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Publications

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

Export 126 results:
Author Title Type [ Year(Asc)]
Filters: Keyword is Genetic Predisposition to Disease  [Clear All Filters]
2021
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.
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.
Schrag, A., Martino D., Apter A., Ball J., Bartolini E., Benaroya-Milshtein N., et al. (2019).  European Multicentre Tics in Children Studies (EMTICS): protocol for two cohort studies to assess risk factors for tic onset and exacerbation in children and adolescents.. Eur Child Adolesc Psychiatry. 28(1), 91-109.
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.
Fountoulakis, K. N., Panagiotidis P., Kimiskidis V., Nimatoudis I., & Gonda X. (2019).  Neurological soft signs in familial and sporadic schizophrenia.. Psychiatry Res. 272, 222-229.
Stamou, M. I., Plummer L., Koika V., Galli-Tsinopoulou A., & Georgopoulos N. A. (2019).  A novel FGF8 mutation in a female patient with isolated congenital anosmia.. Hormones (Athens). 18(2), 241-244.
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.
Rikos, D., Siokas V., Aloizou A-M., Tsouris Z., Aslanidou P., Koutsis G., et al. (2019).  TREM2 R47H (rs75932628) variant is unlikely to contribute to Multiple Sclerosis susceptibility and severity in a large Greek MS cohort.. Mult Scler Relat Disord. 35, 116-118.
2018
Sarri, C. A., Papadopoulos G. E., Papa A., Tsakris A., Pervanidou D., Baka A., et al. (2018).  Amino acid signatures in the HLA class II peptide-binding region associated with protection/susceptibility to the severe West Nile Virus disease.. PLoS One. 13(10), e0205557.
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.
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.
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.
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.
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.
Kartanou, C., Karadima G., Koutsis G., Breza M., Papageorgiou S. G., Paraskevas G. P., et al. (2018).  Screening for the C9ORF72 repeat expansion in a greek frontotemporal dementia cohort.. Amyotroph Lateral Scler Frontotemporal Degener. 19(1-2), 152-154.
2017
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.
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.
Aung, T., Ozaki M., Lee M. Chin, Schlötzer-Schrehardt U., Thorleifsson G., Mizoguchi T., et al. (2017).  Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.. Nat Genet. 49(7), 993-1004.
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.
Sarri, C. A., Roussaki-Schulze A., Vasilopoulos Y., Zafiriou E., Patsatsi A., Stamatis C., et al. (2017).  Netherton Syndrome: A Genotype-Phenotype Review.. Mol Diagn Ther. 21(2), 137-152.

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