Publications

Geethakumari, A. M., Sultana, A., Fatima, A., Uddin, S. M. N., Abdulhakim, S., Mohamed, A.,…Biswas, K. H. (2025). A BRET-based Mpro biosensor containing a nanobody and tandem cleavage sites shows an increased cleavage rate [Article]. Sensors and Actuators Reports, 9, Article 100315.

Dave, N., Innan, N., Behera, B. K., Mumtaz, S., Al-Kuwari, S., & Farouk, A. (2025). Optimizing Low-Energy Carbon IIOT systems with quantum algorithms: performance evaluation and noise robustness. IEEE Internet of Things Journal, 1.

Publication | arXiv

al., A. I. S. E. (2025). Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging.

Ana et. al., A. I. S. e. (2025). Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology.

Naja, K., Anwardeen, N., Albagha, O., & Elrayess, M. A. (2025). Lipid subclasses differentiate insulin resistance by Triglyceride–Glucose index. Metabolites, 15. 

Shadab, M., Ben-Mahmoud, A., Martínez Völter, L. N., Abbasi, A. A., Ku, B., Ejaz, A., Latif, Z., Gupta, V., Owrang, D., Jang, M. H., Zhang, Z., Mohammad, R., Houlden, H., Kim, H. G., & Vona, B. (2025). Recurrent and novel pathogenic variants in genes involved with hearing loss in the pakistani population. Molecular Diagnosis and Therapy.

Koval, A., Mamadalieva, N. Z., Mamadalieva, R., Jalilov, F., & Katanaev, V. L. (2025). Success and controversy of natural products as therapeutic modulators of wnt signaling and its interplay with oxidative stress: Comprehensive review across compound classes and experimental systems. Antioxidants, 14.

Arredouani, A. (2025). GLP-1 receptor agonists, are we witnessing the emergence of a paradigm shift for neuro-cardio-metabolic disorders?. Pharmacology and Therapeutics, 269. 

Ghasemi, M.-R., Fateh, S. T., Ben-Mahmoud, A., Gupta, V., Stühn, L. G., Lesca, G., Chatron, N., Platzer, K., Edery, P., Sadeghi, H., Isidor, B., Cogné, B., Schulz, H. L., Krauspe-Stübecke, I., Periyasamy, R., Nampoothiri, S., Mirfakhraie, R., Alijanpour, S., Syrbe, S., …, Kim, H.-G. (2025). Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of CNKSR2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (MRXSHG).