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

Gaël Nicolas

Inserm

ORCID: 0000-0001-9391-7800

Also affiliated with Normandie Université, Université de Rouen Normandie

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.

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Acta Neuropathologica(2022)10.1007/s00401-022-02454-z
Top 10%
2.1DataRank
Top 10%139 citations

Sven J. van der Lee, Duber Gomez‐Fonseca, Itziar de Rojas, Carolina Dalmasso, Benjamin Grenier‐Boley +95 more

Papers

Driven by 12 papers — median percentile 78. Top paper: “Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers”.

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Acta Neuropathologica(2022)10.1007/s00401-022-02454-z
Top 10%
2.1DataRank
Top 10%139 citations

Sven J. van der Lee, Duber Gomez‐Fonseca, Itziar de Rojas, Carolina Dalmasso, Benjamin Grenier‐Boley +95 more

Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease

JAMA Neurology(2022)10.1001/jamaneurol.2022.1166
N/A
0.681DataRank · unranked
93 citations

Michaël E. Belloy, Benjamin Grenier‐Boley, Itziar de Rojas, Atahualpa Castillo-Morales, Iris E. Jansen +95 more

Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

Nature Communications(2024)10.1038/s41467-024-46354-0
N/A
0.568DataRank · unranked
43 citations

Henriette Aksnes, Reza Maroofian, Lauren C. LaMonica, Luís Seabra, Anette Siggervåg +55 more

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

medRxiv(2022)10.1101/2022.03.08.22271043
Top 35%
0.564DataRank
Top 35%12 citations

Sven J. van der Lee, Duber Gomez‐Fonseca, Itziar de Rojas, Carolina Dalmasso, Benjamin Grenier‐Boley +95 more

Brain malformations and seizures by impaired chaperonin function of TRiC

Science(2024)10.1126/science.adp8721
N/A
0.489DataRank · unranked
25 citations

Piere Rodriguez-Aliaga, Weimin Yuan, Lena Franken, Kamil K. Zajt, Dimah Hasan +82 more

A mutation in the iron-responsive element of ALAS2 is a modifier of disease severity in a patient suffering from CLPX associated erythropoietic protoporphyria

Haematologica(2021)10.3324/haematol.2020.272450
N/A
0.477DataRank · unranked
23 citations

Sara Luscieti, Xènia Ferrer-Cortés, Gaël Nicolas, Hana Manceau, Katell Peoc’h +6 more

ARID1B-related disorder in 87 adults: Natural history and self-sustainability

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101873
N/A
0.292DataRank · unranked
6 citations

M. Gösgens, Alexander J.M. Dingemans, P. Striano, Antonella Riva, C. Mignot +81 more

Benchmark of computational methods to detect digenism in sequencing data

European Journal of Human Genetics(2025)10.1038/s41431-025-01834-9
N/A
0.165DataRank · unranked
2 citations

Donald F. Conrad, Anaı̈s Baudot, Elisabeth Tournier‐Lasserve, Principal investigators, Emmanuelle Génin +30 more

Polygenic Hazard Score for Predicting Age-associated Risk of Alzheimer’s Disease in European Populations: Development and Validation

medRxiv(2025)10.1101/2025.07.28.25332293
N/A
0.104DataRank · unranked
1 citations

Shahram Bahrami, Espen Hagen, Julian Fuhrer, Vera Fominykh, Alexey Shadrin +95 more

RRP12 Variants Are Associated With Autosomal Recessive Brain Calcifications

Movement Disorders(2025)10.1002/mds.70058
N/A
0DataRank · unranked
4 citations

Paola Rinchetti, Mathieu Anheim, Anna Klingseisen, Ouhaïd Lagha‐Boukbiza, Zhidong Cen +15 more

Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease

Acta Neuropathologica Communications(2021)10.1186/s40478-021-01294-4
N/A
0DataRank · unranked
40 citations

Sébastien Feuillette, Laëtitia Miguel, Catherine Schramm, Ségolène Pernet, Olivier Quenez +9 more

CLPX regulates erythroid heme synthesis by control of mitochondrial heme synthesis enzymes and iron utilization

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.09.289660
N/A
0DataRank · unranked
1 citations

Mark Perfetto, Aidan Danoff, Hector A. Bergonia, Samantha Gillis, Gaël Nicolas +5 more