Peter Emil Becker
Impact in
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- Genetic Neurodegenerative Diseases
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- Neurogenetic and Muscular Disorders Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- Genetic Neurodegenerative Diseases 11
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- Muscle Physiology and Disorders 5
- Ion channel regulation and function 3
- Mitochondrial Function and Pathology 3
- 14-3-3 protein interactions 1
- Co-authors
- J. Michael Schr�der (1 shared paper)Carsten G. Bönnemann (1 shared paper)Knut Brockmann (1 shared paper)Gudrun Schreiber (1 shared paper)Karin Neubert (1 shared paper)Edgar Brunner (1 shared paper)Paul Eberlé (2 shared papers)FP Lenz (1 shared paper)
- Journals
- Human Genetics (8 papers)European Archives of Psychiatry and Clinical Neuroscience (4 papers)Neuromuscular Disorders (1 paper)Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin (1 paper)Journal of Neurology (1 paper)
- Partner nations
- GermanyUnited States
In The Last Decade
Peter Emil Becker
27 papers receiving 442 citations
Peers
Comparison fields: 5 of 75
- Cellular and Molecular Neuroscience 138
- Genetics 74
- Molecular Biology 316
- Cardiology and Cardiovascular Medicine 90
- Neurology 47
Countries citing papers authored by Peter Emil Becker
This map shows the geographic impact of Peter Emil Becker'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 Peter Emil Becker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter Emil Becker more than expected).
Fields of papers citing papers by Peter Emil Becker
This network shows the impact of papers produced by Peter Emil Becker. 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 Peter Emil Becker. The network helps show where Peter Emil Becker may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter Emil Becker, 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 29 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1955 | 163 | |
| 2 | 2007 | 63 | |
| 3 | 1967 | 45 | |
| 4 | 1972 | 35 | |
| 5 | 1972 | 32 | |
| 6 | Paramyotonia congenita : (Eulenburg) | 1970 | 23 |
| 7 | 1979 | 22 | |
| 8 | Myotonia congenita and syndromes associated with myotonia: Clinical-genetic studies of the nondystrophic myotonias | 1977 | 16 |
| 9 | 1986 | 15 | |
| 10 | 1973 | 14 | |
| 11 | 1966 | 14 | |
| 12 | [Estimation of mutation rate in muscular dystrophy]. | 1955 | 12 |
| 13 | 1964 | 9 | |
| 14 | 2007 | 9 | |
| 15 | 1952 | 9 | |
| 16 | 1985 | 8 | |
| 17 | 2000 | 7 | |
| 18 | 1964 | 7 | |
| 19 | Zur Geschichte der Rassenhygiene | 1988 | 6 |
| 20 | 1971 | 5 |
About Peter Emil Becker
Peter Emil Becker is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Genetics, Neurology and Genetics, having authored 29 papers that have together received 534 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (11 papers), Muscle Physiology and Disorders (5 papers), Ion channel regulation and function (3 papers), Mitochondrial Function and Pathology (3 papers), Neurogenetic and Muscular Disorders Research (2 papers), Biotin and Related Studies (1 paper), 14-3-3 protein interactions (1 paper) and Behavioral Health and Interventions (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (138 citations), Genetics (74 citations), Molecular Biology (316 citations), Cardiology and Cardiovascular Medicine (90 citations) and Neurology (47 citations). Peter Emil Becker has collaborated with scholars based in Germany and United States. Frequent co-authors include J. Michael Schr�der, Carsten G. Bönnemann, Knut Brockmann, Gudrun Schreiber, Karin Neubert, Edgar Brunner, Paul Eberlé, FP Lenz, Hans Orthner and Dieter Müller. Their work appears in journals such as Human Genetics, European Archives of Psychiatry and Clinical Neuroscience, Neuromuscular Disorders, Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin and Journal of 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.