B. Alsabah

Identification of a novel founder variant in DNAI2 cause primary ciliary dyskinesia in five consanguineous families derived from a single tribe descendant of Arabian Peninsula

H. Omran, P. Pennekamp, Dalal A Al-Mutairi, 2022, Frontiers in Genetics.

Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia

H. Omran, F. Alkuraya, P. Pennekamp, 2014, Nature Genetics.

A homozygous SP7/OSX mutation causes osteogenesis and dentinogenesis imperfecta with craniofacial anomalies

Marc N. Wein, B. Alsabah, Dalal A. Al-Mutairi, 2024, JBMR plus.

Novel pathogenic variants of DNAH5 associated with clinical and genetic spectra of primary ciliary dyskinesia in an Arab population

H. Omran, P. Pennekamp, B. Alsabah, 2024, Frontiers in genetics.

Mapping the Most Common Founder Variant in RSPH9 That Causes Primary Ciliary Dyskinesia in Multiple Consanguineous Families of Bedouin Arabs

H. Omran, P. Pennekamp, B. Alsabah, 2023, Journal of clinical medicine.