Ralph Holme
Royal National Institute for Deaf People(GB)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Hearing Loss and Rehabilitation, Congenital heart defects research, Vestibular and auditory disorders, Retinal Development and Disorders
Most-Cited Works
- → Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D(2001)431 cited
- → Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31(2003)339 cited
- → Why Is There No Cure for Tinnitus?(2019)188 cited
- → Hearing loss and tinnitus: 250 million people and a US$10 billion potential market(2005)116 cited
- → Progressive Hearing Loss and Increased Susceptibility to Noise-Induced Hearing Loss in Mice Carrying a Cdh23 but not a Myo7a Mutation(2004)112 cited
- → Elongation of hair cell stereocilia is defective in the mouse mutant whirler(2002)91 cited
- → Hearing Protection, Restoration, and Regeneration: An Overview of Emerging Therapeutics for Inner Ear and Central Hearing Disorders(2019)83 cited
- → Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice(2002)71 cited
- → Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration(2003)45 cited
- → The global hearing therapeutic pipeline: 2021(2021)38 cited