(2023) Novel missense mutation in NKX2.6 gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease. Gene Reports.

(2020) Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients. Applied biochemistry and biotechnology. pp. 896-906. ISSN 1559-0291

(2020) Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease. Applied biochemistry and biotechnology. ISSN 1559-0291

(2018) Novel Point Mutations in the Gene in Pediatric Patients with Non-Familial Congenital Heart Disease. Medicina (Kaunas, Lithuania). ISSN 1648-9144

(2016) A Novel Nonsense Mutation in Exon 5 of KIND1 Gene in an Iranian Family with Kindler Syndrome. Archives of Iranian medicine. pp. 403-8. ISSN 1735-3947

(2016) Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients. Research in cardiovascular medicine. e29134. ISSN 2251-9572

(2016) Mitochondrial mutations in tRNAGlu and Cytochrome b genes associated with Iranian Congenial Heart Disease. International Cardiovascular Research Journal. pp. 193-198.

(2013) Apolipoprotein E gene polymorphism in iranian coronary atherosclerosis patients candidate for coronary artery bypass graft. Iranian Journal of Basic Medical Sciences. pp. 841-844.