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Author Details

Eric R Gamazon
Vanderbilt University Medical Center
2009
173
46
PMIDPaper TitleJournal TitlePublished Year
36413071IMMerge: merging imputation data at scale.Bioinformatics2023
36413071IMMerge: merging imputation data at scale.Bioinformatics2023
38017547A phenome-wide scan reveals convergence of common and rare variant associations.Genome Med2023
37828025ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.Nat Commun2023
37961453Mapping the landscape of lineage-specific dynamic regulation of gene expression using single-cell transcriptomics and application to genetics of complex disease.medRxiv2023
37961219Integrating population-level and cell-based signatures for drug repositioning.bioRxiv2023
37473490Identification of drug repurposing candidates for the treatment of anxiety: A genetic approach.Psychiatry Res2023
37090430Towards mechanistic models of mutational effects: Deep learning on Alzheimer's Aβ peptide.Comput Struct Biotechnol J2023
37398182The broad impact of cell death genes on the human disease phenome.medRxiv2023
37398170Minimum entropy framework identifies a novel class of genomic functional elements and reveals regulatory mechanisms at human disease loci.bioRxiv2023
36797672Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.BMC Genomics2023
36993467A Transcriptomic Atlas of the Human Brain Reveals Genetically Determined Aspects of Neuropsychiatric Health.medRxiv2023
37100056Integrative genetic analysis identifies FLVCR1 as a plasma-membrane choline transporter in mammals.Cell Metab2023
38017547A phenome-wide scan reveals convergence of common and rare variant associations.Genome Med2023
37961453Mapping the landscape of lineage-specific dynamic regulation of gene expression using single-cell transcriptomics and application to genetics of complex disease.medRxiv2023
37961219Integrating population-level and cell-based signatures for drug repositioning.bioRxiv2023
37828025ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon.Nat Commun2023
37090430Towards mechanistic models of mutational effects: Deep learning on Alzheimer's Aβ peptide.Comput Struct Biotechnol J2023
36993467A Transcriptomic Atlas of the Human Brain Reveals Genetically Determined Aspects of Neuropsychiatric Health.medRxiv2023
37100056Integrative genetic analysis identifies FLVCR1 as a plasma-membrane choline transporter in mammals.Cell Metab2023
37473490Identification of drug repurposing candidates for the treatment of anxiety: A genetic approach.Psychiatry Res2023
37398182The broad impact of cell death genes on the human disease phenome.medRxiv2023
37398170Minimum entropy framework identifies a novel class of genomic functional elements and reveals regulatory mechanisms at human disease loci.bioRxiv2023
36797672Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome.BMC Genomics2023
34520569A transcriptome-wide association study identifies novel candidate susceptibility genes for prostate cancer risk.Int J Cancer2022
35525699A Local Genetic Correlation Analysis Provides Biological Insights Into the Shared Genetic Architecture of Psychiatric and Substance Use Phenotypes.Biol Psychiatry2022
36357675Rare and common genetic determinants of metabolic individuality and their effects on human health.Nat Med2022
35383711Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension.Pharmacogenet Genomics2022
35669036Modeling mutational effects on biochemical phenotypes using convolutional neural networks: application to SARS-CoV-2.iScience2022
35318325Integrative transcriptomic, evolutionary, and causal inference framework for region-level analysis: Application to COVID-19.NPJ Genom Med2022
34520569A transcriptome-wide association study identifies novel candidate susceptibility genes for prostate cancer risk.Int J Cancer2022
35217801An analysis of genetically regulated gene expression and the role of co-expression networks across 16 psychiatric and substance use phenotypes.Eur J Hum Genet2022
35157052Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.Hum Mol Genet2022
35383711Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension.Pharmacogenet Genomics2022
35669036Modeling mutational effects on biochemical phenotypes using convolutional neural networks: application to SARS-CoV-2.iScience2022
35525699A Local Genetic Correlation Analysis Provides Biological Insights Into the Shared Genetic Architecture of Psychiatric and Substance Use Phenotypes.Biol Psychiatry2022
36357675Rare and common genetic determinants of metabolic individuality and their effects on human health.Nat Med2022
35318325Integrative transcriptomic, evolutionary, and causal inference framework for region-level analysis: Application to COVID-19.NPJ Genom Med2022
35157052Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes.Hum Mol Genet2022
35217801An analysis of genetically regulated gene expression and the role of co-expression networks across 16 psychiatric and substance use phenotypes.Eur J Hum Genet2022
33369091An integrative systems-based analysis of substance use: eQTL-informed gene-based tests, gene networks, and biological mechanisms.Am J Med Genet B Neuropsychiatr Genet2021
34285202Contextualizing genetic risk score for disease screening and rare variant discovery.Nat Commun2021
33532766Modeling mutational effects on biochemical phenotypes using convolutional neural networks: application to SARS-CoV-2.bioRxiv2021
33531486Author Correction: Genetic architecture of host proteins involved in SARS-CoV-2 infection.Nat Commun2021
33624746E-MAGMA: an eQTL-informed method to identify risk genes using genome-wide association study summary statistics.Bioinformatics2021
33951428Multi-omic analysis elucidates the genetic basis of hydrocephalus.Cell Rep2021
34045472Multilayer modelling of the human transcriptome and biological mechanisms of complex diseases and traits.NPJ Syst Biol Appl2021
34032508Revisiting Some Useful Statistical Guidelines in <i>Circulation Research</i> in Response to a Changing Landscape.Circ Res2021
33927746Deep Learning Enables Fast and Accurate Imputation of Gene Expression.Front Genet2021
33499903Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.Genome Biol2021
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Collaborators

Nancy J Cox
Vanderbilt University Medical Center
Co-authored papers 92
Mary Eileen Dolan
University of Chicago
Co-authored papers 34
Hae Kyung Im
Co-authored papers 32
Anuar Konkashbaev
Co-authored papers 17
Eske M Derks
Co-authored papers 17
Jennifer E Below
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Co-authored papers 12
Patrick Evans
Co-authored papers 12
Dan L Nicolae
Co-authored papers 12
Heather E Wheeler
Co-authored papers 11
Dan Zhou
Co-authored papers 10
Claudia Langenberg
Co-authored papers 10
Lea K Davis
Vanderbilt University Medical Center, Tennessee Vanderbilt Genetics Institute
Co-authored papers 10
Nicholas J Wareham
Co-authored papers 9
Benjamin M Neale
Massachusetts General Hospital
Co-authored papers 9
Craig L Hanis
Co-authored papers 8
Mark J Ratain
University of Chicago
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Shaun Purcell
Brigham and Women's Hospital
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Heather M Highland
Co-authored papers 7
Chunyu Liu
Boston University School of Public Health
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Edwin H Cook
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Jeremiah M Scharf
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Graeme I Bell
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Mark I McCarthy
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Dongmei Yu
Co-authored papers 6
Danielle Posthuma
Co-authored papers 6
Larisa H Cavallari
Department of Pharmacotherapy and Translational Research, University of Florida
Co-authored papers 6
Lisa Bastarache
Vanderbilt University Medical Center
Co-authored papers 6
Carol A Mathews
Co-authored papers 6
Andrew D Skol
The University of Chicago
Co-authored papers 6
Michiaki Kubo
Co-authored papers 6
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