F. Ghasemi

Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH).

J. Bragança, M. Khatami, M. Heidari, 2022, Physiology international.

In-silico study to identify the pathogenic single nucleotide polymorphisms in the coding region of CDKN2A gene

M. Khatami, M. Heidari, Reyhane Chamani, 2021 .

Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)

S. Merat, S. Zeinali, M. Khatami, 2021, Journal of clinical laboratory analysis.