Manju Ghosh
Portsmouth Hospitals NHS Trust(GB)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, RNA regulation and disease, Genetics and Neurodevelopmental Disorders, RNA and protein synthesis mechanisms, Connexins and lens biology
Most-Cited Works
- → Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function(2002)473 cited
- → Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC(2002)175 cited
- Risk factors for severe acute lower respiratory tract infection in under-five children.(2001)
- → Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome(2001)148 cited
- → Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39(2009)120 cited
- → Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness(2005)110 cited
- → Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes(2011)104 cited
- → Mutations of human TMHS cause recessively inherited non-syndromic hearing loss(2006)100 cited
- → Mutational spectrum ofMYO15A: the large N-terminal extension of myosin XVA is required for hearing(2007)91 cited
- Clinical profile and frequency of delta f508 mutation in Indian children with cystic fibrosis.(2003)