome medicine, 2022-05, Vol.14 (1), p.53-53, Article 53

2022

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Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety

Frontiers in genetics, 2021-09, Vol.12, p.740134-740134

2021

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Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy

Frontiers in neuroscience, 2021-08, Vol.15, p.722592-722592

2021

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Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants

BMC medicine, 2022-02, Vol.20 (1), p.68-68, Article 68

2022

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GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea

Human molecular genetics, 2013-09, Vol.22 (18), p.3609-3623

2013

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Genome-wide Mendelian randomization identifies actionable novel drug targets for psychiatric disorders

Neuropsychopharmacology (New York, N.Y.), 2023-01, Vol.48 (2), p.270-280

2023

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Mendelian Randomization Study Using Dopaminergic Neuron‐Specific eQTL Nominates Potential Causal Genes for Parkinson's Disease

Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk

In vivo study sheds new light on the dendritic spine pathology hypothesis of schizophrenia

Down-Regulation of SIRT1 Gene Expression in Major Depressive Disorder

SZDB: A Database for Schizophrenia Genetic Research

SZDB2.0: an updated comprehensive resource for schizophrenia research

Functional variants fine‐mapping and gene function characterization provide insights into the role of ZNF323 in schizophrenia pathogenesis

Regulatory mechanisms of major depressive disorder risk variants

The schizophrenia susceptibility gene NAGA regulates dendritic spine density: further evidence for the dendritic spine pathology of schizophrenia

The integrated landscape of causal genes and pathways in schizophrenia

Integration of GWAS and brain eQTL identifies FLOT1 as a risk gene for major depressive disorder

Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes

A missense variant in NDUFA6 confers schizophrenia risk by affecting YY1 binding and NAGA expression

Proteome-wide Association Study Provides Insights Into the Genetic Component of Protein Abundance in Psychiatric Disorders

Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder

Transcriptome-wide association study identifies new susceptibility genes and pathways for depression

Genome wide association study identifies four loci for early onset schizophrenia

Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia

Integrative analyses of major histocompatibility complex loci in the genome-wide association studies of major depressive disorder

Functional genomic analysis delineates regulatory mechanisms of GWAS-identified bipolar disorder risk variants

Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety

Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy

Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants

GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea

Genome-wide Mendelian randomization identifies actionable novel drug targets for psychiatric disorders

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