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Βιογραφικό Σημείωμα

Ανάπτυξη | Σύμπτυξη

Ανθούλα Χατζηκυριακίδου

Αναπληρώτρια Καθηγήτρια, Τμήμα Ιατρικής

Προσωπικά Στοιχεία

Εικόνα chatzikyra

- 2310999013
chatzikyra@auth.gr
Scopus ID8906520900
PubMed IDChatzikyriakidou+A
https://orcid.org/0000-0002-4194-4222
Γνωστικό Αντικείμενο:
Ιατρική Βιολογία-Ιατρική Γενετική
Επιστημονική Ειδίκευση:
- Επιστήμη ζωής
- Βιολογία και βιοχημεία

Εκπαίδευση

Προπτυχιακές Σπουδές

2000	Βιολογίας Βιολογίας Αριστοτέλειο Ελλάδα

Διδακτορικό Δίπλωμα

2004	Διδακτορικό Ιατρικής Ιωαννίνων Ελλάδα

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

Διδακτικό Έργο

Μαθήματα Χειμερινού εξαμήνου ακαδημαϊκού έτους 2021–22

	ΤΜΗΜΑ ΙΑΤΡΙΚΗΣ
ΙΑ0273	ΙΑΤΡΙΚΗ ΒΙΟΛΟΓΙΑ
ΙΑ0429	ΚΛΙΝΙΚΗ ΓΕΝΕΤΙΚΗ
ΙΑ1001	Ιατρική Βιολογία

	ΤΜΗΜΑ ΟΔΟΝΤΙΑΤΡΙΚΗΣ
100102C	ΙΑΤΡΙΚΗ ΒΙΟΛΟΓΙΑ
100201C	ΙΑΤΡΙΚΗ ΓΕΝΕΤΙΚΗ
100413C	ΙΑΤΡΙΚΗ ΓΕΝΕΤΙΚΗ

	MSc HUMAN REPRODUCTION
PMHRA003	Γενετική της Αναπαραγωγής και Βλαστικά Κύτταρα

	ΠΜΣ "ΕΡΕΥΝΗΤΙΚΗ ΜΕΘΟΔΟΛΟΓΙΑ ΣΤΗΝ ΙΑΤΡΙΚΗ ΚΑΙ ΣΤΙΣ ΕΠΙΣΤΗΜΕΣ ΥΓΕΙΑΣ"
ΙΜΑ023	Βασικές εργαστηριακές μέθοδοι και δεξιότητες

Μαθήματα Εαρινού εξαμήνου ακαδημαϊκού έτους 2021–22

	ΤΜΗΜΑ ΙΑΤΡΙΚΗΣ
ΙΑ0255	ΓΕΝΕΤΙΚΗ
ΙΑ1020	Ιατρική Γενετική

	ΤΜΗΜΑ ΟΔΟΝΤΙΑΤΡΙΚΗΣ
100102C	ΙΑΤΡΙΚΗ ΒΙΟΛΟΓΙΑ
100201C	ΙΑΤΡΙΚΗ ΓΕΝΕΤΙΚΗ
100413C	ΙΑΤΡΙΚΗ ΓΕΝΕΤΙΚΗ

Επίβλεψη Εργασιών

Εργασίες Φοιτητών εντός ΑΠΘ

Σε εξέλιξη

Διδακτορικό

Μελέτη των βιολογικών μηχανισμών και του ρόλου του μκροπεριβάλλοντος στην ανάπτυξη, εξέλιξη και θεραπευτική αντιμετώπιση κολοορθικών όγκων
Χωρίς τίτλο

2020–2021

Μεταπτυχιακό

Μελέτη συσχέτισης του πολυμορφισμού CCND1 rs9344 (G870A) με τη γενετική βάση του θηλώδους καρκινώματος του θυροειδούς αδένα

2019–2020

Μεταπτυχιακό

Μελέτη συσχέτισης του πολυμορφισμού rs127099, ο οποίος χαρτογραφείται ανοδικά του γονιδίου CYP24A1, με τη γενετική βάση του πρωτοπαθούς υπερπαραθυροειδισμού

Ερευνητικά Έργα

Συμμετοχή
2012–2015	Thessaloniki Eye Study: Μελέτη επίπτωσης
2010–2014	Υποτροφίες Αριστείας - Βραβεία Αριστείας & Καινοτομίας από την Επιτροπή Ερευνών του Α.Π.Θ

Δημοσιεύσεις

(2021)

Άρθρο σε Περιοδικό

Li Zheng, Wang Zhenxun, Lee Mei Chin, Zenkel Matthias, Peh Esther, Ozaki Mineo, Topouzis Fotios, Nakano Satoko, Chan Anita, Chen Shuwen, Williams Susan E. I, Orr Andrew, Nakano Masakazu, Kobakhidze Nino, Zarnowski Tomasz, Popa-Cherecheanu Alina, Mizoguchi Takanori, Manabe Shin-ichi, Hayashi Ken, Kazama Shigeyasu, Inoue Kenji, Mori Yosai, Miyata Kazunori, Sugiyama Kazuhisa, Higashide Tomomi, Chihara Etsuo, Ideta Ryuichi, Ishiko Satoshi, Yoshida Akitoshi, Tokumo Kana, Kiuchi Yoshiaki, Ohashi Tsutomu, Sakurai Toshiya, Sugimoto Takako, Chuman Hideki, Aihara Makoto, Inatani Masaru, Mori Kazuhiko, Ikeda Yoko, Ueno Morio, Gaston Daniel, Rafuse Paul, Shuba Lesya, Saunders Joseph, Nicolela Marcelo, Chichua George, Tabagari Sergo, Founti Panayiota, Sim Kar Seng, Meah Wee Yang, Soo Hui Meng, Chen Xiao Yin, Chatzikyriakidou Anthoula, Keskini Christina, Pappas Theofanis, Anastasopoulos Eleftherios, Lambropoulos Alexandros, Panagiotou Evangelia S, Mikropoulos Dimitrios, Kosior-Jarecka Ewa, Cheong Augustine, Li Yuanhan, Lukasik Urszula, Nongpiur Monisha E, Husain Rahat, Perera Shamira A, Álvarez Lydia, García Montserrat, González-Iglesias Héctor, Cueto Andrés F. V, Cueto Luis F. V, Martinón-Torres Federico, Salas Antonio, Oguz Çilingir, Tamcelik Nevbahar, Atalay Eray, Batu Bilge, Irkec Murat, Aktas Dilek, Kasim Burcu, Astakhov Yury S, Astakhov Sergei Y, Akopov Eugeny L, Giessl Andreas, Mardin Christian, Hellerbrand Claus, Cooke Bailey Jessica N, Igo Robert P, Haines Jonathan L, Edward Deepak P, Heegaard Steffen, Davila Sonia, Tan Patrick, Kang Jae H, Pasquale Louis R, Kruse Friedrich E, Reis André, Carmichael Trevor R, Hauser Michael, Ramsay Michele, Mossböck Georg, Yildirim Nilgun, Tashiro Kei, Konstas Anastasios-Georgios, Coca-Prados Miguel, Foo Jia Nee, Kinoshita Shigeru, Sotozono Chie, Kubota Toshiaki, Dubina Michael, Ritch Robert, Wiggs Janey L, Pasutto Francesca, Schlötzer-Schrehardt Ursula, Ho Ying Swan, Aung Tin, Tam Wai Leong, Khor Chiea Chuen (2021). Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye. JAMA. τόμ.325 αρ.8 σ.753.

(2019)

Άρθρο σε Περιοδικό

Chatzikyriakidou Anthoula, Chorti A, Papavramidis Theodosios (2019). Association of IRAK1 Gene Polymorphism rs3027898 With Papillary Cancer Restricted to the Thyroid Gland: A Pilot Study. In vivo. τόμ.33 αρ.6 σ.2281-2285.

(2016)

Άρθρο σε Περιοδικό

Chatzikyriakidou Anthoula, Voulgari P.V, Drosos A (2016). Evidence of ERBB3 gene association with rheumatoid arthritis predisposition. International Journal of Rheumatic Diseases. τόμ. 19 αρ.2 σ.146–149.

(2015)

Άρθρο σε Περιοδικό

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. τόμ. 19 αρ.11 σ.641-5.
Aung T, Ozaki M, Mizoguchi T, Chatzikyriakidou Anthoula, Lampropoulos Alexandros, Anastasopoulos E, Coleman AL, Wilson MR, Rhee DJ, Kang JH, May-Bolchakova I, Heegaard S, Mori K, Alward WL, Jonas JB, Xu L, Liebmann JM, Chowbay B, Schaeffeler E, Schwab M, Lerner F, Wang N, Yang Z, Frezzotti P, Kinoshita S, Fingert JH, Inatani M, Tashiro K, Reis A, Edward DP, Pasquale LR, Kubota T, Wiggs JL, Pasutto F, Topouzis Fotios, Dubina M, Craig JE, Yoshimura N, Sundaresan P, John SW, Ritch R, Hauser MA, Khor CC (2015). A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics. τόμ.47 σ. 387–392.
Chatzikyriakidou Anthoula, Aidinidou Louiza, Giannopoulos Andreas, Papadopoulou-Legmpelou Kyriaki, Kalinderi Kallirhoe, Fidani Styliani (2015). Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients. Cardiology in the Young. τόμ.25 αρ.04 σ.681-683.
Founti Panagiota, Haidich Anna-Bettina, Chatzikyriakidou Anthoula, Salonikiou Angeliki, Anastasopoulos Eleftherios, Pappas Theofanis, Lambropoulos Alexandros, Viswanathans Ananth, Topouzis Fotios (2015). Ethnic-based differences in the association of LOXL1 polymorphisms with pseudoexfoliation/pseudoexfoliative glaucoma: a meta-analysis. Annals of Human Genetics. τόμ. 79 αρ.6 σ.431-50.
Founti Panayota, Haidich Anna-Bettina, Chatzikyriakidou Anthoula, Salonikiou Angeliki, Anastasopoulos Eleftherios, Pappas Theofanis, Lampropoulos Alexandros, Viswanathan Ananth C, Topouzis Fotios (2015). Ethnicity-based differences in the association of LOXL1 polymorphisms with pseudoexfoliation/pseudoexfoliative glaucoma: a meta-analysis. Annals of Human Genetics. Vol.79 αρ.6 σ.431-450.

(2014)

Άρθρο σε Περιοδικό

Chatzikyriakidou Anthoula, Voulgari PV, Drosos A (2014). Non-HLA genes in ankylosing spondylitis: what meta-analyses have shown?. Clinical and Experimental Rheumatology. Vol.32 αρ.5.
Chatzikyriakidou Anthoula, Voulgari P.V, Drosos A (2014). Lack of association of the GSDMB gene at locus 17q12 with predisposition to rheumatoid arthritis. Clinical and Experimental Rheumatology. τόμ. 32 αρ. 3 σ.447.
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 αρ. 4 σ. 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. τόμ. 46 αρ.9 σ. 986-96.
Vakalis K, Bechlioulis A, Naka K.K, Chatzikyriakidou Anthoula, Gartzonika K, Vezyraki P, Kolios George, Pappas Konstantinos, Katsouras C.S, Georgiou I, Michalis L.K (2014). Role of 9p21 and 2q36 variants and arterial stiffness in the prediction of coronary artery disease. European Journal of Clinical Investigation. τόμ. 44 αρ. 8 σ.784-794.

(2013)

Άρθρο σε Περιοδικό

Chatzikyriakidou Anthoula, Voulgari P.V, Lampropoulos Alexandros, Georgiou I, Drosos A. A (2013). Validation of the TAGAP rs212389 polymorphism in rheumatoid arthritis susceptibility. Joint Bone Spine. Vol. 80 αρ.5 σ. 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 αρ. 1 σ. 123.
Chatzikyriakidou Anthoula, Voulgari P.V, Lampropoulos Alexandros, Drosos A. A (2013). Genetics in rheumatoid arthritis beyond HLA-genes: What meta-analyses have shown?. Seminars in Arthritis and Rheumatism. Vol. 43 αρ. 1 σ. 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 αρ. 11 σ. 11-14.

(2012)

Άρθρο σε Περιοδικό

Bechlioulis Aris, Naka Katerina K, Kalantaridou S. N, Chatzikyriakidou Anthoula, Papanikolaou Odysseas, Kaponis Apostolos, Vakalis Konstantinos V, Vezyraki Patra, Gartzonika Konstantina, Mavridis Anestis, Georgiou Ioannis, Michalis Lampros K (2012). Short-term hormone therapy improves sCD40L and endothelial function in early menopausal women: Potential role of estrogen receptor polymorphisms. Maturitas. Vol. 71 αρ. 4 σ. 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 αρ. 9 σ. 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 αρ. 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 αρ.1 σ. 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 αρ. 1 σ. 40-45.

(2011)

Άρθρο σε Περιοδικό

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 αρ. 5 σ. 894.
Chatzikyriakidou Anthoula, Voulgari P.V, Drosos A. A (2011). What is the role of HLA-B27 in spondyloarthropathies?. Autoimmunity Reviews. Vol. 10 αρ. 8 σ. 464–468.

(2010)

Άρθρο σε Περιοδικό

Bechlioulis Aris, Kalantaridou Sophia N, Naka Katerina K, Chatzikyriakidou Anthoula, Calis K.A, Makrigiannakis Antonios, Papanikolaou Odysseas, Kaponis Apostolos, Katsouras Christos, Georgiou I, Chrousos George P, Michalis Lampros K (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 αρ. 3 σ. 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 αρ. 5 σ. 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 αρ. 5 σ. 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. σ. 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. Human Reproduction. Vol. 25 αρ. 12 σ. 3129-3133.

(2009)

Άρθρο σε Περιοδικό

Chatzikyriakidou Anthoula, Kollios K.D, Georgiou I (2009). Novel Human Pathological Mutations: Symbol: SLC3A1, Disease: Cystinuria. Human Genetics. Vol. 126 αρ. 2 σ. 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 αρ. 4 σ. 645-648.

(2008)

Άρθρο σε Περιοδικό

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 αρ. 1 σ. 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 αρ. 3 σ. 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 αρ. 3 σ. 174–176.

(2007)

Άρθρο σε Περιοδικό

Chatzikyriakidou Anthoula, Georgiou I, Voulgari P.V, Papadopoulos Christodoulos, 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 αρ. 11 σ. 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 αρ. 6 σ. 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 αρ. 6 σ. 589-595.

(2006)

Άρθρο σε Περιοδικό

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 αρ. 6 σ. 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 αρ. 5 σ. 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 αρ. 2 σ. 554–557.

(2005)

Άρθρο σε Περιοδικό

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 αρ. 4 σ. 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 Testing. Vol. 9 αρ. 3 σ. 175-184.
Chatzikyriakidou Anthoula, Sofikitis N, Georgiou I (2005). Human Gene Mutations: Symbol: SLC3A1, Disease: Cystinuria. Human Genetics. τόμ. 116 αρ. 6 σ. 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. τόμ. 51 αρ. 2 σ. 416-423.

(2004)

Άρθρο σε Περιοδικό

Chatzikyriakidou Anthoula, Sofikitis Nikolaos, Georgiou Ioannis (2004). Human Gene Mutations: Gene Symbol: SLC3A1, SLC7A9 Disease: Cystinuria. Human Genetics. Vol. 116 αρ. 6 σ. 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 αρ. 1 σ. 61–64.

(2003)

Άρθρο σε Περιοδικό

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 αρ. 12 σ. 5976-5980.

(2002)

Άρθρο σε Περιοδικό

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 αρ. 11 σ. 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 αρ. 4 σ. 218-226.

Άρθρο σε Περιοδικό

Kougioumtsidou Niki, Vavoulidis Eleftherios, Nasioutziki Maria, Symeonidou Marianthi, Pratilas Georgios Chrysostomos, Mareti Evangelia, Petousis Stamatios, Chatzikyriakidou Anthoula, Gkrimpizis Grigorios, Theodoridis Theodoros, Miliaras Dimosthenis, Dinas Konstantinos, Zepiridis Leonidas. DNA methylation patterns of RAR ‐β2 and RASSF1A gene promoters in FNAB samples from Greek population with benign or malignant breast lesions. Diagnostic Cytopathology.

Ενημερώθηκε: 2022-04-12