1. Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion. (2nd January 2022) Authors: Hemmati, Sara; Khakpour, Golnaz; Nadjafi-Semnani, Fatemeh; Gordiz, Arzhang; Sajadi, Masoome; Abdi, Fatemeh Journal: Ophthalmic genetics Issue: Volume 43:Number 1(2022) Page Start: 140 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Methylomics of breast cancer: Seeking epimarkers in peripheral blood of young subjects. Issue 3 (March 2017) Authors: Khakpour, Golnaz; Noruzinia, Mehrdad; Izadi, Pantea; Karami, Fatemeh; Ahmadvand, Mohammad; Heshmat, Ramin; Amoli, Mahsa M; Tavakkoly-Bazzaz, Javad Journal: Tumor biology Issue: Volume 39:Issue 3(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Over expression of circulating miR-155 predicts prognosis in diffuse large B-cell lymphoma. (July 2018) Authors: Ahmadvand, Mohammad; Eskandari, Mahsa; Pashaiefar, Hossein; Yaghmaie, Marjan; Manoochehrabadi, Saba; Khakpour, Golnaz; Sheikhsaran, Fatemeh; Montazer Zohour, Mostafa Journal: Leukemia research Issue: Volume 70(2018) Page Start: 45 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗