Ute Grasshoff
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and rare skin diseases.
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Dermatology top 10%
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 4
- Genetic Syndromes and Imprinting 3
- Neurogenetic and Muscular Disorders Research 2
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- Chromatin Remodeling and Cancer 3
- Ubiquitin and proteasome pathways 2
- Co-authors
- Michael von Bonin (10 shared papers)Andreas Dufke (7 shared papers)Andreas Tzschach (6 shared papers)H. Enders (1 shared paper)María del Carmen Boente (1 shared paper)Karl‐Heinz Grzeschik (1 shared paper)Dorothea Bornholdt (1 shared paper)Arne König (1 shared paper)
- Journals
- European Journal of Human Genetics (3 papers)Journal of Medical Genetics (2 papers)Cytogenetic and Genome Research (1 paper)British Journal of Haematology (1 paper)Genome Research (1 paper)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
Ute Grasshoff
27 papers receiving 815 citations
Peers
Comparison fields: 5 of 71
- Genetics 485
- Dermatology 57
- Molecular Biology 434
- Pediatrics, Perinatology and Child Health 87
- Cell Biology 77
Countries citing papers authored by Ute Grasshoff
This map shows the geographic impact of Ute Grasshoff'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 Ute Grasshoff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ute Grasshoff more than expected).
Fields of papers citing papers by Ute Grasshoff
This network shows the impact of papers produced by Ute Grasshoff. 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 Ute Grasshoff. The network helps show where Ute Grasshoff may publish in the future.
Co-authors
The 25 scholars most cited alongside Ute Grasshoff, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 196 | |
| 2 | 2010 | 123 | |
| 3 | 2008 | 110 | |
| 4 | 2012 | 70 | |
| 5 | 2010 | 48 | |
| 6 | 2009 | 47 | |
| 7 | 2013 | 38 | |
| 8 | 2011 | 35 | |
| 9 | 2013 | 33 | |
| 10 | 2014 | 28 | |
| 11 | 2003 | 26 | |
| 12 | 2021 | 17 | |
| 13 | 2012 | 12 | |
| 14 | 2019 | 11 | |
| 15 | 2018 | 9 | |
| 16 | 2012 | 7 | |
| 17 | 2019 | 7 | |
| 18 | 2012 | 6 | |
| 19 | 2020 | 6 | |
| 20 | 2015 | 5 |
About Ute Grasshoff
Ute Grasshoff is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Oncology and Genetics, having authored 29 papers that have together received 851 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (3 papers), Chromatin Remodeling and Cancer (3 papers), Ubiquitin and proteasome pathways (2 papers), Genetic Neurodegenerative Diseases (2 papers) and Neurogenetic and Muscular Disorders Research (2 papers). The work is most often cited by research in Genetics (485 citations), Dermatology (57 citations), Molecular Biology (434 citations), Pediatrics, Perinatology and Child Health (87 citations) and Cell Biology (77 citations). Ute Grasshoff has collaborated with scholars based in Germany, France and United States. Frequent co-authors include Michael von Bonin, Andreas Dufke, Andreas Tzschach, H. Enders, María del Carmen Boente, Karl‐Heinz Grzeschik, Dorothea Bornholdt, Arne König, Gianluca Tadini and Katja Höfling. Their work appears in journals such as European Journal of Human Genetics, Journal of Medical Genetics, Cytogenetic and Genome Research, British Journal of Haematology and Genome Research.
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.