Δημοσιεύσεις

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

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Journal Article
Tsekmekidou, X., Tsetsos F., Koufakis T., Karras S. N., Georgitsi M., Papanas N., et al. (2020).  Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population.. J Steroid Biochem Mol Biol. 198, 105549.
Roumeliotis, A. K., Roumeliotis S. K., Panagoutsos S. A., Tsetsos F., Georgitsi M., Manolopoulos V., et al. (2018).  Association of ALOX12 gene polymorphism with all-cause and cardiovascular mortality in diabetic nephropathy.. Int Urol Nephrol. 50(2), 321-329.
Roumeliotis, S., Roumeliotis A., Stamou A., Panagoutsos S., Manolopoulos V. G., Tsetsos F., et al. (2021).  Association of rs11780592 Polymorphism in the Human Soluble Epoxide Hydrolase Gene (EPHX2) with Oxidized LDL and Mortality in Patients with Diabetic Chronic Kidney Disease.. Oxid Med Cell Longev. 2021, 8817502.
Tsetsos, F., Roumeliotis A., Tsekmekidou X., Alexouda S., Roumeliotis S., Theodoridis M., et al. (2020).  Genetic variation in CARD8, a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus. Diabetes and Vascular Disease Research. 17(6), 147916412097089.
Tsetsos, F., Roumeliotis A., Tsekmekidou X., Alexouda S., Roumeliotis S., Theodoridis M., et al. (2020).  Genetic variation in CARD8, a gene coding for an NLRP3 inflammasome-associated protein, alters the genetic risk for diabetic nephropathy in the context of type 2 diabetes mellitus. Diab Vasc Dis Res. 17(6), 1479164120970892.
Tsetsos, F., Padmanabhuni S. S., Alexander J., Karagiannidis I., Tsifintaris M., Topaloudi A., et al. (2016).  Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis.. Front Neurosci. 10, 340.
Topaloudi, A., Zagoriti Z., Flint A. Camille, Martinez M. Belle, Yang Z., Tsetsos F., et al. (2021).  Myasthenia gravis genome-wide association study implicates AGRN as a risk locus.. J Med Genet.
Alexander, J., Potamianou H., Xing J., Deng L., Karagiannidis I., Tsetsos F., et al. (2016).  Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology.. Front Neurosci. 10, 428.
Tsekmekidou, X., Tsetsos F., Koufakis T., Georgitsi M., Papanas N., Papazoglou D., et al. (2021).  Variants in clock genes could be associated with lower risk of type 2 diabetes in an elderly Greek population.. Maturitas. 152, 20-25.

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Τμήμα Ιατρικής, Πανεπιστημιούπολη ΑΠΘ, T.K. 54124, Θεσσαλονίκη
 

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