A Mavrou
Impact in
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- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- RNA Research and Splicing
- RNA modifications and cancer
- Cancer-related gene regulation
- Congenital heart defects research
- RNA and protein synthesis mechanisms
Papers in
- Genetics 8
- Genetics and Neurodevelopmental Disorders 4
- Genomic variations and chromosomal abnormalities 4
- Genetic Syndromes and Imprinting 2
- Neurogenetic and Muscular Disorders Research 2
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- Congenital heart defects research 2
- Co-authors
- Maryam Hamdollah‐Zadeh (1 shared paper)Jon Oxley (1 shared paper)David O. Bates (1 shared paper)Michael Ladomery (1 shared paper)Sebastian Oltean (1 shared paper)Gopinath Damodaran (1 shared paper)SJ Harper (1 shared paper)David Gillatt (1 shared paper)
- Journals
- Acta Paediatrica (1 paper)Annals of Human Genetics (1 paper)Pediatric Research (1 paper)Epidemiology (1 paper)European Journal of Paediatric Neurology (1 paper)
- Partner nations
- GreeceUnited StatesSwitzerland
In The Last Decade
A Mavrou
16 papers receiving 288 citations
Peers
Comparison fields: 5 of 60
- Genetics 104
- Molecular Biology 172
- Cancer Research 35
- Genetics 23
- Emergency Medicine 20
Countries citing papers authored by A Mavrou
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
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-authors
The 25 scholars most cited alongside A Mavrou, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 121 | |
| 2 | 2004 | 32 | |
| 3 | 2010 | 29 | |
| 4 | 2009 | 22 | |
| 5 | 2013 | 15 | |
| 6 | 2007 | 14 | |
| 7 | 2004 | 12 | |
| 8 | 1992 | 12 | |
| 9 | 10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach. | 2008 | 9 |
| 10 | Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH). | 2006 | 5 |
| 11 | Unilateral microtia in an infant with trisomy 18 mosaicism. | 2009 | 5 |
| 12 | Juvenile idiopathic arthritis-type disease associated with chromosomal aberrations. | 2008 | 4 |
| 13 | 1996 | 3 | |
| 14 | Conventional cytogenetics and fluorescence in situ hybridization in persistent cytopenias and myelodysplastic syndromes in childhood. | 2005 | 3 |
| 15 | 1999 | 2 | |
| 16 | Chromosome fragility and predisposition to childhood malignancies. | 1998 | 2 |
About A Mavrou
A Mavrou is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Pulmonary and Respiratory Medicine, having authored 16 papers that have together received 290 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Acute Myeloid Leukemia Research (3 papers), Autism Spectrum Disorder Research (2 papers), Genetic Syndromes and Imprinting (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (104 citations), Molecular Biology (172 citations), Cancer Research (35 citations), Genetics (23 citations) and Emergency Medicine (20 citations). A Mavrou has collaborated with scholars based in Greece, United States and Switzerland. Frequent co-authors include Maryam Hamdollah‐Zadeh, Jon Oxley, David O. Bates, Michael Ladomery, Sebastian Oltean, Gopinath Damodaran, SJ Harper, David Gillatt, Karen Brakspear and Roya Babaei‐Jadidi. Their work appears in journals such as Acta Paediatrica, Annals of Human Genetics, Pediatric Research, Epidemiology and European Journal of Paediatric Neurology.
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.