Author details

Full Name

Kent D Taylor

Affiliation

ORCID

Career Start Year

1981

Papers

429

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37351609	Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts.	Ann Am Thorac Soc	2023
36379261	Infertility and treatments used have minimal effects on first-trimester placental DNA methylation and gene expression.	Fertil Steril	2023
37848499	Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA.		2023
37601969	Multiset correlation and factor analysis enables exploration of multi-omics data.	Cell Genom	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37662416	Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies.	bioRxiv	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
37582364	Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma.	Cell Metab	2023
37709864	Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.	Nat Genet	2023
38074621	The ICAM1 HFpEF risk variant and inflammatory biomarkers.		2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	2023
37770635	Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.	Nat Genet	2023
37609271	The Relationship of Duffy Gene Polymorphism, High Sensitivity C-Reactive Protein, and Long-term Outcomes.	medRxiv	2023
37216410	Canonical correlation analysis for multi-omics: Application to cross-cohort analysis.	PLoS Genet	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36716967	DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.	J Thromb Haemost	2023
36778386	Structural variation across 138,134 samples in the TOPMed consortium.	Res Sq	2023
37466697	Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential.	Cancer Epidemiol Biomarkers Prev	2023
36882149	Missense Genetic Variation of ICAM1 and Incident Heart Failure.	J Card Fail	2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
36635319	Secretory leukocyte protease inhibitor and risk of heart failure in the Multi-Ethnic Study of Atherosclerosis.	Sci Rep	2023
36698131	Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis.	Respir Res	2023
37005925	Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).	Metabolomics	2023
37126548	The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.	Sci Adv	2023
36747810	Structural variation across 138,134 samples in the TOPMed consortium.	bioRxiv	2023
36798214	Multivariate adaptive shrinkage improves cross-population transcriptome prediction for transcriptome-wide association studies in underrepresented populations.	bioRxiv	2023
36463326	Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis.	Int J Obes (Lond)	2023
37046083	Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.	Nature	2023
36791419	Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.	Diabetes	2023
37425716	Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects.	bioRxiv	2023
37292936	Genome-wide association identifies novel ROP risk loci in a multi-ethnic cohort.	Res Sq	2023
36723951	Association of Rare Protein-Truncating DNA Variants in APOB or PCSK9 With Low-density Lipoprotein Cholesterol Level and Risk of Coronary Heart Disease.	JAMA Cardiol	2023
37526028	Myocardial Fibrosis and Cardiomyopathy Risk: A Genetic Link in the MESA.	Circ Heart Fail	2023
37502922	Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA.	Res Sq	2023
37498674	Genetic modification of inflammation- and clonal hematopoiesis-associated cardiovascular risk.	J Clin Invest	2023
37546893	Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.	medRxiv	2023
35087136	Upregulated heme biosynthesis increases obstructive sleep apnea severity: a pathway-based Mendelian randomization study.	Sci Rep	2022
35658476	Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease.	Circ Res	2022
35654975	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.	Nat Genet	2022
35591888	A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data.	NAR Genom Bioinform	2022
35697868	Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function.	Nature Genetics	2022
35952728	Association of polygenic risk scores with incident atherosclerotic cardiovascular disease events among individuals with coronary artery calcium score of zero: The multi-ethnic study of atherosclerosis.	Prog Cardiovasc Dis	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
36154123	Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.	Circulation	2022
35501457	Lymphocyte activation gene-3-associated protein networks are associated with HDL-cholesterol and mortality in the Trans-omics for Precision Medicine program.	Commun Biol	2022
35998269	Nontargeted and Targeted Metabolomic Profiling Reveals Novel Metabolite Biomarkers of Incident Diabetes in African Americans.	Diabetes	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
36268164	Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022