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

Jean Khoury

Cleveland Clinic

ORCID: 0000-0001-5334-2942

Also affiliated with The Neurological Institute

MedicineImmunology and MicrobiologyBiochemistry, 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 4%percentile
0.660Author 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.

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis

Brain(2023)10.1093/brain/awad292
Top 30%
0.660DataRank
Top 30%23 citations

Eduardo Pérez‐Palma, Tobias Brünger, Ludovica Montanucci, Cornelius Gati, Chiara Klöckner +41 more

Papers

Driven by 6 papers — median percentile 70. Top paper: “SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis”.

SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis

Brain(2023)10.1093/brain/awad292
Top 30%
0.660DataRank
Top 30%23 citations

Eduardo Pérez‐Palma, Tobias Brünger, Ludovica Montanucci, Cornelius Gati, Chiara Klöckner +41 more

Novel de novo TREX1 mutation in a patient with retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations mimicking demyelinating disease

Multiple Sclerosis and Related Disorders(2021)10.1016/j.msard.2021.103015
N/A
0DataRank · unranked
9 citations

Jean Khoury, Rula A. Hajj‐Ali, Richard A. Prayson, Sunil K. Srivastava, Justis P. Ehlers +6 more

GLUT1 and cerebral glucose hypometabolism in human focal cortical dysplasia is associated with hypermethylation of key glucose regulatory genes

Research Square(2024)10.21203/rs.3.rs-4946501/v1
N/A
0DataRank · unranked
1 citations

Rosemary Westcott, David Skvasik, Ishant Khurana, Jean Khoury, Ingmar Blümcke +3 more

Genome-wide association meta-analyses of drug-resistant epilepsy

EBioMedicine(2025)10.1016/j.ebiom.2025.105675
N/A
0DataRank · unranked
12 citations

Andreja Avberšek, Remi Stevelink, Helena Martins Custodio, Siwei Chen, Doug Speed +88 more

GLUT1 and Cerebral Glucose Hypometabolism in Human Focal Cortical Dysplasia Is Associated with Hypermethylation of Key Glucose Regulatory Genes

Molecular Neurobiology(2025)10.1007/s12035-025-04871-z
N/A
0DataRank · unranked
1 citations

Rosemary Westcott, David Skvasik, Ishant Khurana, Jean Khoury, Ingmar Blümcke +3 more

USP25 in genetic generalized epilepsy: a gene under scrutiny

Brain(2025)10.1093/brain/awaf406
N/A
0DataRank · unranked
1 citations

Jill R. Murrell, Anna J. Prentice, Ingo Helbig, Holger Lerche, Patrick May +90 more