Konrad Oexle
- Aging top 10%
- Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders 7
- Neurology top 10%
- Parkinson's Disease Mechanisms and Treatments 5
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
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- Muscle Physiology and Disorders 8
- Mitochondrial Function and Pathology 5
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- Restless Legs Syndrome Research 8
- Co-authors
- Rémy BruggmannJanine MeienbergGábor MátyásAngelika ZwirnerJames R. ConnorStephanie M. PattonRichard P. AllenAlfried Kohlschütter
- Cited by
- AgingClinical BiochemistryNeurology
- Partner nations
- GermanySwitzerlandAustria
In The Last Decade
Konrad Oexle
57 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 99
- Aging 38
- Clinical Biochemistry 115
- Neurology 192
- Genetics 312
- Genetics 114
Countries citing papers authored by Konrad Oexle
This map shows the geographic impact of Konrad Oexle'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 Konrad Oexle with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Konrad Oexle more than expected).
Fields of papers citing papers by Konrad Oexle
This network shows the impact of papers produced by Konrad Oexle. 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 Konrad Oexle. The network helps show where Konrad Oexle may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Konrad Oexle, 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 | 2025 | 0 | |
| 2 | 2025 | 0 | |
| 3 | 2025 | 0 | |
| 4 | 2024 | 1 | |
| 5 | 2024 | 5 | |
| 6 | 2022 | 6 | |
| 7 | 2022 | 5 | |
| 8 | 2021 | 5 | |
| 9 | 2020 | 39 | |
| 10 | 2020 | 2 | |
| 11 | 2015 | 8 | |
| 12 | 2015 | 2 | |
| 13 | 2015 | 55 | |
| 14 | 2013 | 13 | |
| 15 | 2011 | 3 | |
| 16 | 2010 | 5 | |
| 17 | 2009 | 5 | |
| 18 | 2002 | 4 | |
| 19 | 2000 | 11 | |
| 20 | 1996 | 10 |
About Konrad Oexle
Konrad Oexle is a scholar working on Aging, Clinical Biochemistry and Genetics, having authored 63 papers that have together received 1.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (8 papers), Restless Legs Syndrome Research (8 papers), Metabolism and Genetic Disorders (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Mitochondrial Function and Pathology (5 papers) and Parkinson's Disease Mechanisms and Treatments (5 papers). The work is most often cited by research in Aging (38 citations), Clinical Biochemistry (115 citations) and Neurology (192 citations). Konrad Oexle has collaborated with scholars based in Germany, Switzerland and Austria. Frequent co-authors include Rémy Bruggmann, Janine Meienberg, Gábor Mátyás, Angelika Zwirner, James R. Connor, Stephanie M. Patton, Richard P. Allen, Alfried Kohlschütter, Christoph Hübner and Thomas Meitinger. Their work appears in journals such as Nature Communications, The Journal of Immunology and Diabetes Care.
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.