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Author Details
Full Name
Brien P Riley
Affiliation
Virginia Commonwealth University
ORCID
Career Start Year
1992
Papers
151
H Index
48
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36503694
Relationship between polygenic risk scores and symptom dimensions of schizophrenia and schizotypy in multiplex families with schizophrenia.
Br J Psychiatry
2023
37588130
Integrative Post-Genome-Wide Association Study Analyses Relevant to Psychiatric Disorders: Imputing Transcriptome and Proteome Signals.
Complex Psychiatry
2023
37745400
Improving the discovery of rare variants associated with alcohol problems by leveraging machine learning phenotype prediction and functional information.
bioRxiv
2023
37415601
Identifying potential risk genes and pathways for neuropsychiatric and substance use disorders using intermediate molecular mediator information.
Front Genet
2023
37098020
Case-only exome variation analysis of severe alcohol dependence using a multivariate hierarchical gene clustering approach.
PLoS One
2023
34099189
Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders.
Biol Psychiatry
2022
35608069
Large-scale integration of DNA methylation and gene expression array platforms identifies both <i>cis</i> and <i>trans</i> relationships.
Epigenetics
2022
35396580
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
Nature
2022
35523779
A serotonergic biobehavioral signature differentiates cocaine use disorder participants administered mirtazapine.
Transl Psychiatry
2022
35714915
Genome-wide analysis of schizophrenia and multiple sclerosis identifies shared genomic loci with mixed direction of effects.
Brain Behav Immun
2022
36434002
Examining the source of increased bipolar disorder and major depressive disorder common risk variation burden in multiplex schizophrenia families.
Schizophrenia (Heidelb)
2022
36216875
Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.
Sci Rep
2022
33398649
Recruiting for diversity: a pilot test of recruitment strategies for a national alcohol survey with mail-in genetic data collection.
J Community Genet
2021
33576176
Increasing the resolution and precision of psychiatric genome-wide association studies by re-imputing summary statistics using a large, diverse reference panel.
Am J Med Genet B Neuropsychiatr Genet
2021
33791774
DECO: a framework for jointly analyzing de novo and rare case/control variants, and biological pathways.
Brief Bioinform
2021
32064741
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
Addict Biol
2021
31294817
Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes.
Nicotine Tob Res
2020
33096046
A large-scale genome-wide association study meta-analysis of cannabis use disorder.
Lancet Psychiatry
2020
33067813
Assessing the Role of Long Noncoding RNA in Nucleus Accumbens in Subjects With Alcohol Dependence.
Alcohol Clin Exp Res
2020
32954640
TWAS pathway method greatly enhances the number of leads for uncovering the molecular underpinnings of psychiatric disorders.
Am J Med Genet B Neuropsychiatr Genet
2020
32522981
mTADA is a framework for identifying risk genes from de novo mutations in multiple traits.
Nat Commun
2020
32300216
Retraction Note: 11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.
Sci Data
2020
31092822
Hydro-Seq enables contamination-free high-throughput single-cell RNA-sequencing for circulating tumor cells.
Nat Commun
2019
31710321
Single-cell RNA-sequencing of migratory breast cancer cells: discovering genes associated with cancer metastasis.
Analyst
2019
31017905
Cross-species alcohol dependence-associated gene networks: Co-analysis of mouse brain gene expression and human genome-wide association data.
PLoS One
2019
30801977
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
2019
29321615
Functional Isolation of Tumor-Initiating Cells using Microfluidic-Based Migration Identifies Phosphatidylserine Decarboxylase as a Key Regulator.
Sci Rep
2018
30213503
Cross-species molecular dissection across alcohol behavioral domains.
Alcohol
2018
29905862
Building a schizophrenia genetic network: transcription factor 4 regulates genes involved in neuronal development and schizophrenia risk.
Hum Mol Genet
2018
30482948
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders.
Nat Neurosci
2018
30420987
Morphology-based prediction of cancer cell migration using an artificial neural network and a random decision forest.
Integr Biol (Camb)
2018
29700475
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.
Nat Genet
2018
29405378
Polygenic Risk Score Prediction of Alcohol Dependence Symptoms Across Population-Based and Clinically Ascertained Samples.
Alcohol Clin Exp Res
2018
29173193
Polygenic prediction of the phenome, across ancestry, in emerging adulthood.
Psychol Med
2018
28002544
The Genetic Architecture of Major Depressive Disorder in Han Chinese Women.
JAMA Psychiatry
2017
28226201
Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms.
Alcohol Clin Exp Res
2017
28195579
11,670 whole-genome sequences representative of the Han Chinese population from the CONVERGE project.
Sci Data
2017
28360924
Molecular Genetic Influences on Normative and Problematic Alcohol Use in a Population-Based Sample of College Students.
Front Genet
2017
28350396
Genetic effects influencing risk for major depressive disorder in China and Europe.
Transl Psychiatry
2017
26514393
Dimensionality and Genetic Correlates of Problem Behavior in Low-Income African American Adolescents.
J Clin Child Adolesc Psychol
2017
27869829
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Nat Genet
2017
27080172
Motorized actuation system to perform droplet operations on printed plastic sheets.
Lab Chip
2016
26428293
JEPEGMIX: gene-level joint analysis of functional SNPs in cosmopolitan cohorts.
Bioinformatics
2016
26316594
Meta-analysis of Positive and Negative Symptoms Reveals Schizophrenia Modifier Genes.
Schizophr Bull
2016
27187203
A simple yet accurate correction for winner's curse can predict signals discovered in much larger genome scans.
Bioinformatics
2016
27510097
Scaling and automation of a high-throughput single-cell-derived tumor sphere assay chip.
Lab Chip
2016
25505091
JEPEG: a summary statistics based tool for gene-level joint testing of functional variants.
Bioinformatics
2015
26381263
Integrating mRNA and miRNA Weighted Gene Co-Expression Networks with eQTLs in the Nucleus Accumbens of Subjects with Alcohol Dependence.
PLoS One
2015
26106668
Can Genetics Predict Response to Complex Behavioral Interventions? Evidence from a Genetic Analysis of the Fast Track Randomized Control Trial.
J Policy Anal Manage
2015
26059716
DISTMIX: direct imputation of summary statistics for unmeasured SNPs from mixed ethnicity cohorts.
Bioinformatics
2015
1 - 50 of 151
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Marcella Rietschel
Central Institute of Mental Health, University of Mannheim
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Markus M N??then
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Wolfgang Maier
University Hospital Bonn
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Derek W Morris
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Alan R Sanders
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Nicholas G Martin
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Sven Cichon
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Xiangning Chen
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George Kirov
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Christina M Hultman
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