2006

  • Riazuddin S, Khan SN, Ahmed ZM, Ghosh M, Caution K, Nazli S, Kabra M, Zafar AU, Chen K, Naz S, Paven W, Antonellis A, Pavan WJ, Green ED, Wilcox ER, Friedman PL, Morell RJ, Riazuddin S, Friedman TB. (2006)
  • Mutations in TRIOBP, encoding a putative cytoskeletal organizing protein, are associated with nonsyndromic recessive deafness.
  • Am J Hum Genet 78(1):137-143
  • Ahmed ZM,* Shabbir I,* Khan SN, Riazuddin S, Ghosh M, Kabra M, Morell RJ, Belyantseva IA, Friedman TB, Riazuddin S. (2006)
  • Mutations of human TMHS cause recessively inherited nonsyndromic hearing loss.
  • J Med Genet 43(8):634-640
    * co-first authors
  • Ahmed ZM*, Haywood-Watson II RJL*, Kjellstrom S*, Bush RA, Takada Y, Alagramam KN, Hampton LL, Battey JF, Sieving PA, Friedman TB. (2006)
  • Ames waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts.
  • IOVS 47(7):3074-3084
    * co-first authors
  • Ahmed ZM*, Goodyear R*, Riazuddin S, Lagziel A, Behra M, Burgess SM, Wilcox ER, Riazuddin S, Griffith AJ, Frolenkov G, Belyantseva IA, Richardson G, Friedman TB. (2006)
  • The tip link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.
  • J Neuroscience 26:7022-7034
    * co-first authors
  • Riazuddin S, Ahmed ZM, Fanning AS, Lagziel A, Kitajiri S, Ramzan K, Khan SN, Chattaraj P, Friedman PL, Anderson JM, Belyantseva IA, Forge A, Riazuddin S, Friedman TB. (2006)
  • Tricellulin is a tight-junction protein necessary for hearing.
  • Am J Hum Genet 79(6):1040-1051