Jeroen J Smits

6PUBLICATIONS
13CO-AUTHORS
Genome structure and regulationDevelopmental genetics (incl. sex determination)Gene mappingNeurogeneticsMedical infection agents (incl. prions)
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Publications (6)

|Oct 13, 2025
Genetic Landscape of Robin Sequence: A Systematic Review.

Shirley van de Velde, Aebele B Mink van der Molen, Augusta M A Lachmeijer

|Mar 31, 2025
DDX3X-related neurodevelopmental disorder in males - presenting a new cohort of 19 males and a literature review.

Milou G P Kennis, Dmitrijs Rots, Arjan Bouman

|Oct 05, 2021
Correction to: Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant.

Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting

|Aug 19, 2021
Exploring the missing heritability in subjects with hearing loss, enlarged vestibular aqueducts, and a single or no pathogenic SLC26A4 variant.

Jeroen J Smits, Suzanne E de Bruijn, Cornelis P Lanting

|Jul 08, 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

|Dec 12, 2018
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment.

Jeroen J Smits, Jaap Oostrik, Andy J Beynon

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Frequent Collaborators

3 joint publications

Hannie Kremer

3 joint publications

Suzanne E de Bruijn

2 joint publications

Cornelis P Lanting

2 joint publications

Frans P M Cremers