Rafati M, Mohamadhashem F, Jalilian K, Hoseininasab F, Fakhri L, Hoseini A, Amiri H, Barati Z, Darzi Ramandi S, Mostofinezhad N, Mahmoudi AH, Ghaffari SR. Identification of a novel de novo variant in OTX2 in a patient with congenital microphthalmia using targeted next-generation sequencing followed by prenatal diagnosis. Ophthalmic Genet. 2022 Apr;43(2):262-267. doi: 10.1080/13816810.2021.2002915. Epub 2021 Nov 18. PMID: 34791963.
Mohamadhashem F, Rafati M, Hoseininasab F, Rostami S, Tabatabaie R, Rezai S, Keramatipour M, Ghaffari SR. Primary ovarian insufficiency with t(5;13): a case report and literature review on disrupted genes. Climacteric. 2017 Oct;20(5):498-502. doi: 10.1080/13697137.2017.1316255. Epub 2017 Apr 28. PMID: 28453298.
Rafati M, Mohamadhashem F, Hoseini A, Hoseininasab F, Ghaffari SR. A novel ACVR1 mutation detected by whole exome sequencing in a family with an unusual skeletal dysplasia. Eur J Med Genet. 2016 Jun;59(6-7):330-6. doi: 10.1016/j.ejmg.2016.05.007. Epub 2016 May 13. PMID: 27182040.
Rafati M, Mohamadhashem F, Hoseini A, Ramandi SD, Ghaffari SR. Prenatal Diagnosis of Tyrosinemia Type 1 Using Next Generation Sequencing. Fetal Pediatr Pathol. 2016;35(4):282-5. doi: 10.3109/15513815.2016.1167149. Epub 2016 Apr 19. PMID: 27093575.
Torktaz I, Mohamadhashem F, Esmaeili A, Behjati M, Sharifzadeh S. Virtual screening and pharmacophore design for a novel theoretical inhibitor of macrophage stimulating factor as a metastatic agent. Bioimpacts. 2013;3(3):141-4. doi: 10.5681/bi.2013.026. Epub 2013 Sep 21. PMID: 24163807; PMCID: PMC3786797.