Michael Beck
Impact in
- Physiology top 0.02%
- Lysosomal Storage Disorders Research
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Papers in
- Physiology 223
- Lysosomal Storage Disorders Research 222
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- Metabolism and Genetic Disorders 1
- Co-authors
- Christoph Kampmann (37 shared papers)Atul B Mehta (33 shared papers)Catharina Whybra (36 shared papers)James Edmond Wraith (19 shared papers)Gere Sunder–Plassmann (22 shared papers)Roberto Giugliani (28 shared papers)Markus Ries (18 shared papers)Joseph Muenzer (16 shared papers)
- Journals
- Journal of Inherited Metabolic Disease (24 papers)Molecular Genetics and Metabolism (17 papers)Acta Paediatrica (14 papers)Orphanet Journal of Rare Diseases (12 papers)Human Mutation (8 papers)
- Partner nations
- GermanyUnited KingdomUnited States
In The Last Decade
Michael Beck
227 papers receiving 14.1k citations
Michael Beck's Hit Papers
Peers
Comparison fields: 5 of 123
- Physiology 13k
- Clinical Biochemistry 270
- Cardiology and Cardiovascular Medicine 286
- Anesthesiology and Pain Medicine 73
- Genetics 298
Countries citing papers authored by Michael Beck
This map shows the geographic impact of Michael Beck'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 Michael Beck with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael Beck more than expected).
Fields of papers citing papers by Michael Beck
This network shows the impact of papers produced by Michael Beck. 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 Michael Beck. The network helps show where Michael Beck may publish in the future.
Co-authors
The 25 scholars most cited alongside Michael Beck, 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 232 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey Hit paper breakdown → | 2004 | 667 |
| 2 | Recombinant human acid α-glucosidase Hit paper breakdown → | 2006 | 654 |
| 3 | 2006 | 495 | |
| 4 | 2004 | 461 | |
| 5 | 2007 | 406 | |
| 6 | 2005 | 323 | |
| 7 | 2007 | 315 | |
| 8 | 2006 | 314 | |
| 9 | 2008 | 281 | |
| 10 | 2009 | 263 | |
| 11 | 2008 | 252 | |
| 12 | 2001 | 233 | |
| 13 | 2009 | 233 | |
| 14 | 2004 | 232 | |
| 15 | 2007 | 211 | |
| 16 | 2005 | 209 | |
| 17 | 2003 | 198 | |
| 18 | 2004 | 190 | |
| 19 | 2011 | 186 | |
| 20 | 2003 | 180 |
About Michael Beck
Michael Beck is a scholar working on Physiology, Clinical Biochemistry, Genetics, Nephrology and Cell Biology, having authored 232 papers that have together received 14.9k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (222 papers), Genomics and Rare Diseases (2 papers), Bacteriophages and microbial interactions (1 paper), Salmonella and Campylobacter epidemiology (1 paper), Renal Diseases and Glomerulopathies (1 paper), Hip disorders and treatments (1 paper), Cervical and Thoracic Myelopathy (1 paper) and Metabolism and Genetic Disorders (1 paper). The work is most often cited by research in Physiology (13k citations), Clinical Biochemistry (270 citations), Cardiology and Cardiovascular Medicine (286 citations), Anesthesiology and Pain Medicine (73 citations) and Genetics (298 citations). Michael Beck has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Christoph Kampmann, Atul B Mehta, Catharina Whybra, James Edmond Wraith, Gere Sunder–Plassmann, Roberto Giugliani, Markus Ries, Joseph Muenzer, Andreas Gal and Uma Ramaswami. Their work appears in journals such as Journal of Inherited Metabolic Disease, Molecular Genetics and Metabolism, Acta Paediatrica, Orphanet Journal of Rare Diseases and Human Mutation.
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.