Author details

Full Name

Jerome I Rotter

Affiliation

ORCID

Career Start Year

1975

Papers

952

H Index

143

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37178073	Prevalence of Aortic Valve Calcium and the Long-Term Risk of Incident Severe Aortic Stenosis.	JACC Cardiovasc Imaging	2024
36721044	An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signaling.	Commun Biol	2023
35737188	The association between aging-related monocyte transcriptional networks and comorbidity burden: the Multi-Ethnic Study of Atherosclerosis (MESA).	GeroScience	2023
36444934	Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease.	Hum Mol Genet	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
37756531	Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk.	Diabetes Care	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37841955	A Type 1 Diabetes Polygenic Score Is Not Associated With Prevalent Type 2 Diabetes in Large Population Studies.	J Endocr Soc	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
37660929	Untargeted metabolomic analysis investigating links between unprocessed red meat intake and markers of inflammation.	Am J Clin Nutr	2023
38014529	Type 2 Diabetes Modifies the Association of CAD Genomic Risk Variants With Subclinical Atherosclerosis.	Circ Genom Precis Med	2023
37923804	Identification of circulating proteins associated with general cognitive function among middle-aged and older adults.	Commun Biol	2023
37905118	Determinants of mosaic chromosomal alteration fitness.	medRxiv	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
37992186	Increased plasma branched short-chain fatty acids and improved glucose homeostasis: The Microbiome and Insulin Longitudinal Evaluation Study (MILES).		2023
37904051	Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.	Nat Genet	2023
37804200	Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk.	J Am Heart Assoc	2023
37798236	Associations between avocado intake and measures of glucose and insulin homeostasis in Hispanic individuals with and without type 2 diabetes: Results from the Hispanic Community Health Study/Study of Latinos (HCHS/SOL).	Nutr Metab Cardiovasc Dis	2023
37790568	Heterogeneous effects on type 2 diabetes and cardiovascular outcomes of genetic variants and traits associated with fasting insulin.	Res Sq	2023
37709864	Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.	Nat Genet	2023
37562669	Associations between Metabolomic Biomarkers of Avocado Intake and Glycemia in the Multi-Ethnic Study of Atherosclerosis.	J Nutr	2023
37968697	Circulating metabolites may illustrate relationship of alcohol consumption with cardiovascular disease.	BMC Med	2023
37558891	Methods for estimating insulin resistance from untargeted metabolomics data.		2023
37777527	Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality.	Nat Commun	2023
37961394	Lac-Phe mediates the anti-obesity effect of metformin.	bioRxiv	2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37869564	Multivariate adaptive shrinkage improves cross-population transcriptome prediction and association studies in underrepresented populations.	HGG Adv	2023
37770635	Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.	Nat Genet	2023
37609230	A Multi-Ancestry Polygenic Risk Score for Coronary Heart Disease Based on an Ancestrally Diverse Genome-Wide Association Study and Population-Specific Optimization.	medRxiv	2023
37348055	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	Genetics	2023
37219552	Coronary Artery Calcium Score and Polygenic Risk Score for the Prediction of Coronary Heart Disease Events.	JAMA	2023
36716967	DNA methylation analysis is used to identify novel genetic loci associated with circulating fibrinogen levels in blood.	J Thromb Haemost	2023
36778406	Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.	bioRxiv	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
36893872	Most synonymous allelic variants in HIV tat are not silent.		2023
37398015	Circulating Metabolites May Illustrate Relationship of Alcohol Consumption with Cardiovascular Disease.	medRxiv	2023
37268629	Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.	Nat Commun	2023
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
37397985	Participant-derived cell line transcriptomic analyses and mouse studies reveal a role for ZNF335 in plasma cholesterol statin response.	bioRxiv	2023
37202153	Incidence of Interstitial Lung Abnormalities: The MESA Lung Study.		2023
36702996	Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing.	Nat Genet	2023
36698131	Distinct COPD subtypes in former smokers revealed by gene network perturbation analysis.	Respir Res	2023
37126548	The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.	Sci Adv	2023
37005925	Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).	Metabolomics	2023
37445732	Synonymous Variants of Uncertain Silence.	Int J Mol Sci	2023
37186683	Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease.	Circulation	2023
37052566	Association of Inflammation andÂ Lipoprotein(a) With Aortic ValveÂ Calcification.	JACC Cardiovasc Imaging	2023
36798214	Multivariate adaptive shrinkage improves cross-population transcriptome prediction for transcriptome-wide association studies in underrepresented populations.	bioRxiv	2023