(2019) Novel splicing variant c. 208+2T > C in BBS5 segregates with Bardet-Biedl syndrome in an Iranian family by targeted exome sequencing. Bioscience Reports. p. 10. ISSN 0144-8463

(2018) Genetic identification and molecular modeling characterization reveal a novel PROM1 mutation in Stargardt4-like macular dystrophy. Oncotarget. pp. 122-141.

(2018) Identification of a novel RPGRIP1 mutation in an Iranian family with leber congenital amaurosis by exome sequencing. Journal of Cellular and Molecular Medicine. pp. 1733-1742. ISSN 1582-4934

(2018) A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing. Bmc Medical Genetics. p. 8. ISSN 1471-2350

(2017) MicroRNA-34a targets epithelial to mesenchymal transition-inducing transcription factors (EMT-TFs) and inhibits breast cancer cell migration and invasion. Oncotarget. pp. 21362-21379.

(2016) Prognostic Value of EMT-inducing Transcription Factors (EMT-TFs) in Metastatic Breast Cancer: A Systematic Review and Meta-analysis. Scientific Reports. p. 10. ISSN 2045-2322

(2015) Development of SCAR Markers Based on Improved RAPD Amplification Fragments and Molecular Cloning for Authentication of Herbal Medicines Angelica sinensis, Angelica acutiloba and Levisticum officinale. Natural Product Communications. pp. 1743-1747. ISSN 1934-578X

(2015) Genetic Authentication of Gardenia jasminoides Ellis var. grandiflora Nakai by Improved RAPD-Derived DNA Markers. Molecules. pp. 20219-20229. ISSN 1420-3049