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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Thomas B. Friedman

Laboratory of Molecular Genetics

National Institute on Deafness and Other Communication Disorders

National Institutes of Health

5 Research Court



Name/email consistency: high



  • Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, 5 Research Court, USA;. 1999 - 2011


  1. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes. Schultz, J.M., Bhatti, R., Madeo, A.C., Turriff, A., Muskett, J.A., Zalewski, C.K., King, K.A., Ahmed, Z.M., Riazuddin, S., Ahmad, N., Hussain, Z., Qasim, M., Kahn, S.N., Meltzer, M.R., Liu, X.Z., Munisamy, M., Ghosh, M., Rehm, H.L., Tsilou, E.T., Griffith, A.J., Zein, W.M., Brewer, C.C., Riazuddin, S., Friedman, T.B. J. Med. Genet. (2011) [Pubmed]
  2. Human nonsyndromic sensorineural deafness. Friedman, T.B., Griffith, A.J. Annu. Rev. Genomics. Hum. Genet (2003) [Pubmed]
  3. DFNB3, spectrum of MYO15A recessive mutant alleles and an emerging genotype-phenotype correlation. Friedman, T.B., Hinnant, J.T., Ghosh, M., Boger, E.T., Riazuddin, S., Lupski, J.R., Potocki, L., Wilcox, E.R. Adv. Otorhinolaryngol. (2002) [Pubmed]
  4. DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15. Friedman, T.B., Hinnant, J.T., Fridell, R.A., Wilcox, E.R., Raphael, Y., Camper, S.A. Adv. Otorhinolaryngol. (2000) [Pubmed]
  5. Unconventional myosins and the genetics of hearing loss. Friedman, T.B., Sellers, J.R., Avraham, K.B. Am. J. Med. Genet. (1999) [Pubmed]
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