Sai Prasad
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Vestibular and auditory disorders, Hearing Loss and Rehabilitation, Ear Surgery and Otitis Media, Connexins and lens biology
Most-Cited Works
- → Pendred syndrome, DFNB4, andPDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations(2001)297 cited
- → Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)(1999)269 cited
- → Genotype–phenotype correlations for SLC26A4-related deafness(2007)107 cited
- → GJB2: The spectrum of deafness-causing allele variants and their phenotype(2004)87 cited
- → Genetic testing for hereditary hearing loss: Connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA)(2000)71 cited
- → Pendred syndrome and DFNB4‐mutation screening of SLC26A4 by denaturing high‐performance liquid chromatography and the identification of eleven novel mutations(2003)63 cited
- → The M34T Allele Variant of Connexin 26(2000)50 cited
- → Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31(1998)47 cited
- → Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13)(2001)20 cited
- → Presymptomatic Diagnosis of Nonsyndromic Hearing Loss by Genotyping(1998)12 cited