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Page 1
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.
Fattahi Z, Shearer AE, Babanejad M, Bazazzadegan N, Almadani SN, Nikzat N, Jalalvand K, Arzhangi S, Esteghamat F, Abtahi R, Azadeh B, Smith RJ, Kahrizi K, Najmabadi H. Fattahi Z, et al. Among authors: smith rj. Am J Med Genet A. 2012 Aug;158A(8):1857-64. doi: 10.1002/ajmg.a.34411. Epub 2012 Jun 26. Am J Med Genet A. 2012. PMID: 22736430 Free PMC article.
GJB2 mutations: passage through Iran.
Najmabadi H, Nishimura C, Kahrizi K, Riazalhosseini Y, Malekpour M, Daneshi A, Farhadi M, Mohseni M, Mahdieh N, Ebrahimi A, Bazazzadegan N, Naghavi A, Avenarius M, Arzhangi S, Smith RJ. Najmabadi H, et al. Among authors: smith rj. Am J Med Genet A. 2005 Mar 1;133A(2):132-7. doi: 10.1002/ajmg.a.30576. Am J Med Genet A. 2005. PMID: 15666300
GJB2 mutations in Baluchi population.
Naghavi A, Nishimura C, Kahrizi K, Riazalhosseini Y, Bazazzadegan N, Mohseni M, Smith RJ, Najmabadi H. Naghavi A, et al. Among authors: smith rj. J Genet. 2008 Aug;87(2):195-7. doi: 10.1007/s12041-008-0031-5. J Genet. 2008. PMID: 18776652 No abstract available.
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
Bazazzadegan N, Sheffield AM, Sobhani M, Kahrizi K, Meyer NC, Van Camp G, Hilgert N, Abedini SS, Habibi F, Daneshi A, Nishimura C, Avenarius MR, Farhadi M, Smith RJ, Najmabadi H. Bazazzadegan N, et al. Among authors: smith rj. Am J Med Genet A. 2011 May;155A(5):1202-11. doi: 10.1002/ajmg.a.33209. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484990 Free PMC article. Review.
Did the GJB2 35delG mutation originate in Iran?
Norouzi V, Azizi H, Fattahi Z, Esteghamat F, Bazazzadegan N, Nishimura C, Nikzat N, Jalalvand K, Kahrizi K, Smith RJ, Najmabadi H. Norouzi V, et al. Among authors: smith rj. Am J Med Genet A. 2011 Oct;155A(10):2453-8. doi: 10.1002/ajmg.a.34225. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910243 Free PMC article.
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.
Davarnia B, Babanejad M, Fattahi Z, Nikzat N, Bazazzadegan N, Pirzade A, Farajollahi R, Nishimura C, Jalalvand K, Arzhangi S, Kahrizi K, Smith RJ, Najmabadi H. Davarnia B, et al. Among authors: smith rj. Int J Pediatr Otorhinolaryngol. 2012 Feb;76(2):268-71. doi: 10.1016/j.ijporl.2011.11.019. Epub 2011 Dec 14. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22172221
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
Bazazzadegan N, Nikzat N, Fattahi Z, Nishimura C, Meyer N, Sahraian S, Jamali P, Babanejad M, Kashef A, Yazdan H, Sabbagh Kermani F, Taghdiri M, Azadeh B, Mojahedi F, Khoshaeen A, Habibi H, Reyhanifar F, Nouri N, Smith RJ, Kahrizi K, Najmabadi H. Bazazzadegan N, et al. Among authors: smith rj. Int J Pediatr Otorhinolaryngol. 2012 Aug;76(8):1164-74. doi: 10.1016/j.ijporl.2012.04.026. Epub 2012 Jun 12. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22695344
PDZD7 and hearing loss: More than just a modifier.
Booth KT, Azaiez H, Kahrizi K, Simpson AC, Tollefson WT, Sloan CM, Meyer NC, Babanejad M, Ardalani F, Arzhangi S, Schnieders MJ, Najmabadi H, Smith RJ. Booth KT, et al. Among authors: smith rj. Am J Med Genet A. 2015 Dec;167A(12):2957-65. doi: 10.1002/ajmg.a.37274. Epub 2015 Sep 29. Am J Med Genet A. 2015. PMID: 26416264 Free PMC article.
2,316 results