Thomas Eggermann
Impact in
- Genetics top 0.1%
- Genetic Syndromes and Imprinting
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 208
- Genetic Syndromes and Imprinting 163
- Genomic variations and chromosomal abnormalities 49
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- Epigenetics and DNA Methylation 89
- Co-authors
- Klaus Zerres (98 shared papers)Matthias Begemann (59 shared papers)Gerhard Binder (34 shared papers)Sabine Rudnik‐Schöneborn (23 shared papers)Katja Eggermann (26 shared papers)Deborah Mackay (13 shared papers)Sabrina Spengler (31 shared papers)Eamonn R. Maher (11 shared papers)
- Journals
- European Journal of Human Genetics (18 papers)Clinical Genetics (13 papers)European Journal of Medical Genetics (12 papers)Clinical Epigenetics (10 papers)Journal of Medical Genetics (7 papers)
- Partner nations
- GermanyPolandUnited Kingdom
In The Last Decade
Thomas Eggermann
300 papers receiving 7.1k citations
Thomas Eggermann's Hit Papers
Peers
Comparison fields: 5 of 132
- Genetics 4.6k
- Pediatrics, Perinatology and Child Health 2.2k
- Molecular Biology 3.7k
- Genetics 454
- Biochemistry 284
Countries citing papers authored by Thomas Eggermann
This map shows the geographic impact of Thomas Eggermann'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 Thomas Eggermann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Eggermann more than expected).
Fields of papers citing papers by Thomas Eggermann
This network shows the impact of papers produced by Thomas Eggermann. 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 Thomas Eggermann. The network helps show where Thomas Eggermann may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Eggermann, 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 305 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 392 | |
| 2 | Genomic imprinting disorders: lessons on how genome, epigenome and environment interact Hit paper breakdown → | 2019 | 279 |
| 3 | 1994 | 187 | |
| 4 | 2003 | 165 | |
| 5 | 2008 | 160 | |
| 6 | 2015 | 154 | |
| 7 | 2015 | 143 | |
| 8 | 2004 | 128 | |
| 9 | 1997 | 115 | |
| 10 | 1999 | 114 | |
| 11 | 2006 | 113 | |
| 12 | 2003 | 103 | |
| 13 | 2008 | 101 | |
| 14 | 2009 | 94 | |
| 15 | 2001 | 94 | |
| 16 | 2010 | 93 | |
| 17 | 2008 | 93 | |
| 18 | 2016 | 89 | |
| 19 | 2009 | 84 | |
| 20 | 2014 | 83 |
About Thomas Eggermann
Thomas Eggermann is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Pathology and Forensic Medicine and Plant Science, having authored 305 papers that have together received 7.7k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (163 papers), Prenatal Screening and Diagnostics (106 papers), Epigenetics and DNA Methylation (89 papers), Genomic variations and chromosomal abnormalities (49 papers), Chromosomal and Genetic Variations (20 papers), Amino Acid Enzymes and Metabolism (14 papers), Folate and B Vitamins Research (12 papers) and Tumors and Oncological Cases (12 papers). The work is most often cited by research in Genetics (4.6k citations), Pediatrics, Perinatology and Child Health (2.2k citations), Molecular Biology (3.7k citations), Genetics (454 citations) and Biochemistry (284 citations). Thomas Eggermann has collaborated with scholars based in Germany, Poland and United Kingdom. Frequent co-authors include Klaus Zerres, Matthias Begemann, Gerhard Binder, Sabine Rudnik‐Schöneborn, Katja Eggermann, Deborah Mackay, Sabrina Spengler, Eamonn R. Maher, Andrea Riccio and David Monk. Their work appears in journals such as European Journal of Human Genetics, Clinical Genetics, European Journal of Medical Genetics, Clinical Epigenetics and Journal of Medical Genetics.
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.