N.J.D. Weegerink

Next-Generation Sequencing Identifies Mutations of SMPX, which Encodes the Small Muscle Protein, X-Linked, as a Cause of Progressive Hearing Impairment

Margit Schraders, Stefan A. Haas, N.J.D. Weegerink et al. · The American Journal of Human Genetics · 2011 · 103 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

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

N.J.D. Weegerink, Margit Schraders, Jaap Oostrik et al. · Journal of the Association for Research in Otolaryngology · 2011 · 89 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis

Anne M.M. Oonk, Joop M. Leijendeckers, E.M. Lammers et al. · Hearing Research · 2013 · 40 citations

Life Sciences, Genetics, Molecular Genetics +10

Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family

N.J.D. Weegerink, P.L.M. Huygen, Margit Schraders et al. · Hearing Research · 2011 · 16 citations

Medicine, Audiology, Otolaryngology +14

Phenotype of a Belgian Family With 6p25 Deletion Syndrome

N.J.D. Weegerink, Freya Swinnen, Olivier Vanakker et al. · Annals of Otology Rhinology & Laryngology · 2016 · 13 citations

Life Sciences, Audiology, Genetics +17