Anne‐Karin Kahlert
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- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
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- Genomics and Rare Diseases 2
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 2
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- Biochemical and Molecular Research 2
- Congenital heart defects research 2
- RNA modifications and cancer 1
- CRISPR and Genetic Engineering 1
- Mitochondrial Function and Pathology 1
Anne‐Karin Kahlert
10 papers receiving 143 citations
Peers
Comparison fields: 5 of 41
- Genetics 29
- Neurology 34
- Genetics 60
- Molecular Biology 93
- Clinical Biochemistry 5
Countries citing papers authored by Anne‐Karin Kahlert
This map shows the geographic impact of Anne‐Karin Kahlert'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 Anne‐Karin Kahlert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anne‐Karin Kahlert more than expected).
Fields of papers citing papers by Anne‐Karin Kahlert
This network shows the impact of papers produced by Anne‐Karin Kahlert. 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 Anne‐Karin Kahlert. The network helps show where Anne‐Karin Kahlert may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Anne‐Karin Kahlert, 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 | 2023 | 7 | |
| 2 | 2020 | 45 | |
| 3 | 2020 | 7 | |
| 4 | 2019 | 12 | |
| 5 | 2018 | 6 | |
| 6 | 2018 | 29 | |
| 7 | 2018 | 2 | |
| 8 | 2017 | 11 | |
| 9 | 2017 | 13 | |
| 10 | 2016 | 12 |
About Anne‐Karin Kahlert
Anne‐Karin Kahlert is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology, having authored 10 papers that have together received 144 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Biochemical and Molecular Research (2 papers), Congenital heart defects research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), RNA modifications and cancer (1 paper), CRISPR and Genetic Engineering (1 paper) and Mitochondrial Function and Pathology (1 paper). The work is most often cited by research in Genetics (29 citations), Neurology (34 citations) and Genetics (60 citations). Anne‐Karin Kahlert has collaborated with scholars based in Germany, United States and Sweden. Frequent co-authors include Nataliya Di Donato, Evelin Schröck, Andreas Rump, Andreas Tzschach, Joseph Porrmann, Karl Hackmann, Luisa Mackenroth, Laura Gieldon, Susanne Petri and Hannes Glaß. Their work appears in journals such as PLoS ONE, Cardiovascular Research and Breast Cancer Research and Treatment.
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.