Jawahir Y. Mohamed

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 · 472 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia

Mohammed A. Aldahmesh, Jawahir Y. Mohamed, Hisham Alkuraya et al. · The American Journal of Human Genetics · 2011 · 187 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

Life Sciences, Genetics, Molecular Genetics +17

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

Medicine, Genetics, Molecular Genetics +12

In search of triallelism in Bardet–Biedl syndrome

Leen Abu‐Safieh, Shamsa Al-Anazi, Lama AlAbdi et al. · European Journal of Human Genetics · 2012 · 124 citations

Life Sciences, Genetics, Human Genetics +1