Makanko Komara

Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

Jing Zhang, Tomasz Gambin, Bo Yuan et al. · Human Genetics · 2017 · 62 citations · Full text

Neurodevelopmental Disorders, Intellectual Impairment, Developmental Biology +10

A Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child

Makanko Komara, Aisha Al‐Shamsi, Salma Ben‐Salem et al. · Journal of Molecular Neuroscience · 2015 · 53 citations

Mendelian Disorder, Emirati Child, Genetic Disorder +7

A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract

Jozef Hertecant, Makanko Komara, Aslam Nagi et al. · Meta Gene · 2016 · 27 citations · Full text

Ocular Disease, Genetics, Dync1h1 Gene +18

Analysis of MTHFR and MTRR Gene Polymorphisms in Iranian Ventricular Septal Defect Subjects

Seyyed Reza Pishva, Vasudevan Ramachandran, Ali Etemad et al. · International Journal of Molecular Sciences · 2013 · 24 citations · Full text

A novel aberrant splice site mutation in <i>COL27A1</i> is responsible for Steel syndrome and extension of the phenotype to include hearing loss

Nesrin Gariballa, Afif Ben‐Mahmoud, Makanko Komara et al. · American Journal of Medical Genetics Part A · 2017 · 23 citations