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 Gene Frequency  [Clear All Filters]
2019
Dardiotis, E., Aloizou A-M., Siokas V., Tsouris Z., Rikos D., Marogianni C., et al. (2019).  Paraoxonase-1 genetic polymorphisms in organophosphate metabolism.. Toxicology. 411, 24-31.
Karananou, P., Tramma D., Katafigiotis S., Alataki A., Lambropoulos A., & Papadopoulou-Alataki E. (2019).  The Role of TLR4 Asp299Gly and TLR4 Thr399Ile Polymorphisms in the Pathogenesis of Urinary Tract Infections: First Evaluation in Infants and Children of Greek Origin.. J Immunol Res. 2019, 6503832.
2018
Theodoridou, S., Vyzantiadis T-A., & Vlachaki E. (2018).  Compound Heterozygosity for Silent Cap +1570 (T>C) (HBB: c*96T>C), Codon 39 (C>T) (HBB: c.118C>T) and the Presence of ααα/αα in Greece. A Case Presentation.. Hemoglobin. 42(3), 194-195.
Stefanidis, I., Tziastoudi M., Tsironi E. E., Dardiotis E., Tachmitzi S. V., Fotiadou A., et al. (2018).  The contribution of genetic variants of SLC2A1 gene in T2DM and T2DM-nephropathy: association study and meta-analysis.. Ren Fail. 40(1), 561-576.
Bouziana, S. D., Tziomalos K., Goulas A., Vyzantiadis T-A., Panderi A., & Ηatzitolios A. Ι. (2018).  Major Adipokines and the -420C>G Resistin Gene Polymorphism as Predictors of Acute Ischemic Stroke Severity and In-Hospital Outcome.. J Stroke Cerebrovasc Dis. 27(4), 963-970.
Tsolaki, A. C., Gatzima O., Daniilidou M., Lazarou E., Bamidis P. D., Verykouki E., et al. (2018).  Prevalence of Apolipoprotein E Polymorphisms in Alzheimer's Disease, Mild Cognitive Impairment, and Healthy Elderly: A Northern Greece Study.. Neurodegener Dis. 18(4), 216-224.
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.
2017
Dardiotis, E., Siokas V., Zafeiridis T., Paterakis K., Tsivgoulis G., Dardioti M., et al. (2017).  Integrins AV and B8 Gene Polymorphisms and Risk for Intracerebral Hemorrhage in Greek and Polish Populations.. Neuromolecular Med. 19(1), 69-80.
Alexander, J., Mantzaris D., Georgitsi M., Drineas P., & Paschou P. (2017).  Variant Ranker: a web-tool to rank genomic data according to functional significance.. BMC Bioinformatics. 18(1), 341.
Zervou, M. I., Dimopoulou D. G., Eliopoulos E., Trachana M., Pratsidou-Gkertsi P., Andreou A., et al. (2017).  Τhe genetics of juvenile idiopathic arthritis: Searching for new susceptibility loci.. Mol Med Rep. 16(6), 8793-8798.
2016
Goulielmos, G. N., Chiaroni-Clarke R. C., Dimopoulou D. G., Zervou M. I., Trachana M., Pratsidou-Gertsi P., et al. (2016).  Association of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population.. Pediatr Rheumatol Online J. 14(1), 25.
Gbandi, E., Goulas A., Sevastianos V., Hadziyannis S., Panderi A., Koskinas J., et al. (2016).  Common ABCB1 polymorphisms in Greek patients with chronic hepatitis C infection: A comparison with hyperlipidemic patients and the general population.. Pharmacol Rep. 68(2), 476-82.
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.
Papasavva, T., Martin P., Legler T. J., Liasides M., Anastasiou G., Christofides A., et al. (2016).  Prevalence of RhD status and clinical application of non-invasive prenatal determination of fetal RHD in maternal plasma: a 5 year experience in Cyprus.. BMC Res Notes. 9, 198.
2015
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.
2014
Gkampeta, A., Fidani L., Clarimón J., Kalinderi K., Katopodi T., Zafeiriou D., et al. (2014).  Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population.. Epilepsy Res. 108(10), 1734-9.
Gharahkhani, P., Burdon K. P., Fogarty R., Sharma S., Hewitt A. W., Martin S., et al. (2014).  Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma.. Nat Genet. 46(10), 1120-1125.
Papadopoulos, P., Viennas E., Gkantouna V., Pavlidis C., Bartsakoulia M., Ioannou Z-M., et al. (2014).  Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies.. Nucleic Acids Res. 42(Database issue), D1020-6.
Panoutsopoulou, K., Hatzikotoulas K., Xifara D. Kiara, Colonna V., Farmaki A-E., Ritchie G. R. S., et al. (2014).  Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants.. Nat Commun. 5, 5345.
Chatzikyriakidou, A., Voulgari P. V., & Drosos A. A. (2014).  Lack of association of the autophagy-related gene polymorphism ATG16L1 rs2241880 in RA predisposition.. Rheumatol Int. 34(4), 477-9.
Ballantyne, K. N., Ralf A., Aboukhalid R., Achakzai N. M., Anjos M. J., Ayub Q., et al. (2014).  Toward male individualization with rapidly mutating y-chromosomal short tandem repeats.. Hum Mutat. 35(8), 1021-32.
2013
Doudouliaki, T., Haidopoulou K., Pappa S., Sakellaropoulou A., Tsakiridis P., Emboriadou M., et al. (2013).  Association of the RANTES gene promoter polymorphisms -28C/G and -403G/A with pneumonia in Greek children.. Int J Immunopathol Pharmacol. 26(3), 681-90.
Papagianni, A., Economou M., Tragiannidis A., Karatza E., Samarah F., Gombakis N., et al. (2013).  FcγRIIa and FcγRIIIa polymorphisms in childhood primary immune thrombocytopenia: implications for disease pathogenesis and outcome.. Blood Coagul Fibrinolysis. 24(1), 35-9.
Georgitsi, M., & Patrinos G. P. (2013).  Genetic databases in pharmacogenomics: the Frequency of Inherited Disorders Database (FINDbase).. Methods Mol Biol. 1015, 321-36.
Giza, S., Goulas A., Gbandi E., Effraimidou S., Papadopoulou-Alataki E., Eboriadou M., et al. (2013).  The role of PTPN22 C1858T gene polymorphism in diabetes mellitus type 1: first evaluation in Greek children and adolescents.. Biomed Res Int. 2013, 721604.

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