Genetic Research Center

Sanaz Arzhangi

Education:

• M.Sc. in Nursing  Nursing & Midwifery School, Shahid Beheshti University of Medical Sciences. Tehran,Iran
• B.Sc. in  Nursing Nursing & Midwifery School, Shahid Beheshti University of Medical Sciences. Tehran,Iran

    Research associate

Genetics Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran, from 2001 till now

e-mail address: sanarzhangi@yahoo.com

Tel. No.: 0098-21-22180107

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=6506909356&zone=

Selected publications:

Christina M Sloan-Heggen, Mojgan Babanejad, Maryam Beheshtian, Allen C Simpson, Kevin T Booth, Fariba Ardalani, Kathy L Frees, Marzieh Mohseni, Reza Mozafari, Zohreh Mehrjoo, Leila Jamali, Saeideh Vaziri, Tara Akhtarkhavari, Niloofar Bazazzadegan, Nooshin Nikzat, Sanaz Arzhangi, Farahnaz Sabbagh, Hasan Otukesh, Seyed Morteza Seifati, Hossein Khodaei, Maryam Taghdiri, Nicole C Meyer, Ahmad Daneshi, Mohammad Farhadi, Kimia Kahrizi, Richard JH Smith1, Hela Azaiez, Hossein Najmabadi.” Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran”. J Med Genet. October 2015

Kevin T. Booth, Hela Azaiez, Kimia Kahrizi, Allen C. Simpson, William T.A. Tollefson, Christina M. Sloan, Nicole C. Meyer, Mojgan Babanejad, Fariba Ardalani, Sanaz Arzhangi, Michael J. Schnieders, Hossein Najmabadi , Richard J.H. Smith.” PDZD7 and hearing loss: More than just a modifier”. American Journal of Medical Genetics . SEP 2015.

S.Arzhangi, H. Najmabadi, K. Kahrizi;” Genetic Counseling for Intellectual Disability in

                Iran”  Journal of Genetics in the Third Millennium.Vol 13,  No 1 (2014).

Elinaz AKBARIAZAR, Mohammad Reza EBRAHIMPOUR, Saeedeh AKBARI, Sanaz ARZHANGHI, Seydeh Sedigheh ABEDINI, Hossein NAJMABADI, Kimia KAHRIZI. ” A novel deletion mutation in ASPM gene in an Iranian family with autosomal recessive primary microcephaly.”IRAN  J Child Neurology .Vol 7, No 2 (2013).

Fattahi, Z.a, Shearer, A.E.b, Babanejad, M.a, Bazazzadegan, N.a, Almadani, S.N.c, Nikzat, N.a, Jalalvand, K.a, Arzhangi, S.a, Esteghamat, F.a, Abtahi, R.d, Azadeh, B.e, Smith, R.J.b, Kahrizi, K.a  , Najmabadi, H.   ” Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population” American Journal of Medical Genetics, Part A . August 2012

Davarnia, B., Babanejad, M., Fattahi, Z., Nikzat, N., Bazazzadegan, N., Pirzade, A., Farajollahi, R., Nishimura, C., Jalalvand, K., Arzhangi, S., Kahrizi, K., Smith, R.J.H., Najmabadi, H. ” Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss” International Journal of Pediatric Otorhinolaryngology. 2012,February

Kuss, A.W., Garshasbi, M. Kahrizi, K., Tzschach, A., Behjati, F., Darvish, H., Abbasi-Moheb, L., Puettmann, L., Zecha, A., Weimann, R., Hu, H., Mohseni, M., Abedini, S.S., Rajab, A., Hertzberg, C., Wieczorek, D., Ullmann, R., Ghasemi-Firouzabadi, S., Banihashemi, S., Arzhangi, S., Hadavi, V.k, Bahrami-Monajemi, G.b, Kasiri, M.f, Falah, M., Nikuei, P., Dehghan, A., Sobhani, M.i, Jamali, P., Ropers, H.H., Najmabadi, H. "Autosomal recessive mental retardation: Homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots"Human Genetics . Volume 129, Issue 2, February 2011, Pages 141-148.

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