Personal profile
External positions
Ministry of Health
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):
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SDG 3 Good Health and Well-being
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Dive into the research topics where Laila Bastaki is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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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
Research output
- 5 Article
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Ng, B. G., Zhang, W., Neil, J. E., Danish, M., Marafi, D., Kamal, T. M., Bastaki, L., Al Saffar, M., Yang, E., He, M., Walsh, C. A., Mochida, G. H., & Freeze, H. H. (2026). A homozygous nonsense variant in the oligosaccharyltransferase complex gene, RPN1, causes a congenital disorder of glycosylation. Human Genetics and Genomics Advances, 7(3), Article 100604. https://doi.org/10.1016/j.xhgg.2026.100604Open Access
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Alhaddad, M. E., Mohammad, A., Dashti, K. M., John, S. E., Bahbahani, Y., Abu-Farha, M., Abubaker, J., Thanaraj, T. A., Bastaki, L., Al-Mulla, F., Al-Ali, M., & Ali, H. (2024). Genetic landscape and clinical outcomes of autosomal recessive polycystic kidney disease in Kuwait. Heliyon, 10(13), Article e33898. https://doi.org/10.1016/j.heliyon.2024.e33898Open Access
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Al Habib, F., Elshafie, R. M., Bastaki, L., Salem, A., & Yacoub, M. (2024). rare genes in consanguineous families diagnosed as cardiomyopathy: a comprehensive review of autosomal recessive inheritance. European Journal of Human Genetics, 32, 1401.
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Pandova, M. G., Abduljalil, T., Elshafey, A. E., Abdelmoaty, S. M. A., Albastawisy, H. I., Bastaki, L. A., Alsaleh, H., Kozak, I., & AlMerjan, J. I. (2022). Inherited retinal dystrophies in a Kuwaiti tribe. Ophthalmic Genetics, 43(4), 438-445. https://doi.org/10.1080/13816810.2022.20455094 Scopus citations
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Yu, T. W., Chahrour, M. H., Coulter, M. E., Jiralerspong, S., Okamura-Ikeda, K., Ataman, B., Schmitz-Abe, K., Harmin, D. A., Adli, M., Malik, A. N., D'Gama, A. M., Lim, E. T., Sanders, S. J., Mochida, G. H., Partlow, J. N., Sunu, C. M., Felie, J. M., Rodriguez, J., Nasir, R. H., ... Walsh, C. A. (2013). Using Whole-Exome Sequencing to Identify Inherited Causes of Autism. Neuron, 77(2), 259-273. https://doi.org/10.1016/j.neuron.2012.11.002Open Access375 Scopus citations