Mohammad Aldosari

Novel CENPJ mutation causes Seckel syndrome

Mohammad Aldosari, Ranad Shaheen, Dilek Çolak et al. · Journal of Medical Genetics · 2010 · 161 citations

Developmental Anomaly, Novel Cenpj Mutation, Developmental Biology +15

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

Neuronal ceroid lipofuscinosis caused by MFSD8 mutations: a common theme emerging

Mohammed A. Aldahmesh, Zuhair N. Al‐Hassnan, Mohammad Aldosari et al. · Neurogenetics · 2009 · 44 citations

Neuro-oncology, Molecular Neuroscience, Common Theme +11

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

Ocular manifestations of branchio-oculo-facial syndrome: report of a novel mutation and review of the literature.

Mohammad Aldosari, Mazyad Almazyad, L. Al-Ebdi et al. · PubMed · 2010 · 21 citations · Full text