Sebastian Eck
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetic and phenotypic traits in livestock
- Genomic variations and chromosomal abnormalities
- Genetic Mapping and Diversity in Plants and Animals
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 10
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 1
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- Cancer Genomics and Diagnostics 10
- Co-authors
- Tim M. Strom (9 shared papers)Anna Benet‐Pagès (9 shared papers)Hans Scheffer (2 shared papers)Erika Souche (2 shared papers)Marc Sturm (3 shared papers)Ilse Feenstra (2 shared papers)Helger G. Yntema (2 shared papers)Anniek Corveleyn (2 shared papers)
- Journals
- BMC Genomics (2 papers)European Journal of Human Genetics (2 papers)Gene (1 paper)Genome biology (1 paper)PLoS ONE (1 paper)
- Partner nations
- GermanyUnited StatesAustria
In The Last Decade
Sebastian Eck
22 papers receiving 984 citations
Peers
Comparison fields: 5 of 86
- Genetics 381
- Cancer Research 136
- Genetics 59
- Neurology 37
- Molecular Biology 311
Countries citing papers authored by Sebastian Eck
This map shows the geographic impact of Sebastian Eck'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 Sebastian Eck with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sebastian Eck more than expected).
Fields of papers citing papers by Sebastian Eck
This network shows the impact of papers produced by Sebastian Eck. 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 Sebastian Eck. The network helps show where Sebastian Eck may publish in the future.
Co-authors
The 25 scholars most cited alongside Sebastian Eck, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 342 | |
| 2 | 2011 | 170 | |
| 3 | 2009 | 93 | |
| 4 | 2010 | 92 | |
| 5 | 2013 | 62 | |
| 6 | 2013 | 54 | |
| 7 | 2013 | 51 | |
| 8 | 2011 | 44 | |
| 9 | 2012 | 26 | |
| 10 | 2013 | 20 | |
| 11 | 2013 | 16 | |
| 12 | 2015 | 11 | |
| 13 | 2008 | 6 | |
| 14 | 2012 | 5 | |
| 15 | 2011 | 5 | |
| 16 | 2013 | 4 | |
| 17 | EuroGentest guidelines for diagnostic next generation sequencing | 2014 | 3 |
| 18 | 2010 | 2 | |
| 19 | 2018 | 2 | |
| 20 | 2018 | 2 |
About Sebastian Eck
Sebastian Eck is a scholar working on Genetics, Cancer Research, Molecular Biology, Pathology and Forensic Medicine and Neurology, having authored 25 papers that have together received 1.0k indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (10 papers), Genomics and Rare Diseases (8 papers), Genetic factors in colorectal cancer (4 papers), RNA modifications and cancer (3 papers), Religion, Theology, and Education (2 papers), Religious Education and Schools (2 papers), Acute Myeloid Leukemia Research (2 papers) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (381 citations), Cancer Research (136 citations), Genetics (59 citations), Neurology (37 citations) and Molecular Biology (311 citations). Sebastian Eck has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Tim M. Strom, Anna Benet‐Pagès, Hans Scheffer, Erika Souche, Marc Sturm, Ilse Feenstra, Helger G. Yntema, Anniek Corveleyn, Mariëlle Alders and Gert Matthijs. Their work appears in journals such as BMC Genomics, European Journal of Human Genetics, Gene, Genome biology and PLoS ONE.
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.