Margit Schraders
Radboud University Nijmegen(NL)Radboud University Medical Center(NL)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Vestibular and auditory disorders, Lymphoma Diagnosis and Treatment, Connexins and lens biology, Hearing Loss and Rehabilitation
Most-Cited Works
- → SDH5 , a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma(2009)701 cited
- → Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan(2012)209 cited
- → The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands(2016)145 cited
- → Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss(2012)127 cited
- → Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human(2011)119 cited
- → Next-Generation Sequencing Identifies Mutations of SMPX, which Encodes the Small Muscle Protein, X-Linked, as a Cause of Progressive Hearing Impairment(2011)102 cited
- → Lack of Bcl‐2 expression in follicular lymphoma may be caused by mutations in the BCL2 gene or by absence of the t(14;18) translocation(2005)99 cited
- → Mutations in PTPRQ Are a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB84 and Associated with Vestibular Dysfunction(2010)94 cited
- → Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment(2012)91 cited
- → Genotype–Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations(2011)89 cited