Ute Grasshoff
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and rare skin diseases.
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- Genetic Neurodegenerative Diseases
Papers in
- Genetics 30
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 14
- Genomics and Rare Diseases 8
- Neurogenetic and Muscular Disorders Research 3
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- Chromatin Remodeling and Cancer 4
- Mitochondrial Function and Pathology 3
- Co-authors
- Michael von Bonin (10 shared papers)Andreas Dufke (6 shared papers)H. Enders (2 shared papers)Olaf Horst Riess (8 shared papers)Mauro Paradisi (1 shared paper)Karl‐Heinz Grzeschik (1 shared paper)Michael Hertl (1 shared paper)Dorothea Bornholdt (1 shared paper)
- Journals
- Journal of Medical Genetics (6 papers)European Journal of Human Genetics (5 papers)Genetics in Medicine (3 papers)Human Mutation (2 papers)Molecular Psychiatry (1 paper)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
Ute Grasshoff
46 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 81
- Genetics 810
- Cellular and Molecular Neuroscience 374
- Neurology 234
- Molecular Biology 1.0k
- Developmental Neuroscience 35
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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 295 | |
| 2 | 2007 | 209 | |
| 3 | 2010 | 142 | |
| 4 | 2015 | 114 | |
| 5 | 2011 | 110 | |
| 6 | 2018 | 93 | |
| 7 | 2012 | 76 | |
| 8 | 2020 | 58 | |
| 9 | 2014 | 57 | |
| 10 | 2009 | 56 | |
| 11 | 2009 | 49 | |
| 12 | 2023 | 49 | |
| 13 | 2010 | 48 | |
| 14 | 2013 | 40 | |
| 15 | 2016 | 40 | |
| 16 | 2011 | 39 | |
| 17 | 2021 | 35 | |
| 18 | 2013 | 34 | |
| 19 | 2014 | 32 | |
| 20 | 2003 | 26 |
About Ute Grasshoff
Ute Grasshoff is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Neurology, having authored 50 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (8 papers), Prenatal Screening and Diagnostics (4 papers), Chromatin Remodeling and Cancer (4 papers), Genetic Neurodegenerative Diseases (4 papers), Mitochondrial Function and Pathology (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). The work is most often cited by research in Genetics (810 citations), Cellular and Molecular Neuroscience (374 citations), Neurology (234 citations), Molecular Biology (1.0k citations) and Developmental Neuroscience (35 citations). Ute Grasshoff has collaborated with scholars based in Germany, France and United States. Frequent co-authors include Michael von Bonin, Andreas Dufke, H. Enders, Olaf Horst Riess, Mauro Paradisi, Karl‐Heinz Grzeschik, Michael Hertl, Dorothea Bornholdt, Katja Höfling and Frank Oeffner. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Genetics in Medicine, Human Mutation and Molecular Psychiatry.
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.