A Mavrou

460 total citations
16 papers, 290 citations indexed

About

A Mavrou is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, A Mavrou has authored 16 papers receiving a total of 290 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in A Mavrou's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). A Mavrou is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). A Mavrou collaborates with scholars based in Greece, United States and Switzerland. A Mavrou's co-authors include David O. Bates, Roya Babaei‐Jadidi, Karen Brakspear, Sebastian Oltean, Gopinath Damodaran, Jon Oxley, Michael Ladomery, Maryam Hamdollah‐Zadeh, David Gillatt and SJ Harper and has published in prestigious journals such as Oncogene, Epidemiology and Pediatric Research.

In The Last Decade

A Mavrou

16 papers receiving 288 citations

Peers

Countries citing papers authored by A Mavrou

Since Specialization

Citations

This map shows the geographic impact of A Mavrou's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by A Mavrou with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A Mavrou more than expected).

Fields of papers citing papers by A Mavrou

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A Mavrou. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by A Mavrou. The network helps show where A Mavrou may publish in the future.

Co-authorship network of co-authors of A Mavrou

This figure shows the co-authorship network connecting the top 25 collaborators of A Mavrou. A scholar is included among the top collaborators of A Mavrou based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with A Mavrou. A Mavrou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Serine–arginine protein kinase 1 (SRPK1) inhibition as a potential novel targeted therapeutic strategy in prostate cancer 2014 ·Oncogene ·A Mavrou, Karen Brakspear, Maryam Hamdollah‐Zadeh, Gopinath Damodaran, Roya Babaei‐Jadidi, Jon Oxley, David Gillatt, Michael Ladomery, SJ Harper, David O. Bates, Sebastian Oltean	121
2	A Minimal Set of SNPs for the Noninvasive Prenatal Diagnosis of β‐Thalassaemia 2013 ·Annals of Human Genetics ·(unknown), Carsten W. Lederer, Joanne Traeger‐Synodinos, A Mavrou, Emmanuel Kanavakis, (unknown), (unknown), Marina Kleanthous	15
3	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 2010 ·American Journal of Medical Genetics Part A ·Sophia Kitsiou‐Tzeli, Maria Tzetis, Christalena Sofocleous, Christina Vrettou, (unknown), Κρινιώ Γιαννίκου, Ανδρέας Παμπάνος, A Mavrou, Emmanouil Kanavakis	29
4	A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder 2009 ·European Journal of Paediatric Neurology ·Stavroula Psoni, Patrick J. Willems, Emmanuel Kanavakis, A Mavrou, (unknown), Joanne Traeger‐Synodinos, (unknown), (unknown), Sophia Kitsiou‐Tzeli	22
5	Unilateral microtia in an infant with trisomy 18 mosaicism. 2009 ·PubMed ·(unknown), (unknown), (unknown), A Kolialexi, A Mavrou, Emmanouil Kanavakis, (unknown)	5
6	10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach. 2008 ·PubMed ·Christalena Sofocleous, Sofìa Kitsiou, (unknown), A Kolialexi, (unknown), Elefthería Roma, George Th. Tsangaris, (unknown), Catherine Metaxotou, Emmanouel Kanavakis, A Mavrou	9
7	Juvenile idiopathic arthritis-type disease associated with chromosomal aberrations. 2008 ·PubMed ·(unknown), (unknown), A Kolialexi, (unknown), Constantinos T. Sofocleous, A Mavrou	4
8	Spontaneous Ovulation in a True Hermaphrodite with Normal Male Phenotype and a Rare 46,XX/47,XXY Klinefelter’s Mosaic Karyotype 2007 ·Hormone Research in Paediatrics ·(unknown), (unknown), Kalliopi Stefanaki, (unknown), A Kolialexi, (unknown), A Mavrou, (unknown), George P. Chrousos	14
9	Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH). 2006 ·PubMed ·A Kolialexi, Sofìa Kitsiou, (unknown), (unknown), Elisavet Kouvidi, George Th. Tsangaris, (unknown), A Mavrou	5
10	Conventional cytogenetics and fluorescence in situ hybridization in persistent cytopenias and myelodysplastic syndromes in childhood. 2005 ·PubMed ·(unknown), A Kolialexi, George Th. Tsangaris, Maria Moschovi, Sophia Polychronopoulou, A Mavrou	3
11	Clinical and morphological features of paediatric myelodysplastic syndromes: a review of 34 cases 2004 ·Acta Paediatrica ·Sophia Polychronopoulou, (unknown), Lydia Kossiva, A Mavrou, Dimitra Anagnostou, S Haidas	12
12	Estimating the Population Burden of Injuries 2004 ·Epidemiology ·Eleni Petridou, Nick Dessypris, Constantine Frangakis, Maria Belechri, A Mavrou, Dimitrios Trichopoulos	32
13	22q11 microdeletion syndrome 1999 ·Pediatric Research ·A Kolialexi, (unknown), A Mavrou, (unknown), Catherine Metaxotou	2
14	Chromosome fragility and predisposition to childhood malignancies. 1998 ·PubMed ·A Kolialexi, A Mavrou, (unknown), George Th. Tsangaris, (unknown), Fotini Tzortzatou, (unknown), S Haidas, Catherine Metaxotou	2
15	Secondary malignancies in a child with Hodgkin's disease: Peripheral T-cell lymphoma and myelodysplastic syndrome evolving into acute nonlymphoblastic leukaemia 1996 ·Medical and Pediatric Oncology ·Sophia Polychronopoulou, John P. Panagiotou, (unknown), A Mavrou, Dimitra Anagnostou, Stavros Haidas	3
16	Longitudinal changes in IQ among fragile X males: Clinical evidence of more than one mutation? 1992 ·American Journal of Medical Genetics ·Gene S. Fisch, Lawrence R. Shapiro, Richard J. Simensen, Charles E. Schwartz, J. P. Fryns, Martine Borghgraef, L.M.G. Curfs, Patricia N. Howard‐Peebles, Tadao Arinami, A Mavrou	12

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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