Jennifer E. Huffman

Also affiliated with Harvard University, VA Palo Alto Health Care System, VA Boston Healthcare System, Palo Alto Veterans Institute for Research

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 2%percentile

4.5Author DataRank

Indexed papers

2in 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 2 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.

Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program

Science(2024)10.1126/science.adj1182

Top 7%

3.2DataRank

Top 7%377 citations

Jennifer E. Huffman, Alex A Rodriguez, Mitchell Conery, Molei Liu, Yuk‐Lam Ho +66 more

Papers

Driven by 58 papers — median percentile 88. 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

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Nature Genetics(2022)10.1038/s41588-022-01016-z

N/A

8.1DataRank · unranked

699 citations

Yeda Wu, Nancy Wang, Hariharan Jayashankar, Michael Bennett, Seyed Moeen Nehzati +94 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

Genome-wide association study identifies 48 common genetic variants associated with handedness

Nature Human Behaviour(2020)10.1038/s41562-020-00956-y

N/A

3.7DataRank · unranked

157 citations

Joyce Y. Tung, Nicholas Eriksson, Eva Albrecht, Fazil Alıev, Ole A. Andreassen +95 more

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 more

Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program

Science(2024)10.1126/science.adj1182

Top 7%

3.2DataRank

Top 7%377 citations

Jennifer E. Huffman, Alex A Rodriguez, Mitchell Conery, Molei Liu, Yuk‐Lam Ho +66 more

A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program

PLoS Genetics(2022)10.1371/journal.pgen.1010193

Top 17%

1.2DataRank

Top 17%22 citations

Jie Huang, Catherine Tcheandjieu, Jennifer E. Huffman, Elizabeth Litkowski, Chang Liu +20 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

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

A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program

medRxiv(2021)10.1101/2021.05.18.21257396

N/A

0.506DataRank · unranked

8 citations

Noah L. Tsao, Lauren O. Thomann, Yuk‐Lam Ho, Sudha K. Iyengar, Shiuh‐Wen Luoh +32 more

An African ancestry-specific nonsense variant in CD36 is associated with a higher risk of dilated cardiomyopathy

Nature Genetics(2025)10.1038/s41588-025-02372-2

N/A

0.345DataRank · unranked

9 citations

Liam Gaziano, Zeina R. Al Sayed, Renae Judy, Laura M. Raffield, Kiran J. Biddinger +59 more

Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.03.453690

N/A

0DataRank · unranked

2 citations

Sanan Venkatesh, Manuel Tardáguila, Jia Wen, Jonathan D. Rosen, Amanda L. Tapia +13 more

Evaluation of height as a disease risk factor through a phenome-wide association study of genetically-predicted height

medRxiv(2021)10.1101/2021.08.29.21262793

N/A

0DataRank · unranked

2 citations

Jie Huang, Catherine Tcheandjieu, Jennifer E. Huffman, Elizabeth Litkowski, Yuk‐Lam Ho +19 more

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Nature Genetics(2022)10.1038/s41588-022-01078-z

N/A

0DataRank · unranked

195 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +86 more

Genomics and phenomics of body mass index reveals a complex disease network

Nature Communications(2022)10.1038/s41467-022-35553-2

N/A

0DataRank · unranked

188 citations

Jennifer E. Huffman, Yunfeng Huang, Ítalo Faria do Valle, Themistocles L. Assimes, Sridharan Raghavan +34 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

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 MUC5B Gene Polymorphism, rs35705950-T, Confers Protective Effects Against COVID-19 Hospitalization but Not Severe Disease or Mortality

American Journal of Respiratory and Critical Care Medicine(2022)10.1164/rccm.202109-2166oc

N/A

0DataRank · unranked

44 citations

Jessica Minnier, Emily S. Wan, Jennifer E. Huffman, Lina Gao, Jacob Joseph +42 more

Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin

Journal of the American Society of Nephrology(2022)10.1681/asn.2021040491

N/A

0DataRank · unranked

31 citations

Marta Mariniello, Ayumi Yoshifuji, Guglielmo Schiano, Jennifer Lake, Jonathan Marten +38 more

A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program

PLoS Genetics(2022)10.1371/journal.pgen.1010113

N/A

0DataRank · unranked

27 citations

Noah L. Tsao, Lauren O. Thomann, Yuk‐Lam Ho, Sudha K. Iyengar, Shiuh‐Wen Luoh +32 more

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

Nature Communications(2022)10.1038/s41467-022-28729-3

N/A

0DataRank · unranked

20 citations

Lingyan Chen, Paulina J. Stanczyk, Joanna M. M. Howson, Amy M. Mason, Stephen Burgess +91 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

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

Human Molecular Genetics(2022)10.1093/hmg/ddac100

N/A

0DataRank · unranked

17 citations

Peng Wei, Jennifer A. Brody, Ming‐Huei Chen, Paul S. de Vries, Jennifer E. Huffman +26 more

Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits

Human Molecular Genetics(2022)10.1093/hmg/ddac011

N/A

0DataRank · unranked

18 citations

Sanan Venkatesh, Manuel Tardáguila, Jia Wen, Jonathan D. Rosen, Amanda L. Tapia +13 more

Multi-ancestry meta-analysis identifies 2 novel loci associated with ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

medRxiv(2022)10.1101/2022.02.28.22271647

N/A

0DataRank · unranked

18 citations

Kuan-Han H. Wu, Whitney Hornsby, Brooke N. Wolford, Fred Shen, Wei Zhou +17 more

Genome-wide association study meta-analysis of suicide attempt identifies twelve genome-wide significant loci and implicates genetic risks for specific health factors

medRxiv(2022)10.1101/2022.07.03.22277199

N/A

0DataRank · unranked

9 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 more

GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors

American Journal of Psychiatry(2023)10.1176/appi.ajp.21121266

N/A

0DataRank · unranked

150 citations

Niamh Mullins, Allison E. Ashley‐Koch, Xuejun Qin, Jonathan R. I. Coleman, Andrey A. Shabalin +95 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

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

Cell Genomics(2023)10.1016/j.xgen.2022.100241

N/A

0DataRank · unranked

113 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +83 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

0DataRank · unranked

46 citations

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

Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

Cell Genomics(2023)10.1016/j.xgen.2023.100345

N/A

0DataRank · unranked

22 citations

Kuan-Han Wu, Whitney Hornsby, Brooke N. Wolford, Fred Shen, Wei Zhou +16 more

Genetics of varicose veins reveals polygenic architecture and genetic overlap with arterial and venous disease

Nature Cardiovascular Research(2023)10.1038/s44161-022-00196-5

N/A

0DataRank · unranked

14 citations

Jennifer E. Huffman, Anurag Verma, Kyle A. Sullivan, Alexis Rodriguez, David Kainer +17 more

Novel genetic regulators of fibrinogen synthesis identified by an in vitro experimental platform

Journal of Thrombosis and Haemostasis(2023)10.1016/j.jtha.2022.10.027

N/A

0DataRank · unranked

14 citations

Lori A. Holle, Feng‐Chang Lin, Jennifer E. Huffman, James P. Luyendyk, Matthew J. Flick +5 more

A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

Journal of Thrombosis and Haemostasis(2023)10.1016/j.jtha.2023.11.027

N/A

0DataRank · unranked

8 citations

Gerard Temprano‐Sagrera, Jara Cárcel‐Márquez, Elena Muiño, Natàlia Cullell, Miquel Lledós +91 more

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

medRxiv(2023)10.1101/2023.08.14.23294063

N/A

0DataRank · unranked

2 citations

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

Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

medRxiv(2023)10.1101/2023.06.07.23291095

N/A

0DataRank · unranked

1 citations

Jayna Nicolas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Nature Genetics(2024)10.1038/s41588-024-01975-5

N/A

0DataRank · unranked

51 citations

Joel Rämö, Daria R. Kramarenko, Leonoor F. J. M. Wijdeveld, Jan Haas, Mark Chaffin +55 more

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

Blood(2024)10.1182/blood.2023021452

N/A

0DataRank · unranked

23 citations

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

Factors that modulate platelet reactivity as measured by 5 assay platforms in 3429 individuals

Research and Practice in Thrombosis and Haemostasis(2024)10.1016/j.rpth.2024.102406

N/A

0DataRank · unranked

17 citations

Ming‐Huei Chen, Florian Thibord, Bongani B. Nkambule, Amber Lachapelle, Joseph Grech +9 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

Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

Blood(2024)10.1182/blood.2023022596

N/A

0DataRank · unranked

15 citations

Jayna Nicholas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

UEF eRepo (University of Eastern Finland)(2024)10.17615/k2gw-9005

N/A

0DataRank · unranked

10 citations

James R. Staley, M.E. Jørgensen, T. Tuomi, R. Rauramaa, Robin Young +95 more

Characterization of the phenotypic consequences of the Duffy-null genotype

Blood Advances(2025)10.1182/bloodadvances.2024014399

N/A

0DataRank · unranked

11 citations

Megan M. Shuey, Jennifer E. Huffman, Paul L. Auer, Alex P. Reiner, Laura M. Raffield +1 more

Polygenic scores for obstructive sleep apnoea reveal pathways contributing to cardiovascular disease

EBioMedicine(2025)10.1016/j.ebiom.2025.105790

N/A

0DataRank · unranked

6 citations

Satu Strausz, Geetha Chittoor, Shreyash Gupta, Anne E. Justice, Yana Hrytsenko +30 more

Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleeding

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

N/A

0DataRank · unranked

4 citations

Adam S. Heath, Jennifer E. Huffman, James Baker, Natalie R. Hasbani, Sarah A. Gagliano Taliun +39 more

A semi-empirical Bayes approach for calibrating weak instrumental bias in sex-specific Mendelian randomization studies

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.07.015

N/A

0DataRank · unranked

1 citations

Nuzulul Kurniansyah, Daniel F. Levey, Joel Gelernter, Jennifer E. Huffman, Kelly Cho +5 more

Historical review: more than two decades understanding the genetic architecture of hemostasis and thrombosis

Journal of Thrombosis and Haemostasis(2025)10.1016/j.jtha.2025.11.006

N/A

0DataRank · unranked

1 citations

Florian Thibord, Paul S. de Vries, Jennifer E. Huffman, Alisa S. Wolberg, Charles J. Lowenstein +4 more

The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function

Nature Communications(2020)10.1038/s41467-020-17254-w

N/A

0DataRank · unranked

93 citations

Michael A. Mastrangelo, Sara Ture, Charles O. Smith, Shannon G. Loelius, Rachel A. Berg +14 more

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/5y99-4w88

N/A

0DataRank · unranked

5 citations

Terho Lehtimäki, P. Eline Slagboom, Albert V. Smith, Dennis O. Mook‐Kanamori, Paul Elliott +93 more

FTO genotype is associated with phenotypic variability of body mass index

UNC Libraries(2020)10.17615/yvv7-bx40

N/A

0DataRank · unranked

0 citations

Ayşe Demirkan, David Hadley, Cameron D. Palmer, Sarah E. Medland, Ruth J. F. Loos +27 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

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Publisher(2020)10.17615/tme1-9982

N/A

0DataRank · unranked

0 citations

Keolu Fox, Ping An, Li Li, Marie‐France Hivert, Laura J. Rasmussen‐Torvik +27 more

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function

UNC Libraries(2020)10.17615/d3kg-q519

N/A

0DataRank · unranked

0 citations

Patricia A. Cassano, Jing Zhao, Guðný Eiríksdóttir, Gauti Kjartan Gíslason, Jennifer E. Huffman +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 Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies

UNC Libraries(2020)10.17615/tb6e-th27

N/A

0DataRank · unranked

0 citations

Christina L. Wassel, Tanja Zeller, Lina Zgaga, Eric Boerwinkle, Ben A. Oostra +95 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

A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

medRxiv(2021)10.1101/2020.12.26.20248491

N/A

0DataRank · unranked

16 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +85 more

Jennifer E. Huffman

Indexed papers

Top data-sharing exemplar

Papers