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American Journal of Human Genetics|March 30, 2010
Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunctionMargit Schraders, Jaap Oostrik, Patrick L M Huygen, et al.
Blood|October 23, 2004
Novel chromosomal imbalances in mantle cell lymphoma detected by genome-wide array-based comparative genomic hybridizationMargit Schraders, Rolph Pfundt, Huub M P Straatman, et al.
Haematologica|May 10, 2007
Promoter methylation of PARG1, a novel candidate tumor suppressor gene in mantle-cell lymphomasTim Ripperger, Nils von Neuhoff, Kathrin Kamphues, et al.
Plos One|June 21, 2014
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani familiesSobia Shafique, Saima Siddiqi, Margit Schraders, et al.
Ear and Hearing|September 26, 2014
Nonsyndromic hearing loss caused by USH1G mutations: widening the USH1G disease spectrumAnne Marthe Maria Oonk, Ramon A C van Huet, Joop M Leijendeckers, et al.
American Journal of Human Genetics|February 23, 2010
Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing lossYun Li, Esther Pohl, Redouane Boulouiz, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 PhenotypeJeroen J Smits, Eline van Beelen, Nicole J D Weegerink, et al.
American Journal of Human Genetics|May 10, 2011
Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairmentMargit Schraders, Stefan A Haas, Nicole J D Weegerink, et al.
Hearing Research|January 17, 2017
Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairmentMieke Wesdorp, Jiddeke M van de Kamp, Erik F Hensen, et al.
Science (New York, N.Y.)|July 25, 2009
SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paragangliomaHuai-Xiang Hao, Oleh Khalimonchuk, Margit Schraders, et al.
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