Mohammad Reza Pourreza

Genetic study of the BRAF gene reveals new variants and high frequency of the V600E mutation among Iranian ameloblastoma patients

M. Soltani, M. Tabatabaiefar, L. Shariati, 2018, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Somatic BRAF V600E Mutation in Familial Colorectal Cancer Type X: A New Study in Central Iran

M. Emami, M. Zeinalian, M. Tabatabaiefar, 2021, Jentashapir Journal of Cellular and Molecular Biology.

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 .

Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family

A. Rahimi, M. Tabatabaiefar, M. Noori-Daloii, 2019, Acta Diabetologica.

A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss

R. Salehi, N. Saki, M. Tabatabaiefar, 2018, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper

Ladan Sadeghian, M. Tabatabaiefar, M. Sehhati, 2018, Advanced biomedical research.

A pathogenic variant in the transforming growth factor beta I (TGFBI) in four Iranian extended families segregating granular corneal dystrophy type II: A literature review

G. Yaghoobi, M. Tabatabaiefar, Mohammad Amin Tabatabaiefar, 2020, Iranian journal of basic medical sciences.

GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.

M. Tabatabaiefar, M. Noori-Daloii, M. Hashemzadeh-Chaleshtori, 2018, International journal of pediatric otorhinolaryngology.

A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred.

M. Tabatabaiefar, J. Mohammadi-Asl, Mohammad Amin Tabatabaiefar, 2017, Journal of dermatological science.

Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.

Ladan Sadeghian, M. Tabatabaiefar, P. Tahmasebi, 2019, International journal of pediatric otorhinolaryngology.

Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation

M. Tabatabaiefar, M. Darbouy, Mohammad Reza Pourreza, 2018, Journal of cellular biochemistry.