Projects per year
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Collaborations and top research areas from the last five years
Profiles
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EX-QNRF-PPM-61: Implementing Infectious Disease Pharmacogenomics in Qatar
Jithesh, P. V. (Lead Principal Investigator), Rustom, F. (Principal Investigator), Student-1, G. (Graduate Student), 2, G. S. (Graduate Student), Hadi, H. (Principal Investigator), Koleri, J. (Principal Investigator), Almaslamani, M. (Principal Investigator) & Associate-1, R. (Research Associate)
24/03/26 → 24/03/29
Project: Experimental Development/Translation Research
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HBKU-OVPR-TG-03-46: Investigating DUSP5 as a modulator of cancer immunity in triple negative breast cancer
Al-Muftah, M. A. Y. M. (Lead Principal Investigator), Xue, M. (Post Doctoral Fellow), Pourkarimi, E. (Co-Lead Principal Investigator) & Bougarn, S. (Research Assistant)
1/11/25 → 31/10/27
Project: Experimental Development/Translation Research
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EX-QNRF-GSRA-76: Psoriasis Epidemiology and Associated Comorbidities
El Hajj, N. (Lead Principal Investigator) & Khanjar, B. (Graduate Student)
1/09/25 → 1/09/27
Project: Applied Research
Research output
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Applications of artificial intelligence in rare skin diseases and skin cancers: A scoping review
Alkhateeb, M., Nayeem, A., Alokla, M., El Hajj, N., Alam, T., Ahmed, A., Belhaouari, S. B., Sheikh, J. & Abd-Alrazaq, A., Sept 2026, In: Intelligence-Based Medicine. 15, 100408.Research output: Contribution to journal › Review article › peer-review
Open Access -
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humans
Bonardi, C. M., Møller, R. S., Ruiz-Reig, N., Chai, G., Madsen, C. G., Bayat, A., Hammer, T. B., Fenger, C. D., Gardella, E., Gawlinski, P., Dawidziuk, M., Wiszniewski, W., Bekiesinska-Figatowska, M., Cabet, S., Rossi, M., Lesca, G., Gouy, E., Jepsen, B., Mieszczanek, T. S. & Sanchez Russo, R. & 8 others, , Dec 2026, In: Nature Communications. 17, 1, 862.Research output: Contribution to journal › Article › peer-review
Open Access2 Link opens in a new tab Citations (Scopus) -
Characterization of a Familial Goldenhar Syndrome Case Using Whole-Exome Sequencing
Bejaoui, Y., Al-Sarraj, Y., Al-Hage, J., Bitar, F. F., El Hajj, N., Nemer, G. & Kurban, M., Mar 2026, In: Genes. 17, 3, 299.Research output: Contribution to journal › Article › peer-review
Open Access