Bohlega, Saeed

Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

Alazami, A. M., Patel, N., Shamseldin, H. E., Anazi, S., Al-Dosari, M. S., Alzahrani, F., Hijazi, H., Alshammari, M., Aldahmesh, M. A., Salih, M. A., et al. (2015) · Cell Reports

Genomics and Rare DiseasesHereditary Neurological Disorders

Cited by 465

Consensus guidelines for the diagnosis and treatment of multiple sclerosis

Yamout, B., Alroughani, R., Al-Jumah, M., Khoury, S., Abouzeid, N., Dahdaleh, M., Alsharoqi, I., Inshasi, J., Hashem, S., Zakaria, M., et al. (2013) · Current Medical Research and Opinion

Multiple Sclerosis Research StudiesPolyomavirus and related diseases

Cited by 25

Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues

Bohlega, S., Al-Ajlan, H., & Al-Saif, A. (2014) · European Journal of Human Genetics

Connective tissue disorders researchGenomics and Rare Diseases

Cited by 14