J. Beckmann
Impact in
- Genetics top 0.1%
- Genetic Mapping and Diversity in Plants and Animals
- Molecular Biology top 0.1%
- Muscle Physiology and Disorders
- RNA Research and Splicing
- RNA and protein synthesis mechanisms
Papers in
-
- Muscle Physiology and Disorders 61
- RNA and protein synthesis mechanisms 20
- Genetics 91
- Genetic Mapping and Diversity in Plants and Animals 25
- Genomic variations and chromosomal abnormalities 22
- Genetic Associations and Epidemiology 18
- Co-authors
- M. Soller (21 shared papers)Françoise Fougerousse (28 shared papers)J. L. Weber (1 shared paper)Stylianos E. Antonarakis (10 shared papers)Matthias Soller (2 shared papers)Michel Fardeau (11 shared papers)Daniel Cohen (12 shared papers)Joel L. Sussman (4 shared papers)
- Journals
- Human Molecular Genetics (19 papers)Genomics (14 papers)Neuromuscular Disorders (11 papers)The American Journal of Human Genetics (10 papers)Nature Genetics (9 papers)
- Partner nations
- FranceSwitzerlandUnited States
In The Last Decade
J. Beckmann
290 papers receiving 21.1k citations
J. Beckmann's Hit Papers
Peers
Comparison fields: 5 of 189
- Genetics 5.6k
- Molecular Biology 13.8k
- Cell Biology 3.3k
- Cellular and Molecular Neuroscience 2.6k
- Cardiology and Cardiovascular Medicine 2.3k
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-authors
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
Showing the 20 most-cited of 296 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Targeted Disruption of the Mouse Caspase 8 Gene Ablates Cell Death Induction by the TNF Receptors, Fas/Apo1, and DR3 and Is Lethal Prenatally Hit paper breakdown → | 1998 | 1042 |
| 2 | Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A Hit paper breakdown → | 1995 | 819 |
| 3 | FoldIndex(C): a simple tool to predict whether a given protein sequence is intrinsically unfolded Hit paper breakdown → | 2005 | 793 |
| 4 | A Highly Significant Association between a COMT Haplotype and Schizophrenia Hit paper breakdown → | 2002 | 593 |
| 5 | Familial Hyperglycemia Due to Mutations in Glucokinase -- Definition of a Subtype of Diabetes Mellitus Hit paper breakdown → | 1993 | 581 |
| 6 | A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B Hit paper breakdown → | 1998 | 543 |
| 7 | Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats Hit paper breakdown → | 1991 | 521 |
| 8 | 1997 | 499 | |
| 9 | 1992 | 489 | |
| 10 | 1992 | 458 | |
| 11 | 1999 | 437 | |
| 12 | 2001 | 417 | |
| 13 | 1994 | 397 | |
| 14 | A Higher Mutational Burden in Females Supports a “Female Protective Model” in Neurodevelopmental Disorders Hit paper breakdown → | 2014 | 394 |
| 15 | 1995 | 369 | |
| 16 | 2007 | 328 | |
| 17 | 2000 | 319 | |
| 18 | 1983 | 312 | |
| 19 | 2011 | 310 | |
| 20 | 1978 | 310 |
About J. Beckmann
J. Beckmann is a scholar working on Molecular Biology, Genetics, Cell Biology, Cellular and Molecular Neuroscience and Plant Science, having authored 296 papers that have together received 22.4k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (61 papers), Calpain Protease Function and Regulation (34 papers), Genetic Mapping and Diversity in Plants and Animals (25 papers), Genomic variations and chromosomal abnormalities (22 papers), Genetic Neurodegenerative Diseases (22 papers), Cardiomyopathy and Myosin Studies (20 papers), RNA and protein synthesis mechanisms (20 papers) and Genetic Associations and Epidemiology (18 papers). The work is most often cited by research in Genetics (5.6k citations), Molecular Biology (13.8k citations), Cell Biology (3.3k citations), Cellular and Molecular Neuroscience (2.6k citations) and Cardiology and Cardiovascular Medicine (2.3k 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, Matthias Soller, Michel Fardeau, Daniel Cohen, Joel L. Sussman, Israel Silman and Orna Man. Their work appears in journals such as Human Molecular Genetics, Genomics, Neuromuscular Disorders, The American Journal of Human Genetics and Nature Genetics.
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.