Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Export 56 results:
Συντάκτης Τίτλος Τύπος [ Έτος] Φίλτρα: Keyword is Gene Frequency [Clear All Filters]
Paraoxonase-1 genetic polymorphisms in organophosphate metabolism..
Toxicology. 411, 24-31.
(2019).
(2019). 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.
(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.
(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.
(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.
(2018). The role of IL‑16 gene polymorphisms in endometriosis..
Int J Mol Med. 41(3), 1469-1476.
(2018). Integrins AV and B8 Gene Polymorphisms and Risk for Intracerebral Hemorrhage in Greek and Polish Populations..
Neuromolecular Med. 19(1), 69-80.
(2017). Variant Ranker: a web-tool to rank genomic data according to functional significance..
BMC Bioinformatics. 18(1), 341.
(2017). Τhe genetics of juvenile idiopathic arthritis: Searching for new susceptibility loci..
Mol Med Rep. 16(6), 8793-8798.
(2017). Association of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population..
Pediatr Rheumatol Online J. 14(1), 25.
(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.
(2016).
(2016).
(2016).
(2015).
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.
(2014). Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma..
Nat Genet. 46(10), 1120-1125.
(2014). Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies..
Nucleic Acids Res. 42(Database issue), D1020-6.
(2014). Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants..
Nat Commun. 5, 5345.
(2014). Lack of association of the autophagy-related gene polymorphism ATG16L1 rs2241880 in RA predisposition..
Rheumatol Int. 34(4), 477-9.
(2014). Toward male individualization with rapidly mutating y-chromosomal short tandem repeats..
Hum Mutat. 35(8), 1021-32.
(2014). 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.
(2013). FcγRIIa and FcγRIIIa polymorphisms in childhood primary immune thrombocytopenia: implications for disease pathogenesis and outcome..
Blood Coagul Fibrinolysis. 24(1), 35-9.
(2013). Genetic databases in pharmacogenomics: the Frequency of Inherited Disorders Database (FINDbase)..
Methods Mol Biol. 1015, 321-36.
(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.
(2013).