Abdorrahim Sadeghi

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

Fatemeh Alasti, Abdorrahim Sadeghi, Mohammad Hossein Sanati et al. · The American Journal of Human Genetics · 2008 · 100 citations · Full text

Developmental Biology, Mendelian Disorder, Cytogenetics +8

A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families

Fatemeh Alasti, Mohammad Hossein Sanati, Amir Hossein Behrouzifard et al. · International Journal of Pediatric Otorhinolaryngology · 2007 · 46 citations

Developmental Biology, Recognizable Phenotype, Genetics +11

Association between vitamin D receptor ApaI and TaqI gene polymorphisms and gestational diabetes mellitus in an Iranian pregnant women population

Golzar Rahmannezhad, Farideh Jalali Mashayekhi, Mohammad Taghi Goodarzi et al. · Gene · 2016 · 26 citations

Metabolic Syndrome, Taqi Gene Polymorphisms, Genetic Determinant +10

Association between chemerin rs17173608 and rs4721 gene polymorphisms and gestational diabetes mellitus in Iranian pregnant women

Zahra Hasanvand, Abdorrahim Sadeghi, Mohammad Reza Rezvanfar et al. · Gene · 2018 · 23 citations

Metabolic Syndrome, Genetic Determinant, Genetics +10

Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran

Abdorrahim Sadeghi, Mohammad Hossein Sanati, Fatemeh Alasti et al. · Iranian Journal of Biotechnology · 2009 · 17 citations

Genetics, Genetic Epidemiology, Gjb2 Mutations +25