Majid Al-Fayyadh

Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them?: Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry

L. Jordaens, S. Hohnloser, S. Priori, 2010, Circulation.

Clinical profile and mutation spectrum of long QT syndrome in Saudi Arabia: The impact of consanguinity.

N. Dzimiri, Z. Al-Hassnan, B. Meyer, 2017, Heart rhythm.

Recessively inherited severe aortic aneurysm caused by mutated EFEMP2.

Z. Al-Hassnan, B. Meyer, M. Al-Fayyadh, 2012, The American journal of cardiology.

Hybrid management strategy for percutaneous Fontan completion without surgery: early results.

Z. Al-Halees, B. Alsoufi, C. Canver, 2011, The Annals of thoracic surgery.

Identification of a novel KCNQ1 mutation in a large Saudi family with long QT syndrome: clinical consequences and preventive implications

A. Al-Hazzani, N. Dzimiri, Z. Al-Hassnan, 2013, Clinical genetics.

Outcomes of Damus-Kaye-Stansel anastomosis at time of cavopulmonary connection in single ventricle patients at risk of developing systemic ventricular outflow tract obstruction.

Z. Al-Halees, B. Alsoufi, A. Kalloghlian, 2014, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Identification of a novel homozygous NEXN gene mutation in recessively inherited dilated cardiomyopathy

Z. Al-Hassnan, A. Almesned, S. Tulbah, 2013 .

Identification of novel genomic imbalances in Saudi patients with congenital heart disease

N. Kaya, D. Çolak, B. Levy, 2018, Molecular Cytogenetics.