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1

Maternal epigenetics and fetal and neonatal growth

Kitsiou-Tzeli, Sofia, Tzetis, Maria

Journal:

Current Opinion in Endocrinology Diabetes and Obesity

Year:

2016

Language:

english

File:

PDF, 181 KB

english, 2016

2

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

Sofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, Katerina Anagnostopoulou, Maria Kontodiou, Nadezda Kosyakova, Elisabeth Ewers, Anja Weise, Antonios Garas, Sandro Orru, Thomas Liehr, Aikater

Journal:

Molecular Cytogenetics

Year:

2009

Language:

english

File:

PDF, 65 KB

english, 2009

3

Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion

Sofia Kitsiou-Tzeli, Carolina Sismani, Marios Ioannides, Stavros Bashiardes, Andria Ketoni, Vassiliki Touliatou, Aggeliki Kolialexi, Ariadni Mavrou, Emanuel Kanavakis, Philippos C. Patsalis

Journal:

European Journal of Medical Genetics

Year:

2007

Language:

english

File:

PDF, 690 KB

english, 2007

4

Compound heterozygosity of a paternal submicroscopic deletion and a maternal missense mutation in POR gene: Antley-bixler syndrome phenotype in three sibling fetuses

Tzetis, Maria, Konstantinidou, Anastasia, Sofocleous, Christalena, Kosma, Konstantina, Mitrakos, Anastasios, Tzannatos, Christina, Kitsiou-Tzeli, Sofia

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2016

Language:

english

File:

PDF, 248 KB

english, 2016

5

Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA

Tsipi, Maria, Poulou, Myrto, Fylaktou, Eirini, Kosma, Konstantina, Tsoutsou, Eirini, Pons, Maria-Roser, Kokkinou, Eleftheria, Kitsiou-Tzeli, Sofia, Fryssira, Helen, Tzetis, Maria

Journal:

Journal of the Neurological Sciences

Year:

2018

Language:

english

File:

PDF, 711 KB

english, 2018

6

Molecular cytogenetic characterization and origin of two de novo duplication 9p cases

Tsezou, Aspasia, Kitsiou, Sofia, Galla, Angeliki, Petersen, Michael B., Karadima, Georgia, Syrrou, Maria, Sahl�n, Sigrid, Blennow, Elisabeth

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 2.01 MB

english, 2000

7

FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population

Maria Syrrou, Ioannis Georgiou, Maria Grigoriadou, Michael B. Petersen, Sofia Kitsiou, Gerassimos Pagoulatos, Philippos C. Patsalis

Journal:

Genetic Epidemiology

Year:

1998

Language:

english

File:

PDF, 25 KB

english, 1998

8

Molecular investigation of Angelman syndrome in Greece. Screening for UBE3A mutations: preliminary results

Evmorfia Tzagaraki, Christalena Sofocleous, Nikolaos Vogiatzakis, Sofia Kitsiou, Helen Frysira, George Goulielmos, Emmanouil Kanavakis, Ariadni Mavrou

Journal:

Annals of General Psychiatry

Year:

2008

Language:

english

File:

PDF, 75 KB

english, 2008

9

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

Sofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, Maria Kontodiou, Nadezda Kosyakova, Elisabeth Ewers, Anja Weise, Antonios Garas, Sandro Orru, Thomas Liehr, Aikaterini Metaxotou

Journal:

Molecular Cytogenetics

Year:

2009

Language:

english

File:

PDF, 641 KB

english, 2009

10

Prenatal diagnosis of a de novo partial trisomy 10p12.1–12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH

Sofia Kitsiou-Tzeli, Carolina Sismani, Margarita Karkaletsi, Lina Florentin, Anastassios Anastassiou, George Koumbaris, Paola Enangelidou, Emmanouil Agapitos, P. C. Patsalis, Voula Velissariou

Journal:

Prenatal Diagnosis

Year:

2008

Language:

english

File:

PDF, 94 KB

english, 2008

11

Erratum: Prenatal diagnosis of a de novo partial trisomy 10p12.1–12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH

Sofia Kitsiou-Tzeli, Carolina Sismani, Margarita Karkaletsi, Lina Florentin, Anastassios Anastassiou, George Koumbaris, Paola Evangelidou, Emmanouil Agapitos, P. C. Patsalis, Voula Velissariou

Journal:

Prenatal Diagnosis

Year:

2010

Language:

english

File:

PDF, 24 KB

english, 2010

12

Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines

Sofia Kitsiou, Aggeliki Kolialexi, Ariadni Mavrou

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 103 KB

english, 2004

13

Long-term follow-up of a multifocal hepatic mesenchymal hamartoma producing a-fetoprotein

Andrew Fretzayas, Maria Moustaki, Sofia Kitsiou, Georgia Nychtari, E. Alexopoulou

Journal:

Pediatric Surgery International

Year:

2009

Language:

english

File:

PDF, 194 KB

english, 2009

14

Food allergy-related paediatric constipation: the usefulness of atopy patch test

Ekaterini I. Syrigou, Constantinos Pitsios, Ioanna Panagiotou, Georgios Chouliaras, Sofia Kitsiou, Mary Kanariou, Eleftheria Roma-Giannikou

Journal:

European Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 169 KB

english, 2011

15

Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms’ tumor 1 (WT1) gene

Spyridon Megremis, Andromachi Mitsioni, Irene Fylaktou, Sofia Kitsiou Tzeli, Filadelfia Komianou, Constantinos J. Stefanidis, Emmanuel Kanavakis, Joanne Traeger-Synodinos

Journal:

European Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 123 KB

english, 2011

16

Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population

Emmanuel Kavazarakis, Aspasia Tsezou, Maria Tzetis, Androniki Hadjidimoula, Sofia Kitsiou, Emmanuel Kanavakis, Themistocles Karpathios

Journal:

European Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 66 KB

english, 2000

17

The clinical pattern of group C streptococcal pharyngitis in children

Andrew Fretzayas, Maria Moustaki, Sofia Kitsiou, Georgia Nychtari, Polyxeni Nicolaidou

Journal:

Journal of Infection and Chemotherapy

Year:

2009

Language:

english

File:

PDF, 210 KB

english, 2009

18

Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene

Sofia KITSIOU-TZELI, Patrick WILLEMS, Maria KOSMADAKI, Eleni LEZE, Christine VRETTOU, Emmanuel KANAVAKIS, Alexandra KATSAROU

Journal:

The Journal of Dermatology

Year:

2011

Language:

english

File:

PDF, 290 KB

english, 2011

19

Survivin regulation by HER2 through NF-κB and c-myc in irradiated breast cancer cells

Vassilis Papanikolaou, Dimitrios Iliopoulos, Ioannis Dimou, Stephanie Dubos, Constantine Kappas, Sofia Kitsiou-Tzeli, Aspasia Tsezou

Journal:

Journal of Cellular and Molecular Medicine

Year:

2011

Language:

english

File:

PDF, 793 KB

english, 2011

20

The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization

Tzetis, Maria, Kitsiou-Tzeli, Sofia, Frysira, Helen, Xaidara, Athena, Kanavakis, Emmanuel

Journal:

Expert Review of Molecular Diagnostics

Year:

2012

Language:

english

File:

PDF, 369 KB

english, 2012

21

Sex-reversed phenotype in association with two novel mutations c.2494delA and c.T3004C in the ligand-binding domain of the androgen receptor gene

Angeliki Galani, Christalena Sofocleous, Feneli Karahaliou, Asteroula Papathanasiou, Sofia Kitsiou-Tzeli, Ariadni Kalpini-Mavrou

Journal:

Fertility and Sterility

Year:

2008

Language:

english

File:

PDF, 192 KB

english, 2008

22

Coinheritance of Noonan syndrome and Becker muscular dystrophy

Argirios Dinopoulos, Anna Papadopoulou, Panagiota Manta, Kiki Kekou, Tassos Kanelopoulos, Andreas Fretzayas, Sofia Kitsiou

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 127 KB

english, 2010

23

Further delineation of novel 1p36 rearrangements by array-CGH analysis: Narrowing the breakpoints and clarifying the “extended” phenotype

Krinio Giannikou, Helen Fryssira, Vasilis Oikonomakis, Areti Syrmou, Konstantina Kosma, Maria Tzetis, Sofia Kitsiou-Tzeli, Emmanouel Kanavakis

Journal:

Year:

2012

Language:

english

File:

PDF, 697 KB

english, 2012

24

Distal del(4) (q33) syndrome: Detailed clinical presentation and molecular description with array-CGH

Sofia Kitsiou-Tzeli, Carolina Sismani, George Koumbaris, Marios Ioannides, Emmanuel Kanavakis, Angeliki Kolialexi, Ariadni Mavrou, Vasiliki Touliatou, Philippos C. Patsalis

Journal:

European Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 357 KB

english, 2008

25

Acute acalculous cholecystitis in children with Epstein–Barr virus infection: a role for Gilbert's syndrome?

Achilleas Attilakos, Alexia Prassouli, George Hadjigeorgiou, Evangelia Lagona, Sofia Kitsiou-Tzeli, Angeliki Galla, Anastasia Stasinopoulou, Themistocles Karpathios

Journal:

International Journal of Infectious Diseases

Year:

2009

Language:

english

File:

PDF, 139 KB

english, 2009

26

Cryptic genomic imbalances in patients withde novoor familial apparently balanced translocations and abnormal phenotype

Carolina Sismani, Sofia Kitsiou-Tzeli, Marios Ioannides, Christodoulos Christodoulou, Violetta Anastasiadou, Goula Stylianidou, Eleftheria Papadopoulou, Emanuel Kanavakis, Zoe Kosmaidou-Aravidou, Phil

Journal:

Molecular Cytogenetics

Year:

2008

Language:

english

File:

PDF, 1.01 MB

english, 2008

27

Screening of UBE3A gene in patients referred for Angelman Syndrome

Tzagkaraki, Evmorfia, Sofocleous, Christalena, Helen, Fryssira-Kanioura, Dinopoulos, Argyris, Goulielmos, Georgios, Mavrou, Ariadni, Sofia, Kitsiou-Tzeli, Kanavakis, Emmanuel

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 1.32 MB

english, 2013

28

Novel and known nephrin gene (NPHS1) mutations in two Greek cases with congenital nephrotic syndrome including a complex genotype

FYLAKTOU, IRENE, MEGREMIS, SPYRIDON, MITSIONI, ANDROMACHI, KITSIOU-TZELI, SOFIA, KOSMA, KONSTANTINA, BITSORI, MARIA, STEFANIDIS, CONSTANTINOS J., KANAVAKIS, EMMANUEL, SYNODINOS, JOANNE TRAEGER

Journal:

Journal of Genetics

Year:

2013

Language:

english

File:

PDF, 755 KB

english, 2013

29

Corrigendum to “Screening of UBE3A gene in patients referred for Angelman Syndrome” [Eur J Paediatr Neurol 17 (4) (2013) 366–373]

Tzagkaraki, Evmorfia, Sofocleous, Christalena, Fryssira-Kanioura, Helen, Dinopoulos, Argyris, Goulielmos, Georgios, Mavrou, Ariadni, Kitsiou-Tzeli, Sofia, Kanavakis, Emmanuel

Journal:

European Journal of Paediatric Neurology

Year:

2013

Language:

english

File:

PDF, 170 KB

english, 2013

30

Genetic Polymorphisms in the UGT1A1 Gene and Breast Cancer Risk in Greek Women

Tsezou, Aspasia, Tzetis, Maria, Giannatou, Eirini, Gennatas, Constantinos, Pampanos, Andreas, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia

Journal:

Genetic Testing

Year:

2007

Language:

english

File:

PDF, 67 KB

english, 2007

31

Microduplication 3q13.2q13.31 identified in a male with dysmorphic features and multiple congenital anomalies

Karavitakis, Emmanouil, Kitsiou-Tzeli, Sofia, Xaidara, Athena, Kosma, Konstantina, Makrythanasis, Periklis, Apazidou, Eleni, Kanavakis, Emmanuel, Tzetis, Maria

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 270 KB

english, 2014

32

hTERT regulation by NF-κB and c-myc in irradiated HER2-positive breast cancer cells

Papanikolaou, Vassilis, Athanassiou, Evangelos, Dubos, Stephanie, Dimou, Ioannis, Papathanasiou, Ioanna, Kitsiou-tzeli, Sofia, Kappas, Constantin, Tsezou, Aspasia

Journal:

International Journal of Radiation Biology

Year:

2011

Language:

english

File:

PDF, 1.42 MB

english, 2011

33

Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population

Tsezou, Aspasia, Tzetis, Maria, Giannatou, Eirini, Spanos, Ierotheos, Roma, Eleutheria, Fretzayas, Alexandros, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 72 KB

english, 2009

34

Knowledge and Attitudes towards Prenatal Diagnostic Procedures among Pregnant Women in Greece

Kitsiou-Tzeli, Sofia, Petridou, Eleni T., Karagkiouzis, Thomas, Dessypris, Nick, Makrithanasis, Periklis, Sifakis, Stavros, Kanavakis, Emmanuel

Journal:

Fetal Diagnosis and Therapy

Year:

2010

Language:

english

File:

PDF, 129 KB

english, 2010

35

Nucleotide Variations in the NPHS2 Gene in Greek Children with Steroid-Resistant Nephrotic Syndrome

Megremis, Spyridon, Mitsioni, Andromachi, Mitsioni, Artemis G., Fylaktou, Irene, Kitsiou-Tzelli, Sofia, Stefanidis, Constantinos J., Kanavakis, Emmanuel, Traeger-Synodinos, Joanne

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 21.36 MB

english, 2009

36

UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis

Fretzayas, Andrew, Kitsiou, Sofia, Tsezou, Aspasia, Alexaki, Augustina, Nicolaidou, Polyxeni

Journal:

Scandinavian Journal of Infectious Diseases

Year:

2006

Language:

english

File:

PDF, 278 KB

english, 2006

37

UBE3A, c.1347_1348delGA: a mutation in question

Sofocleous, Christalena, Tzagkaraki, Evmorfia, Kosma, Konstantina, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2016

Language:

english

File:

PDF, 363 KB

english, 2016

38

Constitutive Heterochromatin Polymorphisms in Children with Acute Lymphoblastic Leukemia

Tsezoil, Aspasia, Kitsiou-Tzeli, Sofia, Kosmidis, Helen, Paidousi, Kalliopi, Katsouyanni, Klea, Sinaniotis, Constantine

Journal:

Pediatric Hematology-Oncology

Year:

1993

Language:

english

File:

PDF, 434 KB

english, 1993

39

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases

Tsipi, Maria, Tzetis, Maria, Kosma, Konstantina, Moschos, Marilita, Braoudaki, Maria, Poulou, Myrto, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia

Journal:

Year:

2016

Language:

english

File:

PDF, 280 KB

english, 2016

40

An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Giannikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen

Journal:

Molecular Cytogenetics

Year:

2015

Language:

english

File:

PDF, 916 KB

english, 2015

41

Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Giannikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen

Journal:

Molecular Cytogenetics

Year:

2015

Language:

english

File:

PDF, 294 KB

english, 2015

42

Photocatalytic degradation of the herbicide clopyralid: Kinetics, degradation pathways and ecotoxicity evaluation

Berberidou, Chrysanthi, Kitsiou, Vasiliki, Karahanidou, Sofia, Lambropoulou, Dimitra A., Kouras, Athanasios, Kosma, Christina I., Albanis, Triantafyllos A., Poulios, Ioannis

Journal:

Journal of Chemical Technology & Biotechnology

Year:

2015

Language:

english

File:

PDF, 769 KB

english, 2015

43

Caveolinopathies in Greece

Papadopoulos, Constantinos, Papadimas, George K., Kekou, Kyriaki, Spengos, Konstantinos, Svigou, Maria, Kitsiou-Tzeli, Sofia, Manta, Panagiota

Journal:

The Neurologist

Year:

2015

Language:

english

File:

PDF, 211 KB

english, 2015

44

A Female Patient with Xq28 Microduplication Presenting with Myotubular Myopathy, Confirmed with a Custom-Designed X-array

Kosma, Konstantina, Mitrakos, Anastasios, Sofokleous, Christalena, Papadimas, George, Fryssira, Helena, Kitsiou-Tzeli, Sofia, Tzetis, Maria

Journal:

Neuropediatrics

Year:

2018

Language:

english

File:

PDF, 66 KB

english, 2018