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

Mary E. Haas

Regeneron (United States)

ORCID: 0000-0002-2816-9268

Also affiliated with Kliniken der Stadt Köln, Geisinger Health System

Social SciencesBiochemistry, Genetics and Molecular BiologyMedicinePhysics and Astronomy

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
6.0Author 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.

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations

Nucleic Acids Research(2020)10.1093/nar/gkaa1011
Top 3%
6.0DataRank
Top 3%2013 citations

Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy Durham +27 more

Papers

Driven by 14 papers — median percentile 97. Top paper: “MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations”.

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations

Nucleic Acids Research(2020)10.1093/nar/gkaa1011
Top 3%
6.0DataRank
Top 3%2013 citations

Rohit Sharma, Rahul Gupta, Tslil Ast, Connie Chan, Timothy Durham +27 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

Machine learning enables new insights into clinical significance of and genetic contributions to liver fat accumulation

medRxiv(2020)10.1101/2020.09.03.20187195
N/A
0DataRank · unranked
15 citations

James P. Pirruccello, Sam Friedman, Connor A. Emdin, Veeral Ajmera, Tracey G. Simon +11 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

Lipid nanoparticle-mediated codelivery of Cas9 mRNA and single-guide RNA achieves liver-specific in vivo genome editing of Angptl3

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.2020401118
N/A
0DataRank · unranked
383 citations

Zachary Glass, Jinjin Chen, Mary E. Haas, Xin Jin, Xuewei Zhao +6 more

Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease

Cell Reports Medicine(2021)10.1016/j.xcrm.2021.100437
N/A
0DataRank · unranked
256 citations

Erik Abner, Connor A. Emdin, Émilie Gobeil, Nele Taba, Mary E. Haas +15 more

Machine learning enables new insights into genetic contributions to liver fat accumulation

Cell Genomics(2021)10.1016/j.xgen.2021.100066
N/A
0DataRank · unranked
105 citations

James P. Pirruccello, Sam Friedman, Minxian Wang, Connor A. Emdin, Veeral Ajmera +12 more

A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

medRxiv(2021)10.1101/2020.12.26.20248491
N/A
0DataRank · unranked
16 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +85 more

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Nature Genetics(2022)10.1038/s41588-022-01078-z
N/A
0DataRank · unranked
195 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +86 more

Germline Mutations in CIDEB and Protection against Liver Disease

New England Journal of Medicine(2022)10.1056/nejmoa2117872
N/A
0DataRank · unranked
125 citations

Mary E. Haas, Jonas B. Nielsen, Olukayode Sosina, Minhee Kim, Parsa Akbari +42 more

Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis

Journal of Clinical Investigation(2022)10.1172/jci158788
N/A
0DataRank · unranked
74 citations

Daniel J. Tyrrell, Alexi Vasbinder, Changli Wei, Feriel Presswalla, Hui Wang +37 more

Framework From a Multidisciplinary Approach for Transitioning Variants of Unknown Significance From Clinical Genetic Testing in Kidney Disease to a Definitive Classification

Kidney International Reports(2022)10.1016/j.ekir.2022.06.014
N/A
0DataRank · unranked
5 citations

Ahana Bhan, Lotte E. Tholen, Brian Fang, Guoli Chen, Bryn S. Moore +12 more

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants

Science(2025)10.1126/science.adp4753
N/A
0DataRank · unranked
48 citations

Amin Abedini, Eunji Ha, Ziyuan Ma, Xin Sheng, Bernhard Dumoulin +94 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