Sirous Zeinali

Thalassemia in Iran

Hassan Abolghasemi, Ali Amid, Sirous Zeinali et al. · Journal of Pediatric Hematology/Oncology · 2007 · 219 citations

Medicine, Genetics, Hematology +12

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 · 183 citations

Life Sciences, Genetics, Molecular Genetics +17

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 · 159 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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 · 69 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

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 · 64 citations · Full text

Medicine, Genetics, Molecular Genetics +17