Matan M. Jean

Biochemistry, Genetics and Molecular BiologyNeuroscienceMedicine

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 2 papers. Top paper: “SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice”.

SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice

Journal of Medical Genetics(2023)10.1136/jmg-2023-109264

N/A

0DataRank · unranked

6 citations

Matan M. Jean, Yael Noy, Daniel Halpérin, Yuval Yogev, Ohad Wormser +11 more

Early‐Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1B

Movement Disorders(2025)10.1002/mds.30249

N/A

0DataRank · unranked

1 citations

Noam Hadar, Eyal Kristal, Nicola Roberts, Vadim Dolgin, Ilana Aminov +17 more