Koichiro Wasano

Also affiliated with Tokai University Hospital

NeuroscienceMedicine

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

Cell death-inducing cytotoxicity in truncated KCNQ4 variants associated with DFNA2 hearing loss

Disease Models & Mechanisms(2021)10.1242/dmm.049015

N/A

0DataRank · unranked

10 citations

Koichiro Wasano, Satoe Takahashi, Kazuaki Homma, T Kojima

Functional Studies of Deafness-Associated Pendrin and Prestin Variants

International Journal of Molecular Sciences(2024)10.3390/ijms25052759

N/A

0DataRank · unranked

3 citations

T Kojima, Koichiro Wasano, Kazuaki Homma, Satoe Takahashi

Functional studies of deafness-associated pendrin and prestin variants

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.23.576877

N/A

0DataRank · unranked

2 citations

T Kojima, Koichiro Wasano, Kazuaki Homma, Satoe Takahashi