Zarghuna M A Shinwari

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.

The Phenotype and Outcome of Infantile Cardiomyopathy Caused by a Homozygous ELAC2 Mutation

D. Çolak, E. Faqeih, Z. Al-Hassnan, 2017, Cardiology.

Categorized Genetic Analysis in Childhood-Onset Cardiomyopathy

E. Faqeih, Z. Al-Hassnan, A. Almesned, 2020, Circulation. Genomic and precision medicine.

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

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

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

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

A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy

N. Kaya, D. Çolak, Z. Al-Hassnan, 2016, BMC Medical Genetics.