Asma I. Tahir

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population

Dorota Monies, Mohammed Abouelhoda, Mirna Assoum et al. · The American Journal of Human Genetics · 2019 · 283 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families

Bashayer Al‐Mubarak, Mohamed Abouelhoda, Aisha Omar et al. · Scientific Reports · 2017 · 104 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Recessive Mutations in COL25A1 Are a Cause of Congenital Cranial Dysinnervation Disorder

Jameela Shinwari, Arif O. Khan, Salma Awad et al. · The American Journal of Human Genetics · 2014 · 59 citations · Full text

Life Sciences, Genetics, Neuroscience +12

A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits

Nzioka P. Muiya, Salma M. Wakil, Mohammed Al‐Najai et al. · Gene · 2014 · 46 citations

Medicine, Cardiology, Genetics +14

Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel

Mohamed H. Al‐Hamed, Wesam Kurdi, Nada Alsahan et al. · Journal of Medical Genetics · 2016 · 33 citations · Full text

Medicine, Genetics, Molecular Genetics +17