E. Hammouda
- Molecular Biology top 10%
- Nuclear Structure and Function 2
- RNA Research and Splicing 1
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- Cardiomyopathy and Myosin Studies 1
- Genetics top 10%
- Neurogenetic and Muscular Disorders Research 1
- Cell Biology top 10%
- Developmental Biology top 10%
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- Genetic Neurodegenerative Diseases 1
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- Sports Performance and Training 1
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- Neurological diseases and metabolism 1
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- Cardiovascular and exercise physiology 1
E. Hammouda
4 papers receiving 1.1k citations
Hit Papers
Peers
Comparison fields: 5 of 49
- Molecular Biology 1.1k
- Cardiology and Cardiovascular Medicine 260
- Genetics 99
- Cell Biology 148
- Developmental Biology 17
Countries citing papers authored by E. Hammouda
This map shows the geographic impact of E. Hammouda'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 E. Hammouda with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Hammouda more than expected).
Fields of papers citing papers by E. Hammouda
This network shows the impact of papers produced by E. Hammouda. 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 E. Hammouda. The network helps show where E. Hammouda may publish in the future.
Co-authorship network
The 25 scholars most cited alongside E. Hammouda, 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 | 2009 | 28 | |
| 2 | 2008 | 72 | |
| 3 | [Oculopharyngeal muscular dystrophy: study of patients from seven Spanish families with different GCG expansions in PABP2 gene]. | 2004 | 7 |
| 4 | Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophybreakdown → | 1999 | 1032 |
About E. Hammouda
E. Hammouda is a scholar working on Complementary and alternative medicine, Neurology, Orthopedics and Sports Medicine, Animal Science and Zoology and Genetics, having authored 4 papers that have together received 1.1k indexed citations. Recurring topics across this work include Nuclear Structure and Function (2 papers), Genetic Neurodegenerative Diseases (1 paper), Sports Performance and Training (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), Cardiomyopathy and Myosin Studies (1 paper), Neurological diseases and metabolism (1 paper), Cardiovascular and exercise physiology (1 paper) and RNA Research and Splicing (1 paper). The work is most often cited by research in Molecular Biology (1.1k citations), Cardiology and Cardiovascular Medicine (260 citations), Genetics (99 citations), Cell Biology (148 citations) and Developmental Biology (17 citations). E. Hammouda has collaborated with scholars based in France, Spain and Italy. Frequent co-authors include Shaïda Varnous, Daniela Toniolo, Gisèle Bonne, Henri-Marc Bécane, Cheryl R. Greenberg, Marina Raffaele di Barletta, Michel Fardeau, Françoise Gary, J.A. Urtizberea and Luciano Merlini. Their work appears in journals such as Archives of Physical Medicine and Rehabilitation, Nature Genetics, Neuromuscular Disorders 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.