Eric R. Gamazon
#173,350
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Expert in human genetics, computational biology, functional genomics, cancer biology, neuropsychiatric genomics, statistical genetics, pharmacogenomics
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Eric R. Gamazonbiology Degrees
Biology
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Computational Biology
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Genetics
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Biology
Eric R. Gamazon's Degrees
- PhD Genetics University of California, San Francisco
- Masters Bioinformatics Stanford University
- Bachelors Biology University of California, Berkeley
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Why Is Eric R. Gamazon Influential?
(Suggest an Edit or Addition)According to Wikipedia, Eric R. Gamazon is a statistical geneticist in Vanderbilt University, with faculty affiliations in the Division of Genetic Medicine, Data Science Institute, and Center for Precision Medicine. He is a Life Member of Clare Hall, Cambridge University after election to a Visiting Fellowship .
Eric R. Gamazon's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- The Genotype-Tissue Expression (GTEx) project (2013) (6030)
- The Genotype-Tissue Expression (GTEx) pilot analysis: Multitissue gene regulation in humans (2015) (3904)
- Genetic effects on gene expression across human tissues (2017) (2841)
- Genetic effects on gene expression across human tissues (2017) (2841)
- Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS (2010) (1210)
- A gene-based association method for mapping traits using reference transcriptome data (2015) (1160)
- Obesity-associated variants within FTO form long-range functional connections with IRX3 (2014) (1070)
- The genetic architecture of type 2 diabetes (2016) (927)
- Human polymorphism at microRNAs and microRNA target sites. (2013) (330)
- Using an atlas of gene regulation across 44 human tissues to inform complex disease- and trait-associated variation (2018) (319)
- Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture (2013) (280)
- Genome-wide association study of obsessive-compulsive disorder (2013) (256)
- Identification, Replication, and Functional Fine-Mapping of Expression Quantitative Trait Loci in Primary Human Liver Tissue (2011) (249)
- Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases (2016) (242)
- Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study (2013) (232)
- SCAN: SNP and copy number annotation (2010) (229)
- The impact of sex on gene expression across human tissues (2020) (220)
- Gastric colonisation with a restricted commensal microbiota replicates the promotion of neoplastic lesions by diverse intestinal microbiota in the Helicobacter pylori INS-GAS mouse model of gastric carcinogenesis (2013) (206)
- Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record (2017) (205)
- The impact of rare variation on gene expression across tissues (2016) (197)
- Comparison of Breast Cancer Molecular Features and Survival by African and European Ancestry in The Cancer Genome Atlas (2017) (178)
- Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases (2015) (167)
- Enrichment of Cis-Regulatory Gene Expression SNPs and Methylation Quantitative Trait Loci Among Bipolar Disorder Susceptibility Variants (2012) (165)
- Population differences in microRNA expression and biological implications (2011) (154)
- A Quantitative Proteome Map of the Human Body (2019) (143)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (134)
- Campylobacter jejuni Type VI Secretion System: Roles in Adaptation to Deoxycholic Acid, Host Cell Adherence, Invasion, and In Vivo Colonization (2012) (127)
- Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. (2015) (123)
- Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci (2010) (115)
- The Missing Association: Sequencing‐Based Discovery of Novel SNPs in VKORC1 and CYP2C9 That Affect Warfarin Dose in African Americans (2011) (115)
- Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals (2011) (113)
- Exploiting the GTEx resources to decipher the mechanisms at GWAS loci (2019) (111)
- Genome-wide association study of Tourette Syndrome (2012) (102)
- The impact of human copy number variation on gene expression. (2015) (99)
- On sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy. (2012) (98)
- Genetic architecture of microRNA expression: implications for the transcriptome and complex traits. (2012) (98)
- Genomics of alternative splicing: evolution, development and pathophysiology (2013) (97)
- ExprTarget: An Integrative Approach to Predicting Human MicroRNA Targets (2010) (78)
- A unified framework for joint-tissue transcriptome-wide association and Mendelian Randomization analysis (2020) (77)
- A Genome-wide Association Study of Early-Onset Breast Cancer Identifies PFKM as a Novel Breast Cancer Gene and Supports a Common Genetic Spectrum for Breast Cancer at Any Age (2014) (77)
- Local genetic effects on gene expression across 44 human tissues (2016) (72)
- Mapping the proteo-genomic convergence of human diseases (2021) (72)
- Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait. (2014) (70)
- Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs (2016) (66)
- Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits (2019) (64)
- A gene co-expression network-based analysis of multiple brain tissues reveals novel genes and molecular pathways underlying major depression (2019) (63)
- Ethnicity-specific pharmacogenetics: the case of warfarin in African Americans (2013) (62)
- Platinum Sensitivity–Related Germline Polymorphism Discovered via a Cell-Based Approach and Analysis of Its Association with Outcome in Ovarian Cancer Patients (2011) (61)
- Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity (2016) (60)
- Functional genetic screen of human diversity reveals that a methionine salvage enzyme regulates inflammatory cell death (2012) (60)
- A Study of CNVs As Trait-Associated Polymorphisms and As Expression Quantitative Trait Loci (2011) (59)
- Genetic variant in folate homeostasis is associated with lower warfarin dose in African Americans. (2014) (56)
- Variants Affecting Exon Skipping Contribute to Complex Traits (2012) (55)
- Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. (2016) (54)
- Integration of Cell Line and Clinical Trial Genome-Wide Analyses Supports a Polygenic Architecture of Paclitaxel-Induced Sensory Peripheral Neuropathy (2012) (54)
- Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease (2021) (54)
- Genetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liver. (2014) (53)
- Clinical and Genome-Wide Analysis of Cisplatin-Induced Peripheral Neuropathy in Survivors of Adult-Onset Cancer (2017) (53)
- Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer (2019) (53)
- Genome-wide Meta-analysis Identifies Variants Associated with Platinating Agent Susceptibility Across Populations (2011) (52)
- Genetic association signal near NTN4 in Tourette syndrome (2014) (51)
- Cytotoxic and Pathogenic Properties of Klebsiella oxytoca Isolated from Laboratory Animals (2014) (51)
- A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology (2016) (51)
- Genetic architecture of host proteins involved in SARS-CoV-2 infection (2020) (47)
- SLC25A39 is necessary for mitochondrial glutathione import in mammalian cells (2021) (46)
- Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx. (2015) (46)
- PACdb: a database for cell-based pharmacogenomics. (2010) (45)
- Novel genetic predictors of venous thromboembolism risk in African Americans. (2016) (43)
- Poly‐Omic Prediction of Complex Traits: OmicKriging (2013) (43)
- A genome-wide integrative study of microRNAs in human liver (2013) (43)
- A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk (2017) (43)
- Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci (2015) (43)
- Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers. (2011) (42)
- Consistency in large pharmacogenomic studies (2016) (41)
- Network models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseases (2013) (41)
- The impact of microRNA expression on cellular proliferation (2014) (41)
- An exponential combination procedure for set-based association tests in sequencing studies. (2012) (41)
- Comprehensive genetic analysis of cytarabine sensitivity in a cell-based model identifies polymorphisms associated with outcome in AML patients. (2013) (40)
- The limits of genome-wide methods for pharmacogenomic testing (2012) (39)
- Linking the genetic architecture of cytosine modifications with human complex traits. (2014) (39)
- On Using Local Ancestry to Characterize the Genetic Architecture of Human Traits: Genetic Regulation of Gene Expression in Multiethnic or Admixed Populations. (2019) (36)
- Trans-population analysis of genetic mechanisms of ethnic disparities in neuroblastoma survival. (2012) (36)
- Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci (2012) (35)
- Genetic Variation That Predicts Platinum Sensitivity Reveals the Role of miR-193b* in Chemotherapeutic Susceptibility (2012) (34)
- Widespread dose-dependent effects of RNA expression and splicing on complex diseases and traits (2019) (33)
- Inferred divergent gene regulation in archaic hominins reveals potential phenotypic differences (2019) (33)
- Genome-wide association study of obsessive-compulsive disorder (2013) (33)
- Regulation of Insulin Receptor Pathway and Glucose Metabolism by CD36 Signaling (2018) (32)
- Copy number polymorphisms and anticancer pharmacogenomics (2011) (31)
- Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines (2016) (31)
- Population differences in platinum toxicity as a means to identify novel genetic susceptibility variants (2010) (30)
- Genetic risk factors for type 2 diabetes: a trans-regulatory genetic architecture? (2012) (30)
- Identification of a Variant in KDR Associated with Serum VEGFR2 and Pharmacodynamics of Pazopanib (2014) (30)
- Mixed Effects Modeling of Proliferation Rates in Cell-Based Models: Consequence for Pharmacogenomics and Cancer (2012) (30)
- Whole-genome studies identify solute carrier transporters in cellular susceptibility to paclitaxel (2012) (30)
- Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers. (2013) (28)
- eMAGMA: An eQTL-informed method to identify risk genes using genome-wide association study summary statistics (2019) (28)
- Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations, and clinical studies (2019) (27)
- Identification of novel germline polymorphisms governing capecitabine sensitivity (2012) (25)
- SCAN database: facilitating integrative analyses of cytosine modification and expression QTL (2015) (25)
- Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity (2014) (25)
- Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2017) (25)
- Structural architecture of SNP effects on complex traits. (2014) (25)
- Genome-Wide Local Ancestry Approach Identifies Genes and Variants Associated with Chemotherapeutic Susceptibility in African Americans (2011) (24)
- The regulatory effect of miRNAs is a heritable genetic trait in humans (2012) (24)
- Metabolic co-essentiality mapping identifies c12orf49 as a regulator of SREBP processing and cholesterol metabolism (2020) (22)
- Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2018) (21)
- A pharmacogene database enhanced by the 1000 Genomes Project. (2009) (21)
- Clinical Translation of Cell‐Based Pharmacogenomic Discovery (2012) (21)
- Genetic variation associated with euphorigenic effects of d-amphetamine is associated with diminished risk for schizophrenia and attention deficit hyperactivity disorder (2014) (20)
- Genome-wide interrogation of longitudinal FEV1 in children with asthma. (2014) (19)
- Comprehensive Survey of SNPs in the Affymetrix Exon Array Using the 1000 Genomes Dataset (2010) (19)
- Clinical and Genome-wide Analysis of Cisplatin-induced Tinnitus Implicates Novel Ototoxic Mechanisms (2019) (19)
- Transcriptomic Imputation of Bipolar Disorder and Bipolar subtypes reveals 29 novel associated genes (2017) (19)
- Bid maintains mitochondrial cristae structure and function and protects against cardiac disease in an integrative genomics study (2018) (18)
- MicroRNA biogenesis and cellular proliferation. (2015) (18)
- Global biobank analyses provide lessons for computing polygenic risk scores across diverse cohorts (2021) (17)
- Differential expression of systemic inflammatory mediators in amputees with chronic residual limb pain (2017) (17)
- Meta-analysis fine-mapping is often miscalibrated at single-variant resolution (2022) (17)
- GRIK5 Genetically Regulated Expression Associated with Eye and Vascular Phenomes: Discovery through Iteration among Biobanks, Electronic Health Records, and Zebrafish. (2019) (17)
- Ethnic Variation of TET2 SNP rs2454206 and Association with Clinical Outcome in Childhood AML: A Report from the Children’s Oncology Group (2015) (17)
- An eQTL-based method identifies CTTN and ZMAT3 as pemetrexed susceptibility markers. (2012) (16)
- Post-GWAS analysis of six substance use traits improves the identification and functional interpretation of genetic risk loci. (2019) (16)
- STAMS: STRING-assisted module search for genome wide association studies and application to autism (2016) (15)
- Integrative Genomics: Quantifying Significance of Phenotype-Genotype Relationships from Multiple Sources of High-Throughput Data (2013) (15)
- A Transcriptome-Wide Association Study Identifies Candidate Susceptibility Genes for Pancreatic Cancer Risk (2020) (14)
- DNA methylation profiles are associated with complex regional pain syndrome following traumatic injury. (2019) (14)
- An analysis of genetically regulated gene expression across multiple tissues implicates novel gene candidates in Alzheimer’s disease (2020) (13)
- Genome-wide approaches in pharmacogenomics: heritability estimation and pharmacoethnicity as primary challenges. (2012) (13)
- Gene and MicroRNA Perturbations of Cellular Response to Pemetrexed Implicate Biological Networks and Enable Imputation of Response in Lung Adenocarcinoma (2018) (13)
- Discovery and Functional Assessment of Gene Variants in the Vascular Endothelial Growth Factor Pathway (2014) (13)
- Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humans (2016) (12)
- An ancestry‐based approach for detecting interactions (2018) (12)
- Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development (2017) (11)
- The Convergence of eQTL Mapping, Heritability Estimation and Polygenic Modeling: Emerging Spectrum of Risk Variation in Bipolar Disorder (2013) (11)
- Genome-wide discovery of genetic variants affecting tamoxifen sensitivity and their clinical and functional validation. (2013) (11)
- Distant regulatory effects of genetic variation in multiple human tissues (2016) (11)
- Multi-omic analysis elucidates the genetic basis of hydrocephalus (2021) (11)
- Genetic architecture of host proteins interacting with SARS-CoV-2 (2020) (11)
- Genetic Susceptibility to Type 2 Diabetes and Breast Cancer Risk in Women of European and African Ancestry (2012) (10)
- Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use. (2018) (10)
- Contextualizing genetic risk score for disease screening and rare variant discovery (2021) (9)
- Integrative Network-Based Analysis Reveals Gene Networks and Novel Drug Repositioning Candidates for Alzheimer Disease (2021) (9)
- Integrating Cell-Based and Clinical Genome-Wide Studies to Identify Genetic Variants Contributing to Treatment Failure in Neuroblastoma Patients (2014) (9)
- SNP-based heritability estimation: measurement noise, population stratification, and stability (2016) (9)
- Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma (2017) (9)
- Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping (2017) (9)
- SCAN: a systems biology approach to pharmacogenomic discovery. (2013) (9)
- PrediXcan: Trait Mapping Using Human Transcriptome Regulation (2015) (8)
- A pharmacogenetic study of aldehyde oxidase I in patients treated with XK469. (2014) (8)
- Functionally oriented analysis of cardiometabolic traits in a trans-ethnic sample (2019) (8)
- Rare and common genetic determinants of metabolic individuality and their effects on human health (2022) (8)
- A transcriptome-wide association study of Alzheimer’s disease using prediction models of relevant tissues identifies novel candidate susceptibility genes (2021) (7)
- Genome-Wide Association Study Identifies Pharmacogenomic Loci Linked with Specific Antihypertensive Drug Treatment and New-Onset Diabetes (2016) (7)
- Best practices for multi-ancestry, meta-analytic transcriptome-wide association studies: Lessons from the Global Biobank Meta-analysis Initiative (2021) (7)
- The Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations (2017) (7)
- Genetically regulated expression in late-onset Alzheimer’s disease implicates risk genes within known and novel loci (2021) (6)
- Alternative Splicing and Genome Evolution (2016) (6)
- Biomolecular Systems of Disease Buried Across Multiple GWAS Unveiled by Information Theory and Ontology (2010) (6)
- Deep Learning Enables Fast and Accurate Imputation of Gene Expression (2021) (5)
- A genome‐wide sib‐pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13 (2015) (5)
- Abstract 15518: Novel SNPs Associated with Warfarin Dose in a Large Multicenter Cohort of African Americans: Genome Wide Association Study and Replication Results (2011) (5)
- Hepatocyte gene expression and DNA methylation as ancestry-dependent mechanisms in African Americans (2019) (5)
- Translating pharmacogenomics discoveries into the clinic: an implementation framework (2013) (5)
- Multilayer modelling of the human transcriptome and biological mechanisms of complex diseases and traits (2021) (5)
- Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts (2023) (5)
- CD36 maintains the gastric mucosa and associates with gastric disease (2021) (5)
- Genome-wide association meta-analysis identifies novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation (2021) (5)
- The genetic architecture of human infectious diseases and pathogen-induced cellular phenotypes (2020) (4)
- Comprehensive Evaluation of the Contribution of X Chromosome Genes to Platinum Sensitivity (2011) (4)
- Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls (2018) (4)
- An integrative systems‐based analysis of substance use: eQTL‐informed gene‐based tests, gene networks, and biological mechanisms (2020) (4)
- On Using Local Ancestry to Characterize the Genetic Architecture of Human Phenotypes: Genetic Regulation of Gene Expression in Multiethnic or Admixed Populations as a Model (2018) (4)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (4)
- Genome-wide discovery of genetic variants affecting tamoxifen sensitivity and their clinical and functional validation. (2013) (4)
- A Local Genetic Correlation Analysis Provides Biological Insights Into the Shared Genetic Architecture of Psychiatric and Substance Use Phenotypes (2022) (4)
- Electronic health record phenotypes associated with genetically regulated expression of CFTR and application to cystic fibrosis (2020) (4)
- Integrated analysis of genetic variation and gene expression reveals novel variant for increased warfarin dose requirement in African Americans (2017) (4)
- A transcriptome‐wide association study identifies novel candidate susceptibility genes for prostate cancer risk (2021) (3)
- Uncovering the role of admixture in disease and drug response: Association of hepatocyte gene expression and DNA methylation with African Ancestry in African Americans (2018) (3)
- Genome-wide association studies in women of African ancestry identified 3 q 26 . 21 as a novel susceptibility locus for oestrogen receptor negative breast cancer (2017) (3)
- Transcriptome‐wide association analysis offers novel opportunities for clinical translation of genetic discoveries on mental disorders (2020) (3)
- Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation (2018) (3)
- Modeling mutational effects on biochemical phenotypes using convolutional neural networks: application to SARS-CoV-2 (2021) (3)
- A transcriptome-wide association study identifies novel blood-based gene biomarker candidates for Alzheimer's disease risk. (2021) (3)
- 128 Genome-wide Association Study Reveals Genetic Risk Factors for Trigeminal Neuralgia (2021) (3)
- Comparison of Breast CancerMolecular Features and Survival byAfrican and EuropeanAncestry in The Cancer GenomeAtlas (2017) (3)
- Genetic predictors of gene expression associated with risk of bipolar disorder (2016) (2)
- Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (2)
- A genome-wide integrative study of microRNAs in human liver (2013) (2)
- Genomic Variants of Cytarabine Sensitivity Associated with Treatment-Related Mortality in Pediatric AML: A Report from the Children's Oncology Group (2020) (2)
- Gene Expression Imputation with Generative Adversarial Imputation Nets (2020) (2)
- Publicly available GWAS summary statistics, harmonized and imputed to GTEx v8' variant reference (2020) (2)
- Genome-wide association study of cisplatin-induced peripheral neuropathy (CIPN) in testicular cancer survivors. (2016) (2)
- An analysis of genetically regulated gene expression and the role of co-expression networks across 16 psychiatric and substance use phenotypes (2022) (2)
- Metabolic coessentiality mapping identifies C12orf49 as a regulator of SREBP processing and cholesterol metabolism (2020) (2)
- Multi-tissue transcriptome analyses identify genetic mechanisms underlying neuropsychiatric traits (2019) (1)
- Abstract B11: Replication of previously identified breast cancer susceptibility loci in a breast cancer case-control study on women of African ancestry (2014) (1)
- An Ancestry Based Approach for Detecting Interactions (2016) (1)
- Neural-Network-Directed Genetic Programmer for Discovery of Governing Equations (2022) (1)
- The regulatory effect of miRNAs is a heritable genetic trait in humans (2012) (1)
- Variation in protein-coding sequence and the genetic basis of cisplatin-induced toxicities among testicular cancer survivors (TCS) in the Platinum Study. (2016) (1)
- Abstract 2761: Germline polymorphism discovered via a cell-based genome-wide approach predicts platinum response in ovarian and head and neck cancers (2010) (1)
- Genome-wide association study (GWAS) of cisplatin-related hearing loss in testicular cancer survivors (TCS) to reveal associated variant in Wolfram syndrome 1 (WFS1) gene. (2016) (1)
- Preclinical Development Genetic Variation That Predicts Platinum Sensitivity Reveals the Role of miR-193 b in Chemotherapeutic Susceptibility (2012) (1)
- Revisiting Some Useful Statistical Guidelines in Circulation Research in Response to a Changing Landscape (2021) (1)
- Towards mechanistic models of mutational effects: Deep Learning on Alzheimer’s Aβ peptide (2021) (1)
- Integrative genetic analysis identifies FLVCR1 as an essential component of choline transport in mammals (2022) (1)
- Novel diabetes gene discovery through comprehensive characterization and integrative analysis of longitudinal gene expression changes (2022) (1)
- Shared Genetic Control of Brain Activity During Sleep and Insulin Secretion: A Laboratory-Based Family Study (2017) (1)
- Alterations in White Matter and Total Brain Volumes Underlie Genetic Risk of Hydrocephalus (2020) (1)
- An Integrative Network-based Analysis Reveals Gene Networks, Biological Mechanisms, and Novel Drug Targets in Alzheimer’s Disease (2019) (1)
- A Coding Polymorphism in PFAS (The Gene Encoding Phosphoribosylformylglycinamidine Synthase) Is a Determinant of Prostacyclin Dose (2016) (0)
- Genome-Wide Association Study of Gilles de la Tourette Syndrome (IN10-1.002) (2012) (0)
- Integrative transcriptomic, evolutionary, and causal inference framework for region-level analysis: Application to COVID-19 (2022) (0)
- Abstract PL07-02: Whole genome approaches to identify pharmacogenomic markers of anticancer agents (2011) (0)
- The genetic architecture of neuropsychiatric traits: mechanism, polygenicity, and genome function (2016) (0)
- IMMerge: merging imputation data at scale (2022) (0)
- The regulatory genome constrains protein sequence evolution: implications for the search for disease-associated genes (2020) (0)
- A systematic analysis of genetically regulated differences in gene expression and the role of co-expression networks across 16 psychiatric disorders and substance use phenotypes (2021) (0)
- Integrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivity (2014) (0)
- Mechanistic Deep Learning Framework on Cell Traits Derived from Single-Cell Mass Cytometry Data (2022) (0)
- Hypergraph Factorisation for Multi-Tissue Gene Expression Imputation (2022) (0)
- Detecting context-dependent gene regulation (2021) (0)
- 243-LB: Characterization and Genetic Validation of Gene Expression Changes across Diabetes Development (2019) (0)
- Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. (2016) (0)
- 41 EXPLORING THE ROLE OF GENETIC REGULATION OF GENE EXPRESSION IN SUBSTANCE USE AND DEPENDENCE (2019) (0)
- Evidence of selection on splicing-associated loci in human populations and relevance to disease loci mapping (2017) (0)
- Small science: high stakes. (2012) (0)
- Abstract A46: Genomic ancestry is associated with risk group and survival in children with neuroblastoma (2011) (0)
- A Functional Analysis of Variants Associated with Therapy-Induced Second Malignancies After Hodgkin Lymphoma Identified by a Genome-Wide Scan (2010) (0)
- Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk (2019) (0)
- A Transcriptomic Atlas of the Human Brain Reveals Genetically Determined Aspects of Neuropsychiatric Health (2023) (0)
- Identifying genes that underlie Primary Open-Angle Glaucoma using genetically determined gene expression (2018) (0)
- MYELOID NEOPLASIA Comprehensive genetic analysis of cytarabine sensitivity in a cell-based model identi fi es polymorphisms associated with outcome in AML patients (2013) (0)
- Identification of a genetic variant associated with treatment outcome in ovarian cancer: the potential role of cholesterol metabolism as a determinant of response to chemotherapy (2012) (0)
- Abstract 2486: African ancestry is associated with high-risk disease and event-free survival in children with neuroblastoma (2012) (0)
- 1 An Ancestry Based Approach for Detecting Interactions 1 2 (2016) (0)
- Abstract 1643: MicroRNA processing genes and implications for complex traits (2012) (0)
- The Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations (2017) (0)
- Phenome-Wide Scan Identifies Hematologic Traits Associated with Genetically-Determined Expression of BCL-2 Family Genes (2022) (0)
- Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension (2019) (0)
- Optimizing Genetic Analyses of Serum Lipids in Longitudinal Data. (2020) (0)
- A transcriptome-wide association study of Alzheimer’s disease using prediction models of relevant tissues identifies novel candidate susceptibility genes (2021) (0)
- Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci (2015) (0)
- Analysis of Genetically Determined Gene Expression Suggests Role of Inflammatory Processes in Etiology of Exfoliation Syndrome (2020) (0)
- Expression Quantitative Trait Loci Analysis of Stable Warfarin Dose Identifies Novel Associations : Finding Signal within the Noise (2013) (0)
- Identification of a genetic variant associated with treatment outcome in ovarian cancer: the potential role of cholesterol metabolism as a determinant of response to chemotherapy (2012) (0)
- Evaluation of ICD codes and phecodes for the identification of pancreatic cancer in a large genomic database. (2020) (0)
- Genome-Wide Association Study of Gilles de la Tourette Syndrome (2012) (0)
- Multilayer modelling and analysis of the human transcriptome (2020) (0)
- Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies (2020) (0)
- Abstract 4731: Population specific microRNA expression and biological implications (2011) (0)
- Abstract 4582: Enrichment of colorectal cancer and inflammatory bowel disease risk variants in colon expression quantitative trait loci in African Americans (2015) (0)
- Presidential Trainee Awards (PT 001–024) Attended 4:30 pm – 5:00 pm Displayed March 19 – 21, 2014 (2014) (0)
- THE X CHROMOSOME IN NEURODEGENERATION (2022) (0)
- Translating pharmacogenomics discoveries into the clinic: an implementation framework (2013) (0)
- Identifying Genes that Underlie Exfoliation Syndrome using Genetically Determined Gene Expression (2019) (0)
- A unified framework for joint-tissue transcriptome-wide association and Mendelian randomization analysis (2020) (0)
- Integrative genetic analysis identifies FLVCR1 as a plasma-membrane choline transporter in mammals. (2023) (0)
- 6A MULTI-TISSUE NETWORK-BASED ANALYSIS OF RISK GENES FOR MAJOR DEPRESSION (2019) (0)
- M52 EMAGMA: A NOVEL METHOD TO INTEGRATE GENETIC AND TRANSCRIPTOMIC INFORMATION (2019) (0)
- Mapping Using Human Transcriptome Regulation (2015) (0)
- Genome-wide association study (GWAS) of chemotherapy-induced Raynaud's phenomenon (RP) to reveal shared pathways with cardiovascular disease (CVD). (2017) (0)
- Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer (2019) (0)
- Relationship of divergent ancestral genetic variation on chromosome 6p22 and racial disparities in survival in neuroblastoma. (2012) (0)
- NEUROIMAGING TRANSCRIPTOME WIDE ASSOCIATION STUDIES HIGHLIGHT CONGENITAL NEUROLOGIC DRIVERS OF VISUAL HALLUCINATIONS IN LRRK2 PARKINSON'S DISEASE (2022) (0)
- Author response: Bid maintains mitochondrial cristae structure and function and protects against cardiac disease in an integrative genomics study (2018) (0)
- Response to Knoppers et al. (2012) (0)
- Analysis of genetically determined gene expression suggests role of inflammatory processes in exfoliation syndrome (2020) (0)
- The impact of microRNA expression on cellular proliferation (2014) (0)
- SEX DIFFERENCES AT THE MOLECULAR LEVEL: LESSONS FROM THE HUMAN TRANSCRIPTOME (2019) (0)
- Abstract 1875: Identifying genetic variants contributing to cellular susceptibility to tamoxifen using a genome-wide cell-based model (2012) (0)
- Pharmacokinetic (PK) modeling of serum platinum to reveal extent of long-term exposure and associated comorbidities after cisplatin treatment. (2018) (0)
- Hepatocyte gene expression and DNA methylation as ancestry-dependent mechanisms in African Americans (2019) (0)
- Multilayer modelling of the human transcriptome and biological mechanisms of complex diseases and traits (2021) (0)
- Tissue‐specific genetically regulated expression in late‐onset Alzheimer’s disease implicates risk genes within known and 30 novel loci (2020) (0)
- Evaluation of ICD codes and phecodes for the identification of pancreatic cystic tumors in a large genomic database (2020) (0)
- M27 AN INTEGRATIVE NETWORK-BASED ANALYSIS REVEALS GENE NETWORKS, BIOLOGICAL MECHANISMS, AND DRUG TARGETS IN ALZHEIMER'S DISEASE (2019) (0)
- Gene and MicroRNA Perturbations of Cellular Response to Pemetrexed Implicate Biological Networks and Enable Imputation of Response in Lung Adenocarcinoma (2018) (0)
- Exploiting the GTEx resources to decipher the mechanisms at GWAS loci (2021) (0)
- Abstract 1881: Integration of cell line and Cancer and Leukemia Group B 40101 clinical trial genome-wide association analyses implicates multiple loci in paclitaxel-induced peripheral neuropathy (2012) (0)
- Abstract P1-05-11: Comprehensive comparison of breast cancer molecular portraits by African and European ancestry in the cancer genome atlas (2017) (0)
- Author Correction: Genetic architecture of host proteins involved in SARS-CoV-2 infection (2021) (0)
- Integrative transcriptomic, evolutionary, and causal inference framework for region-level analysis: Application to COVID-19 (2022) (0)
- Characterizing an inverse axis between orthogonal sources of genetic risk (2015) (0)
- An analysis of genetically regulated gene expression across multiple tissues implicates novel gene candidates in Alzheimer’s disease (2020) (0)
- Modeling mutational effects on biochemical phenotypes using convolutional neural networks: application to SARS-CoV-2 (2022) (0)
- Abstract 5452: Functional genome-wide approach identifies genes associated with chemotherapeutic susceptibility in individuals of African descent (2011) (0)
- SA77 MULTI-TISSUE TRANSCRIPTOME ANALYSIS REVEALS GENETIC MECHANISMS OF NEUROPSYCHIATRIC TRAITS (2019) (0)
- Genomics of alternative splicing: evolution, development and pathophysiology (2014) (0)
- Multi-omic analysis elucidates the genetic basis of hydrocephalus. (2021) (0)
- Databases and ontologies SCAN : SNP and copy number annotation (2009) (0)
- Abstract 3636: Systems biology approach links genetic, epigenetic, and transcriptomic features to tamoxifen sensitivity. (2013) (0)
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