Sirous Zeinali
Pasteur Institute of Iran(IR)
Publications by Year
Research Areas
Hemoglobinopathies and Related Disorders, Skin and Cellular Biology Research, Iron Metabolism and Disorders, Prenatal Screening and Diagnostics, CRISPR and Genetic Engineering
Most-Cited Works
- → Therapeutic targeting of angiogenesis molecular pathways in angiogenesis-dependent diseases(2018)262 cited
- → Thalassemia in Iran(2007)218 cited
- → Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families(2017)182 cited
- → Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort(2015)158 cited
- → Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations(2010)91 cited
- → Targeted deletion of BCL11A gene by CRISPR-Cas9 system for fetal hemoglobin reactivation: A promising approach for gene therapy of beta thalassemia disease(2019)68 cited
- → Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency(2018)64 cited
- → Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy(2017)57 cited
- → Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages(2016)54 cited
- → Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families(2018)53 cited