Author details

Full Name

Ron Do

Affiliation

ORCID

Career Start Year

2006

Papers

108

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37162979	Quantitative prediction of right ventricular and size and function from the electrocardiogram.	medRxiv	2023
37605270	An atlas of associations between 14 micronutrients and 22 cancer outcomes: Mendelian randomization analyses.		2023
37582372	Prioritization of therapeutic targets for dyslipidemia using integrative multi-omics and multi-trait analysis.		2023
37014069	Causal effect of adiposity on the risk of 19 gastrointestinal diseases: a Mendelian randomization study.		2023
36563696	Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts.	Lancet	2023
37308786	Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program.	Nat Genet	2023
37248299	Polygenic prediction of preeclampsia and gestational hypertension.	Nat Med	2023
37169741	A machine learning model identifies patients in need of autoimmune disease testing using electronic health records.	Nat Commun	2023
37042260	Machine Learning Identifies Plasma Metabolites Associated With Heart Failure in Underrepresented Populations With the <i>TTR</i> V122I Variant.	J Am Heart Assoc	2023
37227948	Cholesterol Contributes to Risk, Severity, and Machine Learning-Driven Diagnosis of Lyme Disease.		2023
36988189	Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits.	Elife	2023
36786746	Genetic Associations Between Smoking- and Glaucoma-Related Traits.	Transl Vis Sci Technol	2023
37546893	Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus.	medRxiv	2023
35331410	Coronary Risk Estimation Based on Clinical Data in Electronic Health Records.	J Am Coll Cardiol	2022
36376295	Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure.	Nat Commun	2022
35526571	Genome-first recall of healthy individuals by polygenic risk score reveals differences in coronary artery calcium.	Am Heart J	2022
35385311	Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.	Sci Adv	2022
35579644	Penetrance of Deleterious Clinical Variants-Reply.	JAMA	2022
36154123	Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.	Circulation	2022
35948364	Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney Disease.	Clin J Am Soc Nephrol	2022
35612836	Statin Use in Relation to Intraocular Pressure, Glaucoma, and Ocular Coherence Tomography Parameters in the UK Biobank.	Investigative Ophthalmology and Visual Science	2022
35987940	A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank.	Commun Biol	2022
35915156	Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.	Nat Med	2022
36712313	Cannabis Use and CKD: Epidemiological Associations and Mendelian Randomization.	Kidney Med	2022
36788979	Short-term prediction of coronary artery disease using serum metabolomic patterns.	Am Heart J Plus	2022
35278270	Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failure.	European Journal of Heart Failure	2022
34727735	Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project.	Stroke	2022
34951958	Overcoming constraints on the detection of recessive selection in human genes from population frequency data.	Am J Hum Genet	2022
35076666	Population-Based Penetrance of Deleterious Clinical Variants.	JAMA	2022
34713709	Derivation and Validation of Genome-Wide Polygenic Score for Ischemic Heart Failure.	J Am Heart Assoc	2021
33493176	Probing the aggregated effects of purifying selection per individual on 1,380 medical phenotypes in the UK Biobank.	PLoS Genet	2021
33704450	Genome-wide polygenic risk score for retinopathy of type 2 diabetes.	Hum Mol Genet	2021
33483510	An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease.	Nat Commun	2021
34005834	Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries.	Hum Mutat	2021
33846329	Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices.	Nat Commun	2021
34089483	Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19.	Infection	2021
33499903	Exploiting the GTEx resources to decipher the mechanisms at GWAS loci.	Genome Biol	2021
32989268	A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations.	Genet Med	2021
33284643	Transethnic Transferability of a Genome-Wide Polygenic Score for Coronary Artery Disease.	Circ Genom Precis Med	2021
33333105	Intraocular Pressure, Glaucoma, and Dietary Caffeine Consumption: A Gene-Diet Interaction Study from the UK Biobank.	Ophthalmology	2021
33333072	Prediction of Incident Heart Failure in TTR Val122Ile Carriers One Year Ahead of Diagnosis in a Multiethnic Biobank.	Am J Cardiol	2021
33432171	Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations.	Nat Med	2021
32498804	Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease.	J Am Coll Cardiol	2020
32226016	Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.	PLoS Genet	2020
32540406	Derivation and validation of genome-wide polygenic score for urinary tract stone diagnosis.	Kidney Int	2020
32917698	Tissue-specific genetic features inform prediction of drug side effects in clinical trials.	Sci Adv	2020
32511564	Acute Kidney Injury in Hospitalized Patients with COVID-19.	medRxiv	2020
31154530	Estimation of metabolic syndrome heritability in three large populations including full pedigree and genomic information.	Hum Genet	2019
31821430	Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry.	JAMA	2019
31653226	HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases.	Genome Biol	2019