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2018
- 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
2017
- 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
2016
- 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
2014
- 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