Gina M. Peloso

Also affiliated with VA Boston Healthcare System

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

15.3Author DataRank

Indexed papers

7in 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 7 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 62 papers — median percentile 52. 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

Transcriptomic signatures across human tissues identify functional rare genetic variation

Science(2020)10.1126/science.aaz5900

N/A

5.0DataRank · unranked

166 citations

Benjamin J. Strober, Jonah Einson, Nathan S. Abell, François Aguet, Alvaro N. Barbeira +183 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

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

Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program

Circulation(2023)10.1161/circulationaha.122.061451

N/A

1.9DataRank · unranked

73 citations

Gina M. Peloso, Jason Linefsky, Jayashri Aragam, Ashley Galloway, Vidisha Tanukonda +21 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

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

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 DNA and RNA sequencing of whole blood elucidates the genetic architecture of gene expression underlying a wide range of diseases

Scientific Reports(2022)10.1038/s41598-022-24611-w

Top 38%

0.509DataRank

Top 38%21 citations

Roby Joehanes, Jiantao Ma, Yuxuan Wang, Xianbang Sun, Amena Keshawarz +15 more

Genetic modification of inflammation and clonal hematopoiesis-associated cardiovascular risk

medRxiv(2022)10.1101/2022.12.08.22283237

N/A

0.416DataRank · unranked

8 citations

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

Whole Genome DNA and RNA Sequencing of Whole Blood Elucidates the Genetic Architecture of Gene Expression Underlying a Wide Range of Diseases

medRxiv(2022)10.1101/2022.04.13.22273841

Top 48%

0.379DataRank

Top 48%9 citations

Roby Joehanes, Jiantao Ma, Yuxuan Wang, Xianbang Sun, Amena Keshawarz +15 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

Key variants via Alzheimer’s Disease Sequencing Project whole genome sequence data

medRxiv(2023)10.1101/2023.08.28.23294631

Top 59%

0.257DataRank

Top 59%4 citations

Chloé Sarnowski, Honghuang Lin, Achilleas Pitsillides, Nancy L. Heard‐Costa, Seung Hoan Choi +14 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

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

Alternative splicing of OAS1 alters the risk for severe COVID-19

medRxiv(2021)10.1101/2021.03.20.21254005

N/A

0DataRank · unranked

17 citations

Guillaume Butler‐Laporte, Atlas Khan, Theodore G. Drivas, Gina M. Peloso, Tomoko Nakanishi +5 more

Polygenic Risk Prediction using Gradient Boosted Trees Captures Non-Linear Genetic Effects and Allele Interactions in Complex Phenotypes

medRxiv(2021)10.1101/2021.07.09.21260288

N/A

0DataRank · unranked

3 citations

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

Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

UNC Libraries(2021)10.17615/shbq-nv48

N/A

0DataRank · unranked

0 citations

Douglas M. Ruderfer, Goo Jun, Ji Zhang, Yun Li, Leslie A. Lange +27 more

Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19

Nature Genetics(2022)10.1038/s41588-021-00996-8

N/A

0DataRank · unranked

129 citations

Guillaume Butler‐Laporte, Atlas Khan, Erola Pairo-Castineira, Theodore G. Drivas, Gina M. Peloso +9 more

Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program

Frontiers in Genetics(2022)10.3389/fgene.2021.777076

N/A

0DataRank · unranked

17 citations

Catherine Tcheandjieu, John E. McGeary, Daniel Posner, Yuk‐Lam Ho, Jin Zhou +12 more

Sugar-Sweetened Beverage Consumption and Plasma Lipoprotein Cholesterol, Apolipoprotein, and Lipoprotein Particle Size Concentrations in US Adults

Journal of Nutrition(2022)10.1093/jn/nxac166

N/A

0DataRank · unranked

15 citations

Daniel I. Chasman, Gina M. Peloso, Mark A. Herman, Josée Dupuis, Alice H. Lichtenstein +6 more

Genome-wide discovery for diabetes-dependent triglycerides-associated loci

PLoS ONE(2022)10.1371/journal.pone.0275934

N/A

0DataRank · unranked

13 citations

Kaavya Paruchuri, Sara Haidermota, Rachel Bernardo, Stephen S. Rich, Gina M. Peloso +2 more

Family history aggregation unit-based tests to detect rare genetic variant associations with application to the Framingham Heart Study

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.001

N/A

0DataRank · unranked

4 citations

Han Chen, Gina M. Peloso, James B. Meigs, Alexa Beiser, Sudha Seshadri +3 more

Genome-wide Discovery for Diabetes-Dependent Triglycerides-Associated Loci

medRxiv(2022)10.1101/2022.01.06.22268848

N/A

0DataRank · unranked

1 citations

Kaavya Paruchuri, Sara Haidermota, Rachel Bernardo, Stephen S. Rich, Gina M. Peloso +2 more

Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of multiple cardiovascular disease risk factors

medRxiv(2022)10.1101/2022.03.29.22273133

N/A

0DataRank · unranked

1 citations

B Kavitha, Siqi Hu, Roi Isaac, Minxian Wang, Xiaomi Du +16 more

Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure

Nature Communications(2023)10.1038/s41467-023-39253-3

N/A

0DataRank · unranked

129 citations

Gina M. Peloso, Alexandre C. Pereira, Hesam Dashti, Claudia Giambartolomei, Eleanor Wheeler +30 more

Human gain-of-function variants in HNF1A confer protection from diabetes but independently increase hepatic secretion of atherogenic lipoproteins

Cell Genomics(2023)10.1016/j.xgen.2023.100339

N/A

0DataRank · unranked

20 citations

B Kavitha, Siqi Hu, Roi Isaac, Lynne Krohn, Minxian Wang +17 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.003

N/A

0DataRank · unranked

15 citations

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

Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease

Circulation(2023)10.1161/circulationaha.123.064168

N/A

0DataRank · unranked

12 citations

Jacqueline S. Dron, Brandon K. Bellows, Amit V. Khera, Junxiu Liu, Pallavi Balte +27 more

Genetic and clinical factors underlying a self-reported family history of heart disease

European Journal of Preventive Cardiology(2023)10.1093/eurjpc/zwad096

N/A

0DataRank · unranked

7 citations

Romit Bhattacharya, Christopher Marnell, Megan Wong, Sara Haidermota, Mark Trinder +5 more

Bayesian multivariate genetic analysis improves translational insights

iScience(2023)10.1016/j.isci.2023.107854

N/A

0DataRank · unranked

1 citations

Satoshi Koyama, Whitney Hornsby, Rohan Bhukar, Sumeet Kheterpal, Buu Truong +6 more

Frequency of Variants in Mendelian Alzheimer’s Disease Genes within the Alzheimer’s Disease Sequencing Project (ADSP)

medRxiv(2023)10.1101/2023.10.24.23297227

N/A

0DataRank · unranked

6 citations

Alexandra Scalici, Yanbing Wang, Honghuang Lin, Achilleas Pitsillides, Nancy L. Heard‐Costa +16 more

Human Plasma Proteomic Profile of Clonal Hematopoiesis

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.25.550557

N/A

0DataRank · unranked

5 citations

Amélie Vromman, Ngoc Quynh Nguyen, Art Schuermans, Thiago Rentz, Shamsudheen Karuthedath Vellarikkal +44 more

Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies

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

Comparison of methods for building polygenic scores for diverse populations

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100355

N/A

0DataRank · unranked

19 citations

Xin Wang, Daniel Posner, Kelly Cho, Jennifer E. Huffman, Michael Gaziano +5 more

Lipid levels and risk of acute pancreatitis using bidirectional Mendelian randomization

Scientific Reports(2024)10.1038/s41598-024-56946-x

N/A

0DataRank · unranked

16 citations

Jacqueline S. Dron, Yuxuan Wang, Seung Hoan Choi, Jennifer E. Huffman, Kelly Cho +4 more

Protein Identification for Stroke Progression via Mendelian Randomization in Million Veteran Program and UK Biobank

Stroke(2024)10.1161/strokeaha.124.047103

N/A

0DataRank · unranked

8 citations

Nimish Adhikari, April Hartley, Hugo J. Aparicio, Daniel Posner, Gibran Hemani +10 more

Proteome-wide association studies for blood lipids and comparison with transcriptome-wide association studies

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100383

N/A

0DataRank · unranked

1 citations

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

The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup

medRxiv(2024)10.1101/2024.03.05.24303738

N/A

0DataRank · unranked

3 citations

Nuzulul Kurniansyah, Matthew Goodman, Brian Spitzer, Jiongming Wang, Adrienne M. Stilp +27 more

Protein identification for stroke progression via Mendelian Randomization in Million Veteran Program and UK Biobank

medRxiv(2024)10.1101/2024.01.31.24302111

N/A

0DataRank · unranked

1 citations

Nimish Adhikari, April Hartley, Hugo J. Aparicio, Dan C. Posner, Gibran Hemani +10 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

UNC Libraries(2024)10.17615/8vh7-3029

N/A

0DataRank · unranked

0 citations

Jordi Merino, J. Dupuis, J.B. Meigs, T. Lehtimäki, Mika Helminen +51 more

A system for phenotype harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) program

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

N/A

0DataRank · unranked

0 citations

Nicola L. Hawley, May E. Montasser, P.A. Peyser, Daniel E. Weeks, Braxton D. Mitchell +67 more

Human plasma proteomic profile of clonal hematopoiesis

Nature Communications(2025)10.1038/s41467-025-66755-z

N/A

0DataRank · unranked

7 citations

Amélie Vromman, Ngoc Quynh Nguyen, Art Schuermans, Linke Li, Thiago Rentz +48 more

Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals

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

N/A

0DataRank · unranked

2 citations

Xihao Li, Zilin Li, Eric Van Buren, Sara Haidermota, Darina Postupaka +95 more

Methylome-wide association analyses of lipids and modifying effects of behavioral factors in diverse race and ethnicity participants

Clinical Epigenetics(2025)10.1186/s13148-025-01859-3

N/A

0DataRank · unranked

1 citations

Jeff Haessler, Jessica I. Lundin, Burcu F. Darst, Eric A. Whitsel, Megan L. Grove +32 more

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

UNC Libraries(2025)10.17615/408w-ez13

N/A

0DataRank · unranked

0 citations

Jessica Lundin, Dawn L. DeMeo, Daniel Levy, Ramachandran S. Vasan, Shih‐Jen Hwang +31 more

Association of an Aquaporin-4 Haplotype with Cognition, Brain Volume, and Dementia Risk in Community-Dwelling Individuals without Dementia

medRxiv(2025)10.64898/2025.12.15.25342248

N/A

0DataRank · unranked

0 citations

Dibya Himali, Lachlan Cribb, Gina M. Peloso, Joanne Ryan, Qiong Yang +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

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

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

N/A

0DataRank · unranked

5 citations

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

Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

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

N/A

0DataRank · unranked

5 citations

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

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

UNC Libraries(2020)10.17615/vn1s-8a35

N/A

0DataRank · unranked

0 citations

Frank J.A. van Rooij, Raha Pazoki, Albert Hofman, Nathan Pankratz, Richard A. Gibbs +51 more

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

UNC Libraries(2020)10.17615/a384-d483

N/A

0DataRank · unranked

0 citations

Jerome I. Rotter, Alex P. Reiner, André G. Uitterlinden, Gonçalo R. Abecasis, Digna R. Velez Edwards +95 more

Common variants at 30 loci contribute to polygenic dyslipidemia

UNC Libraries(2020)10.17615/wktm-vc19

N/A

0DataRank · unranked

0 citations

Pilar Galán, Serkalem Demissie, Eric E. Schadt, Aarti Surti, Luigi Ferrucci +27 more

Association of Exome Sequences With Cardiovascular Traits among Blacks in the Jackson Heart Study

UNC Libraries(2020)10.17615/a9gj-5z87

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Mark J. Daly, James G. Wilson, Hao Mei, Joshua D. Smith +14 more

Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks

UNC Libraries(2020)10.17615/sbz9-wg52

N/A

0DataRank · unranked

0 citations

Rebecca D. Jackson, Valeska Redon, Gina M. Peloso, Joshua C. Bis, Arend Voorman +27 more

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/msaw-3g92

N/A

0DataRank · unranked

0 citations

Patrick Deelen, David J. van Enckevort, Irene Mateo Leach, Gina M. Peloso, Mary F. Feitosa +27 more

Association of Sickle Cell Trait With Chronic Kidney Disease and Albuminuria in African Americans

UNC Libraries(2020)10.17615/0cmb-g360

N/A

0DataRank · unranked

0 citations

Vimal K. Derebail, Carmen A. Peralta, Pierre Fontanillas, Alexander G. Bick, Adolfo Correa +26 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

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

0DataRank · unranked

66 citations

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

Gina M. Peloso

Indexed papers

Top data-sharing exemplar

Papers