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Page 1
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: riazalhosseini y. 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: riazalhosseini y. J Genet. 2008 Aug;87(2):195-7. doi: 10.1007/s12041-008-0031-5. J Genet. 2008. PMID: 18776652 No abstract available.
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: riazalhosseini y. 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.
A novel DFNA5 mutation does not cause hearing loss in an Iranian family.
Van Laer L, Meyer NC, Malekpour M, Riazalhosseini Y, Moghannibashi M, Kahrizi K, Vandevelde A, Alasti F, Najmabadi H, Van Camp G, Smith RJH. Van Laer L, et al. Among authors: riazalhosseini y. J Hum Genet. 2007;52(6):549-552. doi: 10.1007/s10038-007-0137-2. Epub 2007 Apr 11. J Hum Genet. 2007. PMID: 17427029
Association between the DRD2 A1 allele and opium addiction in the Iranian population.
Shahmoradgoli Najafabadi M, Ohadi M, Joghataie MT, Valaie F, Riazalhosseini Y, Mostafavi H, Mohammadbeigi F, Najmabadi H. Shahmoradgoli Najafabadi M, et al. Among authors: riazalhosseini y. Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):39-41. doi: 10.1002/ajmg.b.30117. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15704216
Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability.
Mehvari S, Larti F, Hu H, Fattahi Z, Beheshtian M, Abedini SS, Arzhangi S, Ropers HH, Kalscheuer VM, Auld D, Kahrizi K, Riazalhosseini Y, Najmabadi H. Mehvari S, et al. Among authors: riazalhosseini y. Mol Genet Genomic Med. 2020 Oct;8(10):e1418. doi: 10.1002/mgg3.1418. Epub 2020 Jul 26. Mol Genet Genomic Med. 2020. PMID: 32715656 Free PMC article.
Epigenetically deregulated microRNA-375 is involved in a positive feedback loop with estrogen receptor alpha in breast cancer cells.
de Souza Rocha Simonini P, Breiling A, Gupta N, Malekpour M, Youns M, Omranipour R, Malekpour F, Volinia S, Croce CM, Najmabadi H, Diederichs S, Sahin O, Mayer D, Lyko F, Hoheisel JD, Riazalhosseini Y. de Souza Rocha Simonini P, et al. Among authors: riazalhosseini y. Cancer Res. 2010 Nov 15;70(22):9175-84. doi: 10.1158/0008-5472.CAN-10-1318. Epub 2010 Oct 26. Cancer Res. 2010. PMID: 20978187
Diagnostic values of GHSR DNA methylation pattern in breast cancer.
Botla SK, Gholami AM, Malekpour M, Moskalev EA, Fallah M, Jandaghi P, Aghajani A, Bondar IS, Omranipour R, Malekpour F, Mohajeri A, Babadi AJ, Sahin Ö, Bubnov VV, Najmabadi H, Hoheisel JD, Riazalhosseini Y. Botla SK, et al. Among authors: riazalhosseini y. Breast Cancer Res Treat. 2012 Oct;135(3):705-13. doi: 10.1007/s10549-012-2197-z. Epub 2012 Aug 17. Breast Cancer Res Treat. 2012. PMID: 22899222
109 results