Arabandi Ramesh
University of Madras(IN)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Connexins and lens biology, RNA regulation and disease, Phytochemistry and Biological Activities, Congenital heart defects research
Most-Cited Works
- → Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23(2001)552 cited
- → Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus(2002)144 cited
- → Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human(2011)119 cited
- → Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss(2008)83 cited
- → Mutations of theRDXgene cause nonsyndromic hearing loss at theDFNB24locus(2007)83 cited
- Antioxidant activity measured in different solvent fractions obtained from Mentha spicata Linn.: an analysis by ABTS*+ decolorization assay.(2006)
- → A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus(1995)67 cited
- → Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE(2014)56 cited
- → Consanguineous nuclear families used to identify a new locus for recessive non-syndromic hearing loss on 14q(1995)55 cited
- → New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p(1997)52 cited