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Publications

2007 publications of the Riazuddin and Ahmed labs.

  • Khan SY, Riazuddin S, Tariq M, Anwar S, Shabbir MI, Riazuddin SA, Khan SN, Husnain T, Ahmed ZM, Friedman TB, Riazuddin S. (2007)
  • Autosomal Recessive Nonsyndromic Deafness Locus DFNB63 at Chromosome 11q13.2-q13.3.
  • Hum Genet 120:789-793
  • Ahmed ZM*, Khan SY*, Shabbir MI, Kitajiri S, Kalsoom S, Tasneem S, Shayiq S, Ramesh A, Srisailpathy S, Khan SN, Smith RJ, Riazuddin S, Friedman TB, Riazuddin S. (2007)
  • Mutations in RDX cause nonsyndromic recessive hearing loss.
  • Hum Mutat. 28(5):417-423
    * co-first authors
  • Hertzano R, Dror AA, Montcouquiol M, Ahmed ZM, Ellsworth B, Camper S, Friedman TB, Kelley MW, Avraham KB. (2007)
  • Lhx3, a LIM domain trancription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system.
  • Euro J Neurosci 25(4):999-1005
  • Ahmed ZM*, Nal N*, Erkal E, Alper O, Lüleci G, Dinç O, Chattaraj P, Riazuddin S, Boger E, Kabra M, Ghosh M, Riazuddin S, Morell RJ, Friedman TB. (2007)
  • Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
  • Hum Mutat 28(10):1014-1019
    * co-first authors
  • Rebibo-Sabbah A, Nudelman I, Ahmed ZM, Baasov T, Ben-Yosef T. (2007)
  • In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndrome.
  • Hum Genet 122:373-381
  • Ain Q, Nazli S, Riazuddin S, Jaleel A, Riazuddin SA, Zafar AU, Khan SN, Husnain T, Griffith AJ, Ahmed ZM, Friedman TB, Riazuddin S. (2007)
  • The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.
  • Hum Genet 122:445-450
  • Kitajiri S, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ. (2007)
  • Identities, frequencies, and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan.
  • Clin Genet 72:546-550
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