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Author Details

Jennifer A Smith
2007
224
51
PMIDPaper TitleJournal TitlePublished Year
37956337Epigenetic Aging Is Associated With Measures of Midlife Muscle Volume and Attenuation in CARDIA Study.J Gerontol A Biol Sci Med Sci2024
36782352Polygenic Risk Scores for Alzheimer's Disease and General Cognitive Function Are Associated With Measures of Cognition in Older South Asians.J Gerontol A Biol Sci Med Sci2023
35943854Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI.Brain2023
36444934Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.Hum Mol Genet2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37934796Methods for mediation analysis with high-dimensional DNA methylation data: Possible choices and comparisons.2023
37662265WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.medRxiv2023
38014529Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.Circ Genom Precis Med2023
37579321Associations of Early-Life Adversity With Later-Life Epigenetic Aging Profiles in the Multi-Ethnic Study of Atherosclerosis.2023
37804200Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk.J Am Heart Assoc2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37968697Circulating metabolites may illustrate relationship of alcohol consumption with cardiovascular disease.BMC Med2023
37961350A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.bioRxiv2023
37770635Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.Nat Genet2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
36716967DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.J Thromb Haemost2023
36778386Structural variation across 138,134 samples in the TOPMed consortium.Res Sq2023
36824903Methods for Mediation Analysis with High-Dimensional DNA Methylation Data: Possible Choices and Comparison.2023
37398003Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.medRxiv2023
37268629Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.Nat Commun2023
36702996Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.Nat Genet2023
36479596Epigenome-wide association study of BMI in Black populations from InterGEN and GENOA.Obesity (Silver Spring)2023
37188560Cardiometabolic disease and obesity patterns differentially predict acute kidney injury after total joint replacement: a retrospective analysis.2023
36747810Structural variation across 138,134 samples in the TOPMed consortium.bioRxiv2023
37180517Epigenome-Wide Meta-Analysis Reveals Differential DNA Methylation Associated With Estimated Glomerular Filtration Rate Among African American Men With HIV.Kidney Int Rep2023
36927883Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function: A Meta-analysis of Community-Based Cohorts.Neurology2023
36465006Methods for large-scale single mediator hypothesis testing: Possible choices and comparisons.Genetic Epidemiology2023
37169753meQTL mapping in the GENOA study reveals genetic determinants of DNA methylation in African Americans.Nat Commun2023
37425772Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.medRxiv2023
36670106Deep phenotyping and genomic data from a nationally representative study on dementia in India.Sci Data2023
37487060Alcohol Use and Mortality among Older Couples in the United States: Evidence of Individual and Partner Effects.2023
35085396Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts.Diabetes Care2022
35974141Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning.Mol Psychiatry2022
36304436Prediction of telomere length and telomere attrition using a genetic risk score: The multi-ethnic study of atherosclerosis (MESA).2022
36240765The construction of cross-population polygenic risk scores using transfer learning.American Journal of Human Genetics2022
36240095Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke.Neurology2022
35652341Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension.Hypertension2022
36360196The Interplay of Epigenetic, Genetic, and Traditional Risk Factors on Blood Pressure: Findings from the Health and Retirement Study.Genes (Basel)2022
35511193Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate.Brain2022
36292585Differentially Methylated DNA Regions and Left Ventricular Hypertrophy in African Americans: A HyperGEN Study.Genes (Basel)2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
36285173Sex-specific and generational effects of alcohol and tobacco use on epigenetic age acceleration in the Michigan longitudinal study.2022
36220816Whole genome sequence analysis of blood lipid levels in >66,000 individuals.Nat Commun2022
35877617Assessing the added value of linking electronic health records to improve the prediction of self-reported COVID-19 testing and diagnosis.PLoS ONE2022
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
36268164Erratum: Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.HGG Adv2022
35927319Rare genetic variants explain missing heritability in smoking.Nat Hum Behav2022
35729114A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood.Nat Commun2022
36193739Rare Variants in Genes Encoding Subunits of the Epithelial Na<sup>+</sup> Channel Are Associated With Blood Pressure and Kidney Function.Hypertension2022
35665255DNA Methylation Mediates the Association Between Individual and Neighborhood Social Disadvantage and Cardiovascular Risk Factors.Front Cardiovasc Med2022
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