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Curriculum Vitae

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Anthoula Chatzikyriakidou

Assistant Professor, School of Medicine

Personal Information

chatzikyra@auth.gr
Γνωστικό Αντικείμενο:
Ιατρική Βιολογία-Ιατρική Γενετική
Επιστημονική Ειδίκευση:
- Επιστήμη ζωής
- Βιολογία και βιοχημεία

Education

Προπτυχιακές Σπουδές

2000	Βιολογίας Βιολογίας Αριστοτέλειο Greece

Διδακτορικό Δίπλωμα

2004	Διδακτορικό Ιατρικής Ιωαννίνων Greece

Μετεκπαίδευση

5-10 Ιουλίου 2009: Μετεκπαίδευση στο Εργαστήριο Παθολογικής Ανατομικής – Μοριακής Ιστοπαθολογίας, Ιατρική Σχολή Πανεπιστημίου Θεσσαλίας

21 Ιουνίου - 2 Ιουλίου 2010: Μετεκπαίδευση στο Εργαστήριο Μοριακής και Ιατρικής Γενετικής, Ινστιτούτο Νευρολογίας και Γενετικής, Κύπρος.

Αύγουστος 2010: Μετεκπαίδευση στο Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, USA

Course Work

Courses of Winter semester of 2016–17 academic year

	ΤΜΗΜΑ ΙΑΤΡΙΚΗΣ
ΙΑ0273	Medical Biology

	ΤΜΗΜΑ ΟΔΟΝΤΙΑΤΡΙΚΗΣ
100102C	Medical Biology

Courses of Spring semester of 2016–17 academic year

	ΤΜΗΜΑ ΙΑΤΡΙΚΗΣ
ΙΑ0255	Genetics

	ΤΜΗΜΑ ΟΔΟΝΤΙΑΤΡΙΚΗΣ
100201C	Medical Genetics

Publications

2016

Chatzikyriakidou Anthoula, Voulgari PV, Drosos A (2016). Evidence of ERBB3 gene association with rheumatoid arthritis predisposition. International Journal of Rheumatic Diseases. vol. 19 no.2 p.146–149.

2015

Athanasiou Y, Voskarides K, Chatzikyriakidou Anthoula, Ignatiou A, Demosthenous P, Elia A, Zavros M, Georgiou I, Pierides A, Deltas C (2015). Molecular and clinical investigation of cystinuria in the Greek-Cypriot population. Genet Test Mol Biomarkers. vol. 19 no.11 p.641-5.
Aung T, Ozaki M, Mizoguchi T, Chatzikyriakidou Anthoula, Lambropoulos A, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH, May-Bolchakova I, et al (2015). A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics. vol.47 p. 387–392.
Chatzikyriakidou Anthoula, Aidinidou Louiza, Giannopoulos Andreas, Papadopoulou-Legmpelou Kyriaki, Kalinderi Kallirhoe, Fidani Liana (2015). Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients. Cardiology in the Young. vol.25 no.04 p.681-683.
Founti P, Haidich AB, Chatzikyriakidou Anthoula, Salonikiou A, Anastasopoulos E, Pappas Th, Lambropoulos A, Viswanathans A, Topouzis F (2015). Ethnic-based differences in the association of LOXL1 polymorphisms with pseudoexfoliation/pseudoexfoliative glaucoma: a meta-analysis. Annals of Human Genetics. vol. 79 no.6 p.431-50.

2014

Chatzikyriakidou Anthoula, Voulgari PV, Drosos A (2014). Non-HLA genes in ankylosing spondylitis: what meta-analyses have shown?. Clinical and Experimental Rheumatology.
Chatzikyriakidou Anthoula, Voulgari PV, Drosos A (2014). Lack of association of the GSDMB gene at locus 17q12 with predisposition to rheumatoid arthritis. Clin Exp Rheumatol. vol. 32 no. 3.
Chatzikyriakidou Anthoula, Voulgari P.V, Drosos A. A (2014). Lack of association of the autophagy-related gene polymorphism ATG16L1 rs2241880 in RA predisposition. Rheumatology International. Vol. 34 no. 4 p. 477-479.
Mamoulakis C, Georgiou I, Dimitriadis F, Tsounapi P, Giannakis I, Chatzikyriakidou Anthoula, Antypas S, Sofras F, Takenaka A, Sofikitis N (2014). Genetic analysis of the human Insulin-like 3 gene: absence of mutations in a Greek paediatric cohort with testicular maldescent. Andrologia. vol. 46 no.9 p. 986-96.
Vakalis A, Bechlioulis A, Naka KK, Chatzikyriakidou Anthoula, Gartzonika K, Vezyraki P, Kolios George, Pappas K, Katsouras CS, Georgiou I, Michalis LK (2014). Role of 9p21 and 2q36 variants and arterial stiffness in the prediction of coronary artery disease. European Journal of Clinical Investigation. vol. 44 no. 8 p.784-794.

2013

Chatzikyriakidou Anthoula, Voulgari P.V, Lambropoulos A, Georgiou I, Drosos A. A (2013). Validation of the TAGAP rs212389 polymorphism in rheumatoid arthritis susceptibility. Joint Bone Spine. Vol. 80 no.5 p. 543-544.
Chatzikyriakidou Anthoula, Markoula S, Kyritsis A.P, Georgiou I (2013). Evidence for association of a polymorphism in the 3´-UTR of IL-1R-Associated Kinase (IRAK1) with ischemic stroke. Neurology Asia. Vol. 18 no. 1 p. 123.
Chatzikyriakidou Anthoula, Voulgari P.V, Lambropoulos A, Drosos A. A (2013). Genetics in rheumatoid arthritis beyond HLA-genes: What meta-analyses have shown?. Seminars in Arthritis and Rheumatism. Vol. 43 no. 1 p. 29-38.
Chatzikyriakidou Anthoula, Voulgari P.V, Georgiou I, Drosos A. A (2013). Altered sequence of the ETS1 transcription factor may predispose to rheumatoid arthritis susceptibility. Scandinavian Journal of Rheumatology. Vol. 42 no. 11 p. 11-14.

2012

Bechlioulis A, Naka K.K, Kalantaridou S. N, Chatzikyriakidou Anthoula, Papanikolaou O, Kaponis A, Vakalis K.V, Vezyraki P, Gartzonika K, Mavridis A, Georgiou I, et al (2012). Short-term hormone therapy improves sCD40L and endothelial function in early menopausal women: Potential role of estrogen receptor polymorphisms. Maturitas. Vol. 71 no. 4 p. 389–395.
Chatzikyriakidou Anthoula, Voulgari P.V, Georgiou I, Drosos A. A (2012). miRNAs and related polymorphisms in rheumatoid arthritis susceptibility. Autoimmunity Reviews. Vol. 11 no. 9 p. 636–641.
Eggermann T, Zerres K, Nunes V, Font-Llitjós M, Bisceglia L, Chatzikyriakidou Anthoula, Strologo L.D, Pras E, Creemers J, Palacin M (2012). Clinical utility gene card for: Cystinuria. European Journal of Human Genetics. Vol. 20 no. 2.
Lazaros Leandros A, Xita N.V, Chatzikyriakidou Anthoula, Kaponis A, Grigoriadis N.G, Hatzi E.G, Grigoriadis I.G, Sofikitis N, Zikopoulos K.A, Georgiou I (2012). Association of TNF{alpha}, TNFR1 and TNFR2 polymorphisms with sperm concentration and motility. Journal of Andrology. Vol. 33 no.1 p. 74–80.
Mamoulakis C, Sofikitis N, Tsounapi P, Vlachopoulou E, Chatzikyriakidou Anthoula, Antypas S, Tzortzakakis D, Sofras F, Takenaka A, Georgiou I (2012). The (TAAAA)(n) polymorphism of sex hormone-binding globulin gene is not associated with testicular maldescent. Andrologia. Vol. 45 no. 1 p. 40-45.

2011

Chatzikyriakidou Anthoula, Voulgari P.V, Georgiou I, Drosos A. A (2011). Identification of the semaphorin receptor Plexin-A2 as a candidate gene for susceptibility to ankylosing spondylitis. Clinical and Experimental Rheumatology. Vol. 29 no. 5 p. 894.
Chatzikyriakidou Anthoula, Voulgari P.V, Drosos A. A (2011). What is the role of HLA-B27 in spondyloarthropathies?. Autoimmunity Reviews. Vol. 10 no. 8 p. 464–468.

2010

Bechlioulis A, Kalantaridou S.N, Naka K.K, Chatzikyriakidou Anthoula, Calis K.A, Makrigiannakis A, Papanikolaou O, Kaponis A, Katsouras Ch, Georgiou I, Chrousos G.P, et al (2010). Endothelial function, but not carotid intima-media thickness, is affected early in menopause and is associated with severity of hot flushes. Journal of Clinical Endocrinology and Metabolism. Vol. 95 no. 3 p. 1199-206.
Chatzikyriakidou Anthoula, Voulgari P.V, Georgiou I, Drosos A. A (2010). A polymorphism in the 3´-UTR of interleukin-1 receptor-associated kinase (IRAK1), a target gene of miR-146a, is associated with rheumatoid arthritis susceptibility. Joint Bone Spine. Vol. 77 no. 5 p. 411-413.
Chatzikyriakidou Anthoula, Voulgari P.V, Georgiou I, Drosos A. A (2010). The role of microRNA-146a (miR-146a) and its target IL-1R-associated kinase (IRAK1) in psoriatic arthritis susceptibility. Scandinavian Journal of Immunology. Vol. 71 no. 5 p. 382–385.
Nikolaou K, Kalatzis F.G, Giannakeas N, Markoula S, Chatzikyriakidou Anthoula, Georgiou I, Fotiadis D.I (2010). Polymerase chain reaction (PCR) and sequence specific oligonucleotide probes (SSOP) genotyping assay for detection of genes associated with rheumatoid arthritis and multiple sclerosis. Engineering in Medicine and Biology Society (EMBC), 2010 Annual International Conference of the IEEE. p. 6202 - 6205.
Xita N, Chatzikyriakidou Anthoula, Stavrou I, Zois C, Georgiou I, Tsatsoulis A (2010). The (TTTA)n polymorphism of aromatase (CYP19) gene is associated with age at menarche. Hum Reprod. Vol. 25 no. 12 p. 3129-3133.

2009

Chatzikyriakidou Anthoula, Kollios K.D, Georgiou I (2009). Novel Human Pathological Mutations: Symbol: SLC3A1, Disease: Cystinuria. Human Genetics. Vol. 126 no. 2 p. 335.
Chatzikyriakidou Anthoula, Georgiou I, Voulgari P.V, Drosos A. A (2009). The role of tumor necrosis factor-α (TNF-a) and TNF receptor polymorphisms in susceptibility of ankylosing spondylitis. Clinical and Experimental Rheumatology. Vol. 27 no. 4 p. 645-648.

2008

Chatzikyriakidou Anthoula, Georgiou I, Voulgari P.V, Georgiadis A.N, Argyriou E.S, Drosos A. A (2008). Glucocorticoid receptor variants may predispose to rheumatoid arthritis susceptibility. Scandinavian Journal of Rheumatology. Vol. 38 no. 1 p. 1-5.
Chatzikyriakidou Anthoula, Louizou E, Dedousis G.V.Z, Bisceglia L, Michelakakis H, Georgiou I (2008). An overview of SLC3A1 and SLC7A9 mutations in Greek cystinuria patients. Molecular Genetics and Metabolism. Vol. 95 no. 3 p. 192-193.
Chatzikyriakidou Anthoula, Vakalis K.V, Kolaitis N, Kolios G, Naka K.N, Michalis L.K, Georgiou I (2008). Distinct association of SLC19A1 polymorphism –43T>C with red cell folate levels and of MTHFR polymorphism 677C>T with plasma folate levels. Clinical Biochemistry. Vol. 41 no. 3 p. 174–176.

2007

Chatzikyriakidou Anthoula, Georgiou I, Voulgari P.V, Papadopoulos C.G, Tzavaras T, Drosos A. A (2007). Transcription regulatory polymorphism -43T and in the 5′-flanking region of SLC19A1 gene could affect rheumatoid arthritis patient response to methotrexate therapy. Rheumatology International. Vol. 27 no. 11 p. 1057-1061.
Chatzikyriakidou Anthoula, Georgiou I, Voulgari P.V, Venetsanopoulou A, Drosos A. A (2007). Combined TNF-a and TNFR genotypes could predict RA patient response to anti-TNF-a therapy and explain controversies of studies based on a single polymorphism. Rheumatology. Vol. 46 no. 6 p. 1034-1035.
Tzovaras V, Chatzikyriakidou Anthoula, Bairaktari E, Liberopoulos E.N, Georgiou I, Elisaf M (2007). Absence of SLC22A12 gene mutations in Greek Caucasian patients with primary renal hypouricaemia. Scandinavian Journal of Clinical and Laboratory Investigation. Vol. 67 no. 6 p. 589-595.

2006

Bourantas L.K, Chatzikyriakidou Anthoula, Dasoula A, Syrrou M, Bourantas K.L, Georgiou I (2006). Absence of mutations of the EPO-receptor gene in Greek patients with familiar polycythemia. European Journal of Haematology. Vol. 76 no. 6 p. 537–538.
Chatzikyriakidou Anthoula, Sofikitis N, Kalfakakou V, Siamopoulos K, Georgiou I (2006). Evidence for association of SLC7A9 gene haplotypes with cystinuria manifestation in SLC7A9 mutation carriers. Urological Research. Vol. 34 no. 5 p. 299-303.
Stavrou I, Zois C, Chatzikyriakidou Anthoula, Georgiou I, Tsatsoulis A (2006). Combined estrogen receptor α and estrogen receptor β genotypes influence the age of menarche. Human Reproduction. Vol. 21 no. 2 p. 554–557.

2005

Chatzikyriakidou Anthoula, Yapijakis C, Sofikitis N, Vassilopoulos D, Georgiou I (2005). Real-Time PCR analysis of trinucleotide repeat allele expansions in the androgen receptor gene. Molecular Diagnosis. Vol. 9 no. 4 p. 217-219.
Chatzikyriakidou Anthoula, Sofikitis N, Georgiou I (2005). Identification of novel cystinuria mutations and polymorphisms in SLC3A1 and SLC7A9 genes: Absence of SLC7A10 gene mutations in cystinuric patients. Genetic Test. Vol. 9 no. 3 p. 175-184.
Chatzikyriakidou Anthoula, Sofikitis N, Georgiou I (2005). Human Gene Mutations: Symbol: SLC3A1, Disease: Cystinuria. Human Genetics. vol. 116 no. 6 p. 543.
Xita N, Georgiou I, Chatzikyriakidou Anthoula, Vounatsou M, Papassotiriou G.P, Papassotiriou I, Tsatsoulis A (2005). Effect of Adiponectin Gene Polymorphisms on Circulating Adiponectin and Insulin Resistance Indexes in women with Polycystic Ovary Syndrome. Clinical Chemistry. vol. 51 no. 2 p. 416-423.

2004

Chatzikyriakidou Anthoula, Sofikitis Nikolaos, Georgiou Ioannis (2004). Human Gene Mutations: Gene Symbol: SLC3A1, SLC7A9 Disease: Cystinuria. Human Genetics. Vol. 116 no. 6 p. 543.
Robino C, Varacalli S, Gino Sarah, Chatzikyriakidou Anthoula, Kouvatsi A, Triantaphyllidis C, Di Gaetano C, Crobu F, Matullo G, Piazza A, Torre C (2004). Y-chromosomal STR haplotypes in a population sample from continental Greece, and the islands of Crete and Chios. Forensic Science International. Vol. 145 no. 1 p. 61–64.

2003

Xita Nektaria, Tsatsoulis Agathocles, Chatzikyriakidou Anthoula, Georgiou Ioannis (2003). Association of the (TAAAA)n repeat polymorphism in the sex hormone-binding globulin (SHBG) gene with the polycystic ovary syndrome and relation to SHBG serum levels. The Journal of Clinical Endocrinology & Metabolism. Vol. 88 no. 12 p. 5976-5980.

2002

Sofikitis Nikolaos, Yianakis D, Chatzikyriakidou Anthoula, Baltoyiannis D, Tsabalas S, Tasos A, Georgiou Ioannis, Schradr M, Yamamoto Y, Miyagawa I, Giannakopoulos X (2002). Meiosis and Kleinefelter’s syndrome. Human Reproduction. Vol. 17 no. 11 p. 3006-3007.
Yamamoto Y, Sofikitis Nikolaos, Kaponis A, Georgiou Ioannis, Giannakis D, Mamoulakis Ch, Loutradis D, Yiannakopoulos X, Mio Y, Miyagawa I, Chatzikyriakidou Anthoula (2002). Use of a highly sensitive quantitative telomerase assay in intracytoplasmic sperm injection programmes for the treatment of 47, XXY non-mosaic Klinefelter men. Andrologia. Vol. 34 no. 4 p. 218-226.

Aggiornato: 2017-07-11