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

Stéphanie Baulac

Centre National de la Recherche Scientifique

ORCID: 0000-0001-6430-4693

Also affiliated with Inserm, Sorbonne Université, Assistance Publique – Hôpitaux de Paris, Institut du Cerveau

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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
0.522Author 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.

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.07.487401
Top 37%
0.522DataRank
Top 37%11 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +45 more

Papers

Driven by 11 papers — median percentile 63. Top paper: “Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development”.

Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

Nature Genetics(2023)10.1038/s41588-022-01276-9
N/A
0.709DataRank · unranked
112 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +76 more

Comprehensive multiomic profiling of somatic mutations in malformations of cortical development

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.07.487401
Top 37%
0.522DataRank
Top 37%11 citations

Xiaoxu Yang, Taejeong Bae, Keng Ioi Vong, Swapnil Mittal, Catharina Donkels +45 more

Single-cell genotyping and transcriptomic profiling in focal cortical dysplasia

10.21203/rs.3.rs-4014535/v1
N/A
0.292DataRank · unranked
6 citations

Sara Baldassari, Esther Klingler, Lucia Gomez Teijeiro, Marion Doladilhe, Corentin Raoux +9 more

Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

Brain(2020)10.1093/brain/awaa085
N/A
0DataRank · unranked
32 citations

Felicitas Becker, Heba Morsy, Miriam Schmidts, Katia Hardies, Beyhan Tüysüz +40 more

Analysis of 1386 epileptogenic brain lesions reveals association with DYRK1A and EGFR

Nature Communications(2024)10.1038/s41467-024-54911-w
N/A
0DataRank · unranked
22 citations

Costin Leu, Tobias Brünger, Lucas Hoffmann, Sara Baldassari, Mathilde Chipaux +18 more

WONOEP 2022: Neurotechnology for the diagnosis of epilepsy

Epilepsia(2024)10.1111/epi.18028
N/A
0DataRank · unranked
10 citations

Katja Kobow, Pablo M. Casillas‐Espinosa, Andrew J. Cole, Diego Jiménez‐Jiménez, Hiroki Nariai +8 more

WONOEP appraisal: Genetic insights into early onset epilepsies

Epilepsia(2024)10.1111/epi.18124
N/A
0DataRank · unranked
6 citations

Silvia Cases‐Cunillera, Ganna Balagura, Matthew Coleman, L Rossini, James D. Mills +11 more

WONOEP appraisal: Modeling early onset epilepsies

Epilepsia(2024)10.1111/epi.18063
N/A
0DataRank · unranked
2 citations

Christopher A. Reid, Stéphane Auvin, Peter L. Carlen, Andrew J. Cole, Roza Szlendak +9 more

Targeted suppression of mTORC2 reduces seizures across models of epilepsy

Nature Communications(2023)10.1038/s41467-023-42922-y
N/A
0DataRank · unranked
22 citations

Jacqunae Mays, Alexandre Bacq, Juan A. Osés-Prieto, Stefka Tyanova, Chien-Ju Chen +9 more

Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene

Neurology(2022)10.1212/wnl.0000000000201471
N/A
0DataRank · unranked
55 citations

Ingmar Blümcke, Melodie R. Winawer, Till Hartlieb, Hoon‐Chul Kang, Laura Grisotto +31 more

Defective lipid signalling caused by mutations inPIK3C2Bunderlies focal epilepsy

Brain(2022)10.1093/brain/awac082
N/A
0DataRank · unranked
23 citations

Gaga Kochlamazashvili, Sara Baldassari, Albert Ian Mackintosh, Laura Licchetta, Emanuela Iovino +27 more