Nooshin Nikzat
Education: MSc in Human Genetics, Tehran University of Medical Sciences, Health Faculty, Tehran, Iran, 1999
BSc in Genetics, Jondishapour University, Sciences Faculty, Ahvaz, Iran, 1989
e-mail Address : nikzat2002@yahoo.com
Tel. No.: 021-22180138
Address: Genetic Research Center- USWR- Kudakyar Alley- Daneshju Blvd.- Evin- Tehran- Iran
http://www.scopus.com/authid/detail.url?origin=resultslist&authorId=26031688500&zone= Publications: Babanejad M, Fattahi Z, Bazazzadegan N, Nishimura C, Meyer N, Nikzat N, Sohrabi E, Najmabadi A, Jamali P, Habibi F, Smith RJ, Kahrizi K, Najmabadi H. A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran. Am J Med Genet A. 2012 Oct;158A(10):2485-92. doi: 10.1002/ajmg.a.35572. Epub 2012 Aug 17. PMID:22903915
Jamaldini SH, Babanejad M, Mozaffari R, Nikzat N, Jalalvand K, Badiei A, Sanati H, Shakerian F, Afshari M, Kahrizi K, Najmabadi H. Association of polymorphisms at LDLR locus with coronary artery disease independently from lipid profile. Acta Med Iran. 2014;52(5):352-9. PMID:24902015
Kashef A, Nikzat N, Bazzazadegan N, Fattahi Z, Sabbagh-Kermani F, Taghdiri M, Azadeh B, Mojahedi F, Khoshaeen A, Habibi H, Najmabadi H, Kahrizi K. Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population. Int J Pediatr Otorhinolaryngol. 2015 Feb;79(2):136-8. doi: 10.1016/j.ijporl.2014.11.024. Epub 2014 Dec 3. PMID:25555641
Kahrizi K, Bazazzadegan N, Jamali L, Nikzat N, Kashef A, Najmabadi H. A novel mutation of the USH2C (GPR98) gene in an Iranian family with Usher syndrome type II. J Genet. 2014 Dec;93(3):837-41. No abstract available. PMID:25572244
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. Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. J Med Genet. 2015 Oct 7. pii: jmedgenet-2015-103389. doi: 10.1136/jmedgenet-2015-103389. [Epub ahead of print]. PMID:26445815
http://genetic.uswr.ac.ir/index.jsp?siteid=60&fkeyid=&siteid=60&pageid=9783
|
Links
©All rights reserved to the University of Social Welfare and Rehabilitation Sciences.
Update : 2018/1/16