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Maria Tzetis

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Greece

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Areti Syrmou; Maria Tzetis; Helen Fryssira; Krinio Giannikou; Sophia Kitsiou-Tzeli; Konstantina Kosma; Periklis Makrythanasis; Vasilis Oikonomakis; Emmanuel Kanavakis
Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.
Eirini Tsoutsou; Maria Tzetis; Krinio Giannikou; Emmanuel Kanavakis; Anastasia Kanioura; Konstantina Kosma; Vasilis Oikonomakis; Areti Syrmou; Helen Fryssira
Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation.
Myrto Poulou; Aspasia Destouni; Irini Fylaktou; Emmanuel Kanavakis; Maria Tzetis
Genotyping efficiency of 2 primer sets and an unlabeled oligonucleotide probe for the p.Phe508del in exon 10 of the CFTR gene as determined with high-resolution melting analysis.

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All Publications

2013: Areti Syrmou; Maria Tzetis; Helen Fryssira; Krinio Giannikou; Sophia Kitsiou-Tzeli; Konstantina Kosma; Periklis Makrythanasis; Vasilis Oikonomakis; Emmanuel Kanavakis
Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.
Pediatric research 2013;73(6):772-6.
2013: Eirini Tsoutsou; Maria Tzetis; Krinio Giannikou; Emmanuel Kanavakis; Anastasia Kanioura; Konstantina Kosma; Vasilis Oikonomakis; Areti Syrmou; Helen Fryssira
Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2013;17(3):316-20.
2012: Myrto Poulou; Aspasia Destouni; Irini Fylaktou; Emmanuel Kanavakis; Maria Tzetis
Genotyping efficiency of 2 primer sets and an unlabeled oligonucleotide probe for the p.Phe508del in exon 10 of the CFTR gene as determined with high-resolution melting analysis.
Clinical chemistry 2012;58(10):1490-2.
2012: Krinio Giannikou; Helen Fryssira; Sophia Kitsiou-Tzeli; Konstantina Kosma; Vasilis Oikonomakis; Areti Syrmou; Maria Tzetis; Emmanouel Kanavakis
Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.
Gene 2012;506(2):360-8.
2012: Maria Tzetis; Michael Choulakis; Krinio Giannikou; Aggeliki Kolialexi; Konstantina Kosma; Eleni Leze; Periklis Makrythanasis; Vasilis Oikonomakis; Christalena Sofocleous; Kalliopi Stefanaki; Areti Syrmou; Sophia Kitsiou-Tzeli
An unusual case of Cat-Eye syndrome phenotype and extragonadal mature teratoma: review of the literature.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(7):561-6.
2012: Myrto Poulou; Maria Fotoulaki; Irini Fylaktou; Emmanuel Kanavakis; Maria Tzetis
Cystic fibrosis genetic counseling difficulties due to the identification of novel mutations in the CFTR gene.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2012;11(4):344-8.
2012: Maria Tzetis; Athena Xaidara; Helen Frysira; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis
The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.
Expert review of molecular diagnostics 2012;12(5):449-57.
2012: Sophia Kitsiou-Tzeli; Anastasia E Konstantinidou; Konstantina Kosma; Periklis Makrythanasis; Stavros Sifakis; Christalena Sofocleous; Areti Syrmou; Krinio Giannikou; Maria Tzetis
Familial Pelizaeus-Merzbacher disease caused by a 320.6-kb Xq22.2 duplication and the pathological findings of a male fetus.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(6):494-8.
2011: Ioannis K Litos; Theodore K Christopoulos; Penelope C Ioannou; Emmanuel Kanavakis; Maria Tzetis; Jan Traeger-Synodinos
Quadruple-allele dipstick test for simultaneous visual genotyping of A896G (Asp299Gly) and C1196T (Thr399Ile) polymorphisms in the toll-like receptor-4 gene.
Clinica chimica acta; international journal of clinical chemistry 2011;412(21-22):1968-72.
2011: Argirios Dinopoulos; Efi Alexopoulou; Achilleas Attilakos; Olga Karapanou; Maria Tzetis; Andreas Fretzayas
VPA-induced recurrent pancreatitis in a cystic fibrosis carrier.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2011;15(5):453-5.
2011: Antonia Spiropoulos; Kalliopi Stefanaki; Maria Theodosaki; Maria Tzetis; Stelios Graphakos; Emmanuel Kanavakis; Ioannis Papassotiriou; George Paterakis; Eftichia Petrakou; Eleftheria Roma; Maria N Dimopoulou; Krinio Giannikou; Evgenios Goussetis
Rapid clinical-scale propagation of mesenchymal stem cells using cultures initiated with immunoselected bone marrow CD105+ cells.
Journal of cellular and molecular medicine 2011;15(9):1983-8.
2010: Marios Kaliakatsos; Aristeidis Giannakopoulos; Helen Fryssira; Maria Kanariou; Anna-Venetia Skiathitou; Tania Siahanidou; Krinio Giannikou; Periklis Makrythanasis; Emmanuel Kanavakis; Maria Tzetis
Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH.
Journal of human genetics 2010;55(11):761-3.
2010: Periklis Makrythanasis; Maria Tzetis; Aggeliki Rapti; Athanasios Papatheodorou; Maria Tsipi; Sophia Kitsiou-Tzeli; Alexia Tsiamouri; Myrto Poulou; Charis Roussos; Emmanuel Kanavakis
Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients.
Genetic testing and molecular biomarkers 2010;14(4):577-84.
2010: Sophia Kitsiou-Tzeli; Maria Tzetis; Christalena Sofocleous; Christina Vrettou; Athena Xaidara; Krinio Giannikou; Andreas Pampanos; Ariadni Mavrou; Emmanuel Kanavakis
De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.
American journal of medical genetics. Part A 2010;152A(8):1925-32.
2010: Athanasios Papatheodorou; Periklis Makrythanasis; Marios Kaliakatsos; Aikaterini Dimakou; Dora Orfanidou; Charis Roussos; Emmanuel Kanavakis; Maria Tzetis
Development of novel microarray methodology for the study of mutations in the SERPINA1 and ADRB2 genes--their association with Obstructive Pulmonary Disease and Disseminated Bronchiectasis in Greek patients.
Clinical biochemistry 2010;43(1-2):43-50.
2009: Alexandra Iliadi; Periklis Makrythanasis; Maria Tzetis; Maria Tsipi; Joanne Traeger-Synodinos; Penelope C Ioannou; Aggeliki Rapti; Emmanuel Kanavakis; Theodore K Christopoulos
Association of TLR4 single-nucleotide polymorphisms and sarcoidosis in Greek patients.
Genetic testing and molecular biomarkers 2009;13(6):849-53.
2009: Andreas Pampanos; Konstantina Volaki; Emmanuel Kanavakis; Ourania Papandreou; Sotiris Youroukos; Loretta Thomaidis; Savvas Karkelis; Maria Tzetis; Sophia Kitsiou-Tzeli
A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.
Genetic testing and molecular biomarkers 2009;13(5):611-5.
2009: Aspasia Tsezou; Maria Tzetis; Eirini Giannatou; Ierotheos Spanos; Eleutheria Roma; Alexandros Fretzayas; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population.
Genetic testing and molecular biomarkers 2009;13(1):143-6.
2009: Nina Manolaki; Georgia Nikolopoulou; George L Daikos; Eleni Panagiotakaki; Maria Tzetis; Eleftheria Roma; Emmanuel Kanavakis; Vassiliki Syriopoulou
Wilson disease in children: analysis of 57 cases.
Journal of pediatric gastroenterology and nutrition 2009;48(1):72-7.
2008: Kristina V Krasnov; Maria Tzetis; Jie Cheng; William B Guggino; Garry R Cutting
Localization studies of rare missense mutations in cystic fibrosis transmembrane conductance regulator (CFTR) facilitate interpretation of genotype-phenotype relationships.
Human mutation 2008;29(11):1364-72.
2008: Myrto Poulou; Marios Kaliakatsos; Aspasia Tsezou; Emmanuel Kanavakis; Konstantinos N Malizos; Maria Tzetis
Association of the CALM1 core promoter polymorphism with knee osteoarthritis in patients of Greek origin.
Genetic testing 2008;12(2):263-5.
2008: C Castellani; H Cuppens; Milan Macek Jr.; J J Cassiman; E Kerem; Peter Roy Durie; E Tullis; B M Assael; C Bombieri; A Brown; T Casals; M Claustres; Garry R Cutting; E Dequeker; J Dodge; I Doull; P Farrell; C Ferec; E Girodon; M Johannesson; B Kerem; Michael Knowles; A Munck; P F Pignatti; Dragica Radojkovic; P Rizzotti; M Schwarz; M Stuhrmann; Maria Tzetis; J Zielenski; J S Elborn
Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2008;7(3):179-96.
2008: Aspasia Tsezou; Maria Tzetis; Constantinos Gennatas; E Giannatou; A Pampanos; G Malamis; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Association of repeat polymorphisms in the estrogen receptors alpha, beta (ESR1, ESR2) and androgen receptor (AR) genes with the occurrence of breast cancer.
Breast (Edinburgh, Scotland) 2008;17(2):159-66.
2008: Konstantinos Douros; Ioanna Loukou; Stavros Doudounakis; Maria Tzetis; Kostas N Priftis; Emmanuel Kanavakis
Asthma and pulmonary function abnormalities in heterozygotes for cystic fibrosis transmembrane regulator gene mutations.
International journal of clinical and experimental medicine 2008;1(4):345-9.
2007: Athanasios Papatheodorou; Panagiota Latsi; Christina Vrettou; Aikaterini Dimakou; Alexia Chroneou; Periklis Makrythanasis; Marios Kaliakatsos; Dora Orfanidou; Charis Roussos; Emmanuel Kanavakis; Maria Tzetis
Development of a novel microarray methodology for the study of SNPs in the promoter region of the TNF-alpha gene: their association with obstructive pulmonary disease in Greek patients.
Clinical biochemistry 2007;40(12):843-50.
2007: Takahiro Nakamura; Dongquan Shi; Maria Tzetis; Julio A Rodriguez-Lopez; Yoshinari Miyamoto; Aspasia Tsezou; Antonio Gonzalez; Qing Jiang; Naoyuki Kamatani; John Loughlin; Shiro Ikegawa
Meta-analysis of association between the ASPN D-repeat and osteoarthritis.
Human molecular genetics 2007;16(14):1676-81.
2007: Maria Tzetis; Marios Kaliakatsos; Maria Fotoulaki; Athanasios Papatheodorou; Stavros Doudounakis; Aspasia Tsezou; P Makrythanasis; Emmanuel Kanavakis; Sanda Nousia-Arvanitakis
Contribution of the CFTR gene, the pancreatic secretory trypsin inhibitor gene (SPINK1) and the cationic trypsinogen gene (PRSS1) to the etiology of recurrent pancreatitis.
Clinical genetics 2007;71(5):451-7.
2007: P K Yiallouros; Vassos Neocleous; M Zeniou; T Adamidou; C Costi; C Christophi; Maria Tzetis; E Kanavakis; C Constantinou Deltas
Cystic fibrosis mutational spectrum and genotypic/phenotypic features in Greek-Cypriots, with emphasis on dehydration as presenting symptom.
Clinical genetics 2007;71(3):290-2.
2007: Sophia Kitsiou-Tzeli; Eleanna Giannatou; I Spanos; Polyxeni Nicolaidou; Andreas Fretzayas; Maria Tzetis; Dimitrios Lazaris; Emmanuel Kanavakis; Aspasia Tsezou
Steroid hormones polymorphisms and cholelithiasis in Greek population.
Liver international : official journal of the International Association for the Study of the Liver 2007;27(1):61-8.
2007: Aspasia Tsezou; Maria Tzetis; Eirini Giannatou; Constantinos Gennatas; Andreas Pampanos; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Genetic polymorphisms in the UGT1A1 gene and breast cancer risk in Greek women.
Genetic testing 2007;11(3):303-6.
2006: Marios Kaliakatsos; Maria Tzetis; Emmanuel Kanavakis; Pelagia Fytili; G Chouliaras; Theofilos Karachalios; Konstantinos N Malizos; Aspasia Tsezou
Asporin and knee osteoarthritis in patients of Greek origin.
Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 2006;14(6):609-11.
2005: Ozgur Cogulu; Huseyin Onay; Funda Ozgenc; Emin Karaca; Cumhur Gunduz; Maria Tzetis; Tufan Cankaya; Emmanuel Kanavakis; Ferda Ozkinay
Trigonocephaly and Wilson's disease in two siblings.
Clinical dysmorphology 2005;14(3):161-4.
2004: Eleni Panagiotakaki; Maria Tzetis; Nina Manolaki; Georgios Loudianos; Athanasios Papatheodorou; Emmanuel Manesis; Sanda Nousia-Arvanitakis; Vassiliki Syriopoulou; Emmanuel Kanavakis
Genotype-phenotype correlations for a wide spectrum of mutations in the Wilson disease gene (ATP7B).
American journal of medical genetics. Part A 2004;131(2):168-73.
2004: Margarida D Amaral; Luka A Clarke; Anabela S Ramalho; Sebastian Beck; Fiona C Broackes-Carter; Rebecca Rowntree; Nathalie Mouchel; Sarah Williams; Ann Harris; Maria Tzetis; Bernhard Steiner; Javier Sanz; Sabina Gallati; Malka Nissim-Rafinifa; Batsheva Kerem; Timothy Hefferon; Garry R Cutting; Elisa Goina; Franco Pagani
Quantitative methods for the analysis of CFTR transcripts/splicing variants.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2004;3 Suppl 2():17-23.
2004: Anabela S Ramalho; Sebastian Beck; Carlos M Farinha; Luka A Clarke; Ghanshyam D Heda; Bernhard Steiner; Javier Sanz; Sabina Gallati; Margarida D Amaral; Ann Harris; Maria Tzetis
Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2004;3 Suppl 2():11-5.
2004: Christina Vrettou; Joanne Traeger-Synodinos; Maria Tzetis; Giles Palmer; Christalena Sofocleous; Emmanuel Kanavakis
Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis.
Human mutation 2004;23(5):513-21.
2004: Isabel Carvalho-Oliveira; Alexandra Efthymiadou; Rui Malhó; Paulo Nogueira; Maria Tzetis; Emmanuel Kanavakis; Margarida D Amaral; Deborah Penque
CFTR localization in native airway cells and cell lines expressing wild-type or F508del-CFTR by a panel of different antibodies.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2004;52(2):193-203.
2004: Danijela Radivojevic; Marina Djurisic; Tanja Lalic; Marija Guc-Scekic; Jovan Savic; Predrag Minic; Thalia Antoniadi; Maria Tzetis; Emmanuel Kanavakis
Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis.
Genetic testing 2004;8(3):276-80.
2004: Joshua D Groman; Timothy W Hefferon; Teresa Casals; Lluís Bassas; Xavier Estivill; Marie Des Georges; Caroline Guittard; Monika Koudova; MARGARET D FALLIN; Krisztina Nemeth; Gyorgy Fekete; Ludovit Kadasi; Kenneth Friedman; Martin Schwarz; Cristina Bombieri; Pier Franco Pignatti; Emmanuel Kanavakis; Maria Tzetis; Marianne Schwartz; Giuseppe Novelli; Maria Rosaria D'Apice; Agnieszka Sobczynska-Tomaszewska; Jerzy Bal; Manfred Stuhrmann; Milan Macek Jr.; Mireille Claustres; Garry R Cutting
Variation in a repeat sequence determines whether a common variant of the cystic fibrosis transmembrane conductance regulator gene is pathogenic or benign.
American journal of human genetics 2004;74(1):176-9.
2003: Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Maria Tzetis; Emmanuel Kavazarakis; Angeliki Galla; Aspasia Tsezou
Gilbert's syndrome as a predisposing factor for idiopathic cholelithiasis in children.
Haematologica 2003;88(10):1193-4.
2003: Franco Pagani; Cristiana Stuani; Maria Tzetis; Emmanuel Kanavakis; Alexandra Efthymiadou; Stavros Doudounakis; Teresa Casals; Francisco E Baralle
New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12.
Human molecular genetics 2003;12(10):1111-20.
2003: Emmanuel Kanavakis; Alexandra Efthymiadou; S Strofalis; Stavros Doudounakis; Joanne Traeger-Synodinos; Maria Tzetis
Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individuals.
Clinical genetics 2003;63(5):400-9.
2003: Joanne Traeger-Synodinos; Christina Vrettou; Giles Palmer; Maria Tzetis; Minas Mastrominas; Stephen Davies; Emmanuel Kanavakis
An evaluation of PGD in clinical genetic services through 3 years application for prevention of beta-thalassaemia major and sickle cell thalassaemia.
Molecular human reproduction 2003;9(5):301-7.
2003: Christina Vrettou; Joanne Traeger-Synodinos; Maria Tzetis; George Malamis; Emmanuel Kanavakis
Rapid screening of multiple beta-globin gene mutations by real-time PCR on the LightCycler: application to carrier screening and prenatal diagnosis of thalassemia syndromes.
Clinical chemistry 2003;49(5):769-76.
2002: Georgios Loudianos; Mario Lovicu; Valeria Dessi; Maria Tzetis; Emmanuel Kanavakis; Lucia Zancan; L Zelante; C Galvèz-Galvèz; Antonio Cao
Abnormal mRNA splicing resulting from consensus sequence splicing mutations of ATP7B.
Human mutation 2002;20(4):260-6.
2002: Christina Vrettou; Maria Tzetis; Joanne Traeger-Synodinos; Giles Palmer; Emmanuel Kanavakis
Multiplex sequence variation detection throughout the CFTR gene appropriate for preimplantation genetic diagnosis in populations with heterogeneity of cystic fibrosis mutations.
Molecular human reproduction 2002;8(9):880-6.
2002: G A Palmer; Joanne Traeger-Synodinos; S Davies; Maria Tzetis; Christina Vrettou; Minas Mastrominas; Emmanuel Kanavakis
Pregnancies following blastocyst stage transfer in PGD cycles at risk for beta-thalassaemic haemoglobinopathies.
Human reproduction (Oxford, England) 2002;17(1):25-31.
2001: Maria Tzetis; Alexandra Efthymiadou; Stavros Doudounakis; Emmanuel Kanavakis
Qualitative and quantitative analysis of mRNA associated with four putative splicing mutations (621+3A-->G, 2751+2T-->A, 296+1G-->C, 1717-9T-->C-D565G) and one nonsense mutation (E822X) in the CFTR gene.
Human genetics 2001;109(6):592-601.
2001: Maria Tzetis; Emmanuel Kanavakis; Aspasia Tsezou; Vasilios Ladis; E Pateraki; Theano P Georgakopoulou; Emmanuel Kavazarakis; E Maragoudaki; Themistocles Karpathios; Sophia Kitsiou-Tzeli
Gilbert syndrome associated with beta-thalassemia.
Pediatric hematology and oncology 2001;18(8):477-84.
2001: M D Amaral; P Pacheco; S Beck; C M Farinha; Deborah Penque; P Nogueira; C Barreto; B Lopes; T Casals; J Dapena; S Gartner; C Vásquez; Javier Perez Frias; C Olveira; R Cabanas; X Estivill; Maria Tzetis; E Kanavakis; S Doudounakis; T Dörk; B Tümmler; E Girodon-Boulandet; C Cazeneuve; M Goossens; M Blayau; C Verlingue; I Vieira; C Féréc; M Claustres; M des Georges; C Clavel; P Birembaut; D Hubert; T Bienvenu; M Adoun; J C Chomel; K De Boeck; H Cuppens; J Lavinha
Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study.
Journal of medical genetics 2001;38(11):777-83.
2001: Maria Tzetis; Alexandra Efthymiadou; S Strofalis; P Psychou; A Dimakou; Evi Pouliou; Stavros Doudounakis; Emmanuel Kanavakis
CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease.
Human genetics 2001;108(3):216-21.
2000: Emmanuel Kavazarakis; Aspasia Tsezou; Maria Tzetis; A Hadjidimoula; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Themistocles Karpathios
Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population.
European journal of pediatrics 2000;159(11):873-4.
2000: Aspasia Tsezou; Maria Tzetis; Sophia Kitsiou-Tzeli; Emmanuel Kavazarakis; Angeliki Galla; Emmanuel Kanavakis
A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)(8) allele.
Haematologica 2000;85(3):319.
2000: Georgios Loudianos; Mario Lovicu; P Solinas; Emmanuel Kanavakis; Maria Tzetis; Nina Manolaki; E Panagiotakaki; Themistocles Karpathios; Antonio Cao
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations.
Genetic testing 2000;4(4):399-402.
1999: Emmanuel Kanavakis; Christina Vrettou; Giles Palmer; Maria Tzetis; Minas Mastrominas; Joanne Traeger-Synodinos
Preimplantation genetic diagnosis in 10 couples at risk for transmitting beta-thalassaemia major: clinical experience including the initiation of six singleton pregnancies.
Prenatal diagnosis 1999;19(13):1217-22.
1999: Christina Vrettou; Giles Palmer; Emmanuel Kanavakis; Maria Tzetis; Thalia Antoniadi; Minas Mastrominas; Joanne Traeger-Synodinos
A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosis.
Prenatal diagnosis 1999;19(13):1209-16.
1999: E Maragoudaki; Emmanuel Kanavakis; Joanne Traeger-Synodinos; Christina Vrettou; Maria Tzetis; Anna Metaxotou-Mavrommati; Christos Kattamis
Molecular, haematological and clinical studies of the -101 C --> T substitution of the beta-globin gene promoter in 25 beta-thalassaemia intermedia patients and 45 heterozygotes.
British journal of haematology 1999;107(4):699-706.
1998: Georgios Loudianos; Valeria Dessì; Mario Lovicu; Andrea Angius; Emmanuel Kanavakis; Maria Tzetis; Christos Kattamis; Nina Manolaki; G Vassiliki; Themistocles Karpathios; Antonio Cao; Mario Pirastu
Haplotype and mutation analysis in Greek patients with Wilson disease.
European journal of human genetics : EJHG 1998;6(5):487-91.
1998: Thilo Dörk; E H El-Harith; Manfred Stuhrmann; Milan Macek Jr.; M Egan; Garry R Cutting; Maria Tzetis; E Kanavakis; S Carles; Mireille Claustres; Carolyn Padoa; M Ramsay; J Schmidtke
Evidence for a common ethnic origin of cystic fibrosis mutation 3120+1G-->A in diverse populations.
American journal of human genetics 1998;63(2):656-62.
1998: J C Stephens; D E Reich; D B Goldstein; H D Shin; M W Smith; M Carrington; C Winkler; G A Huttley; R Allikmets; Lynn M Schriml; B Gerrard; M Malasky; M D Ramos; S Morlot; Maria Tzetis; C Oddoux; F S di Giovine; G Nasioulas; D Chandler; M Aseev; M Hanson; L Kalaydjieva; D Glavac; P Gasparini; E Kanavakis; M Claustres; M Kambouris; Harry Ostrer; G Duff; V Baranov; H Sibul; A Metspalu; David Goldman; N Martin; D Duffy; J Schmidtke; X Estivill; S J O'Brien; M Dean
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes.
American journal of human genetics 1998;62(6):1507-15.
1998: Emmanuel Kanavakis; Maria Tzetis; Thalia Antoniadi; G Pistofidis; S Milligos; Christos Kattamis
Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia.
Molecular human reproduction 1998;4(4):333-7.
1997: Emmanuel Kanavakis; Joanne Traeger-Synodinos; Christina Vrettou; E Maragoudaki; Maria Tzetis; Christos Kattamis
Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods.
Molecular human reproduction 1997;3(6):523-8.
1997: Maria Tzetis; Emmanuel Kanavakis; Thalia Antoniadi; Stavros Doudounakis; G Adam; Christos Kattamis
Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations.
Human genetics 1997;99(1):121-5.
1995: Emmanuel Kanavakis; Maria Tzetis; Thalia Antoniadi; Joanne Traeger-Synodinos; S Doudounakis; G Adam; Nikolaos Matsaniotis; Christos Kattamis
Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation.
Human genetics 1995;96(3):364-6.
1995: Maria Tzetis; Emmanuel Kanavakis; Thalia Antoniadi; Joanne Traeger-Synodinos; S Doudounakis; G Adam; Christos Kattamis
Identification of two novel mutations (296 + 1G-C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients.
Molecular and cellular probes 1995;9(4):283-5.
1995: Emmanuel Kanavakis; Maria Tzetis; Thalia Antoniadi; J Trager-Synodinos; Christos Kattamis; S Doudounakis; G Adam
Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation.
Journal of medical genetics 1995;32(5):406-7.
1995: Emmanuel Kanavakis; Joanne Traeger-Synodinos; Maria Tzetis; A Metaxotou-Mavromati; Vasilios Ladis; Christos Kattamis
Molecular characterization of homozygous (high HbA2) beta-thalassemia intermedia in Greece.
Pediatric hematology and oncology 1995;12(1):37-45.
1994: L Stefanis; Emmanuel Kanavakis; Joanne Traeger-Synodinos; Maria Tzetis; A Metaxotou-Mavromati; Christos Kattamis
Hematologic phenotype of the mutations IVS1-n6 (T-->C), IVS1-n110 (G-->A), and CD39 (C-->T) in carriers of beta-thalassemia in Greece.
Pediatric hematology and oncology 1994;11(5):509-17.
1994: Maria Tzetis; Joanne Traeger-Synodinos; Emmanuel Kanavakis; A Metaxotou-Mavromati; Christos Kattamis
The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece.
Hematologic pathology 1994;8(1-2):25-34.
1993: Joanne Traeger-Synodinos; Emmanuel Kanavakis; Maria Tzetis; Antonis Kattamis; Christos Kattamis
Characterization of nondeletion alpha-thalassemia mutations in the Greek population.
American journal of hematology 1993;44(3):162-7.
1991: Joanne Traeger-Synodinos; Maria Tzetis; Emmanuel Kanavakis; A Metaxotou-Mavromati; Christos Kattamis
The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.
British journal of haematology 1991;79(2):302-5.
1988: A Metaxotou-Mavromati; Christos Kattamis; L Matathia; Maria Tzetis; Emmanuel Kanavakis
Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.
Journal of medical genetics 1988;25(3):195-9.