Author details

Full Name

Yongmei Liu

Affiliation

ORCID

Career Start Year

2001

Papers

288

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36758480	Modeling biological age using blood biomarkers and physical measurements in Chinese adults.		2023
35737188	The association between aging-related monocyte transcriptional networks and comorbidity burden: the Multi-Ethnic Study of Atherosclerosis (MESA).	GeroScience	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37868038	The functional impact of rare variation across the regulatory cascade.	Cell Genom	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
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
35822943	Targeted Genome Sequencing Identifies Multiple Rare Variants inÂ Caveolin-1 Associated with Obstructive Sleep Apnea.	Am J Respir Crit Care Med	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
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
35536696	Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis.	Am J Respir Crit Care Med	2022
36052690	Differences in Metabolomic Profiles Between Black and White Women and Risk of Coronary Heart Disease: an Observational Study of Women From Four US Cohorts.	Circ Res	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
35716666	Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits.	Am J Hum Genet	2022
34227900	The Socioeconomic Gradient in Epigenetic Ageing Clocks: Evidence from the Multi-Ethnic Study of Atherosclerosis and the Health and Retirement Study.	Epigenetics	2022
33818294	Epigenome-wide analysis of long-term air pollution exposure and DNA methylation in monocytes: results from the Multi-Ethnic Study of Atherosclerosis.	Epigenetics	2022
34814699	Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease.	Circulation	2022
34415308	Epigenome-wide association study of mitochondrial genome copy number.	Hum Mol Genet	2021
33859359	Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.	Mol Psychiatry	2021
34015820	Benchmarking association analyses of continuous exposures with RNA-seq in observational studies.	Brief Bioinform	2021
34050697	Clonal hematopoiesis associated with epigenetic aging and clinical outcomes.	Aging Cell	2021
33517400	Genome-wide association study of circulating interleukin 6 levels identifies novel loci.	Hum Mol Genet	2021
33937878	Transcriptome prediction performance across machine learning models and diverse ancestries.	Human Genetics and Genomics Advances	2021
33931109	Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci.	Genome Med	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34356065	Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.	Genes (Basel)	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34404112	Bayesian hierarchical models for high-dimensional mediation analysis with coordinated selection of correlated mediators.	Stat Med	2021
34732130	Role of DNA methylation on the association between physical activity and cardiovascular diseases: results from the longitudinal multi-ethnic study of atherosclerosis (MESA) cohort.	BMC Genomics	2021
34887595	Bayesian Sparse Mediation Analysis with Targeted Penalization of Natural Indirect Effects.	J R Stat Soc Ser C Appl Stat	2021
34887417	Meta-analyses identify DNA methylation associated with kidney function and damage.	Nat Commun	2021
34937574	Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes.	Clin Epigenetics	2021
34588469	Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function.	Sci Rep	2021
32888493	Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.	Cell	2020
31733066	Bayesian shrinkage estimation of high dimensional causal mediation effects in omics studies.	Biometrics	2020
32387875	Social regulation of inflammation related gene expression in the multi-ethnic study of atherosclerosis.	Psychoneuroendocrinology	2020
32386347	Comparison of Proteomic Assessment Methods in Multiple Cohort Studies.	Proteomics	2020
32693751	Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke.	Stroke	2020
32525743	Whole Blood DNA Methylation Signatures of Diet Are Associated With Cardiovascular Disease Risk Factors and All-Cause Mortality.	Circ Genom Precis Med	2020
32512511	Low oxygen saturation during sleep reduces CD1D and RAB20 expressions that are reversed by CPAP therapy.	EBioMedicine	2020
32888494	The Polygenic and Monogenic Basis of Blood Traits and Diseases.	Cell	2020
30936141	A Peripheral Blood DNA Methylation Signature of Hepatic Fat Reveals a Potential Causal Pathway for Nonalcoholic Fatty Liver Disease.	Diabetes	2019
31719535	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	Nat Commun	2019
31564435	Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.	Am J Hum Genet	2019
31761615	Association between sleep disordered breathing and epigenetic age acceleration: Evidence from the Multi-Ethnic Study of Atherosclerosis.	EBioMedicine	2019
29988085	Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium.	Mol Psychiatry	2019
30973896	Expression of socially sensitive genes: The multi-ethnic study of atherosclerosis.	PLoS One	2019
31221261	Effects of Calcium, Magnesium, and Potassium Concentrations on Ventricular Repolarization in Unselected Individuals.	J Am Coll Cardiol	2019
31127295	A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.	Hum Mol Genet	2019
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019