(2019) Hereditary Ataxia with a novel Mutation in the Senataxin Gene: A case Report. Iranian Journal of Medical Sciences. pp. 262-264. ISSN 0253-0716

(2019) A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia. Cellular & Molecular Biology Letters. p. 8. ISSN 1425-8153

(2018) Mutation analysis of ECM1 gene in two related iranian patients affected by lipoid proteinosis. Acta Med Iran. pp. 474-477. ISSN 00446025 (ISSN)

(2014) Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family. Cell Journal. pp. 91-94. ISSN 2228-5806

(2011) Detecting Rare Triple Heteroplasmic Substitutions in the Mitochondrial DNA Control Region: A Potential Concern for Forensic DNA Studies. Cell Journal. pp. 103-106. ISSN 2228-5806