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Plos One|August 30, 2018
Grxcr2 is required for stereocilia morphogenesis in the cochleaMatthew R Avenarius, Jae-Yun Jung, Charles Askew, et al.Journal of the Association for Research in Otolaryngology : JARO|July 26, 2011
Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutationsNicole J D Weegerink, Margit Schraders, Jaap Oostrik, et al.Ear and Hearing|January 1, 2014
Similar phenotypes caused by mutations in OTOG and OTOGLAnne M M Oonk, Joop M Leijendeckers, Patrick L M Huygen, et al.European Journal of Human Genetics : EJHG|May 1, 2014
Progressive hearing loss and vestibular dysfunction caused by a homozygous nonsense mutation in CLIC5Celia Zazo Seco, Anne M M Oonk, María Domínguez-Ruiz, et al.Nature Communications|February 18, 2011
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and humanNikoletta Charizopoulou, Andrea Lelli, Margit Schraders, et al.American Journal of Human Genetics|February 9, 2010
Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairmentMargit Schraders, Kwanghyuk Lee, Jaap Oostrik, et al.European Journal of Human Genetics : EJHG|July 16, 2015
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cellsCelia Zazo Seco, Arnaud P Giese, Sobia Shafique, et al.Human Genetics|December 12, 2018
De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairmentJeroen J Smits, Jaap Oostrik, Andy J Beynon, et al.American Journal of Human Genetics|November 6, 2012
Mutations of the gene encoding otogelin are a cause of autosomal-recessive nonsyndromic moderate hearing impairmentMargit Schraders, Laura Ruiz-Palmero, Ersan Kalay, et al.American Journal of Human Genetics|November 6, 2012
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing lossKemal O Yariz, Duygu Duman, Celia Zazo Seco, et al.Pageof 4