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Tarki, S.E. and Far, I.S. and Aminimoghaddam, S. and Fooladi, B. and Sarhangi, N. and Farahani, M.S. and Klashami, Z.N. and Hamidi, A.K. and Amoli, M.M. (2021) Investigating the association of matrix metalloproteinase-2 gene variants with endometriosis in an Iranian population. European Journal of Obstetrics and Gynecology and Reproductive Biology, 258. pp. 353-357.
Mohseni, M. and Yazdani, N. and Asgarbeik, S. and Daneshi, A. and Farhadi, M. and Asghari, A. and Mohebbi, S. and Vahidi, A. and Amoli, M.M. (2020) Sex-dependent association of ACE (I/D) polymorphism with Meniere's disease. Meta Gene, 24.
Rashidi, B.H. and Sarhangi, N. and Aminimoghaddam, S. and Haghollahi, F. and Naji, T. and Amoli, M.M. and Shahrabi-Farahani, M. (2019) Association of vascular endothelial growth factor (VEGF) Gene polymorphisms and expression with the risk of endometriosis: a case�control study. Molecular Biology Reports, 46 (3). pp. 3445-3450.
Abbasi, F. and Habibi, M. and Enayati, S. and Bitarafan, F. and Razzaghy-Azar, M. and Sotodeh, A. and Omran, S.P. and Maroofian, R. and Amoli, M.M. (2018) A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes. Canadian Journal of Diabetes, 42 (3). pp. 272-275.
Abbasi, F. and Habibi, M. and Enayati, S. and Bitarafan, F. and Razzaghy-Azar, M. and Sotodeh, A. and Omran, S.P. and Maroofian, R. and Amoli, M.M. (2018) A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes. Canadian Journal of Diabetes, 42 (3). pp. 272-275.
Aminimoghaddam, S. and Shahrabi-Farahani, M. and Mohajeri-Tehrani, M. and Amiri, P. and Fereidooni, F. and Larijani, B. and Shafiee, G. and Amoli, M.M. (2007) Epistatic interaction between adiponectin and survivin gene polymorphisms in endometrial carcinoma. Pathology Research and Practice, 211 (4). pp. 293-297.
