T. Omran

Point of Care Exome Sequencing Reveals Allelic and Phenotypic Heterogeneity Underlying Mendelian disease in Qatar.

Kamal M. Osman, J. Mezey, J. Malek, 2019, Human molecular genetics.

Human heterologous liver cells transiently improve hyperammonemia and ureagenesis in individuals with severe urea cycle disorders

J. Weitz, M. Yudkoff, A. Schlune, 2018, Journal of Inherited Metabolic Disease.

Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go

M. Schroth, D. Zafeiriou, Y. Chien, 2021, Neuromuscular Disorders.

The re-occurrence of dilated cardiomyopathy in propionic acidemia after liver transplantation requiring heart transplant, first case from Middle East.

Z. Hijazi, Hesham Al-Saloos, T. B. Omran, 2022, Cardiology in the young.

Expert Group Consensus on early diagnosis and management of infantile-onset pompe disease in the Gulf Region

Z. Al-Hassnan, N. Makhseed, Fatma Al Jasmi, 2022, Orphanet Journal of Rare Diseases.