(2024) Repurposing doxycycline for a case of CONDSIAS Syndrome with a novel ADPRHL2 missense mutation. Acta Neurologica Belgica. ISSN 03009009 (ISSN)

(2023) Genetic variants of IL-10, TGFβ, FGF1, ESR1, MMP1 and WNT4 genes and their association with endometriosis in Iranian women. Human Gene.

(2022) Evaluation of miR-146a (rs2910164) polymorphism in coronary artery disease: Case-control and silico analysis. Gene Reports.

(2021) Incomplete penetrance of autosomal recessive anophthalmia in a large consanguineous family. Ophthalmic Genetics.

(2017) Frequency of TNFR1 36 A/G gene polymorphism in azoospermic infertile men: A case-control study. International Journal of Reproductive BioMedicine. pp. 521-526. ISSN 2476-4108 (Print) 2476-3772 (Electronic) 2476-3772 (Linking)

(2017) A Novel Missense Mutation in the ALDH13 Gene Causes Anophthalmia in Two Unrelated Iranian Consanguineous Families. International Journal of Molecular and Cellular Medicine. pp. 131-134. ISSN 2251-9637 (Print) 2251-9645 (Electronic) 2251-9637 (Linking)