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

Fostering Data Sharing

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Fiona Lalloo

Fiona Lalloo

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 12 papers — median percentile 84. Top paper: “A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study”.

A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study

The Lancet Oncology(2021)10.1016/s1470-2045(21)00522-2

N/A

3.0DataRank · unranked

96 citations

Elizabeth Page, Mark N. Brook, Sarah Thomas, Natalie Taylor, Jennifer Pope +95 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

Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

The Lancet Oncology(2021)10.1016/s1470-2045(21)00189-3

N/A

0DataRank · unranked

121 citations

James G. Dowty, Jeanette C. Reece, Grant Lee, Allyson Templeton, John‐Paul Plazzer +95 more

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Communications Biology(2022)10.1038/s42003-022-03978-6

N/A

0DataRank · unranked

15 citations

John F. Pearson, Louise Marquart, Joe Dennis, George A. R. Wiggins, Daniel R. Barnes +95 more

PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

Research Square(2022)10.21203/rs.3.rs-2269143/v1

N/A

0DataRank · unranked

0 citations

Anna Morra, Sofia Khan, Daniel R. Barnes, Manjeet K. Bolla, Joe Dennis +64 more

PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants

npj Breast Cancer(2023)10.1038/s41523-023-00546-x

N/A

0DataRank · unranked

7 citations

Anna Morra, Sofia Khan, Daniel R. Barnes, Manjeet K. Bolla, Joe Dennis +65 more

Head and Neck Cancer: United Kingdom National Multidisciplinary Guidelines, Sixth Edition

The Journal of Laryngology & Otology(2024)10.1017/s0022215123001615

N/A

0DataRank · unranked

51 citations

Stuart C. Winter, Elizabeth Abbey, Hiba Aga, Reshma Agrawal, Derfel ap Dafydd +94 more

Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction

UNC Libraries(2020)10.17615/bg56-kz70

N/A

0DataRank · unranked

19 citations

Trinidad Caldés, Maria A. Caligo, Alessandra Viel, Susan J. Ramus, Kathleen Claes +95 more

Childhood, adolescent, and young adulthood cancer risk in BRCA1 or BRCA2 pathogenic variant carriers

JNCI Journal of the National Cancer Institute(2024)10.1093/jnci/djae306

N/A

0DataRank · unranked

7 citations

Laura Madanat‐Harjuoja, Goska Leslie, Daniel R. Barnes, Manjeet K. Bolla, Joe Dennis +68 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

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)

UNC Libraries(2020)10.17615/rh7v-bc86

N/A

0DataRank · unranked

2 citations

Fiona Lalloo, D. Stoppa-Lyonnet, N. Lindor, C. Casella, I. L. Andrulis +95 more