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

Matthew S. Lebo

Broad Institute

ORCID: 0000-0002-9733-5207

Also affiliated with Brigham and Women's Hospital, Harvard University, Knowledge Foundation, Woman's Hospital, Mass General Brigham

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 1%percentile
12.4Author DataRank

Indexed papers

6in 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 6 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 →

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.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x
Top 2%
8.6DataRank
Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Papers

Driven by 29 papers — median percentile 67. Top paper: “Genomic data in the All of Us Research Program”.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x
Top 2%
8.6DataRank
Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.10.005
Top 11%
1.9DataRank
Top 11%73 citations

Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D. Christensen, Hana Zouk +15 more

The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.001
N/A
0.996DataRank · unranked
23 citations

Charles A. Brunette, Matthew S. Lebo, Katharine MacIsaac, Thomas Yi, Morgan E. Danowski +15 more

Harmonizing variant classification for return of results in the All of Us Research Program

Human Mutation(2021)10.1002/humu.24317
Top 27%
0.738DataRank
Top 27%17 citations

Christina Austin‐Tse, Serra Kim, Matthew S. Lebo, Annette Leon, David R. Murdock +8 more

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

Genetics and context for precision health in Greater Boston

Nature Communications(2025)10.1038/s41467-025-66598-8
Top 51%
0.345DataRank
Top 51%9 citations

Ying Wang, Kaavya Paruchuri, Md Mesbah Uddin, So Mi Jemma Cho, Sarah Urbut +16 more

Returning Actionable Genomic Results in a Research Biobank: Analytic Validity, Clinical Implementation and Resource Utilization

medRxiv(2021)10.1101/2021.08.03.21261489
Top 53%
0.319DataRank
Top 53%4 citations

Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D. Christensen, Hana Zouk +15 more

A framework for integrated clinical risk assessment using population sequencing data

medRxiv(2021)10.1101/2021.08.12.21261563
N/A
0DataRank · unranked
6 citations

Tho Tran, Jackson R. Bernatchez, Keithen E. Shepard, Christopher Koch, Aniruddh P. Patel +10 more

Clinical validation, implementation, and reporting of polygenic risk scores for common diseases

Research Square(2021)10.21203/rs.3.rs-743779/v1
N/A
0DataRank · unranked
2 citations

Limin Hao, Peter Kraft, Gabriel F. Berriz, Elizabeth Hynes, Christopher Koch +15 more

Development of a clinical polygenic risk score assay and reporting workflow

Nature Medicine(2022)10.1038/s41591-022-01767-6
N/A
0DataRank · unranked
198 citations

Peter Kraft, Gabriel F. Berriz, Elizabeth Hynes, Christopher Koch, Prathik K. Vijay Kumar +15 more

Medical Evaluation of Unanticipated Monogenic Disease Risks Identified through Newborn Genomic Screening: Findings from the BabySeq Project

medRxiv(2022)10.1101/2022.03.18.22272284
N/A
0DataRank · unranked
4 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Talia S. Schwartz +13 more

Recommendations for risk allele evidence curation, classification, and reporting from the ClinGen Low Penetrance/Risk Allele Working Group

Genetics in Medicine(2023)10.1016/j.gim.2023.101036
N/A
0DataRank · unranked
70 citations

Marcie Steeves, Pınar Bayrak‐Toydemir, Katherine A. Benson, Bradley P. Coe, Laura K. Conlin +42 more

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.007
N/A
0DataRank · unranked
55 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Melissa Kurtz Uveges +12 more

Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease

Circulation(2023)10.1161/circulationaha.123.064168
N/A
0DataRank · unranked
12 citations

Jacqueline S. Dron, Brandon K. Bellows, Amit V. Khera, Junxiu Liu, Pallavi Balte +27 more

Decoding Genetics, Ancestry, and Geospatial Context for Precision Health

medRxiv(2023)10.1101/2023.10.24.23297096
N/A
0DataRank · unranked
24 citations

Ying Wang, Kaavya Paruchuri, Md Mesbah Uddin, So Mi Jemma Cho, Sarah Urbut +12 more

Preparing to Integrate Generative Pretrained Transformer Series 4 models into Genetic Variant Assessment Workflows: Assessing Performance, Drift, and Nondeterminism Characteristics Relative to Classifying Functional Evidence in Literature

arXiv (Cornell University)(2023)10.48550/arxiv.2312.13521
N/A
0DataRank · unranked
1 citations

Kalotina Machini, Ji-Yeon Shin, Pranav Sriraman, Hamill, Sean, Emma R. Henricks +6 more

Polygenic Risk for Type 2 Diabetes in African Americans

Diabetes(2024)10.2337/db23-0232
N/A
0DataRank · unranked
8 citations

Tian Ge, Amit Patki, Vinodh Srinivasasainagendra, Nicole D. Armstrong, Brittney H. Davis +14 more

Family genetic risk communication and reverse cascade testing in the BabySeq project

Genetics in Medicine(2024)10.1016/j.gim.2024.101350
N/A
0DataRank · unranked
3 citations

Hadley Stevens Smith, Stacey Pereira, Casie A. Genetti, Amy L. McGuire, Alan H. Beggs +38 more

Extracting and calibrating evidence of variant pathogenicity from population biobank data

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.012
N/A
0DataRank · unranked
9 citations

Tian Yu, Lara Brown, Vikas Pejaver, Matthew S. Lebo, Steven M. Harrison +2 more

Electronic health records-based algorithms to screen for U.S. Centers for Disease Control and Prevention tier 1 genetic diseases: a scoping review

Journal of the American Medical Informatics Association(2025)10.1093/jamia/ocaf140
N/A
0DataRank · unranked
5 citations

M Hernandez, Khanh N H Ngo, Anne Fladger, Charles A. Brunette, Sulaiman R Hamarneh +4 more

Precision Grounding: Augmenting Large Language Models with Evidence-Based Databases for Trustworthy Genetic Variant Summarization

medRxiv(2025)10.1101/2025.06.09.25329279
N/A
0DataRank · unranked
1 citations

Anna Andrea Nagy, Michael Oates, Yifei Wang, Xinyi Wang, Joseph M. Plasek +4 more

Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing

Value in Health(2020)10.1016/j.jval.2020.01.017
N/A
0DataRank · unranked
15 citations

Dmitry Dukhovny, Kathryn A. Phillips, Alan H. Beggs, Robert C. Green, Richard B. Parad +27 more

From Expert Knowledge to Validation Resources

Journal of Molecular Diagnostics(2025)10.1016/j.jmoldx.2025.07.006
N/A
0DataRank · unranked
0 citations

Martine Tremblay, Edward R. Lockhart, Swaroop Aradhya, Pınar Bayrak‐Toydemir, Mark Bowser +12 more

An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy

Human Mutation(2020)10.1002/humu.24061
N/A
0DataRank · unranked
19 citations

Naif A. M. Almontashiri, Leslie G. Biesecker, Natalie Berger, Wendy K. Chung, John Garcia +17 more

Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry

Transfusion(2020)10.1111/trf.15839
N/A
0DataRank · unranked
16 citations

Nicholas Gleadall, Judith Aeschlimann, Sunitha Vege, Alba Sanchis‐Juan, Jonathan Stephens +11 more

Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer

Research Square(2020)10.21203/rs.3.rs-100817/v1
N/A
0DataRank · unranked
6 citations

Seyedeh M. Zekavat, Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri +26 more

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record

UNC Libraries(2020)10.17615/4zec-ff92
N/A
0DataRank · unranked
0 citations

Matthew S. Lebo, Samuel Aronson, Laura M. Amendola, Levi A. Garraway, Gail P. Jarvik +10 more

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Nature Medicine(2021)10.1038/s41591-021-01371-0
N/A
0DataRank · unranked
193 citations

Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri, Chen Wang +95 more

Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

Genetics in Medicine(2021)10.1016/j.gim.2021.10.010
N/A
0DataRank · unranked
26 citations

Wanfeng Yu, Andrea M. Oza, Megan Hawley, Prathik K. Vijay Kumar, Christopher Koch +12 more