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CMHS Publications: August 2021

CMHS faculty, students and staff publications

           CMHS faculty, student and staff publications 

Highest impact of the month (Scopus journal metrics)





Papers retrieved from Scopus sorted by publication date

Click on the reference to access papers available in full text in NML's collection


Arnone, D., Galadari, H., Rodgers, C. J., Östlundh, L., Aziz, K. A., Stip, E., & Young, A. H. (2021). Efficacy of onabotulinumtoxinA in the treatment of unipolar major depression: Systematic review, meta-analysis and meta-regression analyses of double-blind randomised controlled trials. Journal of Psychopharmacology, 35(8), 910-918.v


Hashiesh, H. M., Sharma, C., Goyal, S. N., Sadek, B., Jha, N. K., Kaabi, J. A., & Ojha, S. (2021). A focused review on CB2 receptor-selective pharmacological properties and therapeutic potential of β-caryophyllene, a dietary cannabinoid. Biomedicine and Pharmacotherapy, 140.


Khalid, M., Alkaabi, J., Khan, M. A. B., & Adem, A. (2021). Insulin signal transduction perturbations in insulin resistance. International Journal of Molecular Sciences, 22(16).


Pandi, M. T., Koromina, M., Tsafaridis, I., Patsilinakos, S., Christoforou, E., van der Spek, P. J., & Patrinos, G. P. (2021). A novel machine learning-based approach for the computational functional assessment of pharmacogenomic variants. Human Genomics, 15(1).


Selvaraj, S., Arora, T., Casameni Montiel, T., Grey, I., Alfraih, H., Fadipe, M., . . . Östlundh, L. (2021). Early screening for post-stroke depression, and the effect on functional outcomes, quality of life and mortality: A protocol for a systematic review and meta-analysis. BMJ Open, 11(8).


Shmygol, A., & Brosens, J. J. (2021). Proteinase Activated Receptors Mediate the Trypsin-Induced Ca2 + Signaling in Human Uterine Epithelial Cells. Frontiers in Cell and Developmental Biology, 9.


Stringer, R. N., Jurkovicova-Tarabova, B., Souza, I. A., Ibrahim, J., Vacik, T., Fathalla, W. M., . . . Weiss, N. (2021). De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy. Molecular Brain, 14(1).