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

Pål Møller

Norwegian Cancer Society

ORCID: 0000-0001-8211-8237
Biochemistry, Genetics and Molecular BiologyMedicine

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 3%percentile
0.978Author 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.

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

European Journal of Cancer(2021)10.1016/j.ejca.2021.02.022
Top 21%
0.978DataRank
Top 21%23 citations

Mev Dominguez–Valentin, Emma J. Crosbie, Christoph Engel, Stefan Aretz, Finlay Macrae +81 more

Papers

Driven by 6 papers — median percentile 79. Top paper: “Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report”.

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

European Journal of Cancer(2021)10.1016/j.ejca.2021.02.022
Top 21%
0.978DataRank
Top 21%23 citations

Mev Dominguez–Valentin, Emma J. Crosbie, Christoph Engel, Stefan Aretz, Finlay Macrae +81 more

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Genetics in Medicine(2020)10.1038/s41436-020-01029-1
N/A
0DataRank · unranked
43 citations

Emma J. Crosbie, Christoph Engel, Stefan Aretz, Finlay Macrae, Ingrid Winship +83 more

Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for prostate cancer Genetics using novel sumLINK and sumLOD analyses

UNC Libraries(2020)10.17615/cv63-ck59
N/A
0DataRank · unranked
0 citations

Ingrid Oakley‐Girvan, Douglas F. Easton, Gianluca Severi, Stephen N. Thibodeau, Alice S. Whittemore +27 more

Risks of breast and ovarian cancer for women harboring pathogenic missense variants in BRCA1 and BRCA2 compared with those harboring protein truncating variants

Genetics in Medicine(2021)10.1016/j.gim.2021.08.016
N/A
0DataRank · unranked
30 citations

Christoph Engel, Miguel de la Hoya, Paolo Peterlongo, Drakoulis Yannoukakos, Luca Livraghi +56 more

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG)

UNC Libraries(2021)10.17615/ktmt-6886
N/A
0DataRank · unranked
6 citations

Kimberly A. Zuhlke, Nicola J. Camp, Zsofia Kote‐Jarai, Lingyi Lu, Nancy Hamel +45 more

The Risk of Breast Cancer According to Mutation Type and Position in Carriers of a Pathogenic Variant in BRCA1

Current Oncology(2025)10.3390/curroncol32120705
N/A
0DataRank · unranked
2 citations

Adriana Ionelia Apostol, Kelly Metcalfe, Dimitri Jorgji, Cezary Cybulski, Jacek Gronwald +19 more