Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Garshasbi, Masoud  [Clear All Filters]
2024
Hozhabrpour A, Mojbafan M, Palizban F, Vahidnezhad F, Talebi S, Amani M, Garshasbi M, Naghavi A, Khalesi R, Mansouri P, et al. DNA repair-related heritable photosensitivity syndromes: Mutation landscape in a multiethnic cohort of 17 multigenerational families with high degree of consanguinity. DNA Repair (Amst). 2024;136:103633.
Dehghani A, Khajepour F, Dehghani M, Razmara E, Zangouey M, Abadi MFekri Soof, Nezhad RBahram Aba, Dabiri S, Garshasbi M. Hsa-miR-194-5p and hsa-miR-195-5p are down-regulated expressed in high dysplasia HPV-positive Pap smear samples compared to normal cytology HPV-positive Pap smear samples. BMC Infect Dis. 2024;24(1):182.
2023
Hosseinpour S, Razmara E, Heidari M, Rezaei Z, Ashrafi MReza, Dehnavi AZare, Kameli R, Bereshneh AHosseini, Vahidnezhad H, Azizimalamiri R, et al. A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies. Brain Dev. 2023.
Daneshi A, Garshasbi M, Farhadi M, Falavarjani KGhasemi, Vafaee-Shahi M, Almadani N, Zabihi MS, Ghalavand MAmin, Falah M. Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12. BMC Med Genomics. 2023;16(1):235.
Siavashani ESalehi, Ashrafi MReza, Ghabeli H, Heidari M, Garshasbi M. Novel homozygous frameshift variant in the ATCAY gene in an Iranian patient with Cayman cerebellar ataxia; expanding the neuroimaging and clinical features: a case report. BMC Med Genomics. 2023;16(1):226.