Saudi Human Genome



  • A Comprehensive Molecular Research Program for Hereditary Channelopathies in the Kingdom of Saudi Arabia
  • Establishment and Evaluation of a Flash Exome Protocol for Diagnosis of Disease in Critically ill Neonates


  • Characterization of the Clinical and Molecular Basis of Hereditary Bleeding Disorder
  • Genes Underlying Inherited Cystic Kidney Diorder in Saudi Arabia Families
  • Next Generation Premarital Genetic Screening: A Feasibility Study


  • Biomarker and Therapeutic Target Discovery in Patient with Hyper IgE Conditions
  • Metabolic and Molecular Profiling in Patients with Inborn Errors of Metabolism
  • Potential Neuroprotective & Neurotrophic Candidates Against the Toxicity of Beta-Amyloid Peptides Causing Alzheimer’s Disease


  • Autozygome Sequencing for High Throughput of Genes with Biallelic Inactivation in Healthy Humans: Understanding Genetic Influence on Human Phenotypic Variation (The Human Knockout Project)
  • Clinical and Molecular characterization of Genetic Diseases of the Skin
  • Use of Cell Free Fetal DNA (CFFD) for NON-Invasive Prenatal Diagnosis of Inherited Diseases and Aneuploidies