Kristien Verhoeven
Cochlear (Australia)(AU)Macquarie University(AU)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Hearing, Cochlea, Tinnitus, Genetics, Hearing Loss and Rehabilitation, Mitochondrial Function and Pathology, Cellular transport and secretion
Most-Cited Works
- → Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy(2003)452 cited
- → Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2(2006)358 cited
- → Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease(2005)357 cited
- → Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment(1998)339 cited
- → Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity(2007)207 cited
- → A deafness mutation isolates a second role for the tectorial membrane in hearing(2005)138 cited
- → Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10(2003)118 cited
- → Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene(1999)88 cited
- → Autosomal Dominant Inherited Neuropathies With Prominent Sensory Loss and Mutilations(2003)80 cited
- → Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1(2001)67 cited