P. E. Becker
Impact in
- Genetics top 10%
- Neurogenetic and Muscular Disorders Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Genetic Neurodegenerative Diseases
Papers in
-
- Muscle Physiology and Disorders 5
- Mitochondrial Function and Pathology 3
- Ion channel regulation and function 3
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- Genetic Neurodegenerative Diseases 11
- Co-authors
- J. M. Schr�der (1 shared paper)Knut Brockmann (1 shared paper)Edgar Brunner (1 shared paper)Carsten G. Bönnemann (1 shared paper)Gudrun Schreiber (1 shared paper)Karin Neubert (1 shared paper)Paul Eberlé (2 shared papers)F. Lenz (1 shared paper)
- Journals
- Human Genetics (8 papers)European Archives of Psychiatry and Clinical Neuroscience (4 papers)Gastroenterology (2 papers)Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin (1 paper)Neuromuscular Disorders (1 paper)
- Partner nations
- GermanyUnited States
In The Last Decade
P. E. Becker
29 papers receiving 441 citations
Peers
Comparison fields: 5 of 74
- Genetics 74
- Cellular and Molecular Neuroscience 134
- Molecular Biology 307
- Cardiology and Cardiovascular Medicine 87
- Rheumatology 46
Countries citing papers authored by P. E. Becker
This map shows the geographic impact of P. E. 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 P. E. Becker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. E. Becker more than expected).
Fields of papers citing papers by P. E. Becker
This network shows the impact of papers produced by P. E. 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 P. E. Becker. The network helps show where P. E. Becker may publish in the future.
Co-authors
The 25 scholars most cited alongside P. E. 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 30 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1955 | 158 | |
| 2 | 2007 | 60 | |
| 3 | 1967 | 45 | |
| 4 | 1972 | 35 | |
| 5 | 1972 | 31 | |
| 6 | Paramyotonia congenita : (Eulenburg) | 1970 | 23 |
| 7 | 1979 | 21 | |
| 8 | 1986 | 16 | |
| 9 | Myotonia congenita and syndromes associated with myotonia: Clinical-genetic studies of the nondystrophic myotonias | 1977 | 16 |
| 10 | 1973 | 14 | |
| 11 | 1966 | 14 | |
| 12 | [Estimation of mutation rate in muscular dystrophy]. | 1955 | 12 |
| 13 | 1952 | 10 | |
| 14 | 1964 | 9 | |
| 15 | 2007 | 9 | |
| 16 | 1985 | 8 | |
| 17 | 2000 | 7 | |
| 18 | 1964 | 7 | |
| 19 | Zur Geschichte der Rassenhygiene | 1988 | 6 |
| 20 | 1971 | 5 |
About P. E. Becker
P. E. Becker is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Genetics, having authored 30 papers that have together received 528 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (11 papers), Muscle Physiology and Disorders (5 papers), Mitochondrial Function and Pathology (3 papers), Ion channel regulation and function (3 papers), Liver Disease Diagnosis and Treatment (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Behavioral Health and Interventions (1 paper) and Amyotrophic Lateral Sclerosis Research (1 paper). The work is most often cited by research in Genetics (74 citations), Cellular and Molecular Neuroscience (134 citations), Molecular Biology (307 citations), Cardiology and Cardiovascular Medicine (87 citations) and Rheumatology (46 citations). P. E. Becker has collaborated with scholars based in Germany and United States. Frequent co-authors include J. M. Schr�der, Knut Brockmann, Edgar Brunner, Carsten G. Bönnemann, Gudrun Schreiber, Karin Neubert, Paul Eberlé, F. Lenz, Dieter Müller and Rainer Knußmann. Their work appears in journals such as Human Genetics, European Archives of Psychiatry and Clinical Neuroscience, Gastroenterology, Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin and Neuromuscular Disorders.
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.