Ute Grasshoff
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
- Genetic Syndromes and Imprinting
-
- Genetic Neurodegenerative Diseases
Papers in
- Genetics 35
- Genetics and Neurodevelopmental Disorders 20
- Genomics and Rare Diseases 15
- Genomic variations and chromosomal abnormalities 11
- Genetic Syndromes and Imprinting 2
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- Genetic Neurodegenerative Diseases 4
- Hereditary Neurological Disorders 3
- Co-authors
- Michael von Bonin (10 shared papers)Andreas Dufke (6 shared papers)H. Enders (2 shared papers)Olaf Rieß (8 shared papers)Rudolf Happle (1 shared paper)Karl‐Heinz Grzeschik (1 shared paper)Dorothea Bornholdt (1 shared paper)Frank Oeffner (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)Clinical Genetics (1 paper)
- Partner nations
- GermanyFranceNetherlands
In The Last Decade
Ute Grasshoff
46 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 74
- Genetics 881
- Cellular and Molecular Neuroscience 314
- Developmental Neuroscience 37
- Developmental Biology 25
- Pediatrics, Perinatology and Child Health 114
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 | 297 | |
| 2 | 2007 | 209 | |
| 3 | 2010 | 142 | |
| 4 | 2015 | 114 | |
| 5 | 2011 | 111 | |
| 6 | 2018 | 93 | |
| 7 | 2012 | 76 | |
| 8 | 2020 | 58 | |
| 9 | 2014 | 57 | |
| 10 | 2009 | 56 | |
| 11 | 2023 | 51 | |
| 12 | 2009 | 49 | |
| 13 | 2010 | 48 | |
| 14 | 2013 | 40 | |
| 15 | 2016 | 40 | |
| 16 | 2011 | 39 | |
| 17 | 2021 | 36 | |
| 18 | 2013 | 34 | |
| 19 | 2014 | 33 | |
| 20 | 2003 | 26 |
About Ute Grasshoff
Ute Grasshoff is a scholar working on Genetics, Cellular and Molecular Neuroscience, Pediatrics, Perinatology and Child Health, Neurology and Psychiatry and Mental health, having authored 50 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (20 papers), Genomics and Rare Diseases (15 papers), Genomic variations and chromosomal abnormalities (11 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genetic Neurodegenerative Diseases (4 papers), Hereditary Neurological Disorders (3 papers), Genetic Syndromes and Imprinting (2 papers) and Retinal Development and Disorders (2 papers). The work is most often cited by research in Genetics (881 citations), Cellular and Molecular Neuroscience (314 citations), Developmental Neuroscience (37 citations), Developmental Biology (25 citations) and Pediatrics, Perinatology and Child Health (114 citations). Ute Grasshoff has collaborated with scholars based in Germany, France and Netherlands. Frequent co-authors include Michael von Bonin, Andreas Dufke, H. Enders, Olaf Rieß, Rudolf Happle, Karl‐Heinz Grzeschik, Dorothea Bornholdt, Frank Oeffner, Zsuzsanna Zsófia Szalai and Gianluca Tadini. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Genetics in Medicine, Human Mutation and Clinical Genetics.
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.