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The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.
Mahdieh N, Nishimura C, Ali-Madadi K, Riazalhosseini Y, Yazdan H, Arzhangi S, Jalalvand K, Ebrahimi A, Kazemi S, Smith RJ, Najmabadi H. Mahdieh N, et al. Among authors: jalalvand k. Clin Genet. 2004 Jun;65(6):506-8. doi: 10.1111/j.1399-0004.2004.00262.x. Clin Genet. 2004. PMID: 15151513 No abstract available.
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: jalalvand k. 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: jalalvand k. 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
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: jalalvand k. 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.
When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS).
Mohseni M, Akbari M, Booth KT, Babanejad M, Azaiez H, Ardalani F, Arzhangi S, Jalalvand K, Nikzat N, Ghodratpour F, Jamali P, Adeli OA, Habibi H, Kahrizi K, Najmabadi H. Mohseni M, et al. Among authors: jalalvand k. J Hum Genet. 2020 Jul;65(7):609-617. doi: 10.1038/s10038-020-0740-z. Epub 2020 Mar 30. J Hum Genet. 2020. PMID: 32231217 Free PMC article.
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