(2020) Effects of synbiotic supplementation on gut microbiome, serum level of TNF-α, and expression of microRNA-126 and microRNA-146a in patients with type 2 diabetes mellitus: study protocol for a double-blind controlled randomized clinical trial. Trials. p. 324. ISSN 1745-6215

(2020) Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the gene. Ophthalmic genetics. pp. 90-92. ISSN 1744-5094

(2020) Evaluation of miR-181b and miR-126-5p expression levels in T2DM patients compared to healthy individuals: Relationship with NF-κB gene expression. Endocrinologia, diabetes y nutricion. ISSN 2530-0172

(2020) Molecular biomarkers in diabetes mellitus (DM). Medical Journal of the Islamic Republic of Iran.

(2020) A Novel PCNT Frame Shift Variant (c.7511delA) Causing Osteodysplastic Primordial Dwarfism of Majewski Type 2 (MOPD II). Frontiers in Pediatrics.

(2019) Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. American journal of human genetics. pp. 1048-1056. ISSN 1537-6605

(2019) Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss. European journal of medical genetics. p. 103724. ISSN 1878-0849

(2018) Biallelic mutations in early-onset, variably progressive neurodegeneration. Neurology. e319-e330. ISSN 1526-632X

(2018) Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy. Orphanet journal of rare diseases. p. 86. ISSN 1750-1172

(2017) A Novel Loss-of-Function Mutation in HOXB1 Associated with Autosomal Recessive Hereditary Congenital Facial Palsy in a Large Iranian Family. Molecular syndromology. pp. 261-265. ISSN 1661-8769

(2017) A Common Ancestral Asn242Ser Mutation in TMEM67 Identified in Multiple Iranian Families with Joubert Syndrome. Public health genomics. pp. 188-193. ISSN 1662-8063

(2016) Newborn with Supernumerary Marker Chromosome Derived from Chromosomes 11 And 22- A Case Report. Iranian journal of public health. pp. 376-80. ISSN 2251-6085

(2016) A novel mutation in the OFD1 gene in a family with oral-facial-digital syndrome type 1: A case report. Iranian Journal of Public Health. pp. 1359-1366.

(2015) Genetic susceptibility to transient and permanent neonatal diabetes mellitus. International Journal of Pediatrics. pp. 1073-1081.