(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) Genetic analysis of Penthorum chinense Pursh by improved RAPD and ISSR in China. Electronic Journal of Biotechnology. pp. 6-11. ISSN 0717-3458

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