Lia Abbasi Moheb

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Hossein Najmabadi, Hao Hu, Masoud Garshasbi et al. · Nature · 2011 · 975 citations

Neurodegenerative Diseases, Recessive Cognitive Disorders, Genetic Disorder +6

Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome

Lia Abbasi Moheb, Andreas Tzschach, Masoud Garshasbi et al. · European Journal of Human Genetics · 2007 · 57 citations · Full text

Lipid Disorder, Genetic Disorder, Genetics +12

Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability

Aida M. Bertoli‐Avella, José María García-Aznar, Oliver Brandau et al. · European Journal of Human Genetics · 2018 · 28 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Genetic Disorder +8

High Prevalence of the −α^3.7Deletion Among Thalassemia Patients in Iran

Maryam Neishabury, Christian Oberkanins, Lia Abbasi Moheb et al. · Hemoglobin · 2003 · 24 citations

Genetic Disorder, Genetics, Inherited Metabolic Disease +12

Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population

Ali Reza Pouya, Seyedeh Sedigheh Abedini, Neda Mansoorian et al. · European Journal of Medical Genetics · 2009 · 20 citations

Down Syndrome, Family Medicine, Iranian Population +11