Zohreh Sharifi

Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect

Marzieh Mojbafan, Reza Bahmani, Samira Dabbagh Bagheri et al. · Orphanet Journal of Rare Diseases · 2020 · 24 citations · Full text

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

Maryam Abiri, Hassan Saei, Maryam Eghbali et al. · Metabolic Brain Disease · 2019 · 16 citations

Urology, Genetic Disorder, Genetics +9

Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran

Zohreh Sharifi, Mohammad Taheri, Mohammad‐Sadegh Fallah et al. · Journal of Molecular Neuroscience · 2021 · 15 citations

Rare Diseases, Somatic Variant, Mendelian Disorder +10

Single-Nucleotide Polymorphisms in Interleukin 6 (IL-6) Gene Are Associated with Suicide Behavior in an Iranian Population

Mohammad Mahdi Eftekharian, Rezvan Noroozi, Mir Davood Omrani et al. · Journal of Molecular Neuroscience · 2018 · 11 citations

Single-nucleotide Polymorphisms, Iranian Population, Psychiatry +3

Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases

Zohreh Sharifi, Faezeh Rahiminejad, Atefeh Joudaki et al. · Scientific Reports · 2019 · 11 citations · Full text