Sina Narrei

Trends of human brucellosis in Central Iran (2010–2018)

S. Hosseini, M. Zeinalian, M. Khalilian, 2021, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.

A Novel Stop-Gain Mutation in MSH2 Gene Among a Persian Family Fulfilling Classic Amsterdam Criteria for Lynch Syndrome

M. Emami, M. Zeinalian, M. Tabatabaiefar, 2021 .

Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior

M. Tabatabaiefar, Sina Narrei, M. Sehhati, 2022, Neuromuscular Disorders.

Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.

M. Sepehrnejad, M. Tabatabaiefar, Sina Narrei, 2021, Laboratory medicine.

Epigenetics and Common Non Communicable Disease.

M. Tabatabaiefar, Sina Narrei, Mohammad Amin Tabatabaiefar, 2019, Advances in experimental medicine and biology.

Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss

M. Tabatabaiefar, Sina Narrei, Z. Nouri, 2020, Molecular Biology Reports.

A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family

M. Sepehrnejad, M. Tabatabaiefar, Sina Narrei, 2020, BMC Medical Genetics.

Epidemiologic and Histopathologic Feature of Lung Cancer in Central Iran (2012-2018)

M. Zeinalian, M. Khalilian, Sina Narrei, 2020 .

Novel in-frame duplication variant characterization in late infantile metachromatic leukodystrophy using whole-exome sequencing and molecular dynamics simulation

M. Tabatabaiefar, Sina Narrei, Z. Nouri, 2023, PloS one.

A Novel Germline Pathogenic Variant of RECQL4 Gene in an Iranian Pedigree with Familial Squamous Cell Carcinoma: A Brief Report

M. Zeinalian, Sina Narrei, M. Amin, 2023, Iranian journal of medical sciences.