Banan Al‐Younes

Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin et al. · Cell Reports · 2014 · 465 citations · Full text

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed et al. · Human Genetics · 2017 · 296 citations · Full text

Association of a Mutation in <i>LACC1</i> With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis

Salma M. Wakil, Dorota Monies, Mohamed Abouelhoda et al. · Arthritis & Rheumatology · 2014 · 136 citations

Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies

Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya et al. · Genetics in Medicine · 2015 · 109 citations · Full text

Ocular Disease, Retina, Ophthalmology +4

A novel X‐linked disorder with developmental delay and autistic features

Namik Kaya, Dilek Çolak, Albandary AlBakheet et al. · Annals of Neurology · 2011 · 72 citations