Πρωτεύουσες καρτέλες
Ο κατάλογος των δημοσιεύσεων είναι ενδεικτικός και μπορεί να μην περιλαμβάνει το σύνολο των δημοσιεύσεων.
The Polygenic Nature and Complex Genetic Architecture of Specific Learning Disorder..
Brain Sci. 11(5),
(2021).
Myasthenia gravis genome-wide association study implicates AGRN as a risk locus..
J Med Genet.
(2021).
Variants in clock genes could be associated with lower risk of type 2 diabetes in an elderly Greek population..
Maturitas. 152, 20-25.
(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.
(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).
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).
Assessment of association between lipoxygenase genes variants in elderly Greek population and type 2 diabetes mellitus..
Diab Vasc Dis Res. 15(4), 340-343.
(2018).
Variant Ranker: a web-tool to rank genomic data according to functional significance..
BMC Bioinformatics. 18(1), 341.
(2017).
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology..
Front Neurosci. 10, 428.
(2016).
Meta-Analysis of Tourette Syndrome and Attention Deficit Hyperactivity Disorder Provides Support for a Shared Genetic Basis..
Front Neurosci. 10, 340.
(2016).
The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery..
Front Neurosci. 10, 351.
(2016).
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.
(2014).
Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin..
Ann Hematol. 92(1), 53-8.
(2013).
Genomic variation in the MAP3K5 gene is associated with β-thalassemia disease severity and hydroxyurea treatment efficacy..
Pharmacogenomics. 14(5), 469-83.
(2013).
Genetic databases in pharmacogenomics: the Frequency of Inherited Disorders Database (FINDbase)..
Methods Mol Biol. 1015, 321-36.
(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).
Population-specific documentation of pharmacogenomic markers and their allelic frequencies in FINDbase..
Pharmacogenomics. 12(1), 49-58.
(2011).
FINDbase: a worldwide database for genetic variation allele frequencies updated..
Nucleic Acids Res. 39(Database issue), D926-32.
(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).