Πρωτεύουσες καρτέλες
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Association of Gene Polymorphism rs3027898 With Papillary Cancer Restricted to the Thyroid Gland: A Pilot Study..
In Vivo. 33(6), 2281-2285.
(2019).
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome..
Hum Mol Genet. 28(15), 2531-2548.
(2019).
Association of NFKB1 -94ATTG ins/del polymorphism (rs28362491) with pemphigus vulgaris..
Exp Dermatol. 28(8), 972-975.
(2019).
MicroRNA-related polymorphisms in pseudoexfoliation syndrome, pseudoexfoliative glaucoma, and primary open-angle glaucoma..
Ophthalmic Genet. 39(5), 603-609.
(2018).
An Extensive Study of the Functional Polymorphisms of Kinin-Kallikrein System in Rheumatoid Arthritis Susceptibility..
Arch Rheumatol. 33(1), 33-38.
(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).
Evidence of ERBB3 gene association with rheumatoid arthritis predisposition..
Int J Rheum Dis. 19(2), 146-9.
(2016).
Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients..
Cardiol Young. 25(4), 681-3.
(2015).
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome..
Nat Genet. 47(4), 387-92.
(2015).
Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome..
Nat Genet. 47(6), 689.
(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).
Molecular and Clinical Investigation of Cystinuria in the Greek-Cypriot Population..
Genet Test Mol Biomarkers. 19(11), 641-5.
(2015).
Lack of association of the autophagy-related gene polymorphism ATG16L1 rs2241880 in RA predisposition..
Rheumatol Int. 34(4), 477-9.
(2014).
Lack of association of the GSDMB gene at locus 17q12 with predisposition to rheumatoid arthritis..
Clin Exp Rheumatol. 32(3), 447.
(2014).
Role of 9p21 and 2q36 variants and arterial stiffness in the prediction of coronary artery disease..
Eur J Clin Invest. 44(8), 784-94.
(2014).
Non-HLA genes in ankylosing spondylitis: what meta-analyses have shown?.
Clin Exp Rheumatol. 32(5), 735-9.
(2014).
Genetic analysis of the human Insulin-like 3 gene: absence of mutations in a Greek paediatric cohort with testicular maldescent..
Andrologia. 46(9), 986-96.
(2014).
Validation of the TAGAP rs212389 polymorphism in rheumatoid arthritis susceptibility..
Joint Bone Spine. 80(5), 543-4.
(2013).
Genetics in rheumatoid arthritis beyond HLA genes: what meta-analyses have shown?.
Semin Arthritis Rheum. 43(1), 29-38.
(2013).
Novel human pathological mutations. Gene symbol: SLC3A1. Disease: Cystinuria..
Hum Genet. 126(2), 335.
(2009).