Cornelia Kraus
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Connective tissue disorders research
- Developmental Neuroscience top 10%
Papers in
-
- RNA Research and Splicing 8
- RNA regulation and disease 6
- Genetics 37
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 7
- Connective tissue disorders research 6
- Co-authors
- André Reis (41 shared papers)Anita Rauch (18 shared papers)Juliane Hoyer (12 shared papers)Christian T. Thiel (17 shared papers)Christiane Zweier (20 shared papers)Udo Trautmann (9 shared papers)Wolfgang G. Ballhausen (9 shared papers)Martin Zenker (8 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)European Journal of Medical Genetics (5 papers)Journal of Medical Genetics (4 papers)International Journal of Cancer (4 papers)Human Mutation (4 papers)
- Partner nations
- GermanySwitzerlandUnited States
In The Last Decade
Cornelia Kraus
72 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 106
- Genetics 940
- Developmental Neuroscience 56
- Molecular Biology 942
- Pathology and Forensic Medicine 186
- Pediatrics, Perinatology and Child Health 182
Countries citing papers authored by Cornelia Kraus
This map shows the geographic impact of Cornelia Kraus'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 Cornelia Kraus with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cornelia Kraus more than expected).
Fields of papers citing papers by Cornelia Kraus
This network shows the impact of papers produced by Cornelia Kraus. 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 Cornelia Kraus. The network helps show where Cornelia Kraus may publish in the future.
Co-authors
The 25 scholars most cited alongside Cornelia Kraus, 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 77 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 306 | |
| 2 | 2010 | 123 | |
| 3 | 1994 | 105 | |
| 4 | 2001 | 88 | |
| 5 | 2016 | 87 | |
| 6 | 2007 | 72 | |
| 7 | 2010 | 69 | |
| 8 | 2017 | 60 | |
| 9 | 2017 | 59 | |
| 10 | 2018 | 58 | |
| 11 | 2003 | 56 | |
| 12 | 2007 | 53 | |
| 13 | 2004 | 51 | |
| 14 | 1998 | 48 | |
| 15 | 2009 | 45 | |
| 16 | 2006 | 44 | |
| 17 | 2019 | 44 | |
| 18 | 2008 | 41 | |
| 19 | 1998 | 40 | |
| 20 | 1992 | 36 |
About Cornelia Kraus
Cornelia Kraus is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Cell Biology, having authored 77 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (13 papers), RNA Research and Splicing (8 papers), Genetic factors in colorectal cancer (8 papers), Genomics and Rare Diseases (7 papers), RNA regulation and disease (6 papers), Cancer Genomics and Diagnostics (6 papers) and Connective tissue disorders research (6 papers). The work is most often cited by research in Genetics (940 citations), Developmental Neuroscience (56 citations), Molecular Biology (942 citations), Pathology and Forensic Medicine (186 citations) and Pediatrics, Perinatology and Child Health (182 citations). Cornelia Kraus has collaborated with scholars based in Germany, Switzerland and United States. Frequent co-authors include André Reis, Anita Rauch, Juliane Hoyer, Christian T. Thiel, Christiane Zweier, Udo Trautmann, Wolfgang G. Ballhausen, Martin Zenker, Arif B. Ekici and Ulrike Hüffmeier. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Journal of Medical Genetics, International Journal of Cancer and Human Mutation.
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.