Katja Kloth
Impact in
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Connective tissue disorders research
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- Congenital heart defects research
- Mitochondrial Function and Pathology
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
Papers in
- Genetics 15
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 4
- Connective tissue disorders research 2
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- Cellular transport and secretion 4
- Co-authors
- Maja Hempel (9 shared papers)Jonas Denecke (7 shared papers)Davor Lessel (6 shared papers)René Santer (4 shared papers)Jessika Johannsen (7 shared papers)Frederike Leonie Harms (2 shared papers)Christian Kubisch (6 shared papers)Kerstin Kutsche (3 shared papers)
- Journals
- Clinical Genetics (3 papers)European Journal of Medical Genetics (3 papers)Neurogenetics (2 papers)The American Journal of Human Genetics (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- GermanyUnited StatesNetherlands
In The Last Decade
Katja Kloth
29 papers receiving 615 citations
Peers
Comparison fields: 5 of 76
- Genetics 261
- Molecular Biology 306
- Developmental Biology 9
- Cellular and Molecular Neuroscience 58
- Cell Biology 48
Countries citing papers authored by Katja Kloth
This map shows the geographic impact of Katja Kloth'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 Katja Kloth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Katja Kloth more than expected).
Fields of papers citing papers by Katja Kloth
This network shows the impact of papers produced by Katja Kloth. 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 Katja Kloth. The network helps show where Katja Kloth may publish in the future.
Co-authors
The 25 scholars most cited alongside Katja Kloth, 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 91 | |
| 2 | 2021 | 69 | |
| 3 | 2018 | 55 | |
| 4 | 2024 | 42 | |
| 5 | 2019 | 37 | |
| 6 | 2020 | 31 | |
| 7 | 2019 | 27 | |
| 8 | 2019 | 26 | |
| 9 | 2017 | 22 | |
| 10 | 2021 | 22 | |
| 11 | 2021 | 21 | |
| 12 | 2020 | 21 | |
| 13 | 2019 | 20 | |
| 14 | 2018 | 19 | |
| 15 | 2018 | 19 | |
| 16 | 2019 | 14 | |
| 17 | 2021 | 11 | |
| 18 | 2019 | 10 | |
| 19 | 2019 | 10 | |
| 20 | 2021 | 10 |
About Katja Kloth
Katja Kloth is a scholar working on Genetics, Cell Biology, Clinical Biochemistry, Biochemistry and Molecular Biology, having authored 30 papers that have together received 625 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (4 papers), Cellular transport and secretion (4 papers), RNA regulation and disease (3 papers), Metabolism and Genetic Disorders (3 papers), Erythrocyte Function and Pathophysiology (3 papers), Prenatal Screening and Diagnostics (2 papers) and Connective tissue disorders research (2 papers). The work is most often cited by research in Genetics (261 citations), Molecular Biology (306 citations), Developmental Biology (9 citations), Cellular and Molecular Neuroscience (58 citations) and Cell Biology (48 citations). Katja Kloth has collaborated with scholars based in Germany, United States and Netherlands. Frequent co-authors include Maja Hempel, Jonas Denecke, Davor Lessel, René Santer, Jessika Johannsen, Frederike Leonie Harms, Christian Kubisch, Kerstin Kutsche, Fanny Kortüm and Annette E. Bley. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Neurogenetics, The American Journal of Human Genetics and Genetics in Medicine.
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.