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Publications

2009 publications of the Riazuddin and Ahmed labs.

  • Schultz JM, Khan SK, Ahmed ZM, Riazuddin S, Waryah AA, Chhatre D, Starost MF, Ploplis B, Buckley S, Velasquez D, Kabra M, Lee K, Hassan MJ, Ali G, Ansar M, Ghosh M, Wilcox ER, Ahmad W, Merlino G, Leal SM, Riazuddin S, Friedman TB, Morell RJ. (2009)
  • Noncoding mutations of HGF3 are associated with nonsyndromic recessive deafness, DFNB39.
  • American J Hum Genet 85(1):25-39
  • Waryah AM, Rehman A, Ahmed ZM, Bashir ZH, Khan SY, Zafar AU, Riazuddin S, Friedman TB, Riazuddin S. (2009)
  • DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.
  • Clinical Genetics 76(3): 270-5.
  • Khan SY, Riazuddin S, Shahzad M, Ahmed N, Zafar AU, Rehman A, Griffith AJ, Ahmed ZM, Riazuddin S, Friedman TB. (2009)
  • DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
  • Eur J Hum Genet Available online.
  • Riazuddin S, Anwar S, Janssen A, Ahmed ZM, Khan SY, Belyantseva I, Jochen E, Friedman PL, Riazuddin S, Fahlke C, Friedman TB. (2009)
  • Molecular basis of DFNB73: mutations of BSND are associated with nonsyndromic deafness or Bartter syndrome.
  • Am J Hum Genet 85:1-8.
  • Ahmed ZM, Riazuddin S, Khan S, Friedman P, Riazuddin S, Friedman TB. (2009)
  • USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
  • Clin Genet 75:86-91
  • Ahmed ZM, Riazuddin S, Khan S, Friedman P, Riazuddin S, Friedman TB. (2009)
  • USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
  • Clin Genet 75:86-91
  • Choi BY, Ahmed ZM, Riazuddin S, Bhinder MA, Shahzad M, Husnain T, Riazuddin S, Griffith AJ, Friedman TB. (2009)
  • Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
  • Clin Genet 75:237-43
  • Anwar S, Riazuddin S, Ahmed ZM, Tasneem S, Jaleel AU, Khan SY, Griffith AJ, Friedman TB, Riazuddin S. (2009)
  • SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred’s syndrome in Pakistanis.
  • J Hum Genet 54(5): 266-70.
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