Esther Meyer
Impact in
-
- Medical Imaging Techniques and Applications
- Radiation Dose and Imaging
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 20
- Genetic Syndromes and Imprinting 12
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
-
- Epigenetics and DNA Methylation 9
- Co-authors
- Marc Kachelrieß (8 shared papers)Rainer Raupach (6 shared papers)Michael Lell (4 shared papers)Bernhard Schmidt (3 shared papers)Manju A. Kurian (20 shared papers)Eamonn R. Maher (12 shared papers)Shanaz Pasha (8 shared papers)Louise Tee (5 shared papers)
- Journals
- Medical Physics (4 papers)Molecular Genetics and Metabolism (4 papers)Developmental Medicine & Child Neurology (4 papers)Journal of Medical Genetics (3 papers)Molecular Diagnosis (2 papers)
- Partner nations
- United KingdomGermanyUnited States
In The Last Decade
Esther Meyer
50 papers receiving 2.6k citations
Peers
Comparison fields: 5 of 96
- Radiology, Nuclear Medicine and Imaging 586
- Genetics 622
- Biomedical Engineering 963
- Pediatrics, Perinatology and Child Health 319
- Neurology 133
Countries citing papers authored by Esther Meyer
This map shows the geographic impact of Esther Meyer'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 Esther Meyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Esther Meyer more than expected).
Fields of papers citing papers by Esther Meyer
This network shows the impact of papers produced by Esther Meyer. 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 Esther Meyer. The network helps show where Esther Meyer may publish in the future.
Co-authors
The 25 scholars most cited alongside Esther Meyer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 457 | |
| 2 | 2012 | 213 | |
| 3 | 2009 | 184 | |
| 4 | 2009 | 149 | |
| 5 | 2016 | 147 | |
| 6 | 2010 | 125 | |
| 7 | 2015 | 105 | |
| 8 | 2006 | 93 | |
| 9 | 2009 | 88 | |
| 10 | 2010 | 78 | |
| 11 | 2011 | 75 | |
| 12 | 2014 | 70 | |
| 13 | 2012 | 68 | |
| 14 | 2015 | 66 | |
| 15 | 2012 | 63 | |
| 16 | 2015 | 49 | |
| 17 | 2010 | 47 | |
| 18 | Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy. | 2010 | 39 |
| 19 | 2006 | 38 | |
| 20 | 2009 | 36 |
About Esther Meyer
Esther Meyer is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Biomedical Engineering and Cellular and Molecular Neuroscience, having authored 51 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (12 papers), Prenatal Screening and Diagnostics (11 papers), Advanced X-ray and CT Imaging (9 papers), Epigenetics and DNA Methylation (9 papers), Genetics and Neurodevelopmental Disorders (5 papers), Neurological diseases and metabolism (4 papers), Genomics and Rare Diseases (4 papers) and Epilepsy research and treatment (4 papers). The work is most often cited by research in Radiology, Nuclear Medicine and Imaging (586 citations), Genetics (622 citations), Biomedical Engineering (963 citations), Pediatrics, Perinatology and Child Health (319 citations) and Neurology (133 citations). Esther Meyer has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Marc Kachelrieß, Rainer Raupach, Michael Lell, Bernhard Schmidt, Manju A. Kurian, Eamonn R. Maher, Shanaz Pasha, Louise Tee, Yiannis Kyriakou and Thomas Eggermann. Their work appears in journals such as Medical Physics, Molecular Genetics and Metabolism, Developmental Medicine & Child Neurology, Journal of Medical Genetics and Molecular Diagnosis.
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.