Author details

Full Name

Jie Yao

Affiliation

ORCID

Career Start Year

2008

Papers

123

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37546893	Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.	medRxiv	2023
38028628	Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.	Front Genet	2023
37923804	Identification of circulating proteins associated with general cognitive function among middle-aged and older adults.	Commun Biol	2023
37582364	Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma.	Cell Metab	2023
37648373	Ancestral diversity in lipoprotein(a) studies helps address evidence gaps.	Open Heart	2023
37804200	Association Between Whole Blood-Derived Mitochondrial DNA Copy Number, Low-Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk.	J Am Heart Assoc	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
37398003	Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.	medRxiv	2023
36945682	Tracking Epidemiological Characteristics and Risk Factors of Multi-Drug Resistant Bacteria in Intensive Care Units.		2023
36791419	Investigating Gene-Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits.	Diabetes	2023
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
35085396	Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts.	Diabetes Care	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
35594314	Resting heart rate and incident atrial fibrillation: A stratified Mendelian randomization in the AFGen consortium.	PLoS One	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
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
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
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
35399580	Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium.	HGG Adv	2022
36455876	A circadian rhythm-related biomarker for predicting prognosis and immunotherapy efficacy in lung adenocarcinoma.	Aging	2022
34296378	CircTMC5 promotes gastric cancer progression and metastasis by targeting miR-361-3p/RABL6.	Gastric Cancer	2022
35309906	Prognostic Value of Genomic Instability of mA-Related lncRNAs in Lung Adenocarcinoma.	Frontiers in Cell and Developmental Biology	2022
34789503	Obesity Partially Mediates the Diabetogenic Effect of Lowering LDL Cholesterol.	Diabetes Care	2022
35234888	Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study.	Hum Mol Genet	2022
35030478	Development of a prognostic gene signature for hepatocellular carcinoma.	Cancer Treatment and Research Communications	2022
34879218	Determinants of Incident Atherosclerotic Cardiovascular Disease Events Among Those With Absent Coronary Artery Calcium: Multi-Ethnic Study of Atherosclerosis.	Circulation	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
34241534	Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes.	Circ Genom Precis Med	2021
33859359	Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure.	Mol Psychiatry	2021
34165540	Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL.	Hum Mol Genet	2021
33876560	FGL1 as a modulator of plasma D-dimer levels: Exome-wide marker analysis of plasma tPA, PAI-1, and D-dimer.	J Thromb Haemost	2021
34257727	hsa_circ_0060975 is highly expressed and predicts a poor prognosis in gastric cancer.	Oncology Letters	2021
33718426	High Expression of Tumor Abnormal Protein Preoperatively Predicts Poor Prognosis of Patients With Esophageal Squamous Cell Carcinoma.	Frontiers in Surgery	2021
33115273	Genome-Wide Association Study Highlights as a Novel Locus for Lipoprotein(a) Levels-Brief Report.	Arteriosclerosis, Thrombosis, and Vascular Biology	2021
33381925	Genome-wide association study identifying novel variant for fasting insulin and allelic heterogeneity in known glycemic loci in Chilean adolescents: The Santiago Longitudinal Study.	Pediatr Obes	2021
35036986	Association of mitochondrial DNA copy number with cardiometabolic diseases.	Cell Genom	2021
34732054	Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation.	Circ Genom Precis Med	2021
34937574	Associations between DNA methylation and BMI vary by metabolic health status: a potential link to disparate cardiovascular outcomes.	Clin Epigenetics	2021
35117615	Mortality from heart disease following radiotherapy in esophageal carcinoma: a retrospective cohort study in US SEER cancer registry.	Translational Cancer Research	2020
32068817	Predictive Accuracy of a Polygenic Risk Score Compared With a Clinical Risk Score for Incident Coronary Heart Disease.	JAMA	2020
32214851	Increased Expression of TAP Is Predictive of Poor Prognosis in Patients with Non-Small Cell Lung Cancer.	Cancer Management and Research	2020
32441789	Predictors of mortality in hospitalized COVID-19 patients: A systematic review and meta-analysis.	J Med Virol	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
32382064	Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy.	Nat Commun	2020
32822252	Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation.	Circ Genom Precis Med	2020
32701509	X chromosome dosage of histone demethylase KDM5C determines sex differences in adiposity.	J Clin Invest	2020
33186364	Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.	PLoS One	2020