Markus Pfister
HNO-Praxis(DE)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Hearing, Cochlea, Tinnitus, Genetics, Dermatological and Skeletal Disorders, Mitochondrial Function and Pathology, Neonatal Health and Biochemistry
Most-Cited Works
- → GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study(2005)551 cited
- → Occupational Noise, Smoking, and a High Body Mass Index are Risk Factors for Age-related Hearing Impairment and Moderate Alcohol Consumption is Protective: A European Population-based Multicenter Study(2008)278 cited
- → GRM7 variants confer susceptibility to age-related hearing impairment(2008)208 cited
- → Deletion of the Ca2+-activated potassium (BK) α-subunit but not the BKβ1-subunit leads to progressive hearing loss(2004)202 cited
- → Nonmuscle Myosin Heavy-Chain Gene MYH14 Is Expressed in Cochlea and Mutated in Patients Affected by Autosomal Dominant Hearing Impairment (DFNA4)(2004)169 cited
- → The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment(2007)138 cited
- → Feasibility of simultaneous PET/MR imaging in the head and upper neck area(2011)118 cited
- → Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell(2009)108 cited
- → The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells(2003)102 cited
- → Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients(2002)101 cited