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

Adam Ameur

Uppsala University

ORCID: 0000-0001-6085-6749

Also affiliated with Science for Life Laboratory

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
15.1Author 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.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874
Top 1%
12.9DataRank
Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

Papers

Driven by 10 papers — median percentile 95. Top paper: “Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project”.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874
Top 1%
12.9DataRank
Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly

Nature Communications(2020)10.1038/s41467-019-14079-0
Top 9%
2.3DataRank
Top 9%76 citations

Paul Lacaze, Emma M. Rath, Andrew Stone, Marie‐Jo Brion, Adam Ameur +33 more

Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

Nature Communications(2020)10.1038/s41467-020-15707-w
N/A
0.678DataRank · unranked
91 citations

Ruth Huh, Nikolay Oskolkov, Jia Wen, Sergiu Netotea, Paola Giusti‐Rodríguez +15 more

Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps

Genome Research(2024)10.1101/gr.279346.124
N/A
0.396DataRank · unranked
13 citations

Jesper Eisfeldt, Jesse D. Bengtsson, Ming Yin Lun, Christopher M. Grochowski, Medhat Mahmoud +17 more

Single cell long read whole genome sequencing reveals somatic transposon activity in human brain

medRxiv(2024)10.1101/2024.11.11.24317113
N/A
0.208DataRank · unranked
3 citations

Ester Kalef-Ezra, Dominic W. Horner, Xinchang Zheng, Nadine Holmes, Marco Toffoli +8 more

Single cell long read whole genome sequencing reveals somatic transposon activity in human brain

Communications Biology(2025)10.1038/s42003-025-08805-2
N/A
0DataRank · unranked
4 citations

Ester Kalef-Ezra, Dominic W. Horner, Xinchang Zheng, Nadine Holmes, Marco Toffoli +10 more

Translating GWAS-identified loci for cardiac rhythm and rate using an in vivo image- and CRISPR/Cas9-based approach

Scientific Reports(2020)10.1038/s41598-020-68567-1
N/A
0DataRank · unranked
91 citations

Anastasia Emmanouilidou, Eugenia Mazzaferro, Silvia Vicenzi, Ida Höijer, Tiffany Klingström +10 more

A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cells

Cell & Bioscience(2021)10.1186/s13578-021-00716-z
N/A
0DataRank · unranked
14 citations

Jonas Mattisson, Galina Polekhina, Andrew Bakshi, Jonatan Halvardson, Marcus Danielsson +5 more

A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cells

medRxiv(2021)10.1101/2021.06.15.21258995
N/A
0DataRank · unranked
1 citations

Jonas Mattisson, Galina Polekhina, Andrew Bakshi, Jonatan Halvardson, Marcus Danielsson +5 more

Mind the gap: the relevance of the genome reference to resolve rare and pathogenic inversions

medRxiv(2024)10.1101/2024.04.22.24305780
N/A
0DataRank · unranked
1 citations

Jesper Eisfeldt, Jesse D. Bengtsson, Ming Yin Lun, Christopher M. Grochowski, Medhat Mahmoud +14 more