Stephen S. Rich

Also affiliated with University of Virginia Health System, University of Virginia

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

18.7Author DataRank

Indexed papers

29in 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 29 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.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Papers

Driven by 325 papers — median percentile 48. Top paper: “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations”.

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

Cell(2020)10.1016/j.cell.2020.06.045

N/A

8.3DataRank · unranked

739 citations

Laura M. Raffield, Abdou Mousas, Saori Sakaue, Jennifer E. Huffman, Arden Moscati +95 more

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes

Nature Genetics(2021)10.1038/s41588-021-00880-5

N/A

6.1DataRank · unranked

300 citations

Jamie Inshaw, Suna Önengüt-Gümüşcü, Wei‐Min Chen, David Flores Santa Cruz, Hanzhi Yang +26 more

Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging

Genome biology(2021)10.1186/s13059-021-02398-9

N/A

5.8DataRank · unranked

307 citations

Josine L. Min, Rebecca Richmond, Ake T. Lu, Maria Sobczyk, Gail Davies +95 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

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00935-7

N/A

4.0DataRank · unranked

191 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 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

Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease

Nature Communications(2018)10.1038/s41467-018-03911-8

N/A

3.1DataRank · unranked

104 citations

Amit V. Khera, Mark Chaffin, Derek Klarin, Pradeep Natarajan, Krishna Aragam +43 more

Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease

Circulation(2021)10.1161/circulationaha.121.055117

N/A

2.8DataRank · unranked

95 citations

Usman A. Tahir, Alexander G. Bick, Akhil Pampana, Debby Ngo, Mark D. Benson +95 more

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Nature Communications(2021)10.1038/s41467-021-23556-4

N/A

2.7DataRank · unranked

110 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 more

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Nature Genetics(2024)10.1038/s41588-024-01714-w

N/A

2.4DataRank · unranked

193 citations

Zoha Kamali, Tian Xie, Ahmad Vaez, Ariel Williams, Slavina B. Goleva +95 more

Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations

Communications Biology(2022)10.1038/s42003-022-03812-z

N/A

2.3DataRank · unranked

108 citations

Genevieve Lyons, Santiago Romero‐Brufau, Nuzulul Kurniansyah, Jennifer A. Brody, Xiuqing Guo +17 more

An open resource of structural variation for medical and population genetics

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/578674

Top 9%

2.2DataRank

Top 9%44 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +37 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

2.1DataRank · unranked

80 citations

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

A novel voluntary weightlifting model in mice promotes muscle adaptation and insulin sensitivity with simultaneous enhancement of autophagy and mTOR pathway

The FASEB Journal(2020)10.1096/fj.201903055r

N/A

2.1DataRank · unranked

65 citations

Joshua C. Drake, Rebecca J. Wilson, Robert Shute, Bevan M. Lewellen, Mei Zhang +8 more

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

Nature(2023)10.1038/s41586-023-05806-1

N/A

2.1DataRank · unranked

107 citations

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

Association of omega 3 polyunsaturated fatty acids with incident chronic kidney disease: pooled analysis of 19 cohorts

BMJ(2023)10.1136/bmj-2022-072909

Top 11%

1.9DataRank

Top 11%82 citations

Matti Marklund, Liping Huang, Kerry‐Anne Rye, Nicholas Hui, Xiong‐Fei Pan +62 more

Consensus Guidance for Monitoring Individuals With Islet Autoantibody–Positive Pre-Stage 3 Type 1 Diabetes

Diabetes Care(2024)10.2337/dci24-0042

N/A

1.6DataRank · unranked

70 citations

Peter Achenbach, Ananta Addala, Anastasia Albanese-O’Neill, Tadej Battelino, Kirstine J. Bell +61 more

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

1.6DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 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

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

Genetic modification of inflammation- and clonal hematopoiesis–associated cardiovascular risk

Journal of Clinical Investigation(2023)10.1172/jci168597

N/A

1.5DataRank · unranked

77 citations

Trevor P. Fidler, Yunfeng Ruan, Caitlyn Vlasschaert, Tetsushi Nakao, Md Mesbah Uddin +23 more

Association of mitochondrial DNA copy number with cardiometabolic diseases

Cell Genomics(2021)10.1016/j.xgen.2021.100006

N/A

1.4DataRank · unranked

62 citations

Ryan J. Longchamps, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Wei Zhao +33 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

Robust relationship inference in genome-wide association studies

Bioinformatics(2010)10.1093/bioinformatics/btq559

N/A

1.2DataRank · unranked

3850 citations

Josyf C. Mychaleckyj, Stephen S. Rich, Kathy Daly, Michèle Sale, Wei-Min Chen +4 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

A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities

American Journal of Respiratory and Critical Care Medicine(2023)10.1164/rccm.202212-2257oc

N/A

1.2DataRank · unranked

62 citations

Anna L. Peljto, John S. Kim, Hanfei Xu, Catherine L. Debban, Xianfeng Chen +33 more

Incidence of interstitial lung abnormalities: the MESA Lung Study

European Respiratory Journal(2023)10.1183/13993003.01950-2022

N/A

1.1DataRank · unranked

31 citations

Spencer Hansen, Karen Hinckley Stukovsky, David Zhang, Hrudaya Nath, Mary Salvatore +20 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

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

Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

Nature Communications(2023)10.1038/s41467-023-41785-7

N/A

1.1DataRank · unranked

44 citations

Stephanie L. Battle, Wen Shi, Daniela Puiu, Vamsee Pillalamarri, Jiaqi Xie +21 more

The Polygenic and Monogenic Basis of Blood Traits and Diseases

Cell(2020)10.1016/j.cell.2020.08.008

N/A

0.988DataRank · unranked

722 citations

Erik L. Bao, Parsa Akbari, Caleb A. Lareau, Abdou Mousas, Tao Jiang +95 more

Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

PLoS Genetics(2023)10.1371/journal.pgen.1010517

N/A

0.970DataRank · unranked

40 citations

François Aguet, Kristin G. Ardlie, Jiawen Chen, Elaine Cornell, Dan Cruz +22 more

Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

Journal of the American Heart Association(2023)10.1161/jaha.122.029090

N/A

0.920DataRank · unranked

30 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, M M Lai, Kerri L. Wiggins +40 more

Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy

Nature Communications(2020)10.1038/s41467-020-15823-7

N/A

0.843DataRank · unranked

275 citations

Alexander G. Bick, Minxian Wang, Mark Chaffin, Sam Friedman, Jie Yao +14 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

Association of clonal hematopoiesis with chronic obstructive pulmonary disease

Blood(2021)10.1182/blood.2021013531

N/A

0.818DataRank · unranked

232 citations

Dandi Qiao, Joselyn Rojas, Michael C. Honigberg, Adam S. Sperling, Christopher J. Gibson +39 more

Clonal Hematopoiesis Is Associated With Higher Risk of Stroke

Stroke(2021)10.1161/strokeaha.121.037388

N/A

0.801DataRank · unranked

208 citations

Seyedeh M. Zekavat, Jeffrey Haessler, Myriam Fornage, Laura M. Raffield, Md Mesbah Uddin +28 more

Structural variation across 138,134 samples in the TOPMed consortium

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.25.525428

Top 27%

0.737DataRank

Top 27%18 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Chronic obstructive pulmonary disease and related phenotypes: polygenic risk scores in population-based and case-control cohorts

The Lancet Respiratory Medicine(2020)10.1016/s2213-2600(20)30101-6

N/A

0.727DataRank · unranked

126 citations

Phuwanat Sakornsakolpat, Nick Shrine, Brian D. Hobbs, Dawn L. DeMeo, Catherine John +82 more

Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals

Nature Genetics(2023)10.1038/s41588-023-01338-6

N/A

0.727DataRank · unranked

126 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +24 more

Enhanced genetic analysis of type 1 diabetes by selecting variants on both effect size and significance, and by integration with autoimmune thyroid disease

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.05.429962

N/A

0.726DataRank · unranked

18 citations

Jamie Inshaw, Catherine C. Robertson, Jiayuan Zhang, Wei‐Min Chen, Suna Önengüt-Gümüşcü +8 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

A high-resolution HLA reference panel capturing global population diversity enables multi-ethnic fine-mapping in HIV host response

medRxiv(2020)10.1101/2020.07.16.20155606

Top 28%

0.708DataRank

Top 28%15 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Kenichi Yamamoto, Kotaro Ogawa +24 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

0.701DataRank · 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

0.701DataRank · unranked

106 citations

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

Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

Communications Biology(2023)10.1038/s42003-023-05454-1

N/A

0.689DataRank · unranked

22 citations

Alison E. Fohner, Qiong Yang, Jennifer A. Brody, Gail Davies, Jie Yao +52 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

Nature Genetics(2023)10.1038/s41588-023-01553-1

N/A

0.681DataRank · unranked

31 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +46 more

Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.11.013

N/A

0.679DataRank · unranked

21 citations

François Aguet, Sarah Kim-Hellmuth, Brielin C. Brown, Daniel Nachun, Russell P. Tracy +16 more

Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.05.014

N/A

0.663DataRank · unranked

82 citations

Shaila Musharoff, Jeffrey P. Spence, Harold Pimentel, Catherine Tcheandjieu, Hakhamanesh Mostafavi +19 more

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

Human Molecular Genetics(2013)10.1093/hmg/ddt588

N/A

0.650DataRank · unranked

75 citations

A. D. Johnson, B. M. Snively, Jarmo Virtamo, P. L. Auer, Jonas B. Nielsen +34 more

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

Human Genetics(2021)10.1007/s00439-021-02394-w

N/A

0.648DataRank · unranked

74 citations

Stephanie Yang, Christina A. Castellani, Wen Shi, Jon D. Lane, Megan L. Grove +47 more

Population sequencing data reveal a compendium of mutational processes in the human germ line

Science(2021)10.1126/science.aba7408

N/A

0.648DataRank · unranked

74 citations

Ruslan Soldatov, Evan M. Koch, Ryan J. McGinty, Jakob M. Goldmann, Ryan D. Hernandez +38 more

The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

Frontiers in Endocrinology(2022)10.3389/fendo.2022.863893

N/A

0.642DataRank · unranked

21 citations

Shing Wan Choi, Nathalie Chami, Eric Boerwinkle, Myriam Fornage, Susan Redline +36 more

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

Stroke(2020)10.1161/strokeaha.120.029123

N/A

0.637DataRank · unranked

69 citations

Hyacinth I. Hyacinth, Joshua C. Bis, Steven J. Kittner, Braxton D. Mitchell, Yu-Ching Cheng +43 more

Arsenic Exposure, Blood DNA Methylation, and Cardiovascular Disease

Circulation Research(2022)10.1161/circresaha.122.320991

N/A

0.635DataRank · unranked

68 citations

Kiran Makhani, Ángela L. Riffo‐Campos, María Téllez-Plaza, Kathleen Klein, Pooja Subedi +34 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

A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

American Journal of Epidemiology(2021)10.1093/aje/kwab115

N/A

0.631DataRank · unranked

66 citations

Leslie S. Emery, Jai Broome, Erin Buth, Alyna Khan, Cecelia Laurie +67 more

Protein-metabolite association studies identify novel proteomic determinants of metabolite levels in human plasma

Cell Metabolism(2023)10.1016/j.cmet.2023.07.012

N/A

0.609DataRank · unranked

57 citations

Aaron S. Eisman, Usman A. Tahir, Daniel H. Katz, Shuliang Deng, Debby Ngo +35 more

Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

Nature Genetics(2023)10.1038/s41588-022-01282-x

N/A

0.606DataRank · unranked

56 citations

Xingyan Wang, Seon-Kyeong Jang, Bryan C. Quach, J. Dylan Weissenkampen, Chachrit Khunsriraksakul +85 more

Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci

Genome Medicine(2021)10.1186/s13073-021-00877-z

N/A

0.606DataRank · unranked

56 citations

Anna Batorsky, Mi Kyeong Lee, Mindy D Szeto, Xiaoguang Xu, Daniel L. McCartney +37 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.014

N/A

0.605DataRank · unranked

14 citations

Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong +64 more

A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

Blood(2024)10.1182/blood.2023021452

N/A

0.601DataRank · unranked

23 citations

Paula Reventún, Michael R. Brown, Adam S. Heath, Jennifer E. Huffman, Ngoc‐Quynh Le +90 more

Sugar-Sweetened Beverage Consumption May Modify Associations Between Genetic Variants in the CHREBP (Carbohydrate Responsive Element Binding Protein) Locus and HDL-C (High-Density Lipoprotein Cholesterol) and Triglyceride Concentrations

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.120.003288

N/A

0.595DataRank · unranked

11 citations

Gina M. Peloso, Mélanie Guirette, Fumiaki Imamura, Traci M. Bartz, Achilleas Pitsillides +51 more

Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations

Nature Communications(2023)10.1038/s41467-023-38800-2

N/A

0.584DataRank · unranked

48 citations

Michael R. Brown, Taryn Alkis, Astrid M. Manuel, Xihao Li, Usman A. Tahir +31 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

Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups

Nature Communications(2023)10.1038/s41467-023-38990-9

N/A

0.578DataRank · unranked

46 citations

Matthew Goodman, Alyna Khan, Jiongming Wang, Elena V. Feofanova, Joshua C. Bis +38 more

Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes

Journal of the Endocrine Society(2020)10.1210/jendso/bvaa121

N/A

0.572DataRank · unranked

12 citations

Josep M. Mercader, Catherine C. Robertson, Joanne B. Cole, Ling Chen, Suzanne B.R. Jacobs +3 more

Pulmonary emphysema subtypes defined by unsupervised machine learning on CT scans

Thorax(2023)10.1136/thorax-2022-219158

N/A

0.561DataRank · unranked

41 citations

Jie Yang, Pallavi Balte, Eric A. Hoffman, Ani Manichaikul, Yifei Sun +36 more

Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts

Annals of the American Thoracic Society(2023)10.1513/annalsats.202210-857oc

N/A

0.556DataRank · unranked

13 citations

Katherine Pratte, Claudia Flexeder, Hans Petersen, Hong Dang, Yanlin Ma +49 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

0.553DataRank · unranked

39 citations

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

Reporting guidelines for precision medicine research of clinical relevance: the BePRECISE checklist

Nature Medicine(2024)10.1038/s41591-024-03033-3

N/A

0.553DataRank · unranked

39 citations

Zhila Semnani‐Azad, Mario Luca Morieri, Ashley Ng, Abrar Ahmad, Hugo Fitipaldi +18 more

Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis

American Journal of Respiratory and Critical Care Medicine(2022)10.1164/rccm.202108-1907oc

N/A

0.546DataRank · unranked

37 citations

Tianxiao Huan, Daniel L. McCartney, Geetha Chittoor, Maaike de Vries, Lies Lahousse +57 more

Toll-Like Receptor 1 Locus Re-examined in a Genome-Wide Association Study Update on Anti–Helicobacter pylori IgG Titers

Gastroenterology(2022)10.1053/j.gastro.2022.01.011

N/A

0.533DataRank · unranked

34 citations

Michiel C. Mommersteeg, Bingting Yu, Linda Broer, Manon C.W. Spaander, Fabian Frost +28 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

The functional impact of rare variation across the regulatory cascade

Cell Genomics(2023)10.1016/j.xgen.2023.100401

N/A

0.526DataRank · unranked

15 citations

Nicole M. Ferraro, Benjamin J. Strober, François Aguet, Silva Kasela, Marios Arvanitis +33 more

Rare genetic variants explain missing heritability in smoking

Nature Human Behaviour(2022)10.1038/s41562-022-01408-5

N/A

0.520DataRank · unranked

31 citations

Luke M. Evans, Allison Fialkowski, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes +85 more

Association of a Multiancestry Genome-Wide Blood Pressure Polygenic Risk Score With Adverse Cardiovascular Events

Circulation Genomic and Precision Medicine(2022)10.1161/circgen.122.003946

N/A

0.515DataRank · unranked

30 citations

Akhil Pampana, Naman S. Shetty, Marguerite R. Irvin, Pradeep Natarajan, Henry J. Lin +8 more

Protein prediction for trait mapping in diverse populations

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Jeongok G. Logan, Younghoon Kwon, João A.C. Lima, DAVID R. JACOBS, Daniel Duprez +19 more

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Journal of the Indian Institute of Science(2023)10.1007/s41745-023-00356-x

N/A

0DataRank · unranked

12 citations

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Scientific Reports(2023)10.1038/s41598-023-34866-6

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0DataRank · unranked

6 citations

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Respiratory Research(2023)10.1186/s12931-023-02316-6

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0DataRank · unranked

8 citations

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Nutrients(2023)10.3390/nu15122779

N/A

0DataRank · unranked

5 citations

Mackenzie K. Senn, Ani Manichaikul, Chaojie Yang, Rasika A. Mathias, Mimi Phan +7 more

Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.26.546528

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0DataRank · unranked

7 citations

François Aguet, Sarah Kim-Hellmuth, Brielin C. Brown, Daniel Nachun, Russell P. Tracy +16 more

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medRxiv(2023)10.1101/2023.07.13.23292628

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0DataRank · unranked

5 citations

Ernesto Nakayasu, Fran Dong, Kathy Waugh, Javier E. Flores, Lisa Bramer +10 more

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bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.17.553749

N/A

0DataRank · unranked

3 citations

Boran Gao, Qidi Feng, Ani Manichaikul, Gina M. Peloso, Russell P. Tracy +17 more

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UNC Libraries(2023)10.17615/hthq-e624

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0DataRank · unranked

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Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESA

Research Square(2023)10.21203/rs.3.rs-3125948/v1

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0DataRank · unranked

0 citations

Xiaowei Hu, Jeongok G. Logan, Younghoon Kwon, João A.C. Lima, DAVID R. JACOBS +19 more

Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores

medRxiv(2023)10.1101/2023.12.13.23299909

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0DataRank · unranked

0 citations

Benjamin Shea, Michael Elgart, Nuzulul Kurniansyah, Genevieve Lyons, Alanna C. Morrison +32 more

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Nature Metabolism(2024)10.1038/s42255-024-00999-9

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0DataRank · unranked

78 citations

Veronica L. Li, Xuchao Lyu, Xudong Chen, Wei Wei, Fahim Abbasi +22 more

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Communications Medicine(2024)10.1038/s43856-024-00478-y

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0DataRank · unranked

46 citations

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Nature Reviews Endocrinology(2024)10.1038/s41574-024-01045-0

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0DataRank · unranked

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Nature Medicine(2024)10.1038/s41591-024-03032-4

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0DataRank · unranked

24 citations

Paul W. Franks, Norman D. Rosenblum, Norann A. Zaghloul, José C. Florez, Francesco Giorgino +25 more

A Research Roadmap to Address the Heterogeneity of Diabetes and Advance Precision Medicine

The Journal of Clinical Endocrinology & Metabolism(2024)10.1210/clinem/dgae844

N/A

0DataRank · unranked

15 citations

Stephen S. Rich, Barbara Linder, Norann A. Zaghloul, William T. Cefalu, Paul W. Franks

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Science Translational Medicine(2024)10.1126/scitranslmed.adj3385

N/A

0DataRank · unranked

14 citations

Eiichiro Satake, Marcus G. Pezzolesi, Zaipul I. Md Dom, DEVORAH STUCKI, Hiroki Kobayashi +11 more

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American Journal of Respiratory and Critical Care Medicine(2024)10.1164/rccm.202401-0011oc

N/A

0DataRank · unranked

10 citations

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Epigenetics(2024)10.1080/15592294.2024.2333668

N/A

0DataRank · unranked

9 citations

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Diabetologia(2024)10.1007/s00125-024-06338-7

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0DataRank · unranked

8 citations

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ESC Heart Failure(2024)10.1002/ehf2.15073

N/A

0DataRank · unranked

3 citations

João A.C. Lima, Sanjiv J. Shah, David A. Bluemke, Alain G. Bertoni, Yongmei Liu +15 more

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The Journal of Clinical Endocrinology & Metabolism(2024)10.1210/clinem/dgae349

N/A

0DataRank · unranked

7 citations

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JACC Heart Failure(2024)10.1016/j.jchf.2024.08.019

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0DataRank · unranked

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Mokshad Gaonkar, Akhil Pampana, Nirav Patel, Alanna C. Morrison, Alex P. Reiner +22 more

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Journal of Clinical Investigation(2024)10.1172/jci173278

N/A

0DataRank · unranked

5 citations

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Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

Mitochondrion(2024)10.1016/j.mito.2024.101954

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0DataRank · unranked

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Annals of the American Thoracic Society(2024)10.1513/annalsats.202305-417oc

N/A

0DataRank · unranked

2 citations

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Metabolites Link Intake of a Healthy Diet to Better Insulin and Glucose Homeostasis in the Microbiome and Insulin Longitudinal Evaluation Study (MILES)

Current Developments in Nutrition(2024)10.1016/j.cdnut.2024.104462

N/A

0DataRank · unranked

1 citations

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medRxiv(2024)10.1101/2024.03.07.24303870

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0DataRank · unranked

1 citations

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Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

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

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Association analysis of mitochondrial DNA heteroplasmic variants: methods and application

medRxiv(2024)10.1101/2024.01.12.24301233

N/A

0DataRank · unranked

0 citations

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medRxiv(2024)10.1101/2024.01.23.24301689

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0 citations

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medRxiv(2024)10.1101/2024.02.13.24302797

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0 citations

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UNC Libraries(2024)10.17615/y07d-kq52

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C.-T. Liu, A Furniss, R.S. Vasan, P.A. Peyser, Gao Ya +74 more

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UNC Libraries(2024)10.17615/tv1j-wn72

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B.M. Psaty, Bing Yu, Taylor, K.D., Donna K. Arnett, D. Levy +33 more

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UNC Libraries(2024)10.17615/0ea7-3v47

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0 citations

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UNC Libraries(2024)10.17615/mjwt-x036

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0DataRank · unranked

0 citations

W.S. Post, Josyf C. Mychaleckyj, M. FORNAGE, Adrienne Tin, Denyse Thornley‐Brown +22 more

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UNC Libraries(2024)10.17615/0hks-jx94

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0DataRank · unranked

0 citations

Xia Zhou, Geetha Chittoor, Elizabeth C. Oelsner, J. Dupuis, Stephanie J. London +41 more

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UNC Libraries(2024)10.17615/mbk9-3d37

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UNC Libraries(2024)10.17615/wajp-xh91

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UNC Libraries(2024)10.17615/a7t8-mf18

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Mayo Clinic Proceedings(2024)10.1016/j.mayocp.2023.12.020

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0 citations

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Scientific Reports(2024)10.1038/s41598-024-71714-7

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medRxiv(2024)10.1101/2024.09.12.24313561

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0DataRank · unranked

0 citations

Kaitlin S. Potts, Bing Yu, Robert C. Kaplan, Carmen R. Isasi, Qibin Qi +12 more

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UNC Libraries(2024)10.17615/54px-be07

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Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

UNC Libraries(2024)10.17615/vs68-ca81

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0 citations

Ryan L. Minster, Fernando D. Martínez, Dawood Darbar, Juan M. Peralta, Barbara A. Konkle +93 more

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UNC Libraries(2024)10.17615/yx5k-ka41

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0DataRank · unranked

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Taralynn Mack, Margaret F. Doyle, Yash Pershad, Paul L. Auer, Jeong H. Yun +39 more

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medRxiv(2024)10.1101/2024.10.25.24316158

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0 citations

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The Relationship of Duffy Gene Polymorphism with High-Sensitivity C-Reactive Protein, Mortality, and Cardiovascular Outcomes in Black Individuals

UNC Libraries(2024)10.17615/shas-p528

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0 citations

Bjoernar Tuftin, Stephen J. Peterson, Laura M. Raffield, KARL T. KELSEY, Manish A. Parikh +15 more

Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

UNC Libraries(2024)10.17615/b6xd-h115

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

Lume (Universidade Federal do Rio Grande do Sul)(2024)10.17615/anr2-h090

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Diabetologia(2025)10.1007/s00125-025-06462-y

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Type 1 diabetes prediction in autoantibody-positive individuals: performance, time and money matter

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

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0DataRank · unranked

4 citations

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Genetic Risk and Transition Through Preclinical Stages of Type 1 Diabetes

The Journal of Clinical Endocrinology & Metabolism(2025)10.1210/clinem/dgaf392

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Steroid hormone biosynthesis and dietary related metabolites associated with excessive daytime sleepiness

EBioMedicine(2025)10.1016/j.ebiom.2025.105881

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The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.011

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medRxiv(2025)10.1101/2025.06.20.25329522

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Refinement of a Published Gene‐Physical Activity Interaction Impacting HDL‐Cholesterol: Role of Sex and Lipoprotein Subfractions

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Thorax(2025)10.1136/thorax-2025-222990

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Lifestyle Genomics(2025)10.1159/000546100

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Michael R. Brown, Solomon K. Musani, Karen Schwander, Thomas W. Winkler, Mario Sims +93 more

HLA-focused type 1 diabetes genetic risk prediction in populations of diverse ancestry

medRxiv(2025)10.1101/2025.08.07.25333167

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Fibrinogen-Associated Plasma Metabolites and Implications for Coagulation, Inflammation, and Vascular Diseases

medRxiv(2025)10.1101/2025.08.06.25333064

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Sleep-disordered breathing subtypes and future diet quality in the Multi-Ethnic Study of Atherosclerosis

Sleep Health(2025)10.1016/j.sleh.2025.08.003

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Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential.

UNC Libraries(2025)10.17615/fdg0-0818

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MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric

UNC Libraries(2025)10.17615/4609-8b83

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Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

UNC Libraries(2025)10.17615/mztm-gw84

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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

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Blood Cells Molecules and Diseases(2025)10.1016/j.bcmd.2025.102966

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Pulmonary emphysema subtypes defined by unsupervised machine learning on CT scans

UNC Libraries(2025)10.17615/6455-md85

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Genetic Predictors of Response to Oral Insulin for Type 1 Diabetes Prevention

Diabetes Care(2025)10.2337/dc25-2006

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Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participants

10.1101/2025.06.11.25329426

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