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Year Number of Results
2007 1
2011 2
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2015 2
2017 1
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2023 1
2024 0

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Page 1
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H. Sloan-Heggen CM, et al. J Med Genet. 2015 Dec;52(12):823-9. doi: 10.1136/jmedgenet-2015-103389. Epub 2015 Oct 7. J Med Genet. 2015. PMID: 26445815 Free PMC article.
New translocation in acute myeloid leukemia M4 eos.
Bahoush G, Vafapour M, Kariminejad R. Bahoush G, et al. Leuk Res Rep. 2020 Jun 8;14:100209. doi: 10.1016/j.lrr.2020.100209. eCollection 2020. Leuk Res Rep. 2020. PMID: 32566479 Free PMC article.
Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends.
Fattahi Z, Mohseni M, Beheshtian M, Jafarpour A, Jalalvand K, Keshavarzi F, Behravan H, Ghodratpour F, Zare Ashrafi F, Kalhor M, Azad M, Koshki M, Ghaziasadi A, Soveyzi M, Abdollahi A, Kiani SJ, Ataei-Pirkooh A, Rezaeiazhar I, Bokharaei-Salim F, Haghshenas MR, Babamahmoodi F, Mokhames Z, Soleimani A, Elahi Z, 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, Tavangar F, Yaghoubi M, Keramat F, Tavakoli M, Jalali T, Pouriayevali MH, Salehi-Vaziri M, Khorram Khorshid HR, Najafipour R, Malekzadeh R, Kahrizi K, Jazayeri SM, Najmabadi H. Fattahi Z, et al. Arch Iran Med. 2022 Aug 1;25(8):508-522. doi: 10.34172/aim.2022.83. Arch Iran Med. 2022. PMID: 37543873 Free article.
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. 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.
SARS-CoV-2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductions.
Fattahi Z, Mohseni M, Jalalvand K, Aghakhani Moghadam F, Ghaziasadi A, Keshavarzi F, Yavarian J, Jafarpour A, Mortazavi SE, Ghodratpour F, Behravan H, Khazeni M, Momeni SA, Jahanzad I, Moradi A, Tabarraei A, Azimi SA, Kord E, Hashemi-Shahri SM, Azaran A, Yousefi F, Mokhames Z, Soleimani A, Ghafari S, Ziaee M, Habibzadeh S, Jeddi F, Hadadi A, Abdollahi A, Kaydani GA, Soltani S, Mokhtari-Azad T, Najafipour R, Malekzadeh R, Kahrizi K, Jazayeri SM, Najmabadi H. Fattahi Z, et al. Transbound Emerg Dis. 2022 May;69(3):1375-1386. doi: 10.1111/tbed.14104. Epub 2021 May 22. Transbound Emerg Dis. 2022. PMID: 33835709 Free PMC article.
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
Imtiaz A, Belyantseva IA, Beirl AJ, Fenollar-Ferrer C, Bashir R, Bukhari I, Bouzid A, Shaukat U, Azaiez H, Booth KT, Kahrizi K, Najmabadi H, Maqsood A, Wilson EA, Fitzgerald TS, Tlili A, Olszewski R, Lund M, Chaudhry T, Rehman AU, Starost MF, Waryah AM, Hoa M, Dong L, Morell RJ, Smith RJH, Riazuddin S, Masmoudi S, Kindt KS, Naz S, Friedman TB. Imtiaz A, et al. Hum Mol Genet. 2018 Mar 1;27(5):780-798. doi: 10.1093/hmg/ddx440. Hum Mol Genet. 2018. PMID: 29293958 Free PMC article.
Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical Development.
Ivanova EL, Mau-Them FT, Riazuddin S, Kahrizi K, Laugel V, Schaefer E, de Saint Martin A, Runge K, Iqbal Z, Spitz MA, Laura M, Drouot N, Gérard B, Deleuze JF, de Brouwer APM, Razzaq A, Dollfus H, Assir MZ, Nitchké P, Hinckelmann MV, Ropers H, Riazuddin S, Najmabadi H, van Bokhoven H, Chelly J. Ivanova EL, et al. Am J Hum Genet. 2017 Sep 7;101(3):428-440. doi: 10.1016/j.ajhg.2017.07.010. Epub 2017 Aug 17. Am J Hum Genet. 2017. PMID: 28823707 Free PMC article.
Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability.
Rafiq MA, Kuss AW, Puettmann L, Noor A, Ramiah A, Ali G, Hu H, Kerio NA, Xiang Y, Garshasbi M, Khan MA, Ishak GE, Weksberg R, Ullmann R, Tzschach A, Kahrizi K, Mahmood K, Naeem F, Ayub M, Moremen KW, Vincent JB, Ropers HH, Ansar M, Najmabadi H. Rafiq MA, et al. Am J Hum Genet. 2011 Jul 15;89(1):176-82. doi: 10.1016/j.ajhg.2011.06.006. Am J Hum Genet. 2011. PMID: 21763484 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. 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.
15 results