6 specialists found
Dr. Sarah Al-Hashimi
MBBS, MRCP, PhD (Clinical Genetics)
London, UK
Consultant clinical geneticist with 14 years of experience in rare disease diagnosis, with specific expertise in GCC population genetics and consanguinity-related conditions.
Prof. James Whitfield
MD, FRCPath, FRCPCH
Manchester, UK
Professor of haematogenomics with 20 years of clinical and research experience in sickle cell disease, beta-thalassaemia, and inherited blood disorders prevalent in GCC populations.
Dr. Fatima Al-Rashid
MD, PhD, FACMG
Dubai, UAE
Board-certified medical geneticist specialising in hereditary cancer syndromes, with particular focus on BRCA1/2, Lynch syndrome, and familial adenomatous polyposis in Middle Eastern populations.
Dr. Khalid Al-Mansouri
MBChB, MD, FRCP
Riyadh, Saudi Arabia
Consultant cardiologist and cardiovascular geneticist with expertise in inherited cardiac conditions including familial hypercholesterolaemia, hypertrophic cardiomyopathy, and inherited arrhythmia syndromes.
Dr. Amelia Chen
MBBS, FRACP, PhD
London, UK
Specialist in inborn errors of metabolism with extensive experience in phenylketonuria, organic acidaemias, and urea cycle disorders, including populations with consanguinity-related risk.
Dr. Mohammed Al-Farsi
MD, FAAN, Clinical Neurogenetics
Muscat, Oman
Consultant neurologist and clinical neurogenetics specialist with a focus on hereditary ataxias, muscular dystrophies, and neurometabolic disorders prevalent in Omani and broader GCC populations.