Author details

Full Name

Zhe Wang

Affiliation

ORCID

Career Start Year

2016

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37415875	Physical Activity, Sedentary Behavior, and Type 2 Diabetes: Mendelian Randomization Analysis.	J Endocr Soc	2023
38036650	Distilling causality between physical activity traits and obesity via Mendelian randomization.	Commun Med (Lond)	2023
37961350	A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies.	bioRxiv	2023
37802043	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.	Am J Hum Genet	2023
37662265	WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.	medRxiv	2023
37658231	Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.	Hum Genet	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
37425772	Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.	medRxiv	2023
36220816	Whole genome sequence analysis of blood lipid levels in >66,000 individuals.	Nat Commun	2022
36088317	Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.	BMC Med Genomics	2022
35927319	Rare genetic variants explain missing heritability in smoking.	Nat Hum Behav	2022
35729114	A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood.	Nat Commun	2022
35592775	The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.	Front Endocrinol (Lausanne)	2022
34553764	Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.	Hum Mol Genet	2022
33887194	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
33619380	Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities.	Nature Metabolism	2021
34582791	Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.	Am J Hum Genet	2021
34517814	Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.	BMC Genomics	2021
34107879	Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.	BMC Genomics	2021
34087167	Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.	Am J Hum Genet	2021
32510982	Role of Rare and Low-Frequency Variants in Gene-Alcohol Interactions on Plasma Lipid Levels.	Circ Genom Precis Med	2020
31339783	Response Letter Regarding Article, "Metabolomic Pattern Predicts Incident Coronary Heart Disease".	Arteriosclerosis, Thrombosis, and Vascular Biology	2019
31092011	Metabolomic Pattern Predicts Incident Coronary Heart Disease.	Arterioscler Thromb Vasc Biol	2019
31719535	Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration.	Nat Commun	2019
28941034	Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent.	Mol Nutr Food Res	2018
28352986	Genetic associations with lipoprotein subfraction measures differ by ethnicity in the multi-ethnic study of atherosclerosis (MESA).	Hum Genet	2017
27884205	Whole genome sequence analysis of serum amino acid levels.	Genome Biol	2016