23/09/2017
آمار بازدید
 total : 70940
 online : 4
Saghar Firouzabadi
 

Saghar Ghasemi Firouzabadi

PhD student (Medical Genetics): 2010-Now

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences  

MS (Human Genetics) [2000-2004, Genetics Research Center, University of Social Welfare and Rehabilitation Sciences  

BS (Microbiology) [1995-1999, Faculty of Science, Tehran University.

email address: ghasemisaghar@gmail.com

Address: Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Evin, Tehran, Iran

Tel/Fax: 0098-21-22180138

http://www.scopus.com/authid/detail.url?origin=AuthorProfile&authorId=36571628600&zone=

 

Students training:

Ø  Karyotyping

Ø  Chromosome analysis

Ø  FISH

Ø  MLPA

 

Research Projects

Detection of copy number variations in 50 patients with idiopathic autism and mental  retardation using MLPA

Genomic Characterization of some patients with ideopathic mental retardation and normal karyotype  using array CGH technique

Investigation of subtelomeric chromosome rearrangements in 50 patients with idiopathic mental retardation and non consanguineous marriage and 50 normal controls, using Multiplex Ligation Dependent Probe Amplification (MLPA) technique

Investigation of sub-telomeric chromosome abnormalities in children with idiopathic mental retardation and developmental delay using Multiplex Ligation Dependent Probe Amplification (MLPA) technique

Subtelomeric chromosome abnormalities Study in 20 mental retarded patients with unknown etiology using FISH technique.

Cytogenetics Study in 100 Iranian patients referred to Genetic research center.

Investigation of Clinical Heterogeneity and Chromosome Breakage in Some Iranian Patients Referred for Fanconi anemia.

 

 

Publications:

Behjati F, Firouzabadi SG, Kariminejad R, Vameghi R, Sajedi F, Shafaghati Y, Ghasemlou BE, Shojaei A, Jamali P, Bahman I, Najmabadi H. Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization. Indian J Hum Genet. 2013 Oct;19(4):443-8

Darvish H, Movafagh A, Omrani MD, Firouzabadi SG, Azargashb E, Jamshidi J, Khaligh A, Haghnejad L, Naeini NS, Talebi A, Heidari-Rostami HR, Noorollahi-Moghaddam H, Karkheiran S, Shahidi GA, Paknejad SM, Ashrafian H, Abdi S, Kayyal M, Akbari M, Pedram N, Emamalizadeh B. Detection of copy number changes in genes associated with Parkinson's disease in Iranian patients. Neurosci Lett. 2013 Sep 13;551:75-8

 

Darvish H, Heidari A, Hosseinkhani S, Movafagh A, Khaligh A, Jamshidi J, Noorollahi-Moghaddam H, Heidari-Rostami HR, Karkheiran S, Shahidi GA, Togha M, Paknejad SM, Ashrafian H, Abdi S, Firouzabadi SG, Jamaldini SH, Ohadi M. Biased homozygous haplotypes across the human caveolin 1 upstream purine complex in Parkinson's disease. J Mol Neurosci. 2013 Oct;51(2):389-93

 

Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation. Behjati F, Ghasemi Firouzabadi S, Sajedi F, Kahrizi K, Najafi M, Ebrahimizade Ghasemlou B, Shafeghati Y, Behnia F, Mohammadi Arya AR, Karimi H, Hadipour F, Hadipour Z, Jamali P, Kariminejad R, Darvish H, Bahman I, Bagherizadeh E, Najmabadi H, Vameghi R. Iran Red Crescent Med J. 2013 Oct;15(10)

 

Ohadi M, Mirabzadeh A, Esmaeilzadeh-Gharehdaghi E, Rezazadeh M, Hosseinkhanni S, Oladnabi M, Firouzabadi SG, Darvish H. Novel evidence of the involvement of calreticulin in major psychiatric disorders. Prog Neuropsychopharmacol Biol Psychiatry. 2012 Jun 1;37(2):276-81

 

 

Copyright © 2009 U.S.W.R - All rights reserved .University of Social Welfare and Rehabilitation Scienc