Hadia Hijazi

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

TLE6 mutation causes the earliest known human embryonic lethality

Anas M. Alazami, Salma Awad, Serdar Coşkun et al. · Genome biology · 2015 · 216 citations · Full text

Mutation in <i>ADAT3</i>, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus

Anas M. Alazami, Hadia Hijazi, Mohammed S. Al‐Dosari et al. · Journal of Medical Genetics · 2013 · 129 citations

Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

Mohammed A. Aldahmesh, Arif O. Khan, Hisham Alkuraya et al. · The American Journal of Human Genetics · 2013 · 128 citations · Full text

Ophthalmology, Severe Myopia, Genetic Disorder +3

A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in <i>MYO18B</i>

Anas M. Alazami, Amal Y. Kentab, Eissa Faqeih et al. · Journal of Medical Genetics · 2015 · 79 citations