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

Julian R. Sampson

Cardiff University

ORCID: 0000-0002-2902-2348
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 2%percentile
2.7Author 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.

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

EClinicalMedicine(2023)10.1016/j.eclinm.2023.101909
Top 12%
1.7DataRank
Top 12%115 citations

Saskia Haupt, Toni T. Seppälä, Julian R. Sampson, Lone Sunde, Inge Bernstein +95 more

Papers

Driven by 6 papers — median percentile 84. Top paper: “Germline MBD4 deficiency causes a multi-tumor predisposition syndrome”.

Germline MBD4 deficiency causes a multi-tumor predisposition syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.018
N/A
1.9DataRank · unranked
79 citations

Hannah D. West, Edward Chew, Sara Galavotti, Christoffer Flensburg, Judith E. Grolleman +64 more

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

EClinicalMedicine(2023)10.1016/j.eclinm.2023.101909
Top 12%
1.7DataRank
Top 12%115 citations

Saskia Haupt, Toni T. Seppälä, Julian R. Sampson, Lone Sunde, Inge Bernstein +95 more

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

De novo variants in SNAP25 cause an early-onset developmental and epileptic encephalopathy

Genetics in Medicine(2020)10.1038/s41436-020-01020-w
N/A
0DataRank · unranked
47 citations

Heinrich Sticht, Pia Zacher, Bernt Popp, Holly E. Babcock, Dewi P. Bakker +53 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

PIGA Mutations and Glycosylphosphatidylinositol Anchor Dysregulation in Polyposis-Associated Duodenal Tumorigenesis

Molecular Cancer Research(2024)10.1158/1541-7786.mcr-23-0810
N/A
0DataRank · unranked
1 citations

Kyle Chang, Angharad Walters, Joanna J. Hurley, Hannah D. West, Iain Perry +24 more