Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
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Συντάκτης Τίτλος Τύπος [ Έτος] Φίλτρα: Συντάκτης is Georgitsi, Marianthi [Clear All Filters]
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.
(2021). Clinical Profiles and Socio-Demographic Characteristics of Adults with Specific Learning Disorder in Northern Greece..
Brain Sci. 11(5),
(2021).
(2021).
(2021).
(2021). Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population..
J Steroid Biochem Mol Biol. 198, 105549.
(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.
(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.
(2020). 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.
(2019). Neuropathology-driven Whole-genome Sequencing Study Points to Novel Candidate Genes for Healthy Brain Aging..
Alzheimer Dis Assoc Disord. 33(1), 7-14.
(2019). Association of ALOX12 gene polymorphism with all-cause and cardiovascular mortality in diabetic nephropathy..
Int Urol Nephrol. 50(2), 321-329.
(2018). Variant Ranker: a web-tool to rank genomic data according to functional significance..
BMC Bioinformatics. 18(1), 341.
(2017). The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery..
Front Neurosci. 10, 351.
(2016).
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(2014).
Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin..
Ann Hematol. 92(1), 53-8.
(2013). Genetic databases in pharmacogenomics: the Frequency of Inherited Disorders Database (FINDbase)..
Methods Mol Biol. 1015, 321-36.
(2013). Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy..
Pharmacogenomics. 14(5), 469-83.
(2013). Genetics of myasthenia gravis: a case-control association study in the Hellenic population..
Clin Dev Immunol. 2012, 484919.
(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.
(2012). FINDbase: a worldwide database for genetic variation allele frequencies updated..
Nucleic Acids Res. 39(Database issue), D926-32.
(2011). Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase..
Pharmacogenomics. 12(1), 49-58.
(2011). Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach..
Nat Genet. 43(4), 295-301.
(2011). Transcriptional regulation and pharmacogenomics..
Pharmacogenomics. 12(5), 655-73.
(2011).