Katja Eggermann
Impact in
- Genetics top 2%
- Neurogenetic and Muscular Disorders Research
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
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- Prenatal Screening and Diagnostics
Papers in
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- Epigenetics and DNA Methylation 9
- Genetics 22
- Genetic Syndromes and Imprinting 15
- Genomic variations and chromosomal abnormalities 9
- Neurogenetic and Muscular Disorders Research 8
- Co-authors
- Thomas Eggermann (26 shared papers)Klaus Zerres (13 shared papers)Nadine Schönherr (4 shared papers)H Wollmann (8 shared papers)Michael B. Ranke (7 shared papers)Sabine Rudnik‐Schöneborn (9 shared papers)Peter Kaiser (6 shared papers)H. Enders (3 shared papers)
In The Last Decade
Katja Eggermann
43 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 67
- Genetics 430
- Genetics 538
- Pediatrics, Perinatology and Child Health 319
- Molecular Biology 624
- Cellular and Molecular Neuroscience 126
Countries citing papers authored by Katja Eggermann
This map shows the geographic impact of Katja 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 Katja Eggermann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katja Eggermann more than expected).
Fields of papers citing papers by Katja Eggermann
This network shows the impact of papers produced by Katja 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 Katja Eggermann. The network helps show where Katja Eggermann may publish in the future.
Co-authors
The 25 scholars most cited alongside Katja 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 160 | |
| 2 | 1997 | 115 | |
| 3 | 2008 | 93 | |
| 4 | 2021 | 93 | |
| 5 | 2002 | 72 | |
| 6 | 2015 | 66 | |
| 7 | 2009 | 62 | |
| 8 | 2020 | 47 | |
| 9 | 2018 | 47 | |
| 10 | 2021 | 44 | |
| 11 | 2006 | 40 | |
| 12 | 2007 | 37 | |
| 13 | 2000 | 36 | |
| 14 | 2000 | 36 | |
| 15 | 1998 | 27 | |
| 16 | 2022 | 23 | |
| 17 | 2015 | 23 | |
| 18 | 2016 | 22 | |
| 19 | 2002 | 21 | |
| 20 | 2016 | 20 |
About Katja Eggermann
Katja Eggermann is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 45 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (15 papers), Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (9 papers), Epigenetics and DNA Methylation (9 papers), Neurogenetic and Muscular Disorders Research (8 papers), Hereditary Neurological Disorders (5 papers), Chromosomal and Genetic Variations (4 papers) and Congenital Anomalies and Fetal Surgery (4 papers). The work is most often cited by research in Genetics (430 citations), Genetics (538 citations), Pediatrics, Perinatology and Child Health (319 citations), Molecular Biology (624 citations) and Cellular and Molecular Neuroscience (126 citations). Katja Eggermann has collaborated with scholars based in Germany, Poland and Hungary. Frequent co-authors include Thomas Eggermann, Klaus Zerres, Nadine Schönherr, H Wollmann, Michael B. Ranke, Sabine Rudnik‐Schöneborn, Peter Kaiser, H. Enders, T. Grimm and Christopher Betzler. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Journal of Medical Genetics, Journal of Neuromuscular Diseases and Neuromuscular Disorders.
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.