Chiara Klöckner
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Epilepsy research and treatment
Papers in
- Genetics 5
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 1
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- Neuroscience and Neuropharmacology Research 2
- Co-authors
- Johannes R. Lemke (5 shared papers)Ilona Krey (4 shared papers)Konrad Platzer (3 shared papers)Pia Zacher (1 shared paper)Tobias Bartolomaeus (1 shared paper)Diana Le Duc (1 shared paper)Susanne Horn (1 shared paper)Anja Heinze (1 shared paper)
- Journals
- Genetics in Medicine (1 paper)Human Mutation (1 paper)Human Molecular Genetics (1 paper)Communications Biology (1 paper)Bioinformatics (1 paper)
- Partner nations
- GermanyUnited StatesLuxembourg
In The Last Decade
Chiara Klöckner
6 papers receiving 73 citations
Peers
Comparison fields: 5 of 24
- Genetics 38
- Psychiatry and Mental health 16
- Cellular and Molecular Neuroscience 15
- Health Informatics 1
- Clinical Biochemistry 3
Countries citing papers authored by Chiara Klöckner
This map shows the geographic impact of Chiara Klöckner'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 Chiara Klöckner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chiara Klöckner more than expected).
Fields of papers citing papers by Chiara Klöckner
This network shows the impact of papers produced by Chiara Klöckner. 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 Chiara Klöckner. The network helps show where Chiara Klöckner may publish in the future.
Co-authors
The 25 scholars most cited alongside Chiara Klöckner, 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 | 2021 | 34 | |
| 2 | 2023 | 19 | |
| 3 | 2023 | 8 | |
| 4 | 2022 | 5 | |
| 5 | 2024 | 4 | |
| 6 | 2024 | 3 |
About Chiara Klöckner
Chiara Klöckner is a scholar working on Genetics, Cellular and Molecular Neuroscience, Psychiatry and Mental health, Molecular Biology and Infectious Diseases, having authored 6 papers that have together received 73 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Neuroscience and Neuropharmacology Research (2 papers), Epilepsy research and treatment (2 papers), Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (1 paper) and RNA and protein synthesis mechanisms (1 paper). The work is most often cited by research in Genetics (38 citations), Psychiatry and Mental health (16 citations), Cellular and Molecular Neuroscience (15 citations), Health Informatics (1 citation) and Clinical Biochemistry (3 citations). Chiara Klöckner has collaborated with scholars based in Germany, United States and Luxembourg. Frequent co-authors include Johannes R. Lemke, Ilona Krey, Konrad Platzer, Pia Zacher, Tobias Bartolomaeus, Diana Le Duc, Susanne Horn, Anja Heinze, Julia Hentschel and Johannes Rebstock. Their work appears in journals such as Genetics in Medicine, Human Mutation, Human Molecular Genetics, Communications Biology and Bioinformatics.
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.