Nada AbuDheim

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

A novel deletion of the<i>MEN1</i>gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype

Hussein Raef, Minjing Zou, Essa Y. Baitei et al. · Clinical Endocrinology · 2011 · 35 citations · Full text

Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways

Dilek Çolak, Hesham Aldhalaan, Michael Nester et al. · Genomics · 2010 · 27 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

GM2 gangliosidosis in Saudi Arabia: Multiple mutations and considerations for future carrier screening

Namik Kaya, Mohammad Al‐ Owain, Nada AbuDheim et al. · American Journal of Medical Genetics Part A · 2011 · 19 citations

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects

Jawaher Al‐Zahrani, Naji Aldosari, Nada AbuDheim et al. · Molecular Cytogenetics · 2011 · 13 citations · Full text