Hideki Mutai

Also affiliated with Kitasato University

NeuroscienceBiochemistry, 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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 4 papers. Top paper: “Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans”.

Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans

PLoS Genetics(2020)10.1371/journal.pgen.1008643

N/A

0DataRank · unranked

58 citations

Koichiro Wasano, Yukihide Momozawa, Yoichiro Kamatani, Fuyuki Miya, Sawako Masuda +8 more

Pax3 deficiency diminishes melanocytes in the developing mouse cochlea

鐵と鋼 : 日本鐡鋼協會々誌(2023)10.21203/rs.3.rs-2990436/v1

N/A

0DataRank · unranked

0 citations

Erisa Takahashi, Norifumi Tatsumi, Hideki Mutai, Yuko Kondo, Patrick J. Atkinson +6 more

Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea

Scientific Reports(2024)10.1038/s41598-024-52629-9

N/A

0DataRank · unranked

7 citations

Erisa Takahashi, Norifumi Tatsumi, Hideki Mutai, Hiroki Saijo, Yuko Kondo +7 more

ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time

Genetics in Medicine(2025)10.1016/j.gim.2025.101392

N/A

0DataRank · unranked

1 citations

Marina T. DiStefano, Andrea M. Oza, Pamela Ajuyah, Ryan Webb, Enyonam Edoh +76 more