Δημοσιεύσεις

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

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Pavlidou, E., Daponte A., Egea R., Dardiotis E., Hadjigeorgiou G. M., Barbadilla A., et al. (2016).  Genetic polymorphisms of FAS and EVER genes in a Greek population and their susceptibility to cervical cancer: a case control study.. BMC Cancer. 16(1), 923.
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.
Borg, J., Georgitsi M., Aleporou-Marinou V., Kollia P., & Patrinos G. P. (2009).  Genetic recombination as a major cause of mutagenesis in the human globin gene clusters.. Clin Biochem. 42(18), 1839-50.
Lipska, B. S., Iatropoulos P., Maranta R., Caridi G., Ozaltin F., Anarat A., et al. (2013).  Genetic screening in adolescents with steroid-resistant nephrotic syndrome.. Kidney Int. 84(1), 206-13.
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.
Tapper, W., Jones A. V., Kralovics R., Harutyunyan A. S., Zoi K., Leung W., et al. (2015).  Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms.. Nat Commun. 6, 6691.
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., 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.
Dimitroulas, T., Hodson J., Panoulas V. F., Sandoo A., Smith J., & Kitas G. (2017).  Genetic variations in the alanine-glyoxylate aminotransferase 2 (AGXT2) gene and dimethylarginines levels in rheumatoid arthritis.. Amino Acids. 49(6), 1133-1141.
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.
Gkouskou, K. K., Grammatikopoulou M. G., Lazou E., Sanoudou D., Goulis D. G., & Eliopoulos A. G. (2022).  Genetically-Guided Medical Nutrition Therapy in Type 2 Diabetes Mellitus and Pre-diabetes: A Series of -of-1 Superiority Trials.. Front Nutr. 9, 772243.
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., Voulgari P. V., Lambropoulos A., & Drosos A. A. (2013).  Genetics in rheumatoid arthritis beyond HLA genes: what meta-analyses have shown?. Semin Arthritis Rheum. 43(1), 29-38.
Deiana, D., Gessa S., Anardu M., Daniilidis A., Nappi L., D'Alterio M. N., et al. (2019).  Genetics of endometriosis: a comprehensive review.. Gynecol Endocrinol. 35(7), 553-558.
Zagoriti, Z., Georgitsi M., Giannakopoulou O., Ntellos F., Tzartos S. J., Patrinos G. P., et al. (2012).  Genetics of myasthenia gravis: a case-control association study in the Hellenic population.. Clin Dev Immunol. 2012, 484919.
Prapas, N., Karkanaki A., Prapas I., Kalogiannidis I., Katsikis I., & Panidis D. (2009).  Genetics of polycystic ovary syndrome.. Hippokratia. 13(4), 216-23.
Kaplan, A. G., Abdelshehid C. S., Alipanah N., Zamansani T., Lee J., Kolla S. B., et al. (2012).  Genitourinary exam skills training curriculum for medical students: a follow-up study of comfort and skill utilization.. J Endourol. 26(10), 1350-5.
Mili, N., Paschou S. A., Armeni A., Georgopoulos N., Goulis D. G., & Lambrinoudaki I. (2021).  Genitourinary syndrome of menopause: a systematic review on prevalence and treatment.. Menopause. 28(6), 706-716.
Bailey, J. N. Cooke, Loomis S. J., Kang J. H., R Allingham R., Gharahkhani P., Khor C. Chuen, et al. (2016).  Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.. Nat Genet. 48(2), 189-94.
Purrington, K. S., Slager S., Eccles D., Yannoukakos D., Fasching P. A., Miron P., et al. (2014).  Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.. Carcinogenesis. 35(5), 1012-9.
Harold, D., Abraham R., Hollingworth P., Sims R., Gerrish A., Hamshere M. L., et al. (2009).  Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.. Nat Genet. 41(10), 1088-93.
Blue Mountains Eye Study (BMES), Wellcome Trust Case Control Consortium 2 (WTCCC2) (2013).  Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus.. Hum Mol Genet. 22(22), 4653-60.
Furney, S. J., Simmons A., Breen G., Pedroso I., Lunnon K., Proitsi P., et al. (2011).  Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.. Mol Psychiatry. 16(11), 1130-8.
Konstantinidis, K., Tebbe A., Klein C., Scheffer B., Aivaliotis M., Bisle B., et al. (2007).  Genome-Wide Proteomics of Natronomonas pharaonis Genome-Wide Proteomics of Natronomonas pharaonis. Journal of Proteome Research. 6(1), 185 - 193.
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.

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