Simone Berkel
Impact in
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 11
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 2
- Genetic Associations and Epidemiology 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
- Animal Genetics and Reproduction 1
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- Autism Spectrum Disorder Research 5
- Co-authors
- Gudrun Rappold (12 shared papers)Rolf Sprengel (4 shared papers)Stephen W. Scherer (2 shared papers)Ralph Roeth (2 shared papers)Birgit Weiß (2 shared papers)Jennifer Howe (1 shared paper)Wendy Roberts (1 shared paper)Christian R. Marshall (1 shared paper)
- Journals
- Molecular Psychiatry (3 papers)Frontiers in Molecular Neuroscience (1 paper)Pancreatology (1 paper)European Journal of Human Genetics (1 paper)Stem Cell Research (1 paper)
- Partner nations
- GermanyPolandNetherlands
In The Last Decade
Simone Berkel
16 papers receiving 838 citations
Peers
Comparison fields: 5 of 69
- Cognitive Neuroscience 383
- Genetics 494
- Developmental Neuroscience 45
- Biological Psychiatry 25
- Cellular and Molecular Neuroscience 166
Countries citing papers authored by Simone Berkel
This map shows the geographic impact of Simone Berkel'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 Simone Berkel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone Berkel more than expected).
Fields of papers citing papers by Simone Berkel
This network shows the impact of papers produced by Simone Berkel. 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 Simone Berkel. The network helps show where Simone Berkel may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone Berkel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 460 | |
| 2 | 2011 | 123 | |
| 3 | 2015 | 68 | |
| 4 | 2017 | 31 | |
| 5 | 2018 | 28 | |
| 6 | 2021 | 27 | |
| 7 | 2023 | 26 | |
| 8 | 2018 | 21 | |
| 9 | 2015 | 16 | |
| 10 | 2004 | 15 | |
| 11 | 2015 | 14 | |
| 12 | 2021 | 13 | |
| 13 | 2017 | 10 | |
| 14 | 2024 | 4 | |
| 15 | 2025 | 3 | |
| 16 | 2020 | 3 |
About Simone Berkel
Simone Berkel is a scholar working on Genetics, Cognitive Neuroscience, Developmental Neuroscience, Molecular Biology and Cancer Research, having authored 16 papers that have together received 862 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Autism Spectrum Disorder Research (5 papers), CRISPR and Genetic Engineering (2 papers), Genomics and Rare Diseases (2 papers), Genetic Associations and Epidemiology (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper) and Animal Genetics and Reproduction (1 paper). The work is most often cited by research in Cognitive Neuroscience (383 citations), Genetics (494 citations), Developmental Neuroscience (45 citations), Biological Psychiatry (25 citations) and Cellular and Molecular Neuroscience (166 citations). Simone Berkel has collaborated with scholars based in Germany, Poland and Netherlands. Frequent co-authors include Gudrun Rappold, Rolf Sprengel, Stephen W. Scherer, Ralph Roeth, Birgit Weiß, Jennifer Howe, Wendy Roberts, Christian R. Marshall, Volker Endris and Michael von Bonin. Their work appears in journals such as Molecular Psychiatry, Frontiers in Molecular Neuroscience, Pancreatology, European Journal of Human Genetics and Stem Cell 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.