N. Weegerink

Most-cited papers

1. Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment.

   M. Schraders, S. Haas, N. Weegerink, Jaap Oostrik +9 more

   2011American Journal of Human Genetics95 citations Open access

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2. Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations

   N. Weegerink, M. Schraders, Jaap Oostrik, P. Huygen +10 more

   2011Journal of the Association for Research in Otolaryngology76 citations Open access

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3. Phenotypes of Two Dutch DFNA3 Families with Mutations in GJB2

   N. Weegerink, R. Pennings, P. Huygen, L. Hoefsloot +2 more

   2011Annals of Otology, Rhinology and Laryngology11 citations

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4. Phenotype of a Belgian Family With 6p25 Deletion Syndrome

   N. Weegerink, F. Swinnen, O. Vanakker, J. Casselman +1 more

   2016Annals of Otology, Rhinology and Laryngology10 citations Open access

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5. A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 Phenotype

   J. Smits, E. van Beelen, N. Weegerink, Jaap Oostrik +8 more

   2020Otology and Neurotology2 citations Open access

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6. Hereditary Hearing Impairment. Clinical and genetic aspects of DFNA3, DFNB8/10, DFNX4, Muckle-Wells syndrome and otosclerosis

   N. Weegerink

   20130 citations

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