Marcus B. Jones

Also affiliated with Regeneron (United States)

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 6%percentile

0.208Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Insights from the Biorepository and Integrative Genomics pediatric resource

Nature Communications(2025)10.1038/s41467-025-59375-0

Top 65%

0.208DataRank

Top 65%3 citations

Franco Mársico, Akram Mohammed, Lokesh Chinthala, Ernestine K Amos-Abanyie, Aris Baras +95 more

Papers

Driven by 21 papers — median percentile 35. Top paper: “A catalog of associations between rare coding variants and COVID-19 outcomes”.

A catalog of associations between rare coding variants and COVID-19 outcomes

medRxiv(2020)10.1101/2020.10.28.20221804

N/A

1.3DataRank · unranked

31 citations

Julie Horowitz, Nilanjana Banerjee, Rouel Lanche, Anthony Marcketta, Evan K. Maxwell +75 more

Mucus sialylation determines intestinal host-commensal homeostasis

Cell(2022)10.1016/j.cell.2022.02.013

N/A

0.821DataRank · unranked

238 citations

Girak Kim, Samantha Shafer, Zuojia Chen, Satoshi Kubo, Yanlong Ji +45 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

0.793DataRank · unranked

197 citations

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

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0.775DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies

BMC Medicine(2022)10.1186/s12916-022-02535-6

N/A

0.731DataRank · unranked

18 citations

Linda Kachuri, Rebecca E. Graff, Jovia L. Nierenberg, Khanh K. Thai, Stacey Alexeeff +90 more

Germline Mutations in CIDEB and Protection against Liver Disease

New England Journal of Medicine(2022)10.1056/nejmoa2117872

N/A

0.728DataRank · unranked

127 citations

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

Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

Biological Psychiatry(2020)10.1016/j.biopsych.2020.06.026

N/A

0.601DataRank · unranked

54 citations

Alison Merikangas, Shefali S. Verma, Anurag Verma, Renae Judy, Gonçalo R. Abecasis +42 more

Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2123000119

N/A

0.599DataRank · unranked

18 citations

Anurag Verma, Yuanqing Feng, Marcelo C. R. Melo, Michael A. McQuillan, Matthew E.B. Hansen +71 more

Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease

medRxiv(2020)10.1101/2020.12.14.20248176

N/A

0.561DataRank · unranked

41 citations

Jack A. Kosmicki, Amy Damask, Deepika Sharma, Genevieve H. L. Roberts, Anne E. Justice +54 more

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

Nature Communications(2020)10.1038/s41467-020-17315-0

N/A

0.546DataRank · unranked

37 citations

Lars G. Fritsche, Wei Zhou, Joshua Backman, Jack A. Kosmicki, Haocheng Lu +45 more

Exome Sequencing Identifies A Nonsense Variant inDAOAssociated With Reduced Energy Expenditure in American Indians

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa548

N/A

0.518DataRank · unranked

9 citations

Çiğdem Köroğlu, Anup Nair, Jeff Sutherland, Yunhua L. Muller, Pankaj Kumar +13 more

Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis

Nature Genetics(2023)10.1038/s41588-023-01444-5

N/A

0.500DataRank · unranked

27 citations

Olukayode Sosina, Jonas Bovijn, Lætitia Laurent, Vasundhara Sharma, Parsa Akbari +24 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0.464DataRank · unranked

21 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 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

0.425DataRank · unranked

16 citations

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

Impact of natural selection on global patterns of genetic variation, and association with clinical phenotypes, at genes involved in SARS-CoV-2 infection.

Research Square(2021)10.21203/rs.3.rs-673011/v1

N/A

0.361DataRank · unranked

6 citations

Anurag Verma, Yuanqing Feng, Marcelo C. R. Melo, Michael A. McQuillan, Matthew E.B. Hansen +24 more

Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.007

N/A

0.269DataRank · unranked

5 citations

Colleen Morse Kripke, Adam J. Mansfield, Alexander Li, Alexander Lopez, Alicia Hawes +95 more

Insights from the Biorepository and Integrative Genomics pediatric resource

Nature Communications(2025)10.1038/s41467-025-59375-0

Top 65%

0.208DataRank

Top 65%3 citations

Franco Mársico, Akram Mohammed, Lokesh Chinthala, Ernestine K Amos-Abanyie, Aris Baras +95 more

Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways

medRxiv(2025)10.1101/2025.09.16.25335186

N/A

0.104DataRank · unranked

1 citations

David E. Kaplan, Jonas Ghouse, Bao‐Li Loza, Joseph Brancale, Adam Lewis +68 more

Genomic and Transcriptomic Analyses of Colistin-Resistant Clinical Isolates of Klebsiella pneumoniae Reveal Multiple Pathways of Resistance

UNC Libraries(2020)10.17615/y61z-t951

N/A

0DataRank · unranked

0 citations

Susan D. Rudin, Marcus B. Jones, Meredith S. Wright, David van Duin, Robert A. Bonomo +5 more

Transcription factor networks disproportionately enrich for heritability of blood cell phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.09.611392

N/A

0DataRank · unranked

2 citations

Alexis Caulier, Seayoung Lee, Nicole Castano, Emily King, Samantha Joubran +7 more

Genetic and Functional Characterization of ANGPTL7 as a Therapeutic Target for Glaucoma

Research Square(2021)10.21203/rs.3.rs-858876/v1

N/A

0DataRank · unranked

0 citations

Gaurang Patel, Lauren Gurski, Ariane Ayer, Trikaladarshi Persaud, Matthew Still +49 more

Marcus B. Jones

Indexed papers

Top data-sharing exemplar

Papers