Omran M. Rashidi

Comprehensive Computational Analysis of GWAS Loci Identifies CCR2 as a Candidate Gene for Celiac Disease Pathogenesis

Babajan Banaganapalli, Omran M. Rashidi, Omar I. Saadah et al. · Journal of Cellular Biochemistry · 2017 · 19 citations

Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development among Saudi patients

Jumana Y. Al‐Aama, Noor Ahmad Shaik, Babajan Banaganapalli et al. · PLoS ONE · 2017 · 19 citations · Full text

Ak5 Gene, Genetics, Genetic Epidemiology +20

Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects

Nagwa E. A. Gaboon, Babajan Banaganapalli, Khalidah Khalid Nasser et al. · Saudi Journal of Biological Sciences · 2019 · 18 citations · Full text

Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen

Zuhier Awan, Omran M. Rashidi, Bandar Alshehri et al. · Frontiers in Medicine · 2021 · 15 citations · Full text

Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients

Naglaa M. Kamal, Ahmed N. Sahly, Babajan Banaganapalli et al. · Saudi Journal of Biological Sciences · 2019 · 12 citations · Full text