Stéphane Llense
Impact in
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- Muscle Physiology and Disorders
- Nuclear Structure and Function
- RNA Research and Splicing
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
Papers in
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- Muscle Physiology and Disorders 10
- Nuclear Structure and Function 1
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- Cardiomyopathy and Myosin Studies 2
- Co-authors
- France Leturcq (9 shared papers)Nathalie Deburgrave (7 shared papers)Dominique Récan (9 shared papers)Jean‐Claude Kaplan (5 shared papers)Jamel Chelly (4 shared papers)Fatma Daoud (2 shared papers)Cécile Peccate (3 shared papers)Christophe Béroud (2 shared papers)
In The Last Decade
Stéphane Llense
11 papers receiving 345 citations
Peers
Comparison fields: 5 of 21
- Molecular Biology 302
- Genetics 61
- Clinical Biochemistry 9
- Cardiology and Cardiovascular Medicine 40
- Genetics 9
Countries citing papers authored by Stéphane Llense
This map shows the geographic impact of Stéphane Llense'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 Stéphane Llense with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stéphane Llense more than expected).
Fields of papers citing papers by Stéphane Llense
This network shows the impact of papers produced by Stéphane Llense. 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 Stéphane Llense. The network helps show where Stéphane Llense may publish in the future.
Co-authors
The 25 scholars most cited alongside Stéphane Llense, 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 | 2006 | 104 | |
| 2 | 2008 | 71 | |
| 3 | 2007 | 58 | |
| 4 | 2003 | 46 | |
| 5 | 1998 | 33 | |
| 6 | Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy. | 2000 | 14 |
| 7 | 2001 | 12 | |
| 8 | 1997 | 8 | |
| 9 | [Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias]. | 2003 | 6 |
| 10 | 2006 | 3 | |
| 11 | 2006 | 1 |
About Stéphane Llense
Stéphane Llense is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine, Genetics, Nuclear Energy and Engineering and Waste Management and Disposal, having authored 11 papers that have together received 356 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Cardiomyopathy and Myosin Studies (2 papers), Nuclear Structure and Function (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Molecular Biology (302 citations), Genetics (61 citations), Clinical Biochemistry (9 citations), Cardiology and Cardiovascular Medicine (40 citations) and Genetics (9 citations). Stéphane Llense has collaborated with scholars based in France, Croatia and China. Frequent co-authors include France Leturcq, Nathalie Deburgrave, Dominique Récan, Jean‐Claude Kaplan, Jamel Chelly, Fatma Daoud, Cécile Peccate, Christophe Béroud, Luis Garcı́a and Arthur H.M. Burghes. Their work appears in journals such as Neuromuscular Disorders, Neurology, Human Mutation, European Journal of Human Genetics and PubMed.
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.