🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Allan Gordon

Northwestern University

ORCID: 0000-0002-2058-7289

Also affiliated with University of Pennsylvania

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

1in 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 1 indexed paper 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 →

Top data-sharing exemplar

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: “ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)”.

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01172-3
N/A
13.5DataRank · unranked
563 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01171-4
N/A
9.7DataRank · unranked
266 citations

Kristy Lee, Allan Gordon, Laura M. Amendola, Kathy Adelman, Sherri J. Bale +13 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

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z
N/A
4.8DataRank · unranked
196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

Correction to: ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2021)10.1038/s41436-021-01278-8
N/A
1.6DataRank · unranked
29 citations

Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein +13 more

Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study

Circulation(2021)10.1161/circulationaha.121.055562
N/A
1.2DataRank · unranked
49 citations

Giovanni Davogustto, Christian M. Shaffer, Carlos G. Vanoye, Reshma R. Desai, Eric Farber‐Eger +46 more

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2023)10.1016/j.gim.2023.100866
N/A
0.911DataRank · unranked
433 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +9 more

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

Human Molecular Genetics(2013)10.1093/hmg/ddt588
N/A
0.650DataRank · unranked
75 citations

A. D. Johnson, B. M. Snively, Jarmo Virtamo, P. L. Auer, Jonas B. Nielsen +34 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

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535
N/A
0.330DataRank · unranked
8 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100010
N/A
0.269DataRank · unranked
5 citations

Xiaoliang Wang, Pierre Fontanillas, Esther Kim, Sirisak Chanprasert, Allan Gordon +55 more

Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network

Genetic Epidemiology(2020)10.1002/gepi.22360
N/A
0DataRank · unranked
10 citations

Daniel Seung Kim, David R. Crosslin, Ian B. Stanaway, Elisabeth A. Rosenthal, David Carrell +19 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
0DataRank · unranked
17 citations

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

Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2024)10.1016/j.gim.2024.101142
N/A
0DataRank · unranked
13 citations

Kristy Lee, Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung +8 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

ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in Medicine(2025)10.1016/j.gim.2025.101454
N/A
0DataRank · unranked
56 citations

Noura S. Abul‐Husn, Laura M. Amendola, Kyle B. Brothers, Wendy K. Chung, Michael H. Gollob +11 more

Functional Profiling of KCNE1 Variants Informs Population Carrier Frequency of Jervell and Lange-Nielsen Syndrome Type 2

Circulation Genomic and Precision Medicine(2025)10.1161/circgen.125.005219
N/A
0DataRank · unranked
2 citations

Reshma R. Desai, Jordan John, Steven C. Hoffman, Nicolas Fink, Yue Zhang +8 more

Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies

npj Digital Medicine(2021)10.1038/s41746-021-00488-3
N/A
0DataRank · unranked
17 citations

Chen Wang, Atlas Khan, Ning Shang, Zihuai He, Allan Gordon +9 more

Age-Dependent Contributions of Rare and Common Genetic Variation in Atrial Fibrillation

Circulation Genomic and Precision Medicine(2025)10.1161/circgen.124.004958
N/A
0DataRank · unranked
2 citations

Peter F. Aziz, Philip Greenland, Rod Passman, Allan Gordon, Gregory Webster +1 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w
N/A
0DataRank · unranked
8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 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