(2023) Novel missense mutation in<i> NKX2.6</i> gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease. Gene Reports. p. 10.

(2022) Mutational Analysis of the <i>VPREB1</i> Gene of Pre-BCR Complex in a Cohort of Sporadic Pediatric Patients With B-Cell Acute Lymphoblastic Leukemia. Journal of Pediatric Hematology Oncology. pp. 210-219. ISSN 1077-4114

(2022) Mutational and bioinformatics analysis of the <i>NKX2</i>.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH). Physiology International. pp. 261-277. ISSN 2498-602X

(2022) Novel Point Mutations in 3′-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Current Medical Science. pp. 129-143. ISSN 20965230 (ISSN)

(2020) MicroRNAs as a New Molecular Biomarker for Diagnosis and Prognosis of T-cell Acute Lymphoblastic Leukemia (T-ALL): A Systematic Review. Iranian Journal of Pediatric Hematology and Oncology. pp. 184-199. ISSN 2008-8892

(2020) Novel Point Mutations in Mitochondrial <i>MT-CO2</i> Gene May Be Risk Factors for Coronary Artery Disease. Applied Biochemistry and Biotechnology. pp. 1326-1339. ISSN 0273-2289

(2020) Novel Point Mutations of <i>CITED2</i> Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients. Applied Biochemistry and Biotechnology. pp. 896-906. ISSN 0273-2289

(2020) Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis. Journal of cardiovascular and thoracic research. pp. 214-221. ISSN 2008-5117

(2019) Development of One-Step Tetra-primer ARMS-PCR for Simultaneous Detection of the Angiotensin Converting Enzyme (ACE) I/D and rs4343 Gene Polymorphisms and the Correlation with CAD Patients. Avicenna Journal of Medical Biotechnology. pp. 118-123. ISSN 2008-2835 (Print) 2008-4625 (Electronic) 2008-2835 (Linking)

(2018) Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome. Cardiology Journal. pp. 113-119. ISSN 1897-5593

(2017) Mutation Analysis of the Mitochondrial tRNA Genes in Iranian Coronary Atherosclerosis Patients. Iranian Journal of Public Health. pp. 1379-1385. ISSN 2251-6085

(2017) Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR. Iranian Journal of Public Health. pp. 811-819. ISSN 2251-6085

(2016) Mitochondrial genetic variation in iranian infertile men with varicocele. International Journal of Fertility and Sterility. pp. 303-309. ISSN 2008076X (ISSN)

(2016) Polymorphisms in NOS3, MTHFR, APOB and TNF-alpha Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients. Research in cardiovascular medicine. e29134. ISSN 2251-9572 (Print) 2251-9580 (Electronic) 2251-9572 (Linking)

(2015) The POLG polyglutamine tract variants in iranian patients with multiple sclerosis. Iranian Journal of Child Neurology. pp. 37-41. ISSN 17354668 (ISSN)

(2014) Mutation analysis of TNP1 gene in infertile men with varicocele. Iranian Journal of Reproductive Medicine. pp. 257-262. ISSN 16806433 (ISSN)

(2012) The POLG gene polymorphism in Iranian varicocele-associated infertility patients. Iranian Journal of Basic Medical Sciences. pp. 739-744. ISSN 20083874 (ISSN)