Bettina E. Mucha
Impact in
- Nephrology top 0.5%
- Renal Diseases and Glomerulopathies
- Chronic Kidney Disease and Diabetes
- Gout, Hyperuricemia, Uric Acid
- Genetics top 10%
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
- Genetic Associations and Epidemiology
Papers in
- Nephrology 11
- Renal Diseases and Glomerulopathies 11
- Genetics 4
- Genetic and Kidney Cyst Diseases 2
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Friedhelm Hildebrandt (12 shared papers)Fatih Özaltın (5 shared papers)Bernward G. Hinkes (5 shared papers)K Hasselbacher (3 shared papers)Arno Fuchshuber (6 shared papers)Rasheed Gbadegesin (3 shared papers)Christopher N. Vlangos (3 shared papers)Jinhong Liu (3 shared papers)
- Journals
- Kidney International (3 papers)Pediatric Nephrology (2 papers)Journal of the American Society of Nephrology (2 papers)Genetics in Medicine (2 papers)European Journal of Paediatric Neurology (1 paper)
- Partner nations
- United StatesGermanyCanada
In The Last Decade
Bettina E. Mucha
21 papers receiving 2k citations
Peers
Comparison fields: 5 of 57
- Nephrology 1.7k
- Genetics 228
- Clinical Biochemistry 36
- Transplantation 20
- Cell Biology 39
Countries citing papers authored by Bettina E. Mucha
This map shows the geographic impact of Bettina E. Mucha'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 Bettina E. Mucha with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bettina E. Mucha more than expected).
Fields of papers citing papers by Bettina E. Mucha
This network shows the impact of papers produced by Bettina E. Mucha. 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 Bettina E. Mucha. The network helps show where Bettina E. Mucha may publish in the future.
Co-authors
The 25 scholars most cited alongside Bettina E. Mucha, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 460 | |
| 2 | 2007 | 347 | |
| 3 | 2004 | 343 | |
| 4 | 2006 | 175 | |
| 5 | 2008 | 120 | |
| 6 | 2004 | 113 | |
| 7 | 2006 | 105 | |
| 8 | 2003 | 78 | |
| 9 | 2004 | 57 | |
| 10 | 2006 | 54 | |
| 11 | 2013 | 46 | |
| 12 | 2007 | 37 | |
| 13 | 2019 | 31 | |
| 14 | 2000 | 30 | |
| 15 | 2018 | 29 | |
| 16 | 2006 | 24 | |
| 17 | 2018 | 20 | |
| 18 | 2010 | 13 | |
| 19 | 2020 | 10 | |
| 20 | 2018 | 7 |
About Bettina E. Mucha
Bettina E. Mucha is a scholar working on Nephrology, Genetics, Clinical Biochemistry, Reproductive Medicine and Rheumatology, having authored 21 papers that have together received 2.1k indexed citations. Recurring topics across this work include Renal Diseases and Glomerulopathies (11 papers), Genetic and Kidney Cyst Diseases (2 papers), Muscle Physiology and Disorders (2 papers), Epilepsy research and treatment (1 paper), Metabolism and Genetic Disorders (1 paper), Hypothalamic control of reproductive hormones (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Tuberous Sclerosis Complex Research (1 paper). The work is most often cited by research in Nephrology (1.7k citations), Genetics (228 citations), Clinical Biochemistry (36 citations), Transplantation (20 citations) and Cell Biology (39 citations). Bettina E. Mucha has collaborated with scholars based in United States, Germany and Canada. Frequent co-authors include Friedhelm Hildebrandt, Fatih Özaltın, Bernward G. Hinkes, K Hasselbacher, Arno Fuchshuber, Rasheed Gbadegesin, Christopher N. Vlangos, Jinhong Liu, Michael Schultheiß and Rainer G. Ruf. Their work appears in journals such as Kidney International, Pediatric Nephrology, Journal of the American Society of Nephrology, Genetics in Medicine and European Journal of Paediatric Neurology.
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.