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Sofìa Kitsiou
Observed names:
S A Kitsiou,
S Kitsiou,
S. Kitsiou,
Sofia Kitsiou
Institution:
Children's Hospital Agia Sophia
Observed institutions:
National and Kapodistrian University of Athens,
Alexandra Hospital,
Children's Hospital Agia Sophia,
Panagiotis & Aglaia Kyriakou Children's Hospital
OpenAlex ID:
A5113671098
Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy
1999
·
A Tsezou
, Ch Hadjiathanasiou
, et al.
·
Clinical Genetics
·
90
The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
2013
·
M. Reza Sailani
, Periklis Makrythanasis
, et al.
·
Genome Research
·
85
PDF
Association of repeat polymorphisms in the estrogen receptors alpha, beta (ESR1, ESR2) and androgen receptor (AR) genes with the occurrence of breast cancer
2007
·
A. Tsezou
, M. Tzetis
, et al.
·
The Breast
·
41
Antepartum aminophylline treatment for prevention of the respiratory distress syndrome in premature infants
1979
·
E. Hadjigeorgiou
, S. Kitsiou
, et al.
·
American Journal of Obstetrics and Gynecology
·
40
Tetrasomy 18p de novo: Parental Origin and Different Mechanisms of Formation
1996
·
Merete Bugge
, Elisabeth Blennow
, et al.
·
European Journal of Human Genetics
·
39
Food allergy-related paediatric constipation: the usefulness of atopy patch test
2011
·
Ekaterini I. Syrigou
, Constantinos Pitsios
, et al.
·
European Journal of Pediatrics
·
26
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population
1998
·
Maria Syrrou
, Ioannis Georgiou
, et al.
·
Genetic Epidemiology
·
26
Molecular cytogenetic characterization and origin of two de novo duplication 9p cases
2000
·
Aspasia Tsezou
, Sofia Kitsiou
, et al.
·
American Journal of Medical Genetics
·
23
The clinical pattern of group C streptococcal pharyngitis in children
2009
·
Andrew Fretzayas
, Maria Moustaki
, et al.
·
Journal of Infection and Chemotherapy
·
20
Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.
2005
·
A Kolialexi
, G Th Tsangaris
, et al.
·
PubMed
·
17
A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)(8) allele.
2000
·
A Tsezou
, M Tzetis
, et al.
·
PubMed
·
16
10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.
2008
·
C Sofocleous
, S Kitsiou
, et al.
·
PubMed
·
14
Glucose-6-phosphate Dehydrogenase Deficiency and Gilbert Syndrome
2005
·
P. Nicolaidou
, S. Kostaridou
, et al.
·
Pediatric Hematology and Oncology
·
14
Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population
2000
·
Emmanuel Kavazarakis
, Aspasia Tsezou
, et al.
·
European Journal of Pediatrics
·
13
Coinheritance of Noonan syndrome and Becker muscular dystrophy
2009
·
Argirios Dinopoulos
, Anna Papadopoulou
, et al.
·
Neuromuscular Disorders
·
9
A case of Ehlers Danlos syndrome type VI.
2006
·
K Salavoura
, M Valari
, et al.
·
PubMed
·
9
Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome
2007
·
S. Voutoufianakis
, S. Psoni
, et al.
·
European Journal of Paediatric Neurology
·
7
PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol
2009
·
C Christofidou
, C Sofocleous
, et al.
·
Reproductive BioMedicine Online
·
6
Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
2006
·
A Kolialexi
, S Kitsiou
, et al.
·
PubMed
·
6
Unusual association of XYY chromosomal constitution with colobomas of iris, myopia, increased lipoproteins, mental retardation and convulsions.
1986
·
S Kitsiou
, C S Bartsocas
·
PubMed
·
6
SMA prenatal diagnosis: A modified protocol to help differentiation between deletions and gene conversion
2014
·
K. Kekou
, C. Sofocleous
, et al.
·
Molecular and Cellular Probes
·
5
Long-term follow-up of a multifocal hepatic mesenchymal hamartoma producing a-fetoprotein
2009
·
Andrew Fretzayas
, Maria Moustaki
, et al.
·
Pediatric Surgery International
·
5
Complex chromosome rearrangement in a retarded girl with malformations.
1987
·
S Kitsiou
, A Tsezou
, et al.
·
PubMed
·
5
UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis
2006
·
Andrew Fretzayas
, Sofia Kitsiou
, et al.
·
Scandinavian Journal of Infectious Diseases
·
3
Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines
2004
·
Sofia Kitsiou
, Aggeliki Kolialexi
, et al.
·
Prenatal Diagnosis
·
3
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Works count:
34
Citation count:
533
H-index:
13
I10-index:
14
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