Δημοσιεύσεις

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

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Journal Article
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.
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.
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.
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.
Prapas, N., Karkanaki A., Prapas I., Kalogiannidis I., Katsikis I., & Panidis D. (2009).  Genetics of polycystic ovary syndrome.. Hippokratia. 13(4), 216-23.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Lazaridis, I., Mittnik A., Patterson N., Mallick S., Rohland N., Pfrengle S., et al. (2017).  Genetic origins of the Minoans and Mycenaeans.. Nature. 548(7666), 214-218.
Zarkavelis, G., Kotoula V., Kolliou G-A., Papadopoulou K., Tikas I., Karavasilis V., et al. (2019).  Genetic mapping of pancreatic cancer by targeted next-generation sequencing e. ESMO Open. 4(5), e000525.
Gavriilaki, E., Asteris P. G., Touloumenidou T., Koravou E-E., Koutra M., Papayanni P. Georgia, et al. (2021).  Genetic justification of severe COVID-19 using a rigorous algorithm.. Clin Immunol. 226, 108726.
Georgitsi, M., A Willsey J., Mathews C. A., State M., Scharf J. M., & Paschou P. (2016).  The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.. Front Neurosci. 10, 351.
Athyros, V. G., Tziomalos K., Karagiannis A., & Mikhailidis D. P. (2015).  Genetic, epidemiologic and clinical data strongly suggest that fasting or non-fasting triglycerides are independent cardiovascular risk factors.. Curr Med Res Opin. 31(3), 435-8.

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