21/11/2017
آمار بازدید
 total : 76886
 online : 3
Niloofar Bazazzadegan
 

Niloofar Bazazzadegan

PhD by research student in Medical Genetics

Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran,    Iran, from 2012

 

Research associate

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

e-mail: baz1380@yahoo.com

Tel. No.: 0098-21-22180138

Address: Genetic Research Center- University of Social Welfare and Rehabilitation- Kudakyar Alley- Daneshju Blvd.- Evin- Tehran- Iran

http://www.scopus.com/authid/detail.url?origin=resultslist&authorId=13203058500&zone=

 

Cooperation in research project, conference holding, workshop and course training and system set up:

  • Research Experience:
    • Research Field:

§  Human Genetics

§  Molecular Genetics

  • Molecular basis of hearing loss
  • Molecular basis of Alzheimer's disease

§  Cell culture and immortalization

  • Immortalization of MR patients
  • conference holding, workshop and course training

 Certificate of involving in organizing of neurogenetic congress, 23-25 Nov. 2010, Genetics Research Center, USWR, Tehran, Iran.

  • Certificate of involving in teaching- organizing in the workshop on molecular biology techniques, 29 Nov-14 Dec 2008, Tehran.
  • Certificate of involving in teaching-organizing in the workshop on molecular biology techniques, Medical genetics and genetics engineering techniques, 23 Sep- 15 Oct. 2007, Tehran, Iran.
  • Certificate of involving in teaching- organizing in the workshop on molecular biology basic techniques, 24th Nov- 5th Dec. 2006, GRC, USWR, Tehran, Iran.
  • Certificate of involving in teaching- organizing in the workshop on Introduction of practical and theoretical principal of molecular biology basic techniques, 11-15 Aug. 2006, GRC, USWR, Tehran.
  • Certificate for organizing theoretical and practical workshop of molecular diagnosis techniques of some human genetic disorders. 10- 14 June 2000, National Research Centre for Genetic Engineering and Biotechnology, Tehran, Iran.
  • system set up

 

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.

 

  • Selected publications

 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

more

 

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