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Page 1
Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations.
Zare Ashrafi F, Mohseni M, Beheshtian M, Fattahi Z, Ghodratpour F, Keshavarzi F, Behravan H, Kalhor M, Jalalvand K, Azad M, Koshki M, Jafarpour A, Ghaziasadi A, Abdollahi A, Kiani SJ, Ataei-Pirkooh A, Rezaei Azhar I, Bokharaei-Salim F, Haghshenas MR, Babamahmoodi F, Mokhames Z, Soleimani A, Ziaee M, Javanmard D, Ghafari S, Ezani A, Ansari Moghaddam A, Shahraki-Sanavi F, Hashemi Shahri SM, Azaran A, Yousefi F, Moattari A, Moghadami M, Fakhim H, Ataei B, Nasri E, Poortahmasebi V, Varshochi M, Mojtahedi A, Jalilian F, Khazeni M, Moradi A, Tabarraei A, Piroozmand A, Yahyapour Y, Bayani M, Aboofazeli A, Ghafari P, Keramat F, Tavakoli M, Jalali T, Pouriayevali MH, Salehi-Vaziri M, Khorram Khorshid HR, Najafipour R, Malekzadeh R, Kahrizi K, Jazayeri SM, Najmabadi H. Zare Ashrafi F, et al. Among authors: kahrizi k. Arch Iran Med. 2023 Feb 1;26(2):69-75. doi: 10.34172/aim.2023.12. Arch Iran Med. 2023. PMID: 37543926 Free PMC article.
Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation.
Mir A, Kaufman L, Noor A, Motazacker MM, Jamil T, Azam M, Kahrizi K, Rafiq MA, Weksberg R, Nasr T, Naeem F, Tzschach A, Kuss AW, Ishak GE, Doherty D, Ropers HH, Barkovich AJ, Najmabadi H, Ayub M, Vincent JB. Mir A, et al. Among authors: kahrizi k. Am J Hum Genet. 2009 Dec;85(6):909-15. doi: 10.1016/j.ajhg.2009.11.009. Am J Hum Genet. 2009. PMID: 20004765 Free PMC article.
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
Borck G, Ur Rehman A, Lee K, Pogoda HM, Kakar N, von Ameln S, Grillet N, Hildebrand MS, Ahmed ZM, Nürnberg G, Ansar M, Basit S, Javed Q, Morell RJ, Nasreen N, Shearer AE, Ahmad A, Kahrizi K, Shaikh RS, Ali RA, Khan SN, Goebel I, Meyer NC, Kimberling WJ, Webster JA, Stephan DA, Schiller MR, Bahlo M, Najmabadi H, Gillespie PG, Nürnberg P, Wollnik B, Riazuddin S, Smith RJ, Ahmad W, Müller U, Hammerschmidt M, Friedman TB, Riazuddin S, Leal SM, Ahmad J, Kubisch C. Borck G, et al. Among authors: kahrizi k. Am J Hum Genet. 2011 Feb 11;88(2):127-37. doi: 10.1016/j.ajhg.2010.12.011. Epub 2011 Jan 20. Am J Hum Genet. 2011. PMID: 21255762 Free PMC article.
The Iranian human mutation database.
Motazacker MM, Taherzadeh-Fard E, Husseini Z, Behjati F, Esteghamat F, Kahrizi K, Najmabadi H. Motazacker MM, et al. Among authors: kahrizi k. Arch Iran Med. 2007 Jul;10(3):372-5. Arch Iran Med. 2007. PMID: 17604476 No abstract available.
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: kahrizi k. J Genet. 2008 Aug;87(2):195-7. doi: 10.1007/s12041-008-0031-5. J Genet. 2008. PMID: 18776652 No abstract available.
174 results