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

Ariadna Sánchez

University of Edinburgh

ORCID: 0000-0003-0409-1328
MedicineBiochemistry, Genetics and Molecular BiologyComputer Science

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
1.7Author 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.

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 5 papers — median percentile 88. Top paper: “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”.

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

An Exosome-Based Liquid Biopsy for the Detection of Early-Onset Colorectal Cancer: The ENCODER Multicenter Study

Gastroenterology(2025)10.1053/j.gastro.2025.08.013
N/A
0.292DataRank · unranked
6 citations

Francesc Balaguer, Yasuhide Yamada, Takeshi Nagasaka, Yuji Toiyama, Yoshinaga Okugawa +86 more

Familial component of early-onset colorectal cancer: opportunity for prevention

British journal of surgery(2022)10.1093/bjs/znac322
N/A
0DataRank · unranked
20 citations

Marc Martí, Antonino Spinelli, Noel F. F. C. de Miranda, Claire Palles, Alfredo Vivas López +93 more

Epigenome-Wide DNA Methylation Profiling of Normal Mucosa Reveals HLA-F Hypermethylation as a Biomarker Candidate for Serrated Polyposis Syndrome

Journal of Molecular Diagnostics(2022)10.1016/j.jmoldx.2022.03.010
N/A
0DataRank · unranked
3 citations

Eva Hernández‐Illán, Juan José Lozano, Julia Sidorova, Jenifer Muñoz, Yasuyuki Okada +18 more

IDENTIFICATION OF MODIFIER GENE VARIANTS OVERREPRESENTED IN FAMILIAL HYPOMAGNESEMIA WITH HYPERCALCIURIA AND NEPHROCALCINOSIS PATIENTS WITH A MORE AGGRESSIVE RENAL PHENOTYPE

medRxiv(2023)10.1101/2023.11.08.23298254
N/A
0DataRank · unranked
3 citations

Jordi Morata, M. Durán, Joseph Torchia, Raúl Tonda, M Ferrer +6 more