17/11/2017
آمار بازدید
 total : 76416
 online : 1
Seyedeh Sedigheh Abedini
 

Seyedeh Sedigheh Abedini

BSc (Botany): [1999-2003] Faculty of Science, Tehran University. Tehran-Iran.

Master student (Human Genetics): [2003-2006] Genetics Research Center- University of Welfare and Rehabilitation sciences  Tehran-Iran.

PhD student by research (Medical Genetics): Genetics Research Center- University of Welfare and Rehabilitation sciences, Tehran-Iran. [Beginning: 2012]

e-mail: abedini_sedigheh@yahoo.com

Tel. No.: 0098-21-22180138

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


Positions

Research assistant 

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences [2004-up to now]

 MS in Genetic, Employee

Genetics Research Center, University of Social Welfare and Rehabilitation Sciences [2010- up to now]

Training students who are involved in ID (intellectual disability) project

 

Publications

Mehrjoo Z, Akbari MR, Abedini SS, Vaziri S, Kahrizi K, Najmabadi H. Carrier Testing in Known Autosomal Recessive Intellectual Disability Genes in an Iranian Healthy Individual Using Exome Sequencing. Arch Iran Med. 2015;18(10):643-69

Mehrjoo Z, Najmabadi A, Abedini SS, Mohseni M, Kamali K, Najmabadi H, Khorram Khorshid HR. Association Study of the TREM2 Gene and Identification of a Novel Variant in Exon 2 in Iranian Patients with Late-Onset Alzheimer's Disease Med Princ Pract. 2015;24(4):351-354.

Jazayeri R, Hu H, Fattahi Z, Musante L, Abedini SS, Hosseini M, Wienker TF, Ropers HH, Najmabadi H, Kahrizi K. Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with Ataxia. Arch Iran Med. 2015;18(10):670-682.

Abedini SS, Azad M, Hasanzad M, Kahrizi K, Najmabadi H. Determination of SMN2 Copy Numbers in Iranian Spinal Muscular Atrophy Patients Using Multiplex Ligation-Dependent Probe Amplification. G3M. 2015;13(2):3984-3989.

Kakroodi ST,  Vesiehsari MJ,  Abedini SS,  Ghobakhloo S,  Dehghani H,  Keyhani E,  Azarkeivan A,  Zamani F,  Najmabadi H,  Neishabury M.  The role of BCL11A and HBS1L-MYB polymorphisms in predicting blood transfusion requirements of Thalassemia patients with homozygous 5'HS4-LCR/ Xmn1-HBG2 background.G3M 2015;13(2):3990-3993.

more

 

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