Jaap Oostrik

A Mutation in CABP2 , Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment

Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki et al. · The American Journal of Human Genetics · 2012 · 135 citations · Full text

Health Professions, Genetics, Molecular Genetics +14

Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Kemal O. Yariz, Duygu Duman, Celia Zazo Seco et al. · The American Journal of Human Genetics · 2012 · 131 citations · Full text

Medicine, Genetics, Molecular Genetics +9

Mutations of ESRRB Encoding Estrogen-Related Receptor Beta Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB35

Rob W.J. Collin, Ersan Kalay, Muhammad Tariq et al. · The American Journal of Human Genetics · 2008 · 129 citations · Full text

Medicine, Genetics, Molecular Genetics +8

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

Nikoletta Charizopoulou, Andrea Lelli, Margit Schraders et al. · Nature Communications · 2011 · 119 citations · Full text

Life Sciences, Genetics, Neuroscience +17

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