Items where Author is "Akhavan-Niaki, H."

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Article

Khademi, E. and Alehabib, E. and Shandiz, E.E. and Ahmadifard, A. and Andarva, M. and Jamshidi, J. and Rahimi-Aliabadi, S. and Pouriran, R. and Nejad, F.R. and Mansoori, N. and Shahmohammadibeni, N. and Taghavi, S. and Shokraeian, P. and Akhavan-Niaki, H. and Paisán-Ruiz, C. and Darvish, H. and Ohadi, M. (2017) Support for "disease-Only" Genotypes and Excess of Homozygosity at the CYTH4 Primate-Specific GTTT-Repeat in Schizophrenia. Genetic Testing and Molecular Biomarkers.

Dadkhah, T. and Rahimi-Aliabadi, S. and Jamshidi, J. and Ghaedi, H. and Taghavi, S. and Shokraeian, P. and Akhavan-Niaki, H. and Tafakhori, A. and Ohadi, M. and Darvish, H. (2017) A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder. Journal of Affective Disorders, 208. pp. 218-222.

Shahmohammadibeni, N. and Rahimi-Aliabadi, S. and Jamshidi, J. and Emamalizadeh, B. and Shahmohammadibeni, H.A. and Zare Bidoki, A. and Akhavan-Niaki, H. and Eftekhari, H. and Abdollahi, S. and Shekari Khaniani, M. and Shahmohammadibeni, M. and Fazeli, A. and Motallebi, M. and Taghavi, S. and Ahmadifard, A. and Shafiei Zarneh, A.E. and Andarva, M. and Dadkhah, T. and Khademi, E. and Alehabib, E. and Rahimi, M. and Tafakhori, A. and Atakhorrami, M. and Darvish, H. (2016) The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson�s disease in Iranian population. Neurological Sciences, 37 (5). pp. 731-736.

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