Projects per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
External positions
Kuwait University (KU)
… → 2024
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Projects
- 1 Finished
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Studying The Genetics Of Congenital Thoracic Anomalies In Consanguineous Kuwaiti Families Caused By Cilia Dysfunction
Al-Mutairi, D. (PI)
1/09/15 → 1/09/15
Project: General Research › General Research 2014 Cycle 2
Research output
- 5 Article
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Al-Mutairi, D. A., Alsabah, B. H., Pennekamp, P., & Omran, H. (2024). Novel pathogenic variants of DNAH5 associated with clinical and genetic spectra of primary ciliary dyskinesia in an Arab population. Frontiers in Genetics, 15, Article 1396797. https://doi.org/10.3389/fgene.2024.1396797Open Access
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Al-Mutairi, D. A., Alsabah, B. H., Pennekamp, P., & Omran, H. (2023). Mapping the Most Common Founder Variant in RSPH9 That Causes Primary Ciliary Dyskinesia in Multiple Consanguineous Families of Bedouin Arabs. Journal of Clinical Medicine, 12(20), Article 6505. https://doi.org/10.3390/jcm12206505Open Access2 Scopus citations
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Al-Mutairi, D. A., Alsabah, B. H., Alkhaledi, B. A., Pennekamp, P., & Omran, H. (2022). 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. Frontiers in Genetics, 13, Article 1017280. https://doi.org/10.3389/fgene.2022.1017280Open Access11 Scopus citations
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Wallmeier, J., Al-Mutairi, D. A., Chen, C. T., Loges, N. T., Pennekamp, P., Menchen, T., Ma, L., Shamseldin, H. E., Olbrich, H., Dougherty, G. W., Werner, C., Alsabah, B. H., Köhler, G., Jaspers, M., Boon, M., Griese, M., Schmitt-Grohé, S., Zimmermann, T., Koerner-Rettberg, C., ... Omran, H. (2014). Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia. Nature Genetics, 46(6), 646-651. https://doi.org/10.1038/ng.2961217 Scopus citations
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Zariwala, M. A., Gee, H. Y., Kurkowiak, M., Al-Mutairi, D. A., Leigh, M. W., Hurd, T. W., Hjeij, R., Dell, S. D., Chaki, M., Dougherty, G. W., Adan, M., Spear, P. C., Esteve-Rudd, J., Loges, N. T., Rosenfeld, M., Diaz, K. A., Olbrich, H., Wolf, W. E., Sheridan, E., ... Hildebrandt, F. (2013). ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. American Journal of Human Genetics, 93(2), 336-345. https://doi.org/10.1016/j.ajhg.2013.06.007Open Access161 Scopus citations