Author

Andy J. Beynon

Radboud University Medical CenterORCID 0000-0002-3191-6113Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:electronic health records· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Alexandra WinkleriD· 1 shared Bo ZhaoiD· 1 shared Chang Liu· 1 shared Cor W. R. J. Cremers· 1 shared Cris LantingiD· 1 shared Erik de VriezeiD· 1 shared Eva KodermaniD· 1 shared Frans P.M. CremersiD· 1 shared

Activity by Year

2020-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperNeuroscience

Alexandra WinklerORCID

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2 papers

Recent·Most cited

Fast and robust objective EEG audiometry

T. Guyonnet-Hencke, Oscar Portoles, M. de Vries, Eva Koderman, Alexandra Winkler, J. Goodall, Peter Desain, Jordy Thielen, Michael Schulte, Andy J. Beynon, M. van Kesteren

This study develops an EEG system for fast and objective audiometry, showing strong correlation with conventional behavioral tests in elderly patients and young adults.

bioRxiv · May 22, 2024 · PreprintNeuroscience

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

Suzanne E. de Bruijn, Jeroen J. Smits, Chang Liu, Cris Lanting, Andy J. Beynon, Joëlle Blankevoort, Jaap Oostrik, Wouter Koole, Erik de Vrieze, Cor W. R. J. Cremers, Frans P.M. Cremers, Susanne Roosing, Helger G. Yntema, Henricus P. M. Kunst, Bo Zhao, , Hannie Kremer

The paper identifies an in-frame deletion in RIPOR2 as a frequent and highly penetrant cause of adult-onset hearing loss, with implications for genetic therapy.

Journal of Medical Genetics · Jul 6, 2020Peer-reviewedGenetics