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

Matthew Harms

Lourdes University

ORCID: 0000-0002-3395-1633
MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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
6.7Author 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.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8
Top 3%
6.7DataRank
Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Papers

Driven by 14 papers — median percentile 97. Top paper: “A structural variation reference for medical and population genetics”.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8
Top 3%
6.7DataRank
Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5
N/A
5.6DataRank · unranked
143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9
N/A
5.2DataRank · unranked
191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5
N/A
4.9DataRank · unranked
114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7
N/A
1.4DataRank · unranked
9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2
N/A
0.796DataRank · unranked
201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z
N/A
0.779DataRank · unranked
179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

Lipoxins reduce obesity-induced adipose tissue inflammation in 3D-cultured human adipocytes and explant cultures

iScience(2022)10.1016/j.isci.2022.104602
N/A
0.509DataRank · unranked
13 citations

Meenu Rohini Rajan, Madison Clark, Matthew Harms, Alankrita Rani, Jamie Kraft +15 more

Access for ALL in ALS: A large‐scale, inclusive, collaborative consortium to unlock the molecular and genetic mechanisms of amyotrophic lateral sclerosis

Muscle & Nerve(2024)10.1002/mus.28244
N/A
0DataRank · unranked
8 citations

Sabrina Paganoni, Matthew Harms, Neil A. Shneider, Jinsy Andrews, Timothy M. Miller +13 more

C9orf72 in myeloid cells suppresses STING-induced inflammation

Nature(2020)10.1038/s41586-020-2625-x
N/A
0DataRank · unranked
305 citations

Jacqueline G. O’Rourke, Alberto Yáñez, Janet L. Markman, Ritchie Ho, Xinchen Wang +12 more

Dominant mutations in ITPR3 cause Charcot‐Marie‐Tooth disease

Annals of Clinical and Translational Neurology(2020)10.1002/acn3.51190
N/A
0DataRank · unranked
28 citations

Svetlana M. Molchanova, Anya Revah‐Politi, Elaine M. Pereira, Mari Auranen, Jussi Toppila +12 more

LATE BREAKING NEWS E-POSTER PRESENTATION

Neuromuscular Disorders(2020)10.1016/j.nmd.2020.09.011
N/A
0DataRank · unranked
0 citations

Svetlana M. Molchanova, Anya Revah‐Politi, Elaine M. Pereira, Mari Auranen, Jussi Toppila +12 more

DYNATE: Localizing Rare-Variant Association Regions via Multiple Testing Embedded in an Aggregation Tree

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.01.518706
N/A
0DataRank · unranked
0 citations

John Pura, Andrew S. Allen, Kouros Owzar, Jianfeng Lu, Matthew Harms +2 more

DYNATE: Localizing rare‐variant association regions via multiple testing embedded in an aggregation tree

Genetic Epidemiology(2023)10.1002/gepi.22542
N/A
0DataRank · unranked
1 citations

John Pura, Andrew S. Allen, Kouros Owzar, Jianfeng Lu, Matthew Harms +2 more