Irina N. Bespalova

Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

Irina N. Bespalova · Human Molecular Genetics · 2001 · 269 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Linkage and Association of the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene With Autism

Nicolás Ramoz, Jennifer Reichert, Christopher J. Smith et al. · American Journal of Psychiatry · 2004 · 206 citations

Life Sciences, Genetics, Molecular Genetics +17

Effects of Vagus Nerve Stimulation on Progressive Myoclonus Epilepsy of Unverricht‐Lundborg Type

Brien Smith, Rhonna Shatz, Kost Elisevich et al. · Epilepsia · 2000 · 51 citations · Full text

Medicine, Neurology, Neuroscience +16

A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus

Guy Van Camp, Henricus P. M. Kunst, Kris Flothmann et al. · Journal of Medical Genetics · 1999 · 46 citations · Full text

Life Sciences, Audiology, Genetics +11

Pathogenesis of clinical signs in recessive ataxia with saccadic intrusions

Barbara E. Swartz, Sheng Li, Irina N. Bespalova et al. · Annals of Neurology · 2003 · 40 citations

Medicine, Genetics, Neurology +17