A Mavrou - Concepedia

Author

A Mavrou

National and Kapodistrian University of Athens

Also Known As

A Mavrou, A. Mavrou, Ariadne Mavrou

Publications

455

Citations

H-Index

Concepts

All Affiliations

National and Kapodistrian University of Athens Children's Hospital Agia Sophia

About

A Mavrou is an author at National and Kapodistrian University of Athens specializing in medicine, genetics, and developmental delay.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	290
2	Education	1	1	16
3	Public Health	1	1	14
4	Molecular Genetics	1	1	74
5	Molecular Medicine	1	1	27

A Mavrou

Publications

398

Citations

H-Index

Page 1

	Year	Citations
Serine–arginine protein kinase 1 (SRPK1) inhibition as a potential novel targeted therapeutic strategy in prostate cancer A Mavrou, Karen Brakspear, Maryam Hamdollah‐Zadeh, Oncogene UrologyMedicineReceptor Tyrosine KinaseTherapeutic StrategyProstatic Disease	2014	159
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 Sophia Kitsiou‐Tzeli, Maria Tzetis, Christalena Sofocleous, American Journal of Medical Genetics Part A Developmental BiologySyndromic AutismGenetic DisorderGeneticsPediatrics	2010	74
Spontaneous Ovulation in a True Hermaphrodite with Normal Male Phenotype and a Rare 46,XX/47,XXY Klinefelter’s Mosaic Karyotype Ch. Kanaka-Gantenbein, E Papandreou, Kalliopi Stefanaki, Hormone Research in Paediatrics	2007	54
Estimating the Population Burden of Injuries Eleni Petridou, Nick Dessypris, Constantine Frangakis, Epidemiology	2004	38
A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder Stavroula Psoni, Patrick J. Willems, Emmanuel Kanavakis, European Journal of Paediatric Neurology Last ExonMendelian DisorderNovel P.arg970x MutationGenetic DisorderGenetics	2009	27
A Minimal Set of SNPs for the Noninvasive Prenatal Diagnosis of <i>β</i>‐Thalassaemia Thessalia Papasavva, Carsten W. Lederer, Joanne Traeger‐Synodinos, Annals of Human Genetics	2013	16
Longitudinal changes in IQ among fragile X males: Clinical evidence of more than one mutation? Gene S. Fisch, Lawrence R. Shapiro, Richard J. Simensen, American Journal of Medical Genetics Longitudinal ChangesGenetic EpidemiologyDisabilityEducationPsychology	1992	16
10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach. Christalena Sofocleous, Sofìa Kitsiou, Helena Fryssira, PubMed Genetic TestingGeneticsDisabilityGenetic EpidemiologyDevelopmental Disabilities	2008	14

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