Krishna G. Aragam

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 4%percentile

0.829Author DataRank

Indexed papers

3in 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 3 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.

The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium

ESC Heart Failure(2021)10.1002/ehf2.13517

Top 24%

0.829DataRank

Top 24%22 citations

Sonia Shah, Honghuang Lin, Tomasz Czuba, Albert Henry, Daniel I. Swerdlow +95 more

Papers

Driven by 35 papers — median percentile 76. Top paper: “Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants”.

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Nature Genetics(2022)10.1038/s41588-022-01233-6

N/A

7.7DataRank · unranked

721 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri +92 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

Convergence of coronary artery disease genes onto endothelial cell programs

Nature(2024)10.1038/s41586-024-07022-x

N/A

2.0DataRank · unranked

111 citations

Helen Kang, Shi Fang, Ramcharan Singh Angom, Vivian S. Lee, X. Rosa +22 more

Titin Truncating Variants in Adults Without Known Congestive Heart Failure

Journal of the American College of Cardiology(2020)10.1016/j.jacc.2020.01.013

N/A

1.6DataRank · unranked

28 citations

Alexander G. Bick, Mark Chaffin, Krishna G. Aragam, Seung Hoan Choi, Steven A. Lubitz +7 more

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

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

N/A

1.4DataRank · unranked

63 citations

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

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

Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood

Cell(2019)10.1016/j.cell.2019.03.028

N/A

1.0DataRank · unranked

842 citations

Mark Chaffin, Kaitlin H. Wade, Sohail Zahid, Joseph Brancale, Rui Xia +14 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

The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium

ESC Heart Failure(2021)10.1002/ehf2.13517

Top 24%

0.829DataRank

Top 24%22 citations

Sonia Shah, Honghuang Lin, Tomasz Czuba, Albert Henry, Daniel I. Swerdlow +95 more

The impact of non-additive genetic associations on age-related complex diseases

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.12.084608

N/A

0.821DataRank · unranked

14 citations

Ramon Amela, Sílvia Bonàs‐Guarch, Montserrat Puiggròs, Cecilia Salvoro, Irene Miguel-Escalada +16 more

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0.775DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

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

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

N/A

0.754DataRank · unranked

151 citations

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

The impact of non-additive genetic associations on age-related complex diseases

Nature Communications(2021)10.1038/s41467-021-21952-4

N/A

0.731DataRank · unranked

130 citations

Ramon Amela, Sílvia Bonàs‐Guarch, Montserrat Puiggròs, Cecilia Salvoro, Irene Miguel-Escalada +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

0.731DataRank · unranked

130 citations

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

Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation

Nature Genetics(2023)10.1038/s41588-023-01410-1

N/A

0.680DataRank · unranked

92 citations

Takiy-Eddine Berrandou, Adrien Georges, Christopher P. Nelson, Eleni Giannoulatou, Joséphine Henry +52 more

Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank

JAMA Cardiology(2022)10.1001/jamacardio.2022.1061

N/A

0.659DataRank · unranked

80 citations

Sean J. Jurgens, Dimitri Maamari, Liam Gaziano, Seung Hoan Choi, Valerie N. Morrill +6 more

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

medRxiv(2021)10.1101/2021.05.24.21257377

N/A

0.637DataRank · unranked

69 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Elle M. Weeks +87 more

Rare coding variant analysis for human diseases across biobanks and ancestries

Nature Genetics(2024)10.1038/s41588-024-01894-5

N/A

0.614DataRank · unranked

59 citations

Xin Wang, Seung Hoan Choi, Lu‐Chen Weng, Satoshi Koyama, James P. Pirruccello +20 more

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

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

N/A

0.601DataRank · unranked

54 citations

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

Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass

Nature Communications(2023)10.1038/s41467-023-37173-w

N/A

0.568DataRank · unranked

43 citations

Julieta Lazarte, James P. Pirruccello, Lu‐Chen Weng, Seung Hoan Choi, Amelia Weber Hall +11 more

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

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

N/A

0.529DataRank · unranked

33 citations

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

Cardiovascular Disease Knowledge Portal: A Community Resource for Cardiovascular Disease Research

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.123.004181

N/A

0.505DataRank · unranked

28 citations

Carolina Roselli, MacKenzie Brandes, Marc Duby, Quy Hoang, Dongkeun Jang +17 more

Menopausal age and left ventricular remodeling by cardiac magnetic resonance imaging among 14,550 women

American Heart Journal(2020)10.1016/j.ahj.2020.08.005

N/A

0.449DataRank · unranked

19 citations

James P. Pirruccello, Krishna G. Aragam, Amy Sarma, Nandita S. Scott, Malissa J. Wood +2 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

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

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

N/A

0.345DataRank · unranked

9 citations

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

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

medRxiv(2023)10.1101/2023.07.16.23292724

N/A

0.292DataRank · unranked

6 citations

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

Cardiac adaptation to endurance exercise training requires suppression of GDF15 via PGC-1α

Nature Cardiovascular Research(2025)10.1038/s44161-025-00712-3

N/A

0.269DataRank · unranked

5 citations

Haobo Li, Tevis Vitale, James Rhee, Saketh Challa, Claire Castro +31 more

Analysis of cardiac magnetic resonance imaging traits in 29,000 individuals reveals shared genetic basis with dilated cardiomyopathy

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.12.946038

N/A

0.240DataRank · unranked

3 citations

Alexander G. Bick, Minxian Wang, Mark Chaffin, Steven A. Lubitz, Patrick T. Ellinor +4 more

Clinical and Genetic Associations of Deep Learning-Derived Cardiac Magnetic Resonance-Based Left Ventricular Mass

medRxiv(2022)10.1101/2022.01.09.22268962

N/A

0.104DataRank · unranked

1 citations

Julieta Lazarte, James P. Pirruccello, Lu‐Chen Weng, Seung Hoan Choi, Amelia Weber Hall +11 more

Multi-ancestry Multivariate Genome-Wide Analysis Highlights the Role of Common Genetic Variation in Cardiac Structure, Function, and Heart Failure-related Traits

medRxiv(2021)10.1101/2021.08.03.21261508

N/A

0.104DataRank · unranked

1 citations

Noah L. Tsao, Tiffany R. Bellomo, William P. Bone, Krishna G. Aragam, Yifan Yang +11 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

PLoS Genetics(2020)10.1371/journal.pgen.1008629

N/A

0DataRank · unranked

169 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.

Apollo (University of Cambridge)(2020)10.17863/cam.52580

N/A

0DataRank · unranked

0 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 more

An expanded repertoire of intensity-dependent exercise-responsive plasma proteins tied to loci of human disease risk

Scientific Reports(2020)10.1038/s41598-020-67669-0

N/A

0DataRank · unranked

33 citations

Timothy W. Churchill, Ashish Yeri, Claire Lo, Marcel G. Brown, Nicholas Houstis +5 more

The diabetes gene Tcf7l2 organizes gene expression in the liver and regulates amino acid metabolism

Molecular Metabolism(2025)10.1016/j.molmet.2025.102208

N/A

0DataRank · unranked

1 citations

William O’Connor, Pedro Henrique Vendramini, Mareike Schell, Kiran J. Biddinger, Matt Kanke +10 more

The Diabetes Gene Tcf7l2 Organizes Gene Expression in the Liver and Regulates Amino Acid Metabolism

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.03.647067

N/A

0DataRank · unranked

1 citations

William O’Connor, Pedro Henrique Vendramini, Mareike Schell, Kiran J. Biddinger, George Pengo +7 more

Krishna G. Aragam

Indexed papers

Top data-sharing exemplar

Papers