Sarar Mohamed

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed et al. · Human Genetics · 2017 · 296 citations · Full text

A multicenter clinical exome study in unselected cohorts from a consanguineous population of Saudi Arabia demonstrated a high diagnostic yield

Ahmed Alfares, Majid Alfadhel, Tariq Ahmad Wani et al. · Molecular Genetics and Metabolism · 2017 · 90 citations

High Diagnostic Yield, Consanguineous Population, Saudi Arabia +10

Genetic variants in components of the NALCN–UNC80–UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies)

Nuria C. Bramswig, Aida M. Bertoli‐Avella, Beate Albrecht et al. · Human Genetics · 2018 · 60 citations · Full text

Channelopathies, Genetic Variants, Genetic Disorder +8

Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia

Sarar Mohamed, W Elsheikh, Aida I. Al‐Aqeel et al. · Saudi Medical Journal · 2020 · 30 citations · Full text

Tyrosinemia type 1: a rare and forgotten cause of reversible hypertrophic cardiomyopathy in infancy

Sarar Mohamed, Mohammed A Kambal, Nasir AM Al Jurayyan et al. · BMC Research Notes · 2013 · 29 citations · Full text