Samya Hagos

Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice

Ranad Shaheen, Shams Anazi, Tawfeg Ben‐Omran et al. · The American Journal of Human Genetics · 2016 · 70 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs

Salma M. Wakil, Ramesh Ram, Nzioka P. Muiya et al. · Atherosclerosis · 2015 · 68 citations

Life Sciences, Cardiology, Genetics +14

Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases

Lama AlAbdi, Hanan E. Shamseldin, Ebtissal Khouj et al. · Genome Medicine · 2023 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C > T

Salma M. Wakil, Khushnooda Ramzan, Rula Abuthuraya et al. · Gene · 2013 · 32 citations

Life Sciences, Genetics, Neurology +14

A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family

Salma M. Wakil, Saeed Bohlega, Samya Hagos et al. · European Journal of Medical Genetics · 2012 · 30 citations

Life Sciences, Genetics, Molecular Genetics +7