23/09/2017
آمار بازدید
 total : 70925
 online : 4
Noushin Nikzat
 

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

                            nu.nikzat@uswr.ac.ir

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

 

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