Safoura Zardadi

Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population

Masoumeh Falah, S. Morovvati, Sima Rayat, 2022, BMC Cardiovascular Disorders.

Symptomatic care of late-onset Alexander disease presenting with area postrema-like syndrome with prednisolone; a case report

M. Garshasbi, E. Razmara, A. Tavasoli, 2022, BMC Pediatrics.

Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

Navid Almadani, M. Garshasbi, E. Razmara, 2020, Molecular genetics & genomic medicine.

Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report

M. Keramatipour, S. Morovvati, Maryam Hassani Doabsari, 2021, BMC Pediatrics.

Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation

M. Keramatipour, S. Morovvati, Sima Rayat, 2021, BMC medical genomics.

ANXA1 with Anti‐Inflammatory Properties Might Contribute to Parkinsonism

C. Paisán-Ruiz, H. Darvish, E. Alehabib, 2021, Annals of neurology.