Sirous Zeinali

Thalassemia in Iran

Hassan Abolghasemi, Ali Amid, Sirous Zeinali et al. · Journal of Pediatric Hematology/Oncology · 2007 · 218 citations

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

Ricardo Harripaul, Nasim Vasli, Muhammad Rafiq et al. · Molecular Psychiatry · 2017 · 177 citations

Mendelian Disorder, Novel Candidate Genes, Genetic Disorder +6

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Güney Bademci, Joseph Foster, Nejat Mahdieh et al. · Genetics in Medicine · 2015 · 158 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +11

Targeted deletion of BCL11A gene by CRISPR-Cas9 system for fetal hemoglobin reactivation: A promising approach for gene therapy of beta thalassemia disease

Mohammad Khosravi, Maryam Abbasalipour, Jean‐Paul Concordet et al. · European Journal of Pharmacology · 2019 · 68 citations · Full text

Gene Therapies, Gene Deletion Data, Genetics +10

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

Hassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian et al. · Matrix Biology · 2018 · 63 citations · Full text

Mendelian Disorder, Genetic Disorder, Lysyl Hydroxylase 3 +5