Steffen Uebe
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Molecular Biology top 10%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
- Congenital heart defects research
Papers in
-
- RNA Research and Splicing 4
- Renal and related cancers 3
- Epigenetics and DNA Methylation 3
- Genetics 22
- Genomics and Rare Diseases 8
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 4
- Genetic and Kidney Cyst Diseases 3
- Co-authors
- Arif B. Ekici (40 shared papers)André Reis (39 shared papers)Heinrich Sticht (14 shared papers)Juliane Hoyer (7 shared papers)Georgia Vasileiou (9 shared papers)Cornelia Kraus (15 shared papers)Christiane Zweier (11 shared papers)Christian T. Thiel (16 shared papers)
- Journals
- European Journal of Medical Genetics (4 papers)The American Journal of Human Genetics (4 papers)Scientific Reports (3 papers)European Journal of Human Genetics (3 papers)Human Mutation (2 papers)
- Partner nations
- GermanySwitzerlandNetherlands
In The Last Decade
Steffen Uebe
57 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 89
- Genetics 437
- Molecular Biology 722
- Clinical Biochemistry 59
- Cancer Research 118
- Cell Biology 130
Countries citing papers authored by Steffen Uebe
This map shows the geographic impact of Steffen Uebe'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 Steffen Uebe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steffen Uebe more than expected).
Fields of papers citing papers by Steffen Uebe
This network shows the impact of papers produced by Steffen Uebe. 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 Steffen Uebe. The network helps show where Steffen Uebe may publish in the future.
Co-authors
The 25 scholars most cited alongside Steffen Uebe, 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 58 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 114 | |
| 2 | 2014 | 96 | |
| 3 | 2016 | 86 | |
| 4 | 2011 | 65 | |
| 5 | 2015 | 64 | |
| 6 | 2019 | 62 | |
| 7 | 2017 | 59 | |
| 8 | 2018 | 56 | |
| 9 | 2013 | 55 | |
| 10 | 2010 | 47 | |
| 11 | 2019 | 44 | |
| 12 | 2017 | 40 | |
| 13 | 2016 | 35 | |
| 14 | 2014 | 33 | |
| 15 | 2018 | 33 | |
| 16 | 2017 | 30 | |
| 17 | 2016 | 29 | |
| 18 | 2014 | 28 | |
| 19 | 2018 | 27 | |
| 20 | 2015 | 26 |
About Steffen Uebe
Steffen Uebe is a scholar working on Molecular Biology, Genetics, Immunology, Cellular and Molecular Neuroscience and Cell Biology, having authored 58 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (6 papers), Neurological diseases and metabolism (4 papers), RNA Research and Splicing (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Renal and related cancers (3 papers), Epigenetics and DNA Methylation (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). The work is most often cited by research in Genetics (437 citations), Molecular Biology (722 citations), Clinical Biochemistry (59 citations), Cancer Research (118 citations) and Cell Biology (130 citations). Steffen Uebe has collaborated with scholars based in Germany, Switzerland and Netherlands. Frequent co-authors include Arif B. Ekici, André Reis, Heinrich Sticht, Juliane Hoyer, Georgia Vasileiou, Cornelia Kraus, Christiane Zweier, Christian T. Thiel, Rami Abou Jamra and Mandy Krumbiegel. Their work appears in journals such as European Journal of Medical Genetics, The American Journal of Human Genetics, Scientific Reports, European Journal of Human Genetics 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.