Ron Do

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

25.0Author DataRank

Indexed papers

14in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 14 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Papers

Driven by 102 papers — median percentile 58. Top paper: “Analysis of protein-coding genetic variation in 60,706 humans”.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

A High-Coverage Genome Sequence from an Archaic Denisovan Individual

Science(2012)10.1126/science.1224344

Top 2%

7.8DataRank

Top 2%2137 citations

Martin Kircher, Marie-Theres Gansauge, Alexandra P. Lewis, Fernando Racimo, Swapan Mallick +31 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

Nature Medicine(2022)10.1038/s41591-022-01891-3

N/A

6.8DataRank · unranked

363 citations

Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma +78 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Genome-wide association study of thoracic aortic aneurysm and dissection in the Million Veteran Program

Nature Genetics(2023)10.1038/s41588-023-01420-z

N/A

1.4DataRank · unranked

63 citations

Poornima Devineni, Anoop K. Sendamarai, Anthony R. Angueira, Sarah E. Graham, Ying H. Shen +32 more

Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

Stroke(2021)10.1161/strokeaha.120.031792

Top 16%

1.3DataRank

Top 16%38 citations

Jeffrey W. Haessler, Regina Manansala, Kerri L. Wiggins, Arden Moscati, Alexa Beiser +34 more

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Proceedings of the National Academy of Sciences(2017)10.1073/pnas.1705859115

N/A

1.2DataRank · unranked

36 citations

Alisa Manning, Marcio Almeida, Matthew Zawistowski, Katharina Domschke, Tanya M. Teslovich +82 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Nature Communications(2021)10.1038/s41467-021-22339-1

N/A

1.1DataRank · unranked

51 citations

Akhil Pampana, Sarah E. Graham, Sanni Ruotsalainen, James A. Perry, Paul S. de Vries +95 more

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 more

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans

Nature Genetics(2015)10.1038/ng.3186

N/A

0.825DataRank · unranked

244 citations

Daniel Balick, Alexandra P. Lewis, Ankit Malhotra, Shamil R. Sunyaev, David Reich +2 more

Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

Circulation(2022)10.1161/circulationaha.122.059675

N/A

0.701DataRank · unranked

106 citations

Derek Klarin, Jennifer A. Brody, Ming‐Huei Chen, Michael G. Levin, Daniel I. Chasman +82 more

HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases

Genome Biology(2019)10.1186/s13059-019-1844-7

N/A

0.665DataRank · unranked

83 citations

Marie Verbanck, Ron Do, Daniel M. Jordan

A large-scale multi-ethnic genome-wide association study of coronary artery disease

Research Square(2021)10.21203/rs.3.rs-275591/v1

N/A

0.561DataRank · unranked

11 citations

Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni +77 more

Statin Use in Relation to Intraocular Pressure, Glaucoma, and Ocular Coherence Tomography Parameters in the UK Biobank

Investigative Ophthalmology & Visual Science(2022)10.1167/iovs.63.5.31

Top 36%

0.543DataRank

Top 36%13 citations

Marianne T. Neary, Hugues Aschard, Mathew M. Palakkamanil, Ron Do, Janey L. Wiggs +4 more

Genome-first evaluation with exome sequence and clinical data uncovers underdiagnosed genetic disorders in a large healthcare system

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101518

Top 38%

0.505DataRank

Top 38%11 citations

Áine Duffy, Joshua K. Park, Ha My T. Vy, Louis R. Pasquale, Girish N. Nadkarni +3 more

Genome-Wide Polygenic Risk Score for CKD in Individuals with APOL1 High-Risk Genotypes

Clinical Journal of the American Society of Nephrology(2023)10.2215/cjn.0000000000000379

Top 39%

0.490DataRank

Top 39%10 citations

Steven G. Coca, Ashwin Sawant, Ankit Sakhuja, Orlando M. Gutiérrez, Richard Cooper +5 more

Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

Cell Genomics(2023)10.1016/j.xgen.2023.100468

N/A

0.457DataRank · unranked

20 citations

Amy R. Bentley, Charles E. Breeze, François Aguet, Xiaoguang Xu, Girish N. Nadkarni +69 more

Using large-scale population-based data to improve disease risk assessment of clinical variants

Nature Genetics(2025)10.1038/s41588-025-02212-3

Top 42%

0.442DataRank

Top 42%10 citations

Kuan-lin Huang, Julie M. Eggington, Wendy K. Chung, Daniel M. Jordan, Ron Do +1 more

Exome sequence analysis identifies rare coding variants associated with a machine learning-based marker for coronary artery disease

Nature Genetics(2024)10.1038/s41588-024-01791-x

N/A

0.434DataRank · unranked

17 citations

Iain S. Forrest, Ghislain Rocheleau, Ha My T. Vy, Carla Márquez‐Luna, Áine Duffy +9 more

Cholesterol Contributes to Risk, Severity, and Machine Learning-Driven Diagnosis of Lyme Disease

Clinical Infectious Diseases(2023)10.1093/cid/ciad307

N/A

0.373DataRank · unranked

11 citations

Anya J. O’Neal, Joao H. F. Pedra, Ron Do, Iain S. Forrest

Genome-wide Association Study of Thoracic Aortic Aneurysm and Dissection in the Million Veteran Program

Research Square(2022)10.21203/rs.3.rs-1507463/v1

N/A

0.345DataRank · unranked

9 citations

Poornima Devineni, Anoop K. Sendamarai, Anthony R. Angueira, Sarah E. Graham, Ying H. Shen +29 more

Cannabis Use and CKD: Epidemiological Associations and Mendelian Randomization

Kidney Medicine(2022)10.1016/j.xkme.2022.100582

N/A

0.330DataRank · unranked

8 citations

Ishan Paranjpe, Madhumitha Rajagopal, Samir Kamat, Ross O’Hagan, Faris F. Gulamali +7 more

Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrum

medRxiv(2023)10.1101/2023.07.16.23292724

N/A

0.292DataRank · unranked

6 citations

Kathleen M. Cardone, David Y. Zhang, Noah L. Tsao, Sarah Abramowitz, Pranav Sharma +30 more

Genome-Wide Epistatic Interaction between DEF1B and APOL1 High-Risk Genotypes for Chronic Kidney Disease

Clinical Journal of the American Society of Nephrology(2022)10.2215/cjn.03610322

N/A

0.292DataRank · unranked

6 citations

Bridget M. Lin, Faris F. Gulamali, Charles Kooperberg, Mariaelisa Graff, Jenny Wong +18 more

Machine learning–based penetrance of genetic variants

Science(2025)10.1126/science.adm7066

N/A

0.292DataRank · unranked

6 citations

Ha My T. Vy, Ghislain Rocheleau, Daniel M. Jordan, Ben Omega Petrazzini, Girish N. Nadkarni +6 more

Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People With Type 2 Diabetes

Diabetes Care(2024)10.2337/dc23-2274

Top 56%

0.289DataRank

Top 56%5 citations

Ryan B. Hernandez-Cancela, Daniel DiCorpo, David E. Condon, Jordi Merino, Peitao Wu +62 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

The Association of Urinary Sodium Excretion with Glaucoma and Related Traits in a Large United Kingdom Population

Ophthalmology Glaucoma(2024)10.1016/j.ogla.2024.04.010

N/A

0.269DataRank · unranked

5 citations

Mahantesh I. Biradar, Robert Luben, Neeraj Dhaun, Siegfried K. Wagner, Alasdair Warwick +79 more

A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

Communications Biology(2022)10.1038/s42003-022-03820-z

Top 60%

0.246DataRank

Top 60%3 citations

Iain S. Forrest, Áine Duffy, Shantanu Bafna, Amanda Dobbyn, Marie Verbanck +4 more

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

medRxiv(2023)10.1101/2023.08.14.23294063

N/A

0.165DataRank · unranked

2 citations

Rainer Malik, Omar El Bounkari, Natalie R. Hasbani, Jiang Li, Jennifer E. Huffman +60 more

Quantitative prediction of right ventricular and size and function from the electrocardiogram

medRxiv(2023)10.1101/2023.04.25.23289130

N/A

0.165DataRank · unranked

2 citations

Akhil Vaid, Ha My T. Vy, Liam R. Butler, Joshua Lampert, Robert H. Pass +8 more

A tissue-level phenome-wide network map of colocalized genes and phenotypes in the UK Biobank

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.30.441974

Top 72%

0.111DataRank

Top 72%1 citations

Iain S. Forrest, Áine Duffy, Shantanu Bafna, Amanda Dobbyn, Marie Verbanck +4 more

Time-to-Event Genome-Wide Association Study for Incident Cardiovascular Disease in People with Type 2 Diabetes Mellitus

medRxiv(2023)10.1101/2023.07.25.23293180

N/A

0.106DataRank · unranked

1 citations

Ryan B. Hernandez-Cancela, Daniel DiCorpo, David E. Condon, Jordi Merino, Peitao Wu +62 more

Statin use in relation to intraocular pressure, glaucoma, and ocular coherence tomography parameters in the UK Biobank

medRxiv(2021)10.1101/2021.12.12.21267685

Top 78%

0.104DataRank

Top 78%1 citations

Marianne T. Neary, Hugues Aschard, Mathew M. Palakkamanil, Ron Do, Janey L. Wiggs +4 more

Prediction of Incident Heart Failure in TTR Val122Ile Carriers One Year Ahead of Diagnosis in a Multiethnic Biobank

The American Journal of Cardiology(2020)10.1016/j.amjcard.2020.12.015

N/A

0DataRank · unranked

3 citations

Ben Omega Petrazzini, Jagat Narula, Girish N. Nadkarni, Ron Do, Kumardeep Chaudhary

The Association of Alcohol Consumption with Glaucoma and Related Traits

Ophthalmology Glaucoma(2022)10.1016/j.ogla.2022.11.008

N/A

0DataRank · unranked

43 citations

Robert Luben, Alasdair Warwick, Kian Madjedi, Praveen J. Patel, Mahantesh I. Biradar +77 more

Coronary Risk Estimation Based on Clinical Data in Electronic Health Records

Journal of the American College of Cardiology(2022)10.1016/j.jacc.2022.01.021

N/A

0DataRank · unranked

42 citations

Kumardeep Chaudhary, Carla Márquez‐Luna, Iain S. Forrest, Ghislain Rocheleau, Judy H. Cho +4 more

The Association between Serum Lipids and Intraocular Pressure in 2 Large United Kingdom Cohorts

Ophthalmology(2022)10.1016/j.ophtha.2022.04.023

N/A

0DataRank · unranked

40 citations

Kelsey V. Stuart, Sharon Chua, Robert Luben, Alasdair Warwick, Louis R. Pasquale +83 more

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

PLoS Genetics(2020)10.1371/journal.pgen.1008684

N/A

0DataRank · unranked

33 citations

Mariaelisa Graff, Jeffrey Haessler, Steven Buyske, Stephanie A. Bien, Ran Tao +49 more

Genome-first recall of healthy individuals by polygenic risk score reveals differences in coronary artery calcium

American Heart Journal(2022)10.1016/j.ahj.2022.04.006

N/A

0DataRank · unranked

3 citations

Lili Chan, Kumardeep Chaudhary, Aparna Saha, Huei Hsun Wen, Cristina Liriano Cepin +7 more

Penetrance of Deleterious Clinical Variants—Reply

JAMA(2022)10.1001/jama.2022.4634

N/A

0DataRank · unranked

1 citations

Girish N. Nadkarni, Ron Do, Iain S. Forrest

Genome-wide meta-analysis identifies novel maternal risk variants and enables polygenic prediction of preeclampsia and gestational hypertension

medRxiv(2022)10.1101/2022.11.30.22282929

N/A

0DataRank · unranked

3 citations

Buu Truong, Raiyan R. Khan, Brenda Xiao, Laxmi Bhatta, Ha My T. Vy +27 more

Phenome-wide Mendelian randomization study of plasma triglycerides and 2,600 disease traits

medRxiv(2022)10.1101/2022.07.21.22277900

N/A

0DataRank · unranked

1 citations

Shantanu Bafna, Iain S. Forrest, Áine Duffy, Carla Márquez‐Luna, Ben Omega Petrazzini +8 more

CD36 homologs determine microbial resistance to the Lyme disease spirochete

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.09.479763

N/A

0DataRank · unranked

0 citations

Nisha Singh, Iain S. Forrest, Agustín Rolandelli, Xiaowei Wang, Dana K. Shaw +17 more

Short-term prediction of coronary artery disease using serum metabolomic patterns

土木技術(2022)10.1016/j.ahjo.2022.100232

N/A

0DataRank · unranked

0 citations

Akhil Vaid, Joshua K. Park, Carla Márquez‐Luna, Ha My T. Vy, Aparna Saha +8 more

Polygenic prediction of preeclampsia and gestational hypertension

Nature Medicine(2023)10.1038/s41591-023-02374-9

N/A

0DataRank · unranked

127 citations

Buu Truong, Raiyan R. Khan, Brenda Xiao, Laxmi Bhatta, Ha My T. Vy +27 more

A genotype-first approach to exploring Mendelian cardiovascular traits with clear external manifestations

Genetics in Medicine(2020)10.1038/s41436-020-00973-2

N/A

0DataRank · unranked

42 citations

Nihir Patel, Madeline Lui, Arden Moscati, Ron Do, Douglas R. Stewart +6 more

Severe hypertriglyceridemia: Existing and emerging therapies

Pharmacology & Therapeutics(2023)10.1016/j.pharmthera.2023.108544

N/A

0DataRank · unranked

38 citations

Ron Do, Robert S. Rosenson, Waqas Malick

Clinical Trial Design for Triglyceride-Rich Lipoprotein-Lowering Therapies

Journal of the American College of Cardiology(2023)10.1016/j.jacc.2023.02.034

N/A

0DataRank · unranked

35 citations

Ori Waksman, Ron Do, Wolfgang Köenig, Aruna D. Pradhan, Erik S.G. Stroes +2 more

Causal effect of adiposity on the risk of 19 gastrointestinal diseases: a Mendelian randomization study

Obesity(2023)10.1002/oby.23722

N/A

0DataRank · unranked

34 citations

Minku Song, Soyeon Kim, Beomsu Kim, Wonseok Kang, Jong Yeob Kim +6 more

A machine learning model identifies patients in need of autoimmune disease testing using electronic health records

Nature Communications(2023)10.1038/s41467-023-37996-7

N/A

0DataRank · unranked

34 citations

Ben Omega Petrazzini, Áine Duffy, Joshua K. Park, Anya J. O’Neal, Daniel M. Jordan +6 more

Prioritization of therapeutic targets for dyslipidemia using integrative multi-omics and multi-trait analysis

Cell Reports Medicine(2023)10.1016/j.xcrm.2023.101112

N/A

0DataRank · unranked

28 citations

Minku Song, Beomsu Kim, Injeong Shim, Dan Say Kim, Pradeep Natarajan +3 more

Tissue-specific genetic features inform prediction of drug side effects in clinical trials

Science Advances(2020)10.1126/sciadv.abb6242

N/A

0DataRank · unranked

64 citations

Marie Verbanck, Amanda Dobbyn, Hong‐Hee Won, Joshua L. Rein, Iain S. Forrest +4 more

Prediction of Venous Thromboembolism in Diverse Populations Using Machine Learning and Structured Electronic Health Records

Arteriosclerosis Thrombosis and Vascular Biology(2023)10.1161/atvbaha.123.320331

N/A

0DataRank · unranked

24 citations

Ben Omega Petrazzini, Waqas Malick, Robert S. Rosenson, Ron Do, Robert Chen

Quantitative Prediction of Right Ventricular Size and Function From the ECG

Journal of the American Heart Association(2023)10.1161/jaha.123.031671

N/A

0DataRank · unranked

16 citations

Akhil Vaid, Ha My T. Vy, Liam R. Butler, Joshua Lampert, Robert H. Pass +9 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

Phenome-wide Mendelian randomization study of plasma triglyceride levels and 2600 disease traits

eLife(2023)10.7554/elife.80560

N/A

0DataRank · unranked

7 citations

Shantanu Bafna, Iain S. Forrest, Áine Duffy, Carla Márquez‐Luna, Ben Omega Petrazzini +8 more

Genetic Associations Between Smoking- and Glaucoma-Related Traits

Translational Vision Science & Technology(2023)10.1167/tvst.12.2.20

N/A

0DataRank · unranked

9 citations

Kelsey V. Stuart, Victor de Vries, Joëlle Vergroesen, Clara C. Cousins, Pirro G. Hysi +11 more

Machine Learning Identifies Plasma Metabolites Associated With Heart Failure in Underrepresented Populations With the TTR V122I Variant

Journal of the American Heart Association(2023)10.1161/jaha.122.027736

N/A

0DataRank · unranked

3 citations

Ben Omega Petrazzini, Aparna Saha, Akhil Vaid, Ha My T. Vy, Carla Márquez‐Luna +4 more

A deep learning transformer model predicts high rates of undiagnosed rare disease in large electronic health systems

medRxiv(2023)10.1101/2023.12.21.23300393

N/A

0DataRank · unranked

4 citations

Ha My T. Vy, Ron Do, Daniel M. Jordan

Machine Learning Enables Single-Score Assessment of MASLD Presence and Severity

medRxiv(2023)10.1101/2023.10.24.23297423

N/A

0DataRank · unranked

2 citations

Ben Omega Petrazzini, Girish N. Nadkarni, Ghislain Rocheleau, Meena B. Bansal, Ron Do +1 more

Deep learning on electronic medical records identifies distinct subphenotypes of diabetic kidney disease driven by genetic variations in the Rho pathway

medRxiv(2023)10.1101/2023.09.06.23295120

N/A

0DataRank · unranked

0 citations

Xuan Wang, Nanditha Anandakrishnan, Jonathan C. Haydak, Tielman Van Vleck, Stefanie DeFronzo +22 more

Association of genetic risk, lifestyle, and their interaction with obesity and obesity-related morbidities

Cell Metabolism(2024)10.1016/j.cmet.2024.06.004

N/A

0DataRank · unranked

109 citations

Injeong Shim, Akl C. Fahed, Ron Do, Woong-Yang Park, Pradeep Natarajan +3 more

Development of a human genetics-guided priority score for 19,365 genes and 399 drug indications

Nature Genetics(2024)10.1038/s41588-023-01609-2

N/A

0DataRank · unranked

32 citations

Ben Omega Petrazzini, David Stein, Joshua K. Park, Iain S. Forrest, Kyle Gibson +12 more

Associations of Circulating Biomarkers with Disease Risks: a Two-Sample Mendelian Randomization Study

medRxiv(2024)10.1101/2024.06.30.24309729

N/A

0DataRank · unranked

0 citations

Kevin Spehar, Ron Do, Joseph M. Castellano, Kuan-lin Huang, Abdülkadir Elmas

Expanding drug targets for 112 chronic diseases using a machine learning-assisted genetic priority score

Nature Communications(2024)10.1038/s41467-024-53333-y

N/A

0DataRank · unranked

11 citations

Áine Duffy, Ben Omega Petrazzini, Ha My T. Vy, David Stein, Matthew Mort +8 more

Use of Diagnostic Codes for Primary Open-Angle Glaucoma Polygenic Risk Score Construction in Electronic Health Record–Linked Biobanks

American Journal of Ophthalmology(2024)10.1016/j.ajo.2024.06.007

N/A

0DataRank · unranked

10 citations

Joyce Kang, Elaine Han, Urvi Gupta, Kasem Seresirikachorn, Ha My T. Vy +12 more

Integration of observational and causal evidence for the association between adiposity and 17 gastrointestinal outcomes: An umbrella review and meta‐analysis

Obesity Reviews(2024)10.1111/obr.13823

N/A

0DataRank · unranked

7 citations

Inhyeok Lee, Pradeep Natarajan, Ron Do, Yeongkeun Kwon, Jae Il Shin +5 more

Ensemble and consensus approaches to prediction of recessive inheritance for missense variants in human disease

Cell Reports Methods(2024)10.1016/j.crmeth.2024.100914

N/A

0DataRank · unranked

6 citations

Daniel J. Balick, Iain S. Forrest, Judy H. Cho, Ghislain Rocheleau, Daniel M. Jordan +2 more

Evaluation of a machine learning-based metabolic marker for coronary artery disease in the UK Biobank

Atherosclerosis(2024)10.1016/j.atherosclerosis.2024.119103

N/A

0DataRank · unranked

6 citations

Iain S. Forrest, Ben Omega Petrazzini, Áine Duffy, Joshua K. Park, Waqas Malick +5 more

Associations of Circulating Biomarkers with Disease Risks: A Two-Sample Mendelian Randomization Study

International Journal of Molecular Sciences(2024)10.3390/ijms25137376

N/A

0DataRank · unranked

1 citations

Kevin Spehar, Ron Do, Joseph M. Castellano, Kuan‐lin Huang, Abdülkadir Elmas

Muesli Intake May Protect Against Coronary Artery Disease

JACC Advances(2024)10.1016/j.jacadv.2024.100888

N/A

0DataRank · unranked

2 citations

Ben Omega Petrazzini, Shantanu Bafna, Áine Duffy, Iain S. Forrest, Ha My T. Vy +8 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

UNC Libraries(2024)10.17615/8zyz-p282

Top 100%

0DataRank

Top 100%0 citations

Shining Ma, J.C. Bis, Noah L. Tsao, Philip S. Tsao, Yi‐Lwun Ho +81 more

Multimodal fusion learning for long QT syndrome pathogenic genotypes in a racially diverse population

npj Digital Medicine(2024)10.1038/s41746-024-01218-1

N/A

0DataRank · unranked

0 citations

Ha My T. Vy, Alexander W. Charney, Patricia Kovatch, Vivek Y. Reddy, Pushkala Jayaraman +8 more

Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02140-2

N/A

0DataRank · unranked

33 citations

Kathleen M. Cardone, David Zhang, Noah L. Tsao, Sarah Abramowitz, Pranav Sharma +35 more

An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease

Nature Communications(2021)10.1038/s41467-020-20750-8

N/A

0DataRank · unranked

63 citations

William Barrington, Daniel M. Jordan, Noam D. Beckmann, Carmen Argmann, Sander M. Houten +21 more

Genetic evidence informs the direction of therapeutic modulation in drug development

npj Drug Discovery.(2025)10.1038/s44386-025-00027-0

N/A

0DataRank · unranked

2 citations

Áine Duffy, Joshua K. Park, David Stein, Avner Schlessinger, Yuval Itan +6 more

Development of a genetic priority score to predict drug side effects using human genetic evidence

Nature Communications(2025)10.1038/s41467-025-63762-y

N/A

0DataRank · unranked

1 citations

Robert Chen, David Stein, Joshua K. Park, Matthew Mort, Marie Verbanck +7 more

ChatGPT-Assisted Glaucoma Diagnosis: A Health-Equitable Multi-Ancestry Analysis Using Visual Field and Optical Coherence Tomography Data

American Journal of Ophthalmology(2025)10.1016/j.ajo.2025.11.046

N/A

0DataRank · unranked

1 citations

Anthony Fam, Hetince Zhao, NICOLE PAULESCU, Anna Fabczak-Kubicka, Janey L. Wiggs +12 more

Genetic analyses of eight complex diseases using predicted continuous representations of disease

Cell Reports Methods(2025)10.1016/j.crmeth.2025.101115

N/A

0DataRank · unranked

2 citations

Ghislain Rocheleau, Ben Omega Petrazzini, Iain S. Forrest, Joshua K. Park, Áine Duffy +4 more

Pyruvate and related energetic metabolites modulate resilience against high genetic risk for glaucoma

eLife(2025)10.7554/elife.105576

N/A

0DataRank · unranked

9 citations

Nicholas Tolman, Ayellet V. Segrè, Kelsey V. Stuart, Oana A. Zeleznik, Neeru A. Vallabh +14 more

Author response: Pyruvate and Related Energetic Metabolites Modulate Resilience Against High Genetic Risk for Glaucoma

(2025)10.7554/elife.105576.2.sa0

N/A

0DataRank · unranked

0 citations

Nicholas Tolman, Ayellet V. Segrè, Kelsey V. Stuart, Oana A. Zeleznik, Neeru A. Vallabh +14 more

Associations between pathophysiological traits and symptom development in retrospective analysis of V30M and V122I transthyretin amyloidosis

IJC Heart & Vasculature(2025)10.1016/j.ijcha.2025.101663

N/A

0DataRank · unranked

0 citations

Ha My T. Vy, Madhav Subramanian, Parasuram Krishnamoorthy, Son Q. Duong, Ghislain Rocheleau +4 more

The omnicausal model reveals the highly polyfactorial nature of complex diseases

medRxiv(2025)10.1101/2025.08.20.25333988

N/A

0DataRank · unranked

0 citations

Martin Tournaire, Ghislain Rocheleau, Ron Do, Marie Verbanck, Carla Márquez‐Luna

Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas

UNC Libraries(2025)10.17615/yvmq-kt94

N/A

0DataRank · unranked

0 citations

Xiaoguang Xu, Jason G. Umans, Thomas Gilliland, Charles Kooperberg, Mariah Meyer +69 more

Does Age Modify the Relation Between Genetic Predisposition to Glaucoma and Various Glaucoma Traits in the UK Biobank?

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.2.57

N/A

0DataRank · unranked

3 citations

Jae H. Kang, Janey L. Wiggs, Hetince Zhao, Keva Li, Nazlee Zebardast +7 more

Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations

Nature Medicine(2021)10.1038/s41591-020-1133-8

N/A

0DataRank · unranked

65 citations

Anastasia Lucas, Xinyuan Zhang, Kumardeep Chaudhary, Judy H. Cho, Girish N. Nadkarni +36 more

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

UNC Libraries(2020)10.17615/pc2a-ev84

N/A

0DataRank · unranked

0 citations

Jeanette Erdmann, Paul L. Auer, Robert Roberts, John Danesh, Deborah Farlow +27 more

Overcoming constraints on the detection of recessive selection in human genes from population frequency data

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.12.001

N/A

0DataRank · unranked

20 citations

Daniel M. Jordan, Shamil R. Sunyaev, Ron Do, Daniel J. Balick

Genetic pleiotropy of ERCC6 loss‐of‐function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries

Human Mutation(2021)10.1002/humu.24220

N/A

0DataRank · unranked

4 citations

Kumardeep Chaudhary, Ha My T. Vy, Shantanu Bafna, Soyeon Kim, Hong‐Hee Won +7 more

Probing the aggregated effects of purifying selection per individual on 1,380 medical phenotypes in the UK Biobank

PLoS Genetics(2021)10.1371/journal.pgen.1009337

N/A

0DataRank · unranked

4 citations

Daniel M. Jordan, Daniel J. Balick, Ron Do, Ha My T. Vy

Exome sequencing and the genetic basis of complex traits

UNC Libraries(2020)10.17615/2gxf-xr79

N/A

0DataRank · unranked

0 citations

Kiran Garimella, Benjamin M. Neale, Adam Kieżun, Shaun Purcell, Nathan O. Stitziel +14 more

Causal effect of adiposity on the risk of 19 gastrointestinal diseases: a Mendelian randomization study

medRxiv(2021)10.1101/2021.11.19.21266578

N/A

0DataRank · unranked

6 citations

Minku Song, Soyeon Kim, Beomsu Kim, Wonseok Kang, Jong Yeob Kim +6 more

Overcoming constraints on the detection of recessive selection in human genes from population frequency data

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.06.443024

N/A

0DataRank · unranked

3 citations

Daniel M. Jordan, Shamil R. Sunyaev, Ron Do, Daniel J. Balick

Prediction of recessive inheritance for missense variants in human disease

medRxiv(2021)10.1101/2021.10.25.21265472

N/A

0DataRank · unranked

3 citations

Daniel J. Balick, Iain S. Forrest, Judy H. Cho, Ghislain Rocheleau, Daniel M. Jordan +2 more

Genome-wide polygenic risk score method for diabetic kidney disease in patients with type 2 diabetes

medRxiv(2021)10.1101/2021.07.09.21260114

N/A

0DataRank · unranked

0 citations

Sergio Dellepiane, Kumardeep Chaudhary, Alexander Blair, Benjamin Scott Glicksberg, Steven G. Coca +5 more

Common variants associated with plasma triglycerides and risk for coronary artery disease

UNC Libraries(2020)10.17615/3nfp-v503

N/A

0DataRank · unranked

4 citations

Hsing‐Yi Chang, Åsa Johansson, Pierre Fontanillas, Martin L. Buchkovich, Ross M. Fraser +27 more

Machine learning-based marker for coronary artery disease: derivation and validation in two longitudinal cohorts

The Lancet(2022)10.1016/s0140-6736(22)02079-7

N/A

0DataRank · unranked

166 citations

Ben Omega Petrazzini, Áine Duffy, Joshua K. Park, Carla Márquez‐Luna, Daniel M. Jordan +7 more

Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure

Nature Communications(2022)10.1038/s41467-022-34216-6

N/A

0DataRank · unranked

150 citations

Noah L. Tsao, Pankhuri Singhal, Chang Liu, Ha My T. Vy, Ishan Paranjpe +38 more

Population-Based Penetrance of Deleterious Clinical Variants

JAMA(2022)10.1001/jama.2021.23686

N/A

0DataRank · unranked

106 citations

Kumardeep Chaudhary, Ha My T. Vy, Ben Omega Petrazzini, Shantanu Bafna, Daniel M. Jordan +6 more

Ron Do

Indexed papers

Top data-sharing exemplar

Papers