Thomas Eggermann
Impact in
- Genetics top 0.2%
- Genetic Syndromes and Imprinting
- Genetic and Kidney Cyst Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 252
- Genetic Syndromes and Imprinting 179
- Genomic variations and chromosomal abnormalities 54
- Genomics and Rare Diseases 20
-
- Metabolism and Genetic Disorders 22
- Co-authors
- Klaus Zerres (96 shared papers)Matthias Begemann (65 shared papers)Gerhard Binder (39 shared papers)Sabine Rudnik-Schöneborn (24 shared papers)Katja Eggermann (31 shared papers)Deborah Mackay (14 shared papers)Sabrina Spengler (35 shared papers)Eamonn Richard Maher (13 shared papers)
- Journals
- Clinical Genetics (22 papers)European Journal of Human Genetics (22 papers)European Journal of Medical Genetics (13 papers)Journal of Medical Genetics (13 papers)Clinical Epigenetics (12 papers)
- Partner nations
- GermanyUnited KingdomFrance
In The Last Decade
Thomas Eggermann
352 papers receiving 11.7k citations
Thomas Eggermann's Hit Papers
Peers
Comparison fields: 5 of 157
- Genetics 6.8k
- Pediatrics, Perinatology and Child Health 873
- Biochemistry 412
- Clinical Biochemistry 256
- Genetics 461
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 359 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mapping the human genetic architecture of COVID-19 Hit paper breakdown → | 2021 | 656 |
| 2 | Swarm Learning for decentralized and confidential clinical machine learning Hit paper breakdown → | 2021 | 646 |
| 3 | 2002 | 421 | |
| 4 | Clinical and molecular diagnosis, screening and management of Beckwith–Wiedemann syndrome: an international consensus statement Hit paper breakdown → | 2018 | 402 |
| 5 | Diagnosis and management of Silver–Russell syndrome: first international consensus statement Hit paper breakdown → | 2016 | 374 |
| 6 | Genomic imprinting disorders: lessons on how genome, epigenome and environment interact Hit paper breakdown → | 2019 | 303 |
| 7 | 2004 | 256 | |
| 8 | 2010 | 233 | |
| 9 | 2018 | 220 | |
| 10 | 1994 | 192 | |
| 11 | 2003 | 176 | |
| 12 | 2015 | 167 | |
| 13 | 2008 | 164 | |
| 14 | 2015 | 156 | |
| 15 | 2015 | 150 | |
| 16 | 2004 | 136 | |
| 17 | 1997 | 126 | |
| 18 | 2018 | 123 | |
| 19 | 2006 | 120 | |
| 20 | 1999 | 112 |
About Thomas Eggermann
Thomas Eggermann is a scholar working on Genetics, Clinical Biochemistry, Biochemistry, Genetics and Cellular and Molecular Neuroscience, having authored 359 papers that have together received 12.5k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (179 papers), Genomic variations and chromosomal abnormalities (54 papers), Metabolism and Genetic Disorders (22 papers), Genomics and Rare Diseases (20 papers), Amino Acid Enzymes and Metabolism (20 papers), Schizophrenia research and treatment (16 papers), Neurotransmitter Receptor Influence on Behavior (13 papers) and Prenatal Screening and Diagnostics (12 papers). The work is most often cited by research in Genetics (6.8k citations), Pediatrics, Perinatology and Child Health (873 citations), Biochemistry (412 citations), Clinical Biochemistry (256 citations) and Genetics (461 citations). Thomas Eggermann has collaborated with scholars based in Germany, United Kingdom and France. Frequent co-authors include Klaus Zerres, Matthias Begemann, Gerhard Binder, Sabine Rudnik-Schöneborn, Katja Eggermann, Deborah Mackay, Sabrina Spengler, Eamonn Richard Maher, David Monk and Nadine Schönherr. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, European Journal of Medical Genetics, Journal of Medical Genetics and Clinical Epigenetics.
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.