Jeroen J. Smits

Also affiliated with Radboud University Medical Center

NeuroscienceBiochemistry, Genetics and Molecular BiologyMedicine

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 3 papers. Top paper: “Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss”.

Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A variant associated with autosomal dominant hearing loss

European Journal of Human Genetics(2021)10.1038/s41431-021-00891-0

N/A

0.360DataRank · unranked

10 citations

Kelly Nunes, Alex Marcel Moreira Dias, Leandro Ucela Alves, Beatriz de Castro Andrade Mendes, Juliana Sampaio‐Silva +6 more

A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss

Journal of Medical Genetics(2020)10.1136/jmedgenet-2020-106863

N/A

0DataRank · unranked

19 citations

Jeroen J. Smits, Chang Liu, Cris Lanting, Andy J. Beynon, Joëlle Blankevoort +12 more

Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearing

Developmental Cell(2021)10.1016/j.devcel.2021.04.017

N/A

0DataRank · unranked

53 citations

Alex M Rohacek, Matthew A. Caporizzo, Amir Nankali, Jeroen J. Smits, Jaap Oostrik +13 more