S. A. Al Hazzaa

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Colin A. Johnson, Teunis J. P. van Dam, J. Shendure, 2015, Nature Cell Biology.

LOXL3, encoding lysyl oxidase-like 3, is mutated in a family with autosomal recessive Stickler syndrome

F. Alkuraya, F. Alzahrani, H. Tayeb, 2015, Human Genetics.

Pink hypopyon: a sign of Serratia marcescens endophthalmitis.

K. Tabbara, J. A. Gammon, S. A. Al Hazzaa, 1992, The British journal of ophthalmology.

Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping

F. Alkuraya, R. Shaheen, M. Aldahmesh, 2009, Journal of Medical Genetics.

IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome.

Yong Xiong, Fowzan S Alkuraya, F. Alkuraya, 2014, Human molecular genetics.

Etiology of optic atrophy: a prospective observational study from Saudi Arabia

A. Eldali, J. N. Mbekeani, Manzoor Ahmed, 2017, Annals of Saudi medicine.

Signet ring cell adenocarcinoma and bilateral leptomeningeal involvement of optic nerve sheaths.

J. N. Mbekeani, A. Tulbah, S. A. Al Hazzaa, 2015, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

Papillary tumor of the pineal region presenting with Foster Kennedy sign.

J. N. Mbekeani, M. Hassounah, Manzoor Ahmed, 2015, Hematology/oncology and stem cell therapy.