PhD by research student in Medical Genetics
Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran, from 2012
Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran, from 2004 till now
M.Sc. in Biology Science - Cellular and Molecular Biology
Branch of Science and Research, Islamic Azad University, Tehran, Iran, Sep 2001- Jan 2004.
B.Sc. in Cellular and Molecular biology (Microbiology)
North Tehran branch, Islamic Azad University, Tehran, Iran, 1994- July 1998
Tel. No.: 0098-21-22180138
Address: Genetic Research Center- University of Social Welfare and Rehabilitation- Kudakyar Alley- Daneshju Blvd.- Evin- Tehran- Iran
Cooperation in research project, conference holding, workshop and course training and system set up:
§ Human Genetics
§ Molecular Genetics
§ Cell culture and immortalization
Certificate of involving in organizing of neurogenetic congress, 23-25 Nov. 2010, Genetics Research Center, USWR, Tehran, Iran.
o Establishing immortalized cell line (LCL) for MR patients as part of the Intelectual disability project.
o Establishing linkage analysis by STR markers for hearing loss patients as part of the hearing loss project.
Khoshbakht T, Soosanabadi M, Neishaboury M, Kamali K, Karimlou M, Bazazzadegan N, Khorram Khorshid HR, An association study on IL16 gene polymorphisms with the risk of sporadic Alzheimers disease. Avicenna J Med Biotechnol. (2015) Jul-Sep; 7 (3): 128-32
Atie Kashef , Nooshin Nikzat, Niloofar Bazzazadegan, Zohreh Fattahi, Farahnaz Sabbagh-Kermani, Maryam Taghdiri, Batool Azadeh, Faezeh Mojahedi, Atefeh Khoshaeen, Haleh Habibi, Hossein Najmabadi, Kimia Kahrizi, Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of Hearing Loss in Iranian population. International Journal of Pediatric Otorhinolaryngology. 79 (2015):136-138
Farzaneh Larti, Kimia Kahrizi, Luciana Musante, Hao Hu, Elahe Papari, Zohreh Fattahi, Niloofar Bazazzadegan, Zhe Liu, Mehdi Banan, Masoud Garshasbi, Thomas Wienker, Hans-Hilger Ropers, Niels Galjart, Hossein Najmabadi. A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disability. Eur J Hum Genet. (2015) Mar; 23(3):416
Kimia Kahrizi, Niloofar Bazazzadegan, Leila Jamali, Nooshin Nikzat, Atie Kashef, Hossein Najmabadi., 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
Shearer AE, Eppsteiner RW, Booth KT, Ephraim SS, Gurrola J 2nd, Simpson A, Black-Ziegelbein EA, Joshi S, Ravi H, Giuffre AC, Happe S, Hildebrand MS, Azaiez H, Bayazit YA, Erdal ME, Lopez-Escamez JA, Gazquez I, Tamayo ML, Gelvez NY, Leal GL, Jalas C, Ekstein J, Yang T, Usami S, Kahrizi K, Bazazzadegan N, Najmabadi H, Scheetz TE, Braun TA, Casavant TL, LeProust EM, Smith RJ., Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants. Am J Hum Genet. (2014) Oct 2;95(4):445-53.
Mojgan Babanejad, Niloofar Bazazzadegan, Zohreh Fattahi, Nooshin Nikzat, Elahe Sohrabi, Khadijeh Jalalvand, Sanaz Arzhangi, Amin Najmabadi, Richard J.H. Smith, Kimia Kahrizi, Hossein Najmabadi*., A comprehensive study to determine heterogeneity of autosomal recessive non-syndromic hearing loss in Iran. American Journal of Medical Genetics A. (2012) Oct; 158A(10):2485-92
Zohreh Fattah, A. Eliot Shearer , Mojgan Babanejad, Niloofar Bazazzadegan, Seyed Navid Almadani, Nooshin Nikzat, Khadijeh Jalalvand, Sanaz Arzhangi, Fatemehsadat Esteghamat ,Rezvan Abtahi, Batool Azadeh, Richard J.H. Smith, Kimia Kahrizi, Hossein Najmabadi. Screening for MYO15A gene mutations in an autosomal recessive non-syndromic, GJB2 negative Iranian Deaf population. American Journal of Medical Genetics A. (2012) Aug; 158 A(8): 1857-64
Niloofar Bazazzadegan, Nooshin Nikzat, Zohreh Fattahi, Carla Nishimura, Nicole Meyer, Shima Sahraian, Payman Jamali, Mojgan Babanejad, Atie Kashef, Hilda Yazdan, Farahnaz Sabagh, Maryam Taghdiri, Batool Azadeh, Faezeh Mojahedi, Atefeh Khoshaein, Haleh Habibi, Farahnaz Reyhanifar, Narges Nouri, Richard J. H. Smith, Kimia Kahrizi, Hossein Najmabadi. The Spectrum of GJB2 mutations in the Iranian population with Non-Syndromic Hearing Loss - A twelve year study. International Journal of Pediatric Otorhinolaryngology. (2012) Aug; 76(8): 1164-74
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Update : 2018/1/16