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Authors
Charles Kooperberg

Charles Kooperberg

University of Southern California

ORCID: 0000-0002-7986-8560

Also affiliated with Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa, University of Washington, Massachusetts General Hospital, Fred Hutch Cancer Center

Biochemistry, Genetics and Molecular BiologyMedicine

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

14.9Author DataRank

Indexed papers

21in 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 21 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 →

Top data-sharing exemplar

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

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 263 papers — median percentile 59. Top paper: “Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program”.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 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

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Nature Genetics(2020)10.1038/s41588-020-0676-4

N/A

5.3DataRank · unranked

295 citations

Zilin Li, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +88 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

Clonal hematopoiesis associated with epigenetic aging and clinical outcomes

Aging Cell(2021)10.1111/acel.13366

N/A

3.3DataRank · unranked

134 citations

Ake T. Lu, Alexander G. Bick, Pradeep Natarajan, Joshua Weinstock, Mindy D Szeto +29 more

Longitudinal profiling of clonal hematopoiesis provides insight into clonal dynamics

Immunity & Ageing(2022)10.1186/s12979-022-00278-9

N/A

1.7DataRank · unranked

72 citations

Ying Zhou, Alexander G. Bick, Bala Bharathi Burugula, Siddhartha Jaiswal, Pinkal Desai +11 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Nature Communications(2022)10.1038/s41467-022-33510-7

N/A

1.6DataRank · unranked

75 citations

Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park +95 more

Model-based assessment of replicability for genome-wide association meta-analysis

Nature Communications(2021)10.1038/s41467-021-21226-z

N/A

1.5DataRank · unranked

40 citations

Yu Jiang, Mengzhen Liu, J. Dylan Weissenkampen, Scott A. Eckert, Lina Yang +125 more

Clonal Hematopoiesis of Indeterminate Potential (CHIP) and Incident Type 2 Diabetes Risk

Diabetes Care(2023)10.2337/dc23-0805

N/A

1.5DataRank · unranked

71 citations

Alisa K. Manning, Jennifer Wessel, Sridharan Raghavan, Kenneth E. Westerman, Alexander G. Bick +27 more

A large‐scale exome array analysis of venous thromboembolism

Genetic Epidemiology(2019)10.1002/gepi.22187

N/A

1.4DataRank · unranked

27 citations

Jennifer A. Brody, Constance Turman, Marine Germain, Traci M. Bartz, Erin N. Smith +34 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

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.021

N/A

1.3DataRank · unranked

70 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian Wang, Margaret Sunitha Selvaraj +95 more

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Nature Genetics(2022)10.1038/s41588-022-01225-6

N/A

1.2DataRank · unranked

63 citations

Corbin Quick, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +95 more

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature Genetics(2019)10.1038/s41588-018-0307-5

N/A

1.1DataRank · unranked

2128 citations

Mengzhen Liu, HUNT All-In Psychiatry, Yu Jiang, Robbee Wedow, Yue Li +120 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 more

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.011

N/A

1.1DataRank · unranked

34 citations

Anne E. Justice, Kristin L. Young, Eirini Marouli, Xinruo Zhang, Rebecca S. Fine +220 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

Social Isolation and Incident Heart Failure Hospitalization in Older Women: Women’s Health Initiative Study Findings

Journal of the American Heart Association(2022)10.1161/jaha.120.022907

N/A

1.1DataRank · unranked

27 citations

Xiaoyan Leng, Khushnood Faraz, Matthew Allison, Khadijah Breathett, Chloe E. Bird +29 more

Prediagnostic Inflammation and Pancreatic Cancer Survival

JNCI Journal of the National Cancer Institute(2021)10.1093/jnci/djab040

N/A

0.943DataRank · unranked

24 citations

Vicente Morales‐Oyarvide, Natalia Khalaf, Kimberly Perez, Fred K. Tabung, Gloria Y. F. Ho +13 more

The PRIMED Consortium: Reducing disparities in polygenic risk assessment

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.010

N/A

0.893DataRank · unranked

37 citations

Matthew P. Conomos, Sarah C. Nelson, Sally N. Adebamowo, Ananyo Choudhury, David V. Conti +90 more

Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

Hypertension(2022)10.1161/hypertensionaha.122.19324

Top 24%

0.842DataRank

Top 24%29 citations

Xiao Sun, Karen He, Michael R. Brown, Sarah A. Gagliano Taliun, Jacklyn N. Hellwege +95 more

Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

Human Molecular Genetics(2021)10.1093/hmg/ddab252

Top 28%

0.724DataRank

Top 28%20 citations

Yao Hu, Quan Sun, Deepti Jain, Jai Broome, Ming‐Huei Chen +62 more

Women’s Health Initiative Strong and Healthy Pragmatic Physical Activity Intervention Trial for Cardiovascular Disease Prevention: Design and Baseline Characteristics

The Journals of Gerontology Series A(2021)10.1093/gerona/glaa325

N/A

0.683DataRank · unranked

23 citations

Abby C. King, Sally Mackey, Lesley F. Tinker, Mark A. Hlatky, Michael J. Lamonte +6 more

Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study

Scientific Reports(2023)10.1038/s41598-023-39936-3

Top 31%

0.641DataRank

Top 31%32 citations

Helena Bui, Roby Joehanes, Jiantao Ma, Chunyu Liu, Tianxiao Huan +31 more

Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas

Cell Genomics(2024)10.1016/j.xgen.2024.100692

Top 31%

0.635DataRank

Top 31%30 citations

Douglas P. Loesch, Bing Guo, Roland Laboulaye, Diego Véliz-Otani, Jennifer N. French +70 more

Genome-Wide Gene–Diabetes and Gene–Obesity Interaction Scan in 8,255 Cases and 11,900 Controls from PanScan and PanC4 Consortia

Cancer Epidemiology Biomarkers & Prevention(2020)10.1158/1055-9965.epi-20-0275

Top 33%

0.600DataRank

Top 33%10 citations

Lai Jiang, Rachael Z. Stolzenberg‐Solomon, Alan A. Arslan, Laura E. Beane Freeman, Paige M. Bracci +66 more

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

Communications Biology(2022)10.1038/s42003-022-03702-4

Top 34%

0.582DataRank

Top 34%16 citations

Sheila M. Gaynor, Emily M. Russell, Kenneth E. Westerman, Laura M. Raffield, Timothy D. Majarian +88 more

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

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.423783

N/A

0.534DataRank · unranked

11 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian X. Wang, Margaret Sunitha Selvaraj +95 more

Genomic and phenomic landscape of clonal hematopoiesis in over a million ancestrally diverse participants

medRxiv(2022)10.1101/2022.07.29.22278015

Top 37%

0.528DataRank

Top 37%13 citations

Zhi Yu, Joshua S. Weinstock, Abhishek Niroula, Satoshi Koyama, Tetsushi Nakao +83 more

Serial 7-Day Electrocardiogram Patch Screening for AF in High-Risk Older Women by the CHARGE-AF Score

JACC. Clinical electrophysiology(2022)10.1016/j.jacep.2022.08.024

N/A

0.515DataRank · unranked

13 citations

Joseph C. Larson, Jenny Schoenberg, Alejandra Sepúlveda, Lesley Tinker, Matthew T. Wheeler +12 more

Rare variant contribution to the heritability of coronary artery disease

Nature Communications(2024)10.1038/s41467-024-52939-6

N/A

0.513DataRank · unranked

16 citations

Shoa L. Clarke, Gaëlle Auguste, Natalie R. Hasbani, Alanna C. Morrison, Adam S. Heath +95 more

Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.121.003532

Top 38%

0.507DataRank

Top 38%11 citations

Cecelia Laurie, Brandon J. Coombes, Deepti Jain, Matthew P. Conomos, Jennifer A. Brody +30 more

Clonal Hematopoiesis and Cardiovascular Outcomes in Older Women

Journal of the American College of Cardiology(2025)10.1016/j.jacc.2025.07.058

N/A

0.500DataRank · unranked

17 citations

Md Mesbah Uddin, Liying Xue, Yash Pershad, Shengruo Zhang, Jason M. Collins +11 more

Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002680

Top 41%

0.466DataRank

Top 41%13 citations

Colleen M. Sitlani, Heather M. Highland, Dan E. Arking, Steven Buyske, Dawood Darbar +27 more

Women's Health Initiative Strong and Healthy (WHISH): A pragmatic physical activity intervention trial for cardiovascular disease prevention

Contemporary Clinical Trials(2022)10.1016/j.cct.2022.106815

N/A

0.457DataRank · unranked

9 citations

Charles Kooperberg, Andrea Z. LaCroix, Marcia L. Stefanick

Type 2 diabetes polygenic risk score demonstrates context-dependent effects and associations with type 2 diabetes-related risk factors and complications across diverse populations

medRxiv(2025)10.1101/2025.02.15.25322341

N/A

0.342DataRank · unranked

4 citations

Yanwei Cai, Daeeun Kim, Roelof A. J. Smit, Zhe Wang, Kruthika Iyer +68 more

A Type 1 Diabetes Polygenic Score Is Not Associated With Prevalent Type 2 Diabetes in Large Population Studies

Journal of the Endocrine Society(2023)10.1210/jendso/bvad123

N/A

0.326DataRank · unranked

4 citations

Peitao Wu, Josep M. Mercader, Miriam S. Udler, Bianca Porneala, Traci M. Bartz +17 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

medRxiv(2021)10.1101/2021.06.18.21258578

N/A

0.320DataRank · unranked

5 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia Weber Hall, Lu‐Chen Weng +33 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

Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: The Framingham Heart Study

medRxiv(2022)10.1101/2022.04.13.22273839

Top 60%

0.253DataRank

Top 60%4 citations

Helena Bui, Roby Joehanes, Jiantao Ma, Chunyu Liu, Tianxiao Huan +32 more

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits

medRxiv(2022)10.1101/2022.07.26.22278077

N/A

0.182DataRank · unranked

1 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 more

Polygenic risk score for type 2 diabetes shows context-dependent effects across populations

Nature Communications(2025)10.1038/s41467-025-63546-4

N/A

0.165DataRank · unranked

2 citations

Yanwei Cai, Daeeun Kim, Roelof A. J. Smit, Zhe Wang, Kruthika R. Iyer +169 more

Integrating whole genome and transcriptome sequencing to characterize the genetic architecture of isoform variation

Nature Communications(2025)10.1038/s41467-025-64336-8

Top 70%

0.165DataRank

Top 70%2 citations

Roby Joehanes, Jiantao Ma, Jiuyong Xie, Jian Yang, Mengyao Wang +20 more

Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations

Nature Communications(2025)10.1038/s41467-025-64236-x

N/A

0.165DataRank · unranked

2 citations

Sharjeel A. Chaudhry, Μαρία Ιωάννου, Maria Viskadourou, Paula Reventún, Yasminka A. Jakubek +49 more

Association of Pathogenic/Likely Pathogenic Inherited Cardiomyopathy Variants With Heart Failure

Mayo Clinic Proceedings(2025)10.1016/j.mayocp.2025.01.021

N/A

0.153DataRank · unranked

1 citations

Mokshad Gaonkar, Akhil Pampana, Nirav Patel, April P. Carson, Bernhard Haring +18 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

medRxiv(2023)10.1101/2023.06.28.23291966

N/A

0.146DataRank · unranked

1 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Proteome‐wide association study using cis and trans variants and applied to blood cell and lipid‐related traits in the Women's Health Initiative study

Genetic Epidemiology(2024)10.1002/gepi.22578

N/A

0.141DataRank · unranked

1 citations

Chanhwa Lee, Amanda L. Tapia, Alex P. Reiner, Hua Tang, Charles Kooperberg +4 more

Genome-Wide Analysis to Assess if Heavy Alcohol Consumption Modifies the Association between SNPs and Pancreatic Cancer Risk

Cancer Epidemiology Biomarkers & Prevention(2024)10.1158/1055-9965.epi-24-0096

N/A

0.111DataRank · unranked

1 citations

Prosenjit Kundu, David McKean, William Wheeler, Demetrius Albanes, Gabriella Andreotti +47 more

Protein quantitative trait locus analysis in African American and non-Hispanic White individuals

Genome biology(2025)10.1186/s13059-025-03671-x

Top 78%

0.104DataRank

Top 78%1 citations

Mari Johnson, J. Haessler, Aaron J. Molstad, Shih‐Jen Hwang, Roby Joehanes +11 more

Correlates and Consequences of Clonal Hematopoiesis Expansion Rate: A 15-Year Longitudinal Study of 6,986 Women

medRxiv(2025)10.1101/2025.01.12.25320422

N/A

0.104DataRank · unranked

1 citations

Md Mesbah Uddin, Liying Xue, Jeffrey Haessler, Jason M. Collins, Taralynn Mack +15 more

Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study

Diabetologia(2021)10.1007/s00125-021-05635-9

N/A

0DataRank · unranked

39 citations

Sofia F. Dimos, Stephanie A. Bien, Yao Hu, Burcu F. Darst, Linda M. Polfus +26 more

A 584 bp deletion in CTRB2 inhibits chymotrypsin B2 activity and secretion and confers risk of pancreatic cancer

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.09.002

N/A

0DataRank · unranked

34 citations

Jun Zhong, Katelyn E. Connelly, Naomi Gordon, Sumeth Perera, Ehssan Abdolalizadeh +49 more

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

EBioMedicine(2021)10.1016/j.ebiom.2020.103157

N/A

0DataRank · unranked

28 citations

Kelsey Grinde, Jennifer A. Brody, Charles E. Breeze, Laura M. Raffield, Josyf C. Mychaleckyj +68 more

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.007

N/A

0DataRank · unranked

26 citations

Caitlin McHugh, Linda M. Polfus, Laura M. Raffield, Meher Preethi Boorgula, Thomas W. Blackwell +88 more

Robust, flexible, and scalable tests for Hardy–Weinberg equilibrium across diverse ancestries

Genetics(2021)10.1093/genetics/iyab044

N/A

0DataRank · unranked

25 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

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)10.1186/s12864-021-07745-5

N/A

0DataRank · unranked

23 citations

Stephanie A. Bien, Katherine K. Nishimura, Jeffrey Haessler, Chani J. Hodonsky, Antoine Baldassari +29 more

Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations

Genes(2021)10.3390/genes12071049

N/A

0DataRank · unranked

20 citations

Munan Xie, Bryce Rowland, Jonathan D. Rosen, Quan Sun, Jiawen Chen +31 more

Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche

Human Reproduction(2021)10.1093/humrep/deab086

N/A

0DataRank · unranked

15 citations

Diana L. Cousminer, Nora Franceschini, Laura M. Raffield, Guochong Jia, Lindsay Fernández‐Rhodes +20 more

Smoking Modifies Pancreatic Cancer Risk Loci on 2q21.3

Cancer Research(2021)10.1158/0008-5472.can-20-3267

N/A

0DataRank · unranked

17 citations

Prosenjit Kundu, William Wheeler, Alan A. Arslan, Laura E. Beane-Freeman, Paige M. Bracci +72 more

Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program

PLoS ONE(2021)10.1371/journal.pone.0253611

N/A

0DataRank · unranked

8 citations

Han Chen, Mary L. Biggs, Sylvia Wassertheil‐Smoller, Jan Bressler, Marguerite R. Irvin +24 more

A large‐scale transcriptome‐wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine‐mapping

Genetic Epidemiology(2021)10.1002/gepi.22436

N/A

0DataRank · unranked

6 citations

Bryce Rowland, Jonathan D. Rosen, Michael Preuß, Kris Young, Misa Graff +14 more

A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

medRxiv(2021)10.1101/2021.10.31.21265717

N/A

0DataRank · unranked

11 citations

Matthew Goodman, Tanika N. Kelly, Tali Elfassi, Kerri L. Wiggins, Joshua C Bis +32 more

Clonal hematopoiesis is driven by aberrant activation of TCL1A

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.10.471810

N/A

0DataRank · unranked

10 citations

Jayakrishnan Gopakumar, Bala Bharathi Burugula, Md Mesbah Uddin, Nikolaus Jahn, Julia A. Belk +95 more

Mendelian randomisation identifies alternative splicing of the FAS death receptor as a mediator of severe COVID-19

medRxiv(2021)10.1101/2021.04.01.21254789

N/A

0DataRank · unranked

9 citations

Jack Gisby, Artemis Papadaki, Marisa D. Muckian, Erin Macdonald-Dunlop, Jing Hua Zhao +64 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.11.463514

N/A

0DataRank · unranked

3 citations

Xihao Li, Zilin Li, Akhil Pampana, David Y Zhang, Joseph Park +80 more

Transcriptome-wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations

Preprints.org(2021)10.20944/preprints202106.0129.v1

N/A

0DataRank · unranked

2 citations

Munan Xie, Bryce Rowland, Jonathan D. Rosen, Quan Sun, Amanda L. Tapia +30 more

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

Nature Methods(2022)10.1038/s41592-022-01640-x

N/A

0DataRank · unranked

109 citations

Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou +95 more

TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.006

N/A

0DataRank · unranked

106 citations

Jonathan D. Rosen, Quan Sun, Jiawen Chen, Marsha M. Wheeler, Ying Zhou +20 more

Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

Circulation(2022)10.1161/circulationaha.122.059675

N/A

0DataRank · unranked

106 citations

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

A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

Nature Communications(2022)10.1038/s41467-022-31080-2

N/A

0DataRank · unranked

79 citations

Matthew Goodman, Tanika N. Kelly, Tali Elfassy, Kerri L. Wiggins, Joshua C. Bis +32 more

The age-dependent association of risk factors with pancreatic cancer

Annals of Oncology(2022)10.1016/j.annonc.2022.03.276

N/A

0DataRank · unranked

77 citations

John Kim, Qiao-Li Wang, Alice A. Lee, Ana Babić, Laufey T. Ámundadóttir +34 more

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

Circulation(2022)10.1161/circulationaha.121.057261

N/A

0DataRank · unranked

50 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia W. Hall, Lu-Chen Weng +34 more

Contributions of the Women’s Health Initiative to Cardiovascular Research

Journal of the American College of Cardiology(2022)10.1016/j.jacc.2022.05.016

N/A

0DataRank · unranked

25 citations

JoAnn E. Manson, Garnet L. Anderson, Laura D. Baker, Jennifer W. Bea, Charles B. Eaton +16 more

Genetic Landscape of the ACE2 Coronavirus Receptor

Circulation(2022)10.1161/circulationaha.121.057888

N/A

0DataRank · unranked

40 citations

Erin Macdonald-Dunlop, Jiantao Chen, Ranran Zhai, Ting Li, Anne Richmond +64 more

Integration of rare expression outlier-associated variants improves polygenic risk prediction

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medRxiv(2024)10.1101/2024.03.05.24303738

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medRxiv(2024)10.1101/2024.01.09.24300914

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UNC Libraries(2024)10.17615/4eyj-4q61

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UNC Libraries(2024)10.17615/68se-b538

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Digital Commons@Becker (Washington University School of Medicine)(2024)10.17615/2bde-jk53

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UNC Libraries(2024)10.17615/qqnb-a348

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UNC Libraries(2024)10.17615/xwxn-9p09

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UNC Libraries(2024)10.17615/c1sy-3719

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UNC Libraries(2024)10.17615/sf0k-n413

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medRxiv(2024)10.1101/2024.09.12.24313572

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UNC Libraries(2024)10.17615/vs68-ca81

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UNC Libraries(2024)10.17615/f3mg-7f39

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UNC Libraries(2024)10.17615/shas-p528

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UNC Libraries(2024)10.17615/b6xd-h115

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Blood(2025)10.1182/blood.2025028417

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Nature Computational Science(2025)10.1038/s43588-024-00764-8

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The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.004

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Epigenetics(2025)10.1080/15592294.2025.2539234

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The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.022

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Journal of Bone and Mineral Research(2025)10.1093/jbmr/zjaf059

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Journal of Thrombosis and Haemostasis(2025)10.1016/j.jtha.2025.04.029

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The Journal of Clinical Endocrinology & Metabolism(2025)10.1210/clinem/dgaf454

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Genome biology(2025)10.1186/s13059-025-03698-0

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medRxiv(2025)10.1101/2025.10.22.25338594

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UNC Libraries(2020)10.17615/4n1y-v979

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Rayjean J. Hung, Naomi Walsh, Han Zhang, Elizabeth A. Platz, William Wheeler +69 more

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PLoS ONE(2020)10.1371/journal.pone.0230815

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Cancer Epidemiology Biomarkers & Prevention(2020)10.1158/1055-9965.epi-20-0091

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BMC Genomics(2020)10.1186/s12864-020-6626-9

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Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002874

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Amelia Weber Hall, Seung Hoan Choi, Sean J. Jurgens, Jeffrey Haessler, Nathan A. Bihlmeyer +55 more

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medRxiv(2020)10.1101/2020.04.23.20077099

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medRxiv(2020)10.1101/2020.12.09.20246736

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A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.18.146423

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.23.167759

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Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

Integration of rare large-effect expression variants improves polygenic risk prediction

medRxiv(2020)10.1101/2020.12.02.20242990

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Nicole M. Ferraro, Matthew G. Durrant, Abhiram Rao, Matthew Aguirre, Xin Li +12 more

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UNC Libraries(2020)10.17615/4xdt-j376

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Diane M. Becker, Nobuyo Maeda, Christopher J. O’Donnell, D. Y. Lin, Alex P. Reiner +26 more

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Tamar Sofer, Henry J. Lin, Matthew P. Conomos, Nona Sotoodehnia, Eric A. Whitsel +20 more

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UNC Libraries(2020)10.17615/613z-hx36

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Qing Duan, Nicholas A. Johnson, Marc Coram, Lisa Warsinger Martin, Neil Risch +12 more

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UNC Libraries(2020)10.17615/9842-r797

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Jeffrey Haessler, Rebecca Rohde, Lynne R. Wilkens, Peters, Ulrike, Christopher S. Carlson +27 more

A Meta-Analysis and Genome-Wide Association Study of Platelet Count and Mean Platelet Volume in African Americans

UNC Libraries(2020)10.17615/04pm-t231

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Elad Ziv, Michael A. Nalls, Rehan Qayyum, Andrew B. Singleton, Benjamin A. Logsdon +18 more

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UNC Libraries(2020)10.17615/jq1f-ha22

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Tara C. Matise, Dana C. Crawford, Marylyn D. Ritchie, Kari E. North, Lucia A. Hindorff +11 more

Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study

UNC Libraries(2020)10.17615/a0p1-ht56

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Zhao Chen, Robert G. Brzyski, Charles Kooperberg, Christopher S. Carlson, Christina T.L. Chen +6 more

A Systematic Mapping Approach of 16q12.2/FTO and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study

UNC Libraries(2020)10.17615/tw0c-5h88

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UNC Libraries(2020)10.17615/f8pj-t864

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