Projects per year
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Dive into the research topics where Wesal Habbab is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Collaborations and top research areas from the last five years
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Projects
- 1 Finished
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QBRI-CORE-000010: Identifying Potential Biomarkers for Autism Spectrum Disorder
Al, D. A. (Consultant), Hottenga, J. J. (Lead Principal Investigator), Habbab, W. (Research Associate) & Al-Khadairi, G. M. (Research Associate)
8/01/18 → 31/12/25
Project: Experimental Development/Translation Research
Research output
- 5 Article
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Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman
Gupta, V., Ben-Mahmoud, A., Idris, A. B., Hottenga, J.-J., Habbab, W., Alsayegh, A., Kim, H.-G., AL-Mamari, W. & Stanton, L. W., 21 Dec 2024, In: International Journal of Molecular Sciences. 25, 24, 13700.Research output: Contribution to journal › Article › peer-review
Open Access3 Citations (Scopus) -
The genetic landscape of autism spectrum disorder in the Middle Eastern population
Al-Sarraj, Y., Taha, R. Z., Al-Dous, E., Ahram, D., Abbasi, S., Abuazab, E., Shaath, H., Habbab, W., Errafii, K., Bejaoui, Y., AlMotawa, M., Khattab, N., Aqel, Y. A., Shalaby, K. E., Al-Ansari, A., Kambouris, M., Abouzohri, A., Ghazal, I., Tolfat, M. & Alshaban, F. & 2 others, , Mar 2024, In: Frontiers in Genetics. 15, 1363849.Research output: Contribution to journal › Article › peer-review
Open Access8 Citations (Scopus) -
The Anti-Tumor Agent Sodium Selenate Decreases Methylated PP2A, Increases GSK3Y216 Phosphorylation, Including Tau Disease Epitopes and Reduces Neuronal Excitability in SHSY-5Y Neurons
Habbab, W., Aoude, I., Palangi, F., Abdulla, S. & Ahmed, T., 2 Feb 2019, In: International Journal of Molecular Sciences. 20, 4, 14 p., 844.Research output: Contribution to journal › Article › peer-review
12 Citations (Scopus) -
PTBP1: A candidate gene for intellectual disability
Alkhateeb, A. M., Habbab, W., Aburahma, S. K. & Thompson, I. R., Sept 2017, In: Meta Gene. 13, p. 57-62 6 p.Research output: Contribution to journal › Article › peer-review
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Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability
Alkhateeb, A. M., Aburahma, S. K., Habbab, W. & Thompson, I. R., Aug 2016, In: Metabolic Brain Disease. 31, 4, p. 901-907 7 p.Research output: Contribution to journal › Article › peer-review
22 Citations (Scopus)