Christopher Schröder
Impact in
- Molecular Biology top 10%
- Genomics and Phylogenetic Studies
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
- Neurology top 5%
- Neuroblastoma Research and Treatments
Papers in
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- Genetic Neurodegenerative Diseases 5
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- Epigenetics and DNA Methylation 9
- Genomics and Chromatin Dynamics 2
- Muscle Physiology and Disorders 1
- Co-authors
- Sven Rahmann (8 shared papers)Bernhard Horsthemke (8 shared papers)Elsa Leitão (4 shared papers)Sandra Laurentino (2 shared papers)Julia Schicks (1 shared paper)Nina Schlipf (1 shared paper)Peter Bauer (1 shared paper)Christel Depienne (3 shared papers)
- Journals
- Nature Communications (4 papers)Scientific Reports (2 papers)Nature Genetics (2 papers)Epigenetics & Chromatin (2 papers)Communications Biology (1 paper)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
Christopher Schröder
27 papers receiving 1.9k citations
Christopher Schröder's Hit Papers
Peers
Comparison fields: 5 of 115
- Molecular Biology 968
- Neurology 195
- Information Systems and Management 111
- Genetics 272
- Cancer Research 100
Countries citing papers authored by Christopher Schröder
This map shows the geographic impact of Christopher Schröder'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 Christopher Schröder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Schröder more than expected).
Fields of papers citing papers by Christopher Schröder
This network shows the impact of papers produced by Christopher Schröder. 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 Christopher Schröder. The network helps show where Christopher Schröder may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher Schröder, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Bioconda: sustainable and comprehensive software distribution for the life sciences Hit paper breakdown → | 2018 | 847 |
| 2 | 2016 | 354 | |
| 3 | 2015 | 249 | |
| 4 | 2019 | 123 | |
| 5 | 2016 | 73 | |
| 6 | 2012 | 53 | |
| 7 | 2020 | 49 | |
| 8 | 2022 | 31 | |
| 9 | 2017 | 26 | |
| 10 | 2024 | 26 | |
| 11 | 2021 | 23 | |
| 12 | 2017 | 22 | |
| 13 | 2025 | 20 | |
| 14 | 2014 | 17 | |
| 15 | 2020 | 16 | |
| 16 | 2023 | 11 | |
| 17 | 2024 | 10 | |
| 18 | 2022 | 9 | |
| 19 | 2023 | 9 | |
| 20 | 2024 | 9 |
About Christopher Schröder
Christopher Schröder is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Psychiatry and Mental health and Clinical Psychology, having authored 28 papers that have together received 2k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (9 papers), Genetic Neurodegenerative Diseases (5 papers), Genomics and Rare Diseases (3 papers), Genomics and Chromatin Dynamics (2 papers), Bayesian Methods and Mixture Models (2 papers), Epilepsy research and treatment (1 paper), Chromosomal and Genetic Variations (1 paper) and Muscle Physiology and Disorders (1 paper). The work is most often cited by research in Molecular Biology (968 citations), Neurology (195 citations), Information Systems and Management (111 citations), Genetics (272 citations) and Cancer Research (100 citations). Christopher Schröder has collaborated with scholars based in Germany, France and United States. Frequent co-authors include Sven Rahmann, Bernhard Horsthemke, Elsa Leitão, Sandra Laurentino, Julia Schicks, Nina Schlipf, Peter Bauer, Christel Depienne, Tally Lerman‐Sagie and Ludger Klein‐Hitpaß. Their work appears in journals such as Nature Communications, Scientific Reports, Nature Genetics, Epigenetics & Chromatin and Communications Biology.
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.