Rifaat Rawashdeh

Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish

Julie C. Van De Weghe, Tamara D. S. Rusterholz, Brooke Latour et al. · The American Journal of Human Genetics · 2017 · 89 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

The Development of Genetic Counseling Services and Training Program in Saudi Arabia

Alya Qari, Ameera Balobaid, Rifaat Rawashdeh et al. · Journal of Genetic Counseling · 2013 · 23 citations · Full text

Life Sciences, Counselor Education, Genetics +10

The many faces of peroxisomal disorders: Lessons from a large Arab cohort

Jumanah Alshenaifi, Nour Ewida, Shams Anazi et al. · Clinical Genetics · 2018 · 23 citations

Life Sciences, Genetics, Molecular Genetics +16

Lethal digenic mutations in the K⁺ channels Kir4.1 (<i>KCNJ10</i>) and SLACK (<i>KCNT1</i>) associated with severe-disabling seizures and neurodevelopmental delay

Sonia Hasan, Ameera Balobaid, Alessandro Grottesi et al. · Journal of Neurophysiology · 2017 · 18 citations · Full text

Life Sciences, Genetics, Neurology +17