22/09/2017
آمار بازدید
 total : 70804
 online : 4
Recent publications
 

Anvar, N.E., Saliminejad, K., Ohadi, M., Kamali, K., Daneshmand, P., Khorshid, H.R.K. Association between polymorphisms in Interleukin-16 gene and risk of late-onset Alzheimer's disease (2015) Journal of the Neurological Sciences, . Article in Press.

http://www.scopus.com/inward/record.url?eid=2-s2.0-84941779352&partnerID=40&md5=bf2d584755695e717b118ceb171b9734

 

Babanejad, M., Moein, H., Akbari, M.R., Badiei, A., Yaseri, M., Soheilian, M., Najmabadi, H. Investigating the CFH Gene Polymorphisms as a Risk Factor for Age-related Macular Degeneration in an Iranian Population (2015) Ophthalmic Genetics, 6 p. Article in Press.

http://www.scopus.com/inward/record.url?eid=2-s2.0-84938788681&partnerID=40&md5=3f7fb50bda135b5e49ff325a953f9212

 

Nikuei, P., Malekzadeh, K., Rajaei, M., Hilbert, P., Shafeghati, Y. Berardinelli-Seip Congenital Lipodystrophy: Report of an Iranian girl with a novel mutation of BSCL2 Gene (2015) Genetics in the Third Millennium, 13 (2), pp. 4002-4005.

http://www.scopus.com/inward/record.url?eid=2-s2.0-84941105467&partnerID=40&md5=a074b5467e9d17508bb13bcf680b7a9d

 

Kashef, A., Nikzat, N., Bazzazadegan, N., Fattahi, Z., Sabbagh-Kermani, F., Taghdiri, M., Azadeh, B., Mojahedi, F., Khoshaeen, A., Habibi, H., Najmabadi, H., Kahrizi, K. Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of Hearing Loss in Iranian population (2015) International Journal of Pediatric Otorhinolaryngology, 79 (2), pp. 136-138.

http://www.scopus.com/inward/record.url?eid=2-s2.0-84922523691&partnerID=40&md5=621032fc95c10107e204497661e1d7e3

 

Saliminejad, K., Saket, M., Kamali, K., Memariani, T., Khorshid, H.R.K. DNA repair gene XRCC1 and XRCC4 variations and risk of endometriosis: An association study (2015) Gynecologic and Obstetric Investigation, 80, pp. 85-88.

http://www.scopus.com/inward/record.url?eid=2-s2.0-84941996387&partnerID=40&md5=f533c615f393dca8f11ea25aa238619c

 

Ebadifar, A., Khorshid, H.R.K., Kamali, K., Zeinabadi, M.S., Khoshbakht, T., Ameli, N. Maternal supplementary folate intake, methylenetetrahydrofolate reductase (MTHFR) C677t and A1298C polymorphisms and the risk of orofacial cleft in Iranian children (2015) Avicenna Journal of Medical Biotechnology, 7 (2), pp. 80-84.

http://www.scopus.com/inward/record.url?eid=2-s2.0-84924957199&partnerID=40&md5=d999cbb9501a6c19123856a2ab757f2a

 

Adegbola, A., Musante, L., Callewaert, B., Maciel, P., Hu, H., Isidor, B., Picker-Minh, S., Le Caignec, C., Chiaie, B.D., Vanakker, O., Menten, B., Dheedene, A., Bockaert, N., Roelens, F., Decaestecker, K., Silva, J., Soares, G., Lopes, F., Najmabadi, H., Kahrizi, K., Cox, G.F., Angus, S.P., Staropoli, J.F., Fischer, U., Suckow, V., Bartsch, O., Chess, A., Ropers, H.-H., Wienker, T.F., Hübner, C., Kaindl, A.M., Kalscheuer, V.M. Redefining the MED13L syndrome (2015) European Journal of Human Genetics, 23 (10), pp. 1308-1317.

http://www.scopus.com/inward/record.url?eid=2-s2.0-84944171575&partnerID=40&md5=0f24020411f6509c78efd4bbd98a7af7

 

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