Dania S. Khalil

Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature

José Morales, Latifa Al-Sharif, Dania S. Khalil et al. · The American Journal of Human Genetics · 2009 · 239 citations · Full text

Homozygous Mutations, Developmental Biology, Mendelian Disorder +7

A missense mutation in <i>PIK3R5</i> gene in a family with ataxia and oculomotor apraxia

Nada Al Tassan, Dania S. Khalil, Jameela Shinwari et al. · Human Mutation · 2011 · 53 citations

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

Parkinson’s Disease in Saudi Patients: A Genetic Study

Bashayer Al‐Mubarak, Saeed Bohlega, Thamer Alkhairallah et al. · PLoS ONE · 2015 · 29 citations · Full text

Genetic Diseases, Neurodegenerative Diseases, Saudi Population +15

Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles

Arif O. Khan, Dania S. Khalil, Latifa J. Al Sharif et al. · Ophthalmology · 2009 · 25 citations

Extraocular Muscles, Mendelian Disorder, Genetic Disorder +8