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Transcriptome-Wide Association Study Provides Insights Into the Genetic Component of Gene Expression in Anxiety.
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- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.740134
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- Article
Genetic regulatory and biological implications of the 10q24.32 schizophrenia risk locus.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 4, p. 1403, doi. 10.1093/brain/awac352
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- Article
Functional variant rs2270363 on 16p13.3 confers schizophrenia risk by regulating NMRAL1.
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- 2022
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- journal article
Regulatory variants at 2q33.1 confer schizophrenia risk by modulating distal gene TYW5 expression.
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- Brain: A Journal of Neurology, 2022, v. 145, n. 2, p. 770, doi. 10.1093/brain/awab357
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- Article
Integrative Analyses Followed by Functional Characterization Reveal TMEM180 as a Schizophrenia Risk Gene.
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- Schizophrenia Bulletin, 2021, v. 47, n. 5, p. 1364, doi. 10.1093/schbul/sbab032
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- Article
SZDB: A Database for Schizophrenia Genetic Research.
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- Schizophrenia Bulletin, 2017, v. 43, n. 2, p. 459, doi. 10.1093/schbul/sbw102
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- Article
Recent Positive Selection Drives the Expansion of a Schizophrenia Risk Nonsynonymous Variant at SLC39A8 in Europeans.
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- Schizophrenia Bulletin, 2016, v. 42, n. 1, p. 178, doi. 10.1093/schbul/sbv070
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- Article
Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function.
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- Schizophrenia Bulletin, 2015, v. 41, n. 6, p. 1294, doi. 10.1093/schbul/sbv017
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- Article
Common Variants in the MKL1 Gene Confer Risk of Schizophrenia.
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- Schizophrenia Bulletin, 2015, v. 41, n. 3, p. 715, doi. 10.1093/schbul/sbu156
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- Article
Proteome-wide Mendelian randomization reveals the causal effects of immune-related plasma proteins on psychiatric disorders.
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- Human Genetics, 2023, v. 142, n. 6, p. 809, doi. 10.1007/s00439-023-02562-0
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- Article
SZDB2.0: an updated comprehensive resource for schizophrenia research.
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- Human Genetics, 2020, v. 139, n. 10, p. 1285, doi. 10.1007/s00439-020-02171-1
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- Article
Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese.
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- National Science Review, 2019, v. 6, n. 2, p. 257, doi. 10.1093/nsr/nwy127
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- Article
Transcriptome-wide association study identifies new susceptibility genes and pathways for depression.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01411-w
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- Article
Genome wide association study identifies four loci for early onset schizophrenia.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01360-4
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- Article
Functional variants fine‐mapping and gene function characterization provide insights into the role of ZNF323 in schizophrenia pathogenesis.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2021, v. 186, n. 1, p. 28, doi. 10.1002/ajmg.b.32835
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- Article
No association between schizophrenia susceptibility variants and macroscopic structural brain volume variation in healthy subjects.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 2, p. 160, doi. 10.1002/ajmg.b.32387
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- Article
ZNF804A and Schizophrenia Susceptibility in Asian Populations
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 7, p. 794, doi. 10.1002/ajmg.b.32084
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- Article
Functional genomic analysis delineates regulatory mechanisms of GWAS-identified bipolar disorder risk variants.
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- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01057-3
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- Article
Meta-Analysis Indicates That the European GWAS-Identified Risk SNP rs1344706 within ZNF804A Is Not Associated with Schizophrenia in Han Chinese Population.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065780
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- Article
The Interleukin 3 Gene (IL3) Contributes to Human Brain Volume Variation by Regulating Proliferation and Survival of Neural Progenitors.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0050375
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- Article
Apoptotic Engulfment Pathway and Schizophrenia.
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- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0006875
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- Article
Adaptive evolution of interleukin-3 (IL3), a gene associated with brain volume variation in general human populations.
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- Human Genetics, 2016, v. 135, n. 4, p. 377, doi. 10.1007/s00439-016-1644-z
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- Article
The schizophrenia-associated missense variant rs13107325 regulates dendritic spine density.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02137-z
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- Article
Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08666-4
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- Article
Author Correction: Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07401-9
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- Article
Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants.
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- BMC Medicine, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12916-022-02264-w
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- Article
Further evidence for the genetic association between CACNA1/ and schizophrenia.
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- Hereditas, 2018, v. 155, p. 1, doi. 10.1186/s41065-017-0054-0
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- Article
Regulatory Variant rs2535629 in ITIH3 Intron Confers Schizophrenia Risk By Regulating CTCF Binding and SFMBT1 Expression.
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- Advanced Science, 2022, v. 9, n. 6, p. 1, doi. 10.1002/advs.202104786
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- Article
The depression GWAS risk allele predicts smaller cerebellar gray matter volume and reduced SIRT1 mRNA expression in Chinese population.
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- Translational Psychiatry, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41398-019-0675-3
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- Article
The integrated landscape of causal genes and pathways in schizophrenia.
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- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0114-x
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- Article
Bhlhb5 is required for the subtype development of retinal amacrine and bipolar cells in mice.
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- Developmental Dynamics, 2014, v. 243, n. 2, p. 279, doi. 10.1002/dvdy.24067
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- Article
GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3609, doi. 10.1093/hmg/ddt212
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- Article
Mendelian Randomization Study Using Dopaminergic Neuron‐Specific eQTL Nominates Potential Causal Genes for Parkinson's Disease.
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- Movement Disorders, 2022, v. 37, n. 12, p. 2451, doi. 10.1002/mds.29239
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- Article
Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations?
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- Scientific Reports, 2015, p. 11076, doi. 10.1038/srep11076
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- Article
Identification of a Risk Locus at 7p22.3 for Schizophrenia and Bipolar Disorder in East Asian Populations.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.789512
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- Article
Functional genomics elucidates regulatory mechanisms of Parkinson's disease-associated variants.
- Published in:
- 2022
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- Publication type:
- journal article
Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia.
- Published in:
- 2021
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- Publication type:
- journal article
Mendelian Randomization Study Using Dopaminergic Neuron-Specific eQTL Identifies Novel Risk Genes for Schizophrenia.
- Published in:
- Molecular Neurobiology, 2023, v. 60, n. 3, p. 1537, doi. 10.1007/s12035-022-03160-3
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- Publication type:
- Article
Evaluation of European Schizophrenia GWAS Loci in Asian Populations via Comprehensive Meta-Analyses.
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- Molecular Neurobiology, 2017, v. 54, n. 6, p. 4071, doi. 10.1007/s12035-016-9990-3
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- Article
MAOA Variants and Genetic Susceptibility to Major Psychiatric Disorders.
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- Molecular Neurobiology, 2016, v. 53, n. 7, p. 4319, doi. 10.1007/s12035-015-9374-0
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- Article
Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy.
- Published in:
- Frontiers in Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnins.2021.722592
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- Article
LMO4 Functions As a Negative Regulator of Sensory Organ Formation in the Mammalian Cochlea.
- Published in:
- Journal of Neuroscience, 2014, v. 34, n. 30, p. 10072, doi. 10.1523/JNEUROSCI.0352-14.2014
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- Publication type:
- Article