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

Jonathan Marchini

Regeneron (United States)

ORCID: 0000-0003-0610-8322
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
42.5Author 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.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393
Top 1%
10.6DataRank
Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 23 papers — median percentile 98. Top paper: “A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies”.

A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies

PLoS Genetics(2009)10.1371/journal.pgen.1000529
N/A
20.4DataRank · unranked
4142 citations

Peter Donnelly, Jonathan Marchini, Bryan N. Howie

A global reference for human genetic variation

Nature(2015)10.1038/nature15393
Top 1%
10.6DataRank
Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

A map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534
Top 2%
9.1DataRank
Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934
Top 2%
8.3DataRank
Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 more

Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank

The Lancet Respiratory Medicine(2015)10.1016/s2213-2600(15)00283-0
Top 2%
7.7DataRank
Top 2%438 citations

Nick Shrine, Suzanne Miller, Victoria E. Jackson, Ioanna Ntalla, María Soler Artigas +39 more

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

Nature Communications(2015)10.1038/ncomms9111
Top 3%
6.7DataRank
Top 3%386 citations

Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min +234 more

Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns

Nature Communications(2019)10.1038/s41467-019-10461-0
N/A
2.8DataRank · unranked
151 citations

Gökçen Eraslan, Christian M. Page, Jari Lahti, Marius Lahti-Pulkkinen, Esa Hämäläinen +233 more

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

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

Nature Genetics(2012)10.1038/ng.2354
N/A
1.1DataRank · unranked
1873 citations

Christian Fuchsberger, Matthew Stephens, Jonathan Marchini, Gonçalo R. Abecasis, Bryan Howie

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease

Cell(2016)10.1016/j.cell.2016.10.042
N/A
1.1DataRank · unranked
1405 citations

Heather Elding, Tao Jiang, Dave Allen, Dace Ruklisa, Alice L. Mann +78 more

The effects of human population structure on large genetic association studies

Nature Genetics(2004)10.1038/ng1337
N/A
1.0DataRank · unranked
898 citations

Lon R. Cardon, Peter Donnelly, Michael Phillips, Jonathan Marchini

Haplotype estimation for biobank-scale data sets

Nature Genetics(2016)10.1038/ng.3583
N/A
0.831DataRank · unranked
254 citations

Kevin Sharp, Nick Shrine, Martin D. Tobin, Jean-Francois Zagury, Olivier Delaneau +5 more

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

Science(2025)10.1126/science.adp4753
N/A
0.587DataRank · unranked
49 citations

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

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

UNC Libraries(2020)10.17615/n5vd-xm37
N/A
0.477DataRank · unranked
23 citations

Björn O. Eriksen, Ivana Išgum, Annette Peters, Christopher D. O’Donnell, Christa Meisinger +67 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 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

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
0DataRank · unranked
18 citations

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

Genetic risk factors for COVID-19 and influenza are largely distinct

Nature Genetics(2024)10.1038/s41588-024-01844-1
N/A
0DataRank · unranked
14 citations

Anthony Marcketta, Deepika Sharma, Silvio Alessandro Di Gioia, Samantha Batista, Xiaoman Yang +53 more

Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

Science(2021)10.1126/science.abf8683
N/A
0DataRank · unranked
278 citations

Ankit Gilani, Olukayode Sosina, Jack A. Kosmicki, Lori Khrimian, Yi‐Ya Fang +55 more

Risk of lymphoid malignancy associated with cancer predisposition genes

Blood Cancer Journal(2025)10.1038/s41408-025-01283-z
N/A
0DataRank · unranked
8 citations

Raphael Mwangi, Dennis P. Robinson, Cristine Allmer, Allison Rosenthal, Thomas M. Habermann +95 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
0DataRank · unranked
5 citations

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

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

UNC Libraries(2020)10.17615/55vz-3f21
N/A
0DataRank · unranked
0 citations

Richard N. Bergman, Katherine S. Elliott, Harald Grallert, Eleftheria Zeggini, Peter Almgren +27 more