Sofia Kitsiou‐Tzeli

Author

Sofia Kitsiou‐Tzeli

National and Kapodistrian University of Athens

Also Known As

Kitsiou-Tzeli Sofia, SOFIA KITSIOU-TZELI, Sofia KITSIOU-TZELI, Sofia Kitsiou-Tzeli, Sofia Kitsiou-tzeli, Sofia Kitsiou‐Tzeli

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

National and Kapodistrian University of Athens Children's Hospital Agia Sophia University of Thessaly Cyprus Institute of Neurology and Genetics Iaso Children’s Hospital

About

Sofia Kitsiou‐Tzeli is an author at National and Kapodistrian University of Athens specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	547
2	Public Health	3	3	63
3	Allergy	1	1	34
4	Biostatistics	1	1	20
5	Cell Biology	1	1	70

Sofia Kitsiou‐Tzeli

Publications

848

Citations

H-Index

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	Year	Citations
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism Georgia Karadima, Merete Bugge, Peter Nicolaidis, European Journal of Human Genetics Developmental BiologyCytogeneticsGenetic DisorderGeneticsTrisomy 8	1998	131
Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype Carolina Sismani, Sofia Kitsiou‐Tzeli, Marios Ioannides, Molecular Cytogenetics	2008	124
Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families Periklis Makrythanasis, Mari Nelis, Federico Santoni, Human Mutation Array CghRare DiseasesMendelian DisorderGenetic DisorderExome Sequencing	2014	85
Survivin regulation by HER2 through NF-κB and c-myc in irradiated breast cancer cells Vassilis Papanikolaou, Dimitrios Iliopoulos, Ioannis Dimou, Journal of Cellular and Molecular Medicine Breast OncologySurvivin MrnaCancer BiologyTumor BiologyRadiation Medicine	2010	70
Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion Sofia Kitsiou‐Tzeli, Carolina Sismani, Marios Ioannides, European Journal of Medical Genetics Array-cgh AnalysisGenetic DisorderMedicineGeneticsNext-generation Sequencing	2006	62
Acute acalculous cholecystitis in children with Epstein–Barr virus infection: a role for Gilbert's syndrome? Achilleas Attilakos, Alexia Prassouli, George Hadjigeorgiou, International Journal of Infectious Diseases	2008	47
Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA Maria Tsipi, Myrto Poulou, Irene Fylaktou, Journal of the Neurological Sciences Neuro-oncologyFibrosisPhenotypic ExpressionPathologyNeurofibromatosis Type 1	2018	39
Deep‐intronic variants in <i>CNGB3</i> cause achromatopsia by pseudoexon activation Nicole Weisschuh, Marc Sturm, Britta Baumann, Human Mutation	2019	36
Influence of Interleukin 1α (IL-1α), IL-4, and IL-6 Polymorphisms on Genetic Susceptibility to Chronic Osteomyelitis Aspasia Tsezou, Lazaros Poultsides, F. Kostopoulou, Clinical and Vaccine Immunology ImmunologyGenetic EpidemiologyPathologyImmune-related Gene PolymorphismInflammation	2008	34
Further delineation of novel 1p36 rearrangements by array-CGH analysis: Narrowing the breakpoints and clarifying the “extended” phenotype Helen Fryssira, Vasilis Oikonomakis, Areti Syrmou, Gene Array-cgh AnalysisGeneticsFurther DelineationMolecular BiologyMolecular Genetics	2012	33

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