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

Martti Färkkilâ

University of Helsinki

ORCID: 0000-0002-0250-8559

Also affiliated with Helsinki University Hospital, Hospital District of Helsinki and Uusimaa

MedicineBiochemistry, 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
7.1Author DataRank

Indexed papers

2in 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 2 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 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 13 papers — median percentile 76. Top paper: “A genomic mutational constraint map using variation in 76,156 human genomes”.

A genomic mutational constraint map using variation in 76,156 human genomes

Nature(2023)10.1038/s41586-023-06045-0
N/A
9.6DataRank · unranked
1369 citations

Laurent C. Francioli, Julia K. Goodrich, Ryan L. Collins, Masahiro Kanai, Qingbo S. Wang +95 more

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

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Nature Genetics(2022)10.1038/s41588-022-01156-2
N/A
3.7DataRank · unranked
195 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu +95 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

Development and validation of a model to predict incident chronic liver disease in the general population: The CLivD score

Journal of Hepatology(2022)10.1016/j.jhep.2022.02.021
N/A
0.641DataRank · unranked
71 citations

Panu K. Luukkonen, Anna But, Veikko Salomaa, Annie Britton, K. Petersen +10 more

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

medRxiv(2021)10.1101/2021.06.15.21258641
N/A
0.500DataRank · unranked
11 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, María T. Abreu +95 more

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database

Nature Communications(2025)10.1038/s41467-025-61698-x
Top 44%
0.417DataRank
Top 44%14 citations

Moriel Singer‐Berk, Sarah L. Stenton, Julia K. Goodrich, Michael W. Wilson, Jonah Einson +95 more

Narcolepsy as a potential risk factor for Schizophrenia

Translational Psychiatry(2025)10.1038/s41398-025-03259-w
N/A
0.248DataRank · unranked
3 citations

Anniina Tervi, Samuel E. Jones, FinnGen, Aarno Palotie, Mark Daly +95 more

Neoplasia Detection Rate and Risk of Post-endoscopy Esophageal Adenocarcinoma and Neoplasia in a Population-based Cohort Study

Clinical Gastroenterology and Hepatology(2025)10.1016/j.cgh.2025.07.020
N/A
0DataRank · unranked
3 citations

Giola Santoni, Dag Holmberg, Joonas H. Kauppila, Martti Färkkilâ, Nicholas J. Shaheen +2 more