John Rendu
Impact in
- Reproductive Medicine top 2%
- Sperm and Testicular Function
- Genetics top 5%
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
- Neurogenetic and Muscular Disorders Research
Papers in
-
- Muscle Physiology and Disorders 36
- Ion channel regulation and function 10
- CRISPR and Genetic Engineering 4
- Genetics 21
- Genomics and Rare Diseases 16
- Neurogenetic and Muscular Disorders Research 6
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Julien Fauré (30 shared papers)Charles Coutton (7 shared papers)Joël Lunardi (8 shared papers)Marie Bidart (3 shared papers)Pierre‐Simon Jouk (4 shared papers)Pierre F. Ray (2 shared papers)Didier Grünwald (2 shared papers)Virginie Pierre (1 shared paper)
- Journals
- Neuromuscular Disorders (7 papers)Human Mutation (4 papers)Journal of Neuromuscular Diseases (4 papers)Acta Neuropathologica Communications (4 papers)Human Molecular Genetics (3 papers)
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
John Rendu
72 papers receiving 1.7k citations
John Rendu's Hit Papers
Peers
Comparison fields: 5 of 79
- Reproductive Medicine 311
- Genetics 431
- Nephrology 114
- Molecular Biology 700
- Developmental Biology 23
Countries citing papers authored by John Rendu
This map shows the geographic impact of John Rendu'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 John Rendu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Rendu more than expected).
Fields of papers citing papers by John Rendu
This network shows the impact of papers produced by John Rendu. 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 John Rendu. The network helps show where John Rendu may publish in the future.
Co-authors
The 25 scholars most cited alongside John Rendu, 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 80 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella Hit paper breakdown → | 2013 | 364 |
| 2 | 2010 | 119 | |
| 3 | SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation Hit paper breakdown → | 2023 | 109 |
| 4 | 2016 | 87 | |
| 5 | 2014 | 78 | |
| 6 | 2018 | 46 | |
| 7 | 2019 | 41 | |
| 8 | 2015 | 39 | |
| 9 | 2021 | 39 | |
| 10 | 2017 | 38 | |
| 11 | 2016 | 36 | |
| 12 | 2017 | 33 | |
| 13 | 2017 | 33 | |
| 14 | 2020 | 33 | |
| 15 | 2013 | 32 | |
| 16 | 2014 | 31 | |
| 17 | 2018 | 30 | |
| 18 | PFMG2025–integrating genomic medicine into the national healthcare system in France Hit paper breakdown → | 2025 | 26 |
| 19 | 2016 | 24 | |
| 20 | 2018 | 24 |
About John Rendu
John Rendu is a scholar working on Molecular Biology, Genetics, Genetics, Cardiology and Cardiovascular Medicine and Clinical Biochemistry, having authored 80 papers that have together received 1.7k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (36 papers), Genomics and Rare Diseases (16 papers), Ion channel regulation and function (10 papers), Neurogenetic and Muscular Disorders Research (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Cardiomyopathy and Myosin Studies (4 papers), CRISPR and Genetic Engineering (4 papers) and Cardiac electrophysiology and arrhythmias (3 papers). The work is most often cited by research in Reproductive Medicine (311 citations), Genetics (431 citations), Nephrology (114 citations), Molecular Biology (700 citations) and Developmental Biology (23 citations). John Rendu has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Julien Fauré, Charles Coutton, Joël Lunardi, Marie Bidart, Pierre‐Simon Jouk, Pierre F. Ray, Didier Grünwald, Virginie Pierre, Denise Escalier and Nicolas Thierry‐Mieg. Their work appears in journals such as Neuromuscular Disorders, Human Mutation, Journal of Neuromuscular Diseases, Acta Neuropathologica Communications and Human Molecular 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.