Δημοσιεύσεις

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

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Φίλτρα: Συντάκτης is Georgitsi, Marianthi  [Clear All Filters]
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A
Jennings, J. E., Georgitsi M., Holdaway I., Daly A. F., Tichomirowa M., Beckers A., et al. (2009).  Aggressive pituitary adenomas occurring in young patients in a large Polynesian kindred with a germline R271W mutation in the AIP gene.. Eur J Endocrinol. 161(5), 799-804.
Georgitsi, M., De Menis E., Cannavò S., Mäkinen M. J., Tuppurainen K., Pauletto P., et al. (2008).  Aryl hydrocarbon receptor interacting protein (AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas.. Clin Endocrinol (Oxf). 69(4), 621-7.
Tsekmekidou, X., Tsetsos F., Koufakis T., Karras S. N., Georgitsi M., Papanas N., et al. (2020).  Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population.. J Steroid Biochem Mol Biol. 198, 105549.
Roumeliotis, A. K., Roumeliotis S. K., Panagoutsos S. A., Tsetsos F., Georgitsi M., Manolopoulos V., et al. (2018).  Association of ALOX12 gene polymorphism with all-cause and cardiovascular mortality in diabetic nephropathy.. Int Urol Nephrol. 50(2), 321-329.
Roumeliotis, S., Roumeliotis A., Stamou A., Panagoutsos S., Manolopoulos V. G., Tsetsos F., et al. (2021).  Association of rs11780592 Polymorphism in the Human Soluble Epoxide Hydrolase Gene (EPHX2) with Oxidized LDL and Mortality in Patients with Diabetic Chronic Kidney Disease.. Oxid Med Cell Longev. 2021, 8817502.
C
Bonti, E., Giannoglou S., Georgitsi M., Sofologi M., Porfyri G-N., Mousioni A., et al. (2021).  Clinical Profiles and Socio-Demographic Characteristics of Adults with Specific Learning Disorder in Northern Greece.. Brain Sci. 11(5), 
E
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.
F
Georgitsi, M., Viennas E., Antoniou D. I., Gkantouna V., van Baal S., Petricoin E. F., et al. (2011).  FINDbase: a worldwide database for genetic variation allele frequencies updated.. Nucleic Acids Res. 39(Database issue), D926-32.
Radmilovic, M., Zukic B., Petrovic M. Stojiljkov, Bartsakoulia M., Stankovic B., Kotur N., et al. (2013).  Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin.. Ann Hematol. 92(1), 53-8.
G
Georgitsi, M., & Patrinos G. P. (2013).  Genetic databases in pharmacogenomics: the Frequency of Inherited Disorders Database (FINDbase).. Methods Mol Biol. 1015, 321-36.
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.
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.
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.
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.
Tafrali, C., Paizi A., Borg J., Radmilovic M., Bartsakoulia M., Giannopoulou E., et al. (2013).  Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy.. Pharmacogenomics. 14(5), 469-83.
Georgitsi, M., Raitila A., Karhu A., van der Luijt R. B., Aalfs C. M., Sane T., et al. (2007).  Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.. J Clin Endocrinol Metab. 92(8), 3321-5.
H
Borg, J., Papadopoulos P., Georgitsi M., Gutiérrez L., Grech G., Fanis P., et al. (2010).  Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.. Nat Genet. 42(9), 801-5.
K
Borg, J., Phylactides M., Bartsakoulia M., Tafrali C., Lederer C., Felice A. E., et al. (2012).  KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients.. Pharmacogenomics. 13(13), 1487-500.
L
Georgitsi, M., Heliövaara E., Paschke R., Kumar A. V. K., Tischkowitz M., Vierimaa O., et al. (2008).  Large genomic deletions in AIP in pituitary adenoma predisposition.. J Clin Endocrinol Metab. 93(10), 4146-51.
Niola, P., Gross J. A., Lopez J. Pablo, Chillotti C., Deiana V., Manchia M., et al. (2014).  Lithium-induced differential expression of SAT1 in suicide completers and controls is not correlated with polymorphisms in the promoter region of the gene.. Psychiatry Res. 220(3), 1167-8.
M
Georgitsi, M. (2010).  MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations.. Best Pract Res Clin Endocrinol Metab. 24(3), 425-37.
Tsetsos, F., Padmanabhuni S. S., Alexander J., Karagiannidis I., Tsifintaris M., Topaloudi A., et al. (2016).  Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis.. Front Neurosci. 10, 340.
Raitila, A., Lehtonen H. J., Arola J., Heliövaara E., Ahlsten M., Georgitsi M., et al. (2010).  Mice with inactivation of aryl hydrocarbon receptor-interacting protein (Aip) display complete penetrance of pituitary adenomas with aberrant ARNT expression.. Am J Pathol. 177(4), 1969-76.
Georgitsi, M., Raitila A., Karhu A., Tuppurainen K., Mäkinen M. J., Vierimaa O., et al. (2007).  Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations.. Proc Natl Acad Sci U S A. 104(10), 4101-5.

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