Katja Kloth
Impact in
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 9
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 2
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- Congenital heart defects research 2
- RNA regulation and disease 2
- Co-authors
- Maja Hempel (8 shared papers)Jonas Denecke (7 shared papers)Davor Lessel (6 shared papers)René Santer (4 shared papers)Jessika Johannsen (7 shared papers)Christian Kubisch (6 shared papers)Kerstin Kutsche (3 shared papers)Frederike L. Harms (2 shared papers)
- Journals
- The American Journal of Human Genetics (2 papers)Neurogenetics (2 papers)European Journal of Medical Genetics (2 papers)Clinical Genetics (2 papers)Frontiers in Oncology (1 paper)
- Partner nations
- GermanyUnited StatesCanada
In The Last Decade
Katja Kloth
18 papers receiving 253 citations
Peers
Comparison fields: 5 of 59
- Genetics 103
- Clinical Biochemistry 13
- Immunology and Allergy 10
- Cell Biology 28
- Molecular Biology 112
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
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 47 | |
| 2 | 2019 | 23 | |
| 3 | 2019 | 23 | |
| 4 | 2017 | 22 | |
| 5 | 2020 | 19 | |
| 6 | 2021 | 19 | |
| 7 | 2021 | 18 | |
| 8 | 2018 | 18 | |
| 9 | 2019 | 12 | |
| 10 | 2021 | 9 | |
| 11 | 2019 | 9 | |
| 12 | 2019 | 9 | |
| 13 | 2021 | 8 | |
| 14 | 2021 | 5 | |
| 15 | 2018 | 4 | |
| 16 | 2021 | 4 | |
| 17 | 2020 | 3 | |
| 18 | 2021 | 2 | |
| 19 | 2020 | 0 |
About Katja Kloth
Katja Kloth is a scholar working on Genetics, Molecular Biology, Cell Biology, Rheumatology and Physiology, having authored 19 papers that have together received 254 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (2 papers), Metabolism and Genetic Disorders (2 papers), Amino Acid Enzymes and Metabolism (2 papers), Cellular transport and secretion (2 papers), Congenital heart defects research (2 papers), Erythrocyte Function and Pathophysiology (2 papers) and RNA regulation and disease (2 papers). The work is most often cited by research in Genetics (103 citations), Clinical Biochemistry (13 citations), Immunology and Allergy (10 citations), Cell Biology (28 citations) and Molecular Biology (112 citations). Katja Kloth has collaborated with scholars based in Germany, United States and Canada. Frequent co-authors include Maja Hempel, Jonas Denecke, Davor Lessel, René Santer, Jessika Johannsen, Christian Kubisch, Kerstin Kutsche, Frederike L. Harms, Fanny Kortüm and Annette Bley. Their work appears in journals such as The American Journal of Human Genetics, Neurogenetics, European Journal of Medical Genetics, Clinical Genetics and Frontiers in Oncology.
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.