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

Sophie Giraud

Assistance Publique – Hôpitaux de Paris

ORCID: 0000-0003-1243-3084

Also affiliated with Hospices Civils de Lyon, Centre Hospitalier de la Côte Basque, Institut Bergonié, Institut National du Cancer

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 5%percentile
0.538Author DataRank

Indexed papers

3in 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 3 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.

International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma

Journal of Medical Genetics(2021)10.1136/jmedgenet-2020-107652
Top 36%
0.538DataRank
Top 36%11 citations

Eamonn R. Maher, Alberto Cascón, Anne Barlier, Sophie Giraud, Tonino Ercolino +13 more

Papers

Driven by 9 papers — median percentile 64. Top paper: “The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant”.

The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

Genetics in Medicine(2021)10.1038/s41436-021-01198-7
N/A
1.1DataRank · unranked
40 citations

Alexandra J. van den Broek, Julien A M Vos, Daniel R. Barnes, Julian Adlard, Irene L. Andrulis +95 more

Birt-Hogg-Dubé syndrome: diagnosis and management

The Lancet Oncology(2009)10.1016/s1470-2045(09)70188-3
N/A
0.958DataRank · unranked
593 citations

Maurice AM van Steensel, Sophie Giraud, Lennart Friis-Hansen, Stéphane Richard, Silvana Ungari +5 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
0.723DataRank · unranked
123 citations

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

Breast and Prostate Cancer Risks for MaleBRCA1andBRCA2Pathogenic Variant Carriers Using Polygenic Risk Scores

JNCI Journal of the National Cancer Institute(2021)10.1093/jnci/djab147
N/A
0.571DataRank · unranked
44 citations

Valentina Silvestri, Goska Leslie, Lesley McGuffog, Joe Dennis, Xin Yang +95 more

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

Nature Communications(2021)10.1038/s41467-020-20496-3
N/A
0.553DataRank · unranked
39 citations

Michael Lush, Jonathan Beesley, Tracy A. O’Mara, Joe Dennis, Jonathan P. Tyrer +94 more

International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma

Journal of Medical Genetics(2021)10.1136/jmedgenet-2020-107652
Top 36%
0.538DataRank
Top 36%11 citations

Eamonn R. Maher, Alberto Cascón, Anne Barlier, Sophie Giraud, Tonino Ercolino +13 more

Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature Review

The Journal of Clinical Endocrinology & Metabolism(2024)10.1210/clinem/dgae055
N/A
0.538DataRank · unranked
35 citations

Lucie Coppin, Pauline Romanet, Thomas Cuny, Jean-Christophe Maïza, Juliette Abeillon +32 more

Germline mutations in the new E1’ cryptic exon of the VHL gene in patients with tumours of von Hippel-Lindau disease spectrum or with paraganglioma

Journal of Medical Genetics(2020)10.1136/jmedgenet-2019-106519
N/A
0.457DataRank · unranked
20 citations

Bruna Calsina, Shahida K. Flores, Sophie Giraud, Marion Lenglet, Pauline Romanet +21 more

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population

UNC Libraries(2020)10.17615/p3jc-e673
N/A
0DataRank · unranked
0 citations

Zachary S. Fredericksen, Pascaline Berthet, Debra Frost, Audrey Remenieras, Sylvie Mazoyer +27 more