Author

Cris Lanting

Radboud University NijmegenORCID 0000-0001-9397-7766Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Andy J. BeynoniD· 1 shared Bo ZhaoiD· 1 shared Chang Liu· 1 shared Cor W. R. J. Cremers· 1 shared Erik de VriezeiD· 1 shared Frans P.M. CremersiD· 1 shared Hannie KremeriD· 1 shared Helger G. YntemaiD· 1 shared

Activity by Year

2020-2020 · peak 1/yr

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10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

Andy J. BeynonORCID

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1 paper

Recent·Most cited

GeneticsJournal of Medical GeneticsPeer-reviewedJul 6, 2020

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…·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.

20 citations

humanstatistical model

𝕏 PostBluesky