Ingo Kurth
Impact in
- Developmental Biology top 2%
-
- Hereditary Neurological Disorders
Papers in
-
- Hereditary Neurological Disorders 28
- Genetics 31
- Genomics and Rare Diseases 10
- Genetic Syndromes and Imprinting 8
- Co-authors
- Christian Andreas Hübner (23 shared papers)Antje K. Huebner (5 shared papers)Joachim Weis (9 shared papers)Nicole Koch (5 shared papers)Sándor Nietzsche (5 shared papers)Britta Qualmann (5 shared papers)Andreas Gal (7 shared papers)Moritz Hentschke (6 shared papers)
- Journals
- Nature (8 papers)Nature Genetics (8 papers)The American Journal of Human Genetics (7 papers)Journal of Clinical Investigation (6 papers)Clinical Genetics (5 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Ingo Kurth
160 papers receiving 9.8k citations
Ingo Kurth's Hit Papers
Peers
Comparison fields: 5 of 116
- Developmental Biology 108
- Cellular and Molecular Neuroscience 659
- Infectious Diseases 862
- Neurology 430
- Molecular Biology 1.6k
Countries citing papers authored by Ingo Kurth
This map shows the geographic impact of Ingo Kurth'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 Ingo Kurth with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingo Kurth more than expected).
Fields of papers citing papers by Ingo Kurth
This network shows the impact of papers produced by Ingo Kurth. 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 Ingo Kurth. The network helps show where Ingo Kurth may publish in the future.
Co-authors
The 25 scholars most cited alongside Ingo Kurth, 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 172 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment Hit paper breakdown → | 2020 | 1114 |
| 2 | Regulation of endoplasmic reticulum turnover by selective autophagy Hit paper breakdown → | 2015 | 786 |
| 3 | Mapping the human genetic architecture of COVID-19 Hit paper breakdown → | 2021 | 656 |
| 4 | Swarm Learning for decentralized and confidential clinical machine learning Hit paper breakdown → | 2021 | 646 |
| 5 | 2016 | 497 | |
| 6 | Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis Hit paper breakdown → | 2016 | 457 |
| 7 | 2020 | 283 | |
| 8 | 2008 | 276 | |
| 9 | 2010 | 273 | |
| 10 | 2013 | 252 | |
| 11 | 2009 | 215 | |
| 12 | 2021 | 183 | |
| 13 | 2010 | 155 | |
| 14 | 2007 | 136 | |
| 15 | 2015 | 128 | |
| 16 | 2019 | 123 | |
| 17 | Aberrant phase separation and nucleolar dysfunction in rare genetic diseases Hit paper breakdown → | 2023 | 110 |
| 18 | 2005 | 108 | |
| 19 | 2015 | 107 | |
| 20 | 2009 | 97 |
About Ingo Kurth
Ingo Kurth is a scholar working on Cellular and Molecular Neuroscience, Genetics, Molecular Biology, Genetics and Developmental Biology, having authored 172 papers that have together received 10.0k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (28 papers), Genomics and Rare Diseases (10 papers), Genetic Syndromes and Imprinting (8 papers), Cytokine Signaling Pathways and Interactions (5 papers), Ion Transport and Channel Regulation (5 papers), Ion channel regulation and function (4 papers), Muscle Physiology and Disorders (4 papers) and Pain Mechanisms and Treatments (4 papers). The work is most often cited by research in Developmental Biology (108 citations), Cellular and Molecular Neuroscience (659 citations), Infectious Diseases (862 citations), Neurology (430 citations) and Molecular Biology (1.6k citations). Ingo Kurth has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Christian Andreas Hübner, Antje K. Huebner, Joachim Weis, Nicole Koch, Sándor Nietzsche, Britta Qualmann, Andreas Gal, Moritz Hentschke, Theresa Heinrich and Lutz Liebmann. Their work appears in journals such as Nature, Nature Genetics, The American Journal of Human Genetics, Journal of Clinical Investigation and Clinical Genetics.
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.