Scott J. Hebbring

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

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.

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

UNC Libraries(2024)10.17615/8zyz-p282

Top 100%

0DataRank

Top 100%0 citations

Shining Ma, J.C. Bis, Noah L. Tsao, Philip S. Tsao, Yi‐Lwun Ho +81 more

Papers

Driven by 21 papers — median percentile 0. Top paper: “Large-scale genome-wide association study of coronary artery disease in genetically diverse populations”.

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

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Scientific Reports(2020)10.1038/s41598-020-58510-9

N/A

1.6DataRank · unranked

64 citations

Susette Lauwen, Christina Kiel, Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey +95 more

The All of Us Research Program: Data quality, utility, and diversity

Patterns(2022)10.1016/j.patter.2022.100570

N/A

0.874DataRank · unranked

339 citations

Lina Sulieman, David J. Schlueter, Alese E. Halvorson, Jun Qian, Francis Ratsimbazafy +81 more

Genetic and clinical determinants of telomere length

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100201

N/A

0.768DataRank · unranked

26 citations

Jing He, John E. Mayer, Luke Moat, Peter Gerstenberger, Reynor Wilhorn +9 more

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants

Science Translational Medicine(2017)10.1126/scitranslmed.aai8708

N/A

0.740DataRank · unranked

138 citations

Lisa Bastarache, Christian M. Shaffer, Silvana Gaudieri, Yaomin Xu, Andrew M. Glazer +12 more

A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgz326

N/A

0.626DataRank · unranked

64 citations

Ky’Era V. Actkins, Jennifer A. Pacheco, Anna O. Basile, Robert J. Carroll, David R. Crosslin +66 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

Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome‐Wide Association Study and Inverse Variance–Weighted Meta‐Analysis

Arthritis & Rheumatology(2020)10.1002/art.41291

N/A

0.434DataRank · unranked

17 citations

Mingjian Shi, Qiping Feng, Cecilia P. Chung, Ge Liu, Nancy J. Cox +13 more

The All of Us Research Program: data quality, utility, and diversity

medRxiv(2020)10.1101/2020.05.29.20116905

N/A

0.416DataRank · unranked

15 citations

Lina Sulieman, David J. Schlueter, Alese E. Halvorson, Jun Qian, Francis Ratsimbazafy +42 more

An independently validated, portable algorithm for the rapid identification of COPD patients using electronic health records

Scientific Reports(2021)10.1038/s41598-021-98719-w

N/A

0.396DataRank · unranked

13 citations

Emily S. Wan, Michael H. Cho, Sergey Goryachev, Vivian S. Gainer, James G. Linneman +8 more

Orphan nuclear receptor NR2E3 and its small-molecule agonist induce cancer cell apoptosis through regulating p53, IFNα and MYC pathways

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.12.26.573366

N/A

0DataRank · unranked

0 citations

Todd G. Kroll, Linhui Hao, Ansul Sharma, Vivian Zhou, Luke F. Moat +12 more

Familial Renal Glucosuria and Potential Pharmacogenetic Impact on Sodium-Glucose Cotransporter-2 Inhibitors

Kidney360(2024)10.34067/kid.0000000621

N/A

0DataRank · unranked

3 citations

Jamie Fox, Terrie Kitchner, Rachel Gabor, Connie Folz, Shankar Bettadahalli +2 more

Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-024-06408-x

N/A

0DataRank · unranked

0 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +93 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

UNC Libraries(2024)10.17615/8zyz-p282

Top 100%

0DataRank

Top 100%0 citations

Shining Ma, J.C. Bis, Noah L. Tsao, Philip S. Tsao, Yi‐Lwun Ho +81 more

Inhibition of FOXM1 Synergizes with BH3 Mimetics Venetoclax and Sonrotoclax in Killing Multiple Myeloma Cells through Repressing MYC Pathway

Advanced Science(2025)10.1002/advs.202508822

N/A

0DataRank · unranked

3 citations

Yidan Wang, Kathryn Fox, Adam Bissonnette, Luke F. Moat, Terrie Kitchner +12 more

Genetic relationships between systemic lupus erythematosus and a positive antinuclear antibody test in the absence of autoimmune disease

Lupus Science & Medicine(2025)10.1136/lupus-2024-001476

N/A

0DataRank · unranked

0 citations

Gul Karakoc, Ge Liu, Jacy Zanussi, Nancy J. Olsen, Mingjian Shi +10 more

Data from Glutathione S-Transferase T1 and M1: Gene Sequence Variation and Functional Genomics

(2023)10.1158/1078-0432.c.6518125.v1

Top 100%

0DataRank

Top 100%0 citations

Oreste E. Salavaggione, Scott J. Hebbring, Irene Moon, Michelle A.T. Hildebrandt, Bruce W. Eckloff +4 more

The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene

Scientific Reports(2021)10.1038/s41598-021-95154-9

N/A

0DataRank · unranked

11 citations

Chuan Wang, Mingjian Shi, Ali Manouchehri, Katherine T. Murray, Matthew B. Murphy +12 more

Regulatory Polymorphisms in Human DBH Affect Peripheral Gene Expression and Sympathetic Activity

UNC Libraries(2020)10.17615/sfcz-sw07

N/A

0DataRank · unranked

3 citations

David Weinshenker, James G. Wilson, Murray H. Brilliant, Glenn S. Gerhard, Helena Kuivaniemi +12 more

Estimating the efficacy of pharmacogenomics over a lifetime

Frontiers in Medicine(2023)10.3389/fmed.2023.1006743

N/A

0DataRank · unranked

4 citations

John Mayer, Emili Leary, Terrie Kitchner, Richard A. Dart, Murray H. Brilliant +2 more

Genetic association of primary non-response to Anti-TNFα therapy in patients with Inflammatory Bowel Disease

medRxiv(2020)10.1101/2020.06.23.20138495

N/A

0DataRank · unranked

2 citations

Hong Zhang, Carlos A. Rodríguez-Alarcón, Bianca Lec, Juan Avitia, Erin Smithberger +19 more

Scott J. Hebbring

Indexed papers

Top data-sharing exemplar

Papers