Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Association of Gene Polymorphism rs3027898 With Papillary Cancer Restricted to the Thyroid Gland: A Pilot Study..
In Vivo. 33(6), 2281-2285.
(2019).
(2019). Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort..
Neurobiol Aging. 62, 245.e1-245.e7.
(2018).
(2018).
(2018). Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci..
Nat Genet. 49(7), 993-1004.
(2017). Netherton Syndrome: A Genotype-Phenotype Review..
Mol Diagn Ther. 21(2), 137-152.
(2017). Presence of the IVS-I-6-Mutated Allele in Beta-Thalassemia Major Patients Correlates with Extramedullary Hematopoiesis Incidence..
Acta Haematol. 137(3), 175-182.
(2017). Rare Variants in Juvenile Idiopathic Arthritis and Primary Antibody Deficiencies..
J Immunol Res. 2017, 1514294.
(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). 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.
(2016). Surfactant Protein A and B Gene Polymorphisms and Risk of Respiratory Distress Syndrome in Late-Preterm Neonates..
PLoS One. 11(11), e0166516.
(2016). Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients..
Cardiol Young. 25(4), 681-3.
(2015). Ethnicity-Based Differences in the Association of LOXL1 Polymorphisms with Pseudoexfoliation/Pseudoexfoliative Glaucoma: A Meta-Analysis..
Ann Hum Genet. 79(6), 431-50.
(2015).
(2015).
(2015). AQP4 tag single nucleotide polymorphisms in patients with traumatic brain injury..
J Neurotrauma. 31(23), 1920-6.
(2014). Assessment of Parkinson's disease risk loci in Greece..
Neurobiol Aging. 35(2), 442.e9-442.e16.
(2014). Association of LOXL1 polymorphisms with pseudoexfoliation, glaucoma, intraocular pressure, and systemic diseases in a Greek population. The Thessaloniki eye study..
Invest Ophthalmol Vis Sci. 55(7), 4238-43.
(2014). Toward male individualization with rapidly mutating y-chromosomal short tandem repeats..
Hum Mutat. 35(8), 1021-32.
(2014). FcγRIIa and FcγRIIIa polymorphisms in childhood primary immune thrombocytopenia: implications for disease pathogenesis and outcome..
Blood Coagul Fibrinolysis. 24(1), 35-9.
(2013). Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus..
Hum Mol Genet. 22(22), 4653-60.
(2013). An infant with ethylmalonic encephalopathy masquerading as a hematologic disorder..
J Child Neurol. 28(5), 668-71.
(2013).