B. Eymard
About
In The Last Decade
B. Eymard
29 papers receiving 528 citations
Peers
Comparison fields: 5 of 65
- Molecular Biology 239
- Neurology 164
- Cellular and Molecular Neuroscience 156
- Cardiology and Cardiovascular Medicine 93
- Rheumatology 70
Countries citing papers authored by B. Eymard
This map shows the geographic impact of B. Eymard'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 B. Eymard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B. Eymard more than expected).
Fields of papers citing papers by B. Eymard
This network shows the impact of papers produced by B. Eymard. 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 B. Eymard. The network helps show where B. Eymard may publish in the future.
Co-authorship network of co-authors of B. Eymard
This figure shows the co-authorship network connecting the top 25 collaborators of B. Eymard. A scholar is included among the top collaborators of B. Eymard based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with B. Eymard. B. Eymard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 14 | |
| 4 | 21 | |
| 5 | 32 | |
| 6 | 18 | |
| 7 | 6 | |
| 8 | 66 | |
| 9 | 51 | |
| 10 | Desminopathies : What can we learn from a long term follow-up? | 0 |
| 11 | 1 | |
| 12 | 107 | |
| 13 | Congenital myasthenic syndrome type Ia - Clinical phenotyping and genetic epidemiology | 1 |
| 14 | 19 | |
| 15 | ["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data]. | 9 |
| 16 | [Severe cardiomyopathy revealing amylopectinosis. Two cases in adolescents from the same family]. | 12 |
| 17 | [Cardiac involvement in certain muscular diseases. Apropos of 216 cases]. | 6 |
| 18 | [Paraneoplastic myasthenic syndrome]. | 4 |
| 19 | 56 | |
| 20 | [Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]. | 3 |
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.