Andreas Rump
Impact in
- Genetics top 2%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Molecular Biology top 5%
- Sexual Differentiation and Disorders
- RNA Research and Splicing
- RNA modifications and cancer
- Genomics and Chromatin Dynamics
Papers in
-
- Genomics and Chromatin Dynamics 5
- Ubiquitin and proteasome pathways 3
- RNA Research and Splicing 3
- Genetics 28
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 6
- BRCA gene mutations in cancer 6
- Genomics and Rare Diseases 6
- Co-authors
- André Rosenthal (6 shared papers)Evelin Schröck (31 shared papers)Walter Arnold (1 shared paper)Alfred Pühler (1 shared paper)Werner Klipp (1 shared paper)Ursula B. Priefer (1 shared paper)M. Winkelmann (2 shared papers)Koji Muroya (1 shared paper)
- Journals
- European Journal of Medical Genetics (5 papers)Genomics (3 papers)European Journal of Human Genetics (3 papers)Human Molecular Genetics (3 papers)Gene (2 papers)
- Partner nations
- GermanyUnited StatesAustria
In The Last Decade
Andreas Rump
57 papers receiving 2.3k citations
Andreas Rump's Hit Papers
Peers
Comparison fields: 5 of 113
- Genetics 1.1k
- Molecular Biology 1.3k
- Cancer Research 219
- Developmental Biology 34
- Sensory Systems 63
Countries citing papers authored by Andreas Rump
This map shows the geographic impact of Andreas Rump'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 Andreas Rump with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andreas Rump more than expected).
Fields of papers citing papers by Andreas Rump
This network shows the impact of papers produced by Andreas Rump. 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 Andreas Rump. The network helps show where Andreas Rump may publish in the future.
Co-authors
The 25 scholars most cited alongside Andreas Rump, 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 | Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome Hit paper breakdown → | 1997 | 764 |
| 2 | 1988 | 242 | |
| 3 | 2001 | 115 | |
| 4 | 2006 | 104 | |
| 5 | 2012 | 94 | |
| 6 | 2017 | 82 | |
| 7 | 2016 | 80 | |
| 8 | 2005 | 72 | |
| 9 | 2013 | 62 | |
| 10 | 2016 | 58 | |
| 11 | 2009 | 54 | |
| 12 | [The relatively frequent incidence of severe sulfonylurea-induced hypoglycemia in the last 25 years in Switzerland. Results of 2 surveys in Switzerland in 1969 and 1984]. | 1986 | 42 |
| 13 | 2015 | 37 | |
| 14 | 2018 | 31 | |
| 15 | 2003 | 30 | |
| 16 | 2017 | 28 | |
| 17 | 2016 | 27 | |
| 18 | 2019 | 25 | |
| 19 | 2009 | 24 | |
| 20 | 2000 | 23 |
About Andreas Rump
Andreas Rump is a scholar working on Molecular Biology, Genetics, Cancer Research, Pediatrics, Perinatology and Child Health and Oncology, having authored 58 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (6 papers), BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (6 papers), Genomics and Chromatin Dynamics (5 papers), Chromosomal and Genetic Variations (4 papers), Ubiquitin and proteasome pathways (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Genetics (1.1k citations), Molecular Biology (1.3k citations), Cancer Research (219 citations), Developmental Biology (34 citations) and Sensory Systems (63 citations). Andreas Rump has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include André Rosenthal, Evelin Schröck, Walter Arnold, Alfred Pühler, Werner Klipp, Ursula B. Priefer, M. Winkelmann, Koji Muroya, Maki Fukami and Gudrun Rappold. Their work appears in journals such as European Journal of Medical Genetics, Genomics, European Journal of Human Genetics, Human Molecular Genetics and Gene.
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.