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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architectureTrait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWASGenome-wide association study of Tourette's syndromeFunctional genetic screen of human diversity reveals that a methionine salvage enzyme regulates inflammatory cell deathThe impact of human copy number variation on gene expressionLinking the genetic architecture of cytosine modifications with human complex traitsObesity-associated variants within FTO form long-range functional connections with IRX3Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait lociExprtarget: an integrative approach to predicting human microRNA targetsIdentification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissueMixed effects modeling of proliferation rates in cell-based models: consequence for pharmacogenomics and cancerA gene-based association method for mapping traits using reference transcriptome dataNetwork models of genome-wide association studies uncover the topological centrality of protein interactions in complex diseasesGenome-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 signalsA 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.The genetic architecture of type 2 diabetesMeta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.Integrative genomics: quantifying significance of phenotype-genotype relationships from multiple sources of high-throughput dataAn eQTL-based method identifies CTTN and ZMAT3 as pemetrexed susceptibility markers.Ethnicity-specific pharmacogenetics: the case of warfarin in African AmericansThe Relation Between Inflation in Type-I and Type-II Error Rate and Population Divergence in Genome-Wide Association Analysis of Multi-Ethnic Populations.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 carcinogenesisIntegrating cell-based and clinical genome-wide studies to identify genetic variants contributing to treatment failure in neuroblastoma patientsPoly-omic prediction of complex traits: OmicKriging.A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci.Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record.Genetic association signal near NTN4 in Tourette syndromeGenetic factors affecting gene transcription and catalytic activity of UDP-glucuronosyltransferases in human liverOn sharing quantitative trait GWAS results in an era of multiple-omics data and the limits of genomic privacy.Genetic variant in folate homeostasis is associated with lower warfarin dose in African Americans.Campylobacter jejuni type VI secretion system: roles in adaptation to deoxycholic acid, host cell adherence, invasion, and in vivo colonizationGenome-wide association study of obsessive-compulsive disorder.Variants affecting exon skipping contribute to complex traits.Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait.A genome-wide integrative study of microRNAs in human liver.Comprehensive evaluation of the contribution of X chromosome genes to platinum sensitivityIdentification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of PazopanibIntegrative analyses of genetic variation, epigenetic regulation, and the transcriptome to elucidate the biology of platinum sensitivityEnrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait lociPlatinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients
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Q21090200-FABB5127-9445-4FBE-A9D1-1AB7A1CE12CCQ21563317-993EBACE-2A6B-45DC-A3EA-D089C5817F99Q23936582-A16BF6E1-8AC4-476B-B9A7-2B3ABF420FD1Q24294349-2880E3F1-9E20-461A-B406-6644DB4470D6Q27027474-42F86624-2DAB-4F32-917A-53A598CB2BA6Q27301341-FE28CFC0-B6C2-4F41-8FF1-F83487524C53Q28236283-CA206E0B-D5F6-488F-94D7-8BEB58F32CF7Q28266762-2AF2639F-E0D8-42F7-941F-98574C57E701Q28475891-6F826CFD-01A7-484B-908C-AB3AA4BDB7A8Q28478309-A4D99116-EF6B-4CC6-BDBB-F14F6B646E6FQ28480587-1432324C-EDCB-4E4A-9D40-C57F0D9FE49CQ28608356-D81A78CF-32F8-4082-8E9C-A4D103CA6741Q28674016-38226450-1DE9-4DC9-98BB-1700433F8E52Q28943499-F3ACC76E-FF38-41F1-BEFB-ABD05D109E44Q29417036-F59646BD-E9E6-4779-9411-F62469199615Q29583824-ECE7A8D4-6906-4CD6-8339-F83A44440489Q30277730-453D5D41-B606-4B0C-B2A9-3303B435F974Q30540182-642CA483-3852-4162-BF44-659DB4DB62C4Q33398764-9CABCAFE-65A4-4380-9BE8-FBED0FDFBC82Q33591111-1ED814DE-61AC-41B5-85F0-39ADEA8E7896Q33600077-363C7011-A04B-4631-9388-2657DB460384Q33621825-B9ABE201-665C-42FF-9A36-C5BBFBE8ED80Q33645629-D47D2E70-4FF0-44F7-A9AF-20B07B8962E3Q33812687-99FAA99C-401A-4427-A8EF-AE7F12112F5CQ33815392-AA027BF6-197F-40DE-A3D2-F6B626480504Q33883530-0669A5C7-C31A-48C7-965D-610042797C59Q34076218-87D067B2-D24A-47CB-A1C6-C4C2920C0F65Q34211851-2FE18EE1-549B-4EA2-9F71-D2F7FD6B9E6DQ34215240-0D9770CC-0BFF-43DC-9B2F-877D7F780CEDQ34284362-8279A442-92D3-430C-86CD-1B81483A6DC2Q34404851-939132A3-4A7D-4939-9C29-7B2D8276A4B5Q34445418-B4AEBF9C-B990-4998-8B48-CF7888FA5572Q34469030-CCB20862-4FD5-40E6-A010-0B72DEEED06CQ34478063-E644701B-A763-42BF-B798-D95FF4533CDFQ34768681-555D0EF0-8912-4811-9EF5-89398EB489F5Q34816784-F7EDC1CD-8186-409A-B044-271557DAA2C7Q35068932-7159FF74-C6D6-40A7-B9D5-EEEA9C9FEFE5Q35150207-BA824E73-BD20-41C5-9EAF-E949A80D9AF9Q35153816-84095843-7B41-4E20-977A-EC702DBBB5F9Q35177861-C933CB66-05D9-4139-817E-9422FAEFB9ED
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description
expert in human genetics, comp ...... cal genetics, pharmacogenomics
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wetenschapper
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name
Eric R Gamazon
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Eric R Gamazon
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Eric R. Gamazon
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type
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Eric R Gamazon
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Eric R Gamazon
@nl
Eric R. Gamazon
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E Gamazon
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ER Gamazon
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Eric Gamazon
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Gamazon ER
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Eric R Gamazon
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Eric R Gamazon
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Eric R. Gamazon
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P108
P1053
I-6873-2018
P1153
35309924700
P21
P2798
P31
P3829
P496
0000-0003-4204-8734