Esther Meyer
Impact in
- Neurology top 2%
- Neurological diseases and metabolism
- Neurological disorders and treatments
- Clinical Biochemistry top 1%
Papers in
- Genetics 32
- Genetic Syndromes and Imprinting 16
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 8
-
- Prenatal Screening and Diagnostics 14
- Co-authors
- Marc Kachelrieß (8 shared papers)Rainer Raupach (6 shared papers)Michael Lell (4 shared papers)Bernhard T. Schmidt (3 shared papers)Manju Ann Kurian (20 shared papers)Eamonn Richard Maher (12 shared papers)Shanaz S. Pasha (8 shared papers)Louise J. Tee (5 shared papers)
- Journals
- Molecular Genetics and Metabolism (6 papers)Brain (6 papers)Movement Disorders (5 papers)The American Journal of Human Genetics (4 papers)Medical Physics (4 papers)
- Partner nations
- United KingdomGermanyUnited States
In The Last Decade
Esther Meyer
77 papers receiving 5.2k citations
Peers
Comparison fields: 5 of 123
- Neurology 544
- Clinical Biochemistry 383
- Genetics 1.3k
- Cellular and Molecular Neuroscience 848
- Neurology 634
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 78 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 487 | |
| 2 | 2012 | 303 | |
| 3 | 2016 | 263 | |
| 4 | 2009 | 227 | |
| 5 | 2012 | 227 | |
| 6 | 2014 | 216 | |
| 7 | 2013 | 199 | |
| 8 | 2016 | 191 | |
| 9 | 2009 | 183 | |
| 10 | 2016 | 175 | |
| 11 | 2010 | 166 | |
| 12 | 2015 | 140 | |
| 13 | 2010 | 130 | |
| 14 | 2015 | 128 | |
| 15 | 2014 | 127 | |
| 16 | 2013 | 124 | |
| 17 | 2006 | 120 | |
| 18 | 2009 | 115 | |
| 19 | 2017 | 109 | |
| 20 | 2016 | 106 |
About Esther Meyer
Esther Meyer is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Neurology, Molecular Biology and Psychiatry and Mental health, having authored 78 papers that have together received 5.4k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (16 papers), Prenatal Screening and Diagnostics (14 papers), Epigenetics and DNA Methylation (14 papers), Genetics and Neurodevelopmental Disorders (10 papers), Advanced X-ray and CT Imaging (9 papers), Genomics and Rare Diseases (8 papers), Epilepsy research and treatment (7 papers) and Neurological disorders and treatments (7 papers). The work is most often cited by research in Neurology (544 citations), Clinical Biochemistry (383 citations), Genetics (1.3k citations), Cellular and Molecular Neuroscience (848 citations) and Neurology (634 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 T. Schmidt, Manju Ann Kurian, Eamonn Richard Maher, Shanaz S. Pasha, Louise J. Tee, Thomas Eggermann and Fatimah Rahman. Their work appears in journals such as Molecular Genetics and Metabolism, Brain, Movement Disorders, The American Journal of Human Genetics and Medical Physics.
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.