J. Beckmann
- Cell Biology top 0.1%
- Calpain Protease Function and Regulation 35
- Molecular Biology top 0.1%
- Muscle Physiology and Disorders 62
- RNA and protein synthesis mechanisms 21
- RNA modifications and cancer 18
- Genetics top 0.1%
- Genetic Mapping and Diversity in Plants and Animals 23
- Genomic variations and chromosomal abnormalities 22
- Cellular and Molecular Neuroscience top 0.5%
- Genetic Neurodegenerative Diseases 22
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- Cardiomyopathy and Myosin Studies 21
J. Beckmann
282 papers receiving 20.5k citations
Hit Papers
Peers
Comparison fields: 5 of 186
- Cell Biology 3.4k
- Molecular Biology 13.8k
- Genetics 5.3k
- Cellular and Molecular Neuroscience 2.7k
- Cardiology and Cardiovascular Medicine 2.4k
Countries citing papers authored by J. Beckmann
This map shows the geographic impact of J. Beckmann'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 J. Beckmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J. Beckmann more than expected).
Fields of papers citing papers by J. Beckmann
This network shows the impact of papers produced by J. Beckmann. 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 J. Beckmann. The network helps show where J. Beckmann may publish in the future.
Co-authorship network
The 25 scholars most cited alongside J. Beckmann, 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 | From evidence-based to precision medicine: Challenges and opportunities | 2017 | 1 |
| 2 | 2014 | 12 | |
| 3 | A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disordersbreakdown → | 2014 | 375 |
| 4 | 2013 | 36 | |
| 5 | 2012 | 17 | |
| 6 | 2010 | 6 | |
| 7 | Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration | 2009 | 8 |
| 8 | A Single-Base Substitution Within an Intronic Repetitive Element in PRPF31 Causes Dominant Retinitis Pigmentosa With Reduced Penetrance | 2009 | 6 |
| 9 | 2000 | 77 | |
| 10 | Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatallybreakdown → | 1998 | 999 |
| 11 | 1996 | 3 | |
| 12 | 1994 | 44 | |
| 13 | 1994 | 3 | |
| 14 | Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. | 1992 | 11 |
| 15 | RFLP analysis of a hybrid cultivar of pepper (Capsicum annuum) and its use in distinguishing between parental lines and in hybrid identification. | 1990 | 11 |
| 16 | 1988 | 10 | |
| 17 | 1987 | 157 | |
| 18 | Restriction fragment length polymorphisms in dairy cattle genetic improvement. | 1986 | 8 |
| 19 | 1983 | 257 | |
| 20 | 1980 | 3 |
About J. Beckmann
J. Beckmann is a scholar working on Cell Biology, Genetics and Molecular Biology, having authored 289 papers that have together received 21.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (62 papers), Calpain Protease Function and Regulation (35 papers), Genetic Mapping and Diversity in Plants and Animals (23 papers), Genomic variations and chromosomal abnormalities (22 papers), Genetic Neurodegenerative Diseases (22 papers), RNA and protein synthesis mechanisms (21 papers), Cardiomyopathy and Myosin Studies (21 papers) and RNA modifications and cancer (18 papers). The work is most often cited by research in Cell Biology (3.4k citations), Molecular Biology (13.8k citations) and Genetics (5.3k citations). J. Beckmann has collaborated with scholars based in France, Switzerland and United States. Frequent co-authors include M. Soller, Françoise Fougerousse, J. L. Weber, Stylianos E. Antonarakis, Isabelle Richard, Matthias Soller, Michel Fardeau, Jianjun Chen, Margaret M. Tarpey and Peter G. Anderson. Their work appears in journals such as Human Molecular Genetics, Genomics, Neuromuscular Disorders, The American Journal of Human Genetics and Nucleic Acids Research.
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.