Δημοσιεύσεις

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

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Συντάκτης Τίτλος Τύπος [ Έτος(Asc)]
Φίλτρα: Keyword is Polymorphism, Single Nucleotide  [Clear All Filters]
2022
Asteris, P. G., Gavriilaki E., Touloumenidou T., Koravou E-E., Koutra M., Papayanni P. Georgia, et al. (2022).  Genetic prediction of ICU hospitalization and mortality in COVID-19 patients using artificial neural networks.. J Cell Mol Med. 26(5), 1445-1455.
2021
Vizirianakis, I. S., Chatzopoulou F., Papazoglou A. S., Karagiannidis E., Sofidis G., Stalikas N., et al. (2021).  The GEnetic Syntax Score: a genetic risk assessment implementation tool grading the complexity of coronary artery disease-rationale and design of the GESS study.. BMC Cardiovasc Disord. 21(1), 284.
2020
Psoma, E., Koliou G-A., Dimitrakopoulos F-I., Papadopoulou K., Rontogianni D., Bobos M., et al. (2020).  Genetic Variations of Gene Are Associated With Infiltration of Adjacent Tissues and the Clinical Outcome of Patients With Nasopharyngeal Carcinoma.. Anticancer Res. 40(2), 677-688.
Karras, S. N., Koufakis T., Antonopoulou V., Goulis D. G., Alaylıoğlu M., Dursun E., et al. (2020).  Vitamin D receptor Fokl polymorphism is a determinant of both maternal and neonatal vitamin D concentrations at birth.. J Steroid Biochem Mol Biol. 199, 105568.
2019
Chatzikyriakidou, A., Chorti A., & Papavramidis T. (2019).  Association of Gene Polymorphism rs3027898 With Papillary Cancer Restricted to the Thyroid Gland: A Pilot Study.. In Vivo. 33(6), 2281-2285.
Strafella, C., Caputo V., Minozzi G., Milano F., Arcangeli M., Sobhy N., et al. (2019).  Atopic Eczema: Genetic Analysis of , , and in Mediterranean Populations.. Biomed Res Int. 2019, 3457898.
Sapalidis, K., Machairiotis N., Zarogoulidis P., Vasilakaki S., Sardeli C., Koimtzis G., et al. (2019).  Genes' Interactions: A Major Contributor to the Malignant Transformation of Endometriosis.. Int J Mol Sci. 20(8), 
Stratopoulos, A., Kolliopoulou A., Karamperis K., John A., Kydonopoulou K., Esftathiou G., et al. (2019).  Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients.. Pharmacogenomics. 20(11), 791-801.
Chatzopoulou, F., Gioula G., Kioumis I., Chatzidimitriou D., & Exindari M. (2019).  Identification of complement-related host genetic risk factors associated with influenza A(H1N1)pdm09 outcome: challenges ahead.. Med Microbiol Immunol. 208(5), 631-640.
Colijn, J. M., Hollander A. I. den, Demirkan A., Cougnard-Grégoire A., Verzijden T., Kersten E., et al. (2019).  Increased High-Density Lipoprotein Levels Associated with Age-Related Macular Degeneration: Evidence from the EYE-RISK and European Eye Epidemiology Consortia.. Ophthalmology. 126(3), 393-406.
Hadjigeorgiou, G. M., Kountra P-M., Koutsis G., Tsimourtou V., Siokas V., Dardioti M., et al. (2019).  Replication study of GWAS risk loci in Greek multiple sclerosis patients.. Neurol Sci. 40(2), 253-260.
Domvri, K., Porpodis K., Tzimagiorgis G., Chatzopoulou F., Kontakiotis T., Kyriazis G., et al. (2019).  Th2/Th17 cytokine profile in phenotyped Greek asthmatics and relationship to biomarkers of inflammation.. Respir Med. 151, 102-110.
2018
Papazisis, G., Goulas A., Sarrigiannidis A., Bargiota S., Antoniadis D., Raikos N., et al. (2018).  ABCB1 and CYP2D6 polymorphisms and treatment response of psychotic patients in a naturalistic setting.. Hum Psychopharmacol. 33(1), 
Goulielmos, G. N., Zervou M. I., Vazgiourakis V. M., Ghodke-Puranik Y., Garyfallos A., & Niewold T. B. (2018).  The genetics and molecular pathogenesis of systemic lupus erythematosus (SLE) in populations of different ancestry.. Gene. 668, 59-72.
Chatzikyriakidou, A., Founti P., Melidou A., Minti F., Bouras E., Anastasopoulos E., et al. (2018).  MicroRNA-related polymorphisms in pseudoexfoliation syndrome, pseudoexfoliative glaucoma, and primary open-angle glaucoma.. Ophthalmic Genet. 39(5), 603-609.
Katsarou, M-S., Papasavva M., Latsi R., Toliza I., Gkaros A-P., Papakonstantinou S., et al. (2018).  Population-Based Analysis of Cluster Headache-Associated Genetic Polymorphisms.. J Mol Neurosci. 65(3), 367-376.
Matalliotakis, M., Zervou M. I., Eliopoulos E., Matalliotaki C., Rahmioglu N., Kalogiannidis I., et al. (2018).  The role of IL‑16 gene polymorphisms in endometriosis.. Int J Mol Med. 41(3), 1469-1476.
Spoto, B., Ntounousi E., Testa A., Liakopoulos V., D'Arrigo G., Tripepi G., et al. (2018).  The sirtuin1 gene associates with left ventricular myocardial hypertrophy and remodeling in two chronic kidney disease cohorts: a longitudinal study.. J Hypertens. 36(8), 1705-1711.
2017
Goutzelas, Y., Kotsa K., Vasilopoulos Y., Tsekmekidou X., Stamatis C., Yovos J. G., et al. (2017).  Association analysis of FTO gene polymorphisms with obesity in Greek adults.. Gene. 613, 10-13.
Williams, K. M., Bentham G. C. G., Young I. S., McGinty A., McKay G. J., Hogg R., et al. (2017).  Association Between Myopia, Ultraviolet B Radiation Exposure, Serum Vitamin D Concentrations, and Genetic Polymorphisms in Vitamin D Metabolic Pathways in a Multicountry European Study.. JAMA Ophthalmol. 135(1), 47-53.
Tsitlakidis, D., Katopodi T., Goulis D. G., Papadimas I., & Kritis A. (2017).  Association of follicle-stimulating hormone receptor single nucleotide polymorphisms with fertility in Greek men.. J Endocrinol Invest. 40(7), 721-726.
Goulas, A., Agapakis D., Apostolidis A., Gouda D., Anastassiadis S., Trakatelli C., et al. (2017).  Association of the Common Catalase Gene Polymorphism rs1001179 With Glycated Hemoglobin and Plasma Lipids in Hyperlipidemic Patients.. Biochem Genet. 55(1), 77-86.
McKay, G. J., Young I. S., McGinty A., Bentham G. C. G., Chakravarthy U., Rahu M., et al. (2017).  Associations between Serum Vitamin D and Genetic Variants in Vitamin D Pathways and Age-Related Macular Degeneration in the European Eye Study.. Ophthalmology. 124(1), 90-96.
De Roeck, A., Van den Bossche T., van der Zee J., Verheijen J., De Coster W., Van Dongen J., et al. (2017).  Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease.. Acta Neuropathol. 134(3), 475-487.
Mendrinou, E., Patsatsi A., Zafiriou E., Papadopoulou D., Aggelou L., Sarri C., et al. (2017).  FCGR3A-V158F polymorphism is a disease-specific pharmacogenetic marker for the treatment of psoriasis with Fc-containing TNFα inhibitors.. Pharmacogenomics J. 17(3), 237-241.

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