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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.
Shadab, S., Ben-Mahmoud, B., Martínez, M. V., Abbasi, A., Ku, K., Ejaz, E., Latif, L., Gupta, G., Owrang, O., Jang M.-H., J., Zhang, Z., Mohammad, M., Houlden, H., Kim H.-G., K., & Vona, V. (2025). Recurrent and novel pathogenic variants in genes involved with hearing loss in the pakistani population.
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).
Arredouani, A. (2025). GLP-1 receptor agonists, are we witnessing the emergence of a paradigm shift for neuro-cardio-metabolic disorders?.
Awayn, A., Hashish, H., Salem, S., Abod, A., Elgahmasi, E., Ouararhni, O., Abdesselem, A., Abdi, A., & El-Agnaf, E. (2025). Investigating the prevalence of the g2019s mutation in parkinson's disease among a libyan population.
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