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

Judith Favier

Inserm

ORCID: 0000-0001-8190-5853

Also affiliated with Université Paris Cité, Sorbonne Université, Sorbonne Paris Cité, Centre de Recherche des Cordeliers, Vall d'Hebron Hospital Universitari, Vall d'Hebron Institute of Oncology

MedicineBiochemistry, Genetics and Molecular BiologyPhysics and Astronomy

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

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.

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 6 papers — median percentile 64. Top paper: “International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma”.

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

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
0DataRank · unranked
20 citations

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

SDHx mutation and pituitary adenoma: can in vivo 1H-MR spectroscopy unravel the link?

Endocrine Related Cancer(2022)10.1530/erc-22-0198
N/A
0DataRank · unranked
6 citations

Betty Salgues, Małgorzata Marjańska, M. Laloi‐Michelin, Philippe Herman, Lauriane Le Collen +11 more

Similar deficiencies, different outcomes: succinate dehydrogenase loss in adrenal medulla vs. fibroblast cell culture models of paraganglioma

Cancer & Metabolism(2024)10.1186/s40170-024-00369-9
N/A
0DataRank · unranked
8 citations

Sanjana Mahadev Bhat, Yuxiang Zhu, Cristina Correia, Sherry X. Zhou, Brandon Wilbanks +5 more

Approaches to reduce succinate accumulation by restoration of succinate dehydrogenase activity in cultured adrenal cells

Journal of Cell Science(2025)10.1242/jcs.263925
N/A
0DataRank · unranked
1 citations

Leili Rahimi, Fan Feng, Nicole A. Becker, Clifford D.L. Folmes, Judith Favier +2 more

Distinct proteomic and acylproteomic adaptations to succinate dehydrogenase loss in two cell contexts

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.08.01.668168
N/A
0DataRank · unranked
1 citations

Benjamin Madden, M. Cristine Charlesworth, Taro Hitosugi, Judith Favier, L. James Maher +1 more