Santhi K. Ganesh

Also affiliated with Michigan Medicine, Institute of Human Genetics

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 100%percentile

0Author 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.

Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

UNC Libraries(2020)10.17615/gafw-pc57

Top 100%

0DataRank

Top 100%0 citations

Santhi K. Ganesh, Ethan M. Lange, Keolu Fox, Nora Franceschini, Robert B. Wallace +17 more

Papers

Driven by 42 papers — median percentile 0. Top paper: “Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target”.

Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

Nature Genetics(2023)10.1038/s41588-023-01510-y

N/A

1.6DataRank · unranked

100 citations

Derek Klarin, Michael G. Levin, Joshua M. Spin, Yae Hyun Rhee, Alicia Deng +92 more

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3

N/A

0.821DataRank · unranked

50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +95 more

Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture

Circulation Genomic and Precision Medicine(2022)10.1161/circgen.121.003496

N/A

0.806DataRank · unranked

22 citations

Min‐Lee Yang, Michael G. Levin, Catherine Tcheandjieu, Michael R. Mathis, Kristina L. Hunker +86 more

Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

Stroke(2023)10.1161/strokeaha.122.040715

N/A

0.520DataRank · unranked

31 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik Slagsvold Winsvold, John‐Anker Zwart +95 more

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

UNC Libraries(2020)10.17615/aapr-pr41

N/A

0.104DataRank · unranked

1 citations

Niels Grarup, Albert Hofman, Lenore J. Launer, David C. Liewald, Albert V. Smith +76 more

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

UNC Libraries(2020)10.17615/bzr0-ap70

N/A

0DataRank · unranked

3 citations

Elad Ziv, Alan B. Zonderman, Jin Li, Ruth J. F. Loos, Michael A. Nalls +27 more

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

UNC Libraries(2020)10.17615/a03d-0d18

N/A

0DataRank · unranked

1 citations

Daniel L. Dries, Kiang Liu, Xiaofeng Zhu, Charleston W. K. Chiang, Adebowale Adeyemo +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

Genetic association studies of fibromuscular dysplasia identify new risk loci and shared genetic basis with more common vascular diseases

medRxiv(2020)10.1101/2020.09.16.20195701

N/A

0DataRank · unranked

0 citations

Min‐Lee Yang, Takiy-Eddine Berrandou, Mark K. Bakker, Ozan Dikilitas, Soto Romuald Kiando +47 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

Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

UNC Libraries(2020)10.17615/gafw-pc57

Top 100%

0DataRank

Top 100%0 citations

Santhi K. Ganesh, Ethan M. Lange, Keolu Fox, Nora Franceschini, Robert B. Wallace +17 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

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

N/A

0DataRank · unranked

0 citations

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

Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans

UNC Libraries(2020)10.17615/3a58-7n18

N/A

0DataRank · unranked

0 citations

Aaron R. Folsom, Brendan J. Keating, Emile R. Mohler, Steven A. McCarroll, Alex P. Reiner +11 more

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

N/A

0DataRank · unranked

0 citations

Lisa R. Yanek, Kjell Nikus, Salman M. Tajuddin, Jussi Hernesniemi, Dawn Waterworth +95 more

Genetic determinants of the ankle-brachial index: A meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium

UNC Libraries(2020)10.17615/cknt-8a26

N/A

0DataRank · unranked

0 citations

Jane F. Ferguson, Susan Redline, Christina L. Wassel, L. Adrienne Cupples, George Papanicolaou +27 more

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

UNC Libraries(2020)10.17615/s8sd-h432

Top 100%

0DataRank

Top 100%0 citations

Todd L. Edwards, Jin Li, John M. Starr, Eric Boerwinkle, Yingchang Lu +92 more

Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)

UNC Libraries(2020)10.17615/wn5h-av49

N/A

0DataRank · unranked

0 citations

David Couper, Struan F.A. Grant, Tamara B. Harris, Santhi K. Ganesh, Sampath Arepalli +27 more

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

UNC Libraries(2020)10.17615/8mhe-8y03

N/A

0DataRank · unranked

0 citations

Sharon B. Wyatt, Kiang Liu, Adebowale Adeyemo, Brendan J. Keating, Sun Joo Kang +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

Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.016

N/A

0DataRank · unranked

58 citations

Haocheng Lu, Whitney Hornsby, Bradley Crone, Gao T. Wang, Dongchuan Guo +35 more

SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism

Viruses(2021)10.3390/v13112209

N/A

0DataRank · unranked

54 citations

Yu Zuo, Srilakshmi Yalavarthi, Kristina L. Hunker, Jason S. Knight, Yogendra Kanthi +3 more

Current progress in clinical, molecular, and genetic aspects of adult fibromuscular dysplasia

Cardiovascular Research(2021)10.1093/cvr/cvab086

N/A

0DataRank · unranked

48 citations

Piotr Dobrowolski, Heather L. Gornik, Jeffrey W. Olin, David Adlam, Michel Azizi +20 more

Lysyl oxidase interactions with transforming growth factor‐β during angiogenesis are mediated by endothelin 1

The FASEB Journal(2021)10.1096/fj.202001860rr

N/A

0DataRank · unranked

10 citations

Kristina L. Hunker, Isabelle Birt, Chen Lulu, Rohtem Aviram, Shelly Zaffryar‐Eilot +3 more

An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population

Human Molecular Genetics(2021)10.1093/hmg/ddab062

N/A

0DataRank · unranked

7 citations

Wei Zhou, Yi Fu, Chloe Y. Y. Cheung, Yujun Dong, Min‐Lee Yang +15 more

Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.19.488795

N/A

0DataRank · unranked

2 citations

Seong Kyu Han, Or Yaacov, Hanna Berk-Rauch, Prabhu Mathiyalagan, Santhi K. Ganesh +2 more

Genetic risk score for intracranial aneurysms to predict aneurysmal subarachnoid hemorrhage and identify associations with patient characteristics

medRxiv(2022)10.1101/2022.04.29.22274404

N/A

0DataRank · unranked

0 citations

Jos P. Kanning, Gad Abraham, Amy E. Martinsen, Bendik S Winsvold, John‐Anker Zwart +19 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

0DataRank · unranked

91 citations

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

mtPGS: Leverage multiple correlated traits for accurate polygenic score construction

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.08.016

N/A

0DataRank · unranked

27 citations

Santhi K. Ganesh, Xiang Zhou, Chang Xu

Placental transcriptome analysis of hypertensive pregnancies identifies distinct gene expression profiles of preeclampsia superimposed on chronic hypertension

BMC Medical Genomics(2023)10.1186/s12920-023-01522-x

N/A

0DataRank · unranked

9 citations

Elizabeth Langen, Olesya Plazyo, Jóhann E. Guðjónsson, Santhi K. Ganesh, Ashley Hesson

Advancements in the Genetics of Spontaneous Coronary Artery Dissection

Current Cardiology Reports(2023)10.1007/s11886-023-01989-1

N/A

0DataRank · unranked

8 citations

Santhi K. Ganesh, Alexander Katz

Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure

Cell Reports(2023)10.1016/j.celrep.2023.113351

N/A

0DataRank · unranked

8 citations

Seong Kyu Han, Or Yaacov, Hanna Berk-Rauch, Prabhu Mathiyalagan, Santhi K. Ganesh +2 more

Sex-specific genetic architecture of blood pressure

Nature Medicine(2024)10.1038/s41591-024-02858-2

N/A

0DataRank · unranked

46 citations

Chang Xu, Trisha Gupte, Thomas J. Hoffmann, Carlos Iribarren, Xiang Zhou +2 more

From Atherosclerosis to Spontaneous Coronary Artery Dissection: Defining a Clinical and Genetic Risk Spectrum for Myocardial Infarction

Current Atherosclerosis Reports(2024)10.1007/s11883-024-01208-4

N/A

0DataRank · unranked

10 citations

Trisha Gupte, Santhi K. Ganesh, Alexander Katz

Genetic variation in CCDC93 is associated with elevated central systolic blood pressure, impaired arterial relaxation, and mitochondrial dysfunction

PLoS Genetics(2024)10.1371/journal.pgen.1011151

N/A

0DataRank · unranked

1 citations

Min‐Lee Yang, Pengfei Sun, Kristina L. Hunker, Jianping Li, Jia Jia +12 more

Statistical construction of calibrated prediction intervals for polygenic score-based phenotype prediction

Nature Genetics(2025)10.1038/s41588-025-02360-6

N/A

0DataRank · unranked

5 citations

Santhi K. Ganesh, Xiang Zhou, Chang Xu

Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

Nature Communications(2020)10.1038/s41467-020-17558-x

N/A

0DataRank · unranked

102 citations

Min‐Lee Yang, Mark Trinder, Catherine Tcheandjieu, Chang Xu, Andrew Starovoytov +22 more

Peripartum dapagliflozin improves late-life maternal cardiovascular outcomes in a murine model of superimposed preeclampsia

American Journal of Obstetrics and Gynecology(2025)10.1016/j.ajog.2025.03.035

N/A

0DataRank · unranked

2 citations

Ajleeta Sangtani, Ingrid L. Bergin, Elizabeth Langen, Kristina L. Hunker, Nitin Kumar +2 more

Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits

Nature Genetics(2020)10.1038/s41588-020-00738-2

N/A

0DataRank · unranked

49 citations

Eirini Trompouki, Brian J. Abraham, Leandro M. Colli, Kian Hong Kock, William Mallard +28 more

Histologic and morphologic character of pediatric renal artery occlusive disease

Journal of Vascular Surgery(2020)10.1016/j.jvs.2020.02.046

N/A

0DataRank · unranked

16 citations

Amer Heider, David Gordon, Santhi K. Ganesh, Jonathan L. Eliason, James C. Stanley +1 more

Surgical management of pediatric renin-mediated hypertension secondary to renal artery occlusive disease and abdominal aortic coarctation

Journal of Vascular Surgery(2020)10.1016/j.jvs.2020.02.045

N/A

0DataRank · unranked

32 citations

Jonathan L. Eliason, Robert J. Beaulieu, Tatum Jackson, Monita Karmakar, David B. Kershaw +6 more

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia

Cardiovascular Research(2020)10.1093/cvr/cvaa161

N/A

0DataRank · unranked

32 citations

Juliette Albuisson, Takiy-Eddine Berrandou, Délia Dupré, Aurélien Lorthioir, Valentina d’Escamard +32 more

Santhi K. Ganesh

Indexed papers

Top data-sharing exemplar

Papers