Julie Bouron
Impact in
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- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
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- Genetic Neurodegenerative Diseases
Papers in
- Genetics 8
- Genomic variations and chromosomal abnormalities 5
- Connective tissue disorders research 2
- Congenital Ear and Nasal Anomalies 2
- Ocular Disorders and Treatments 2
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- CRISPR and Genetic Engineering 2
- RNA regulation and disease 2
- Co-authors
- Caroline Rooryck (10 shared papers)Benoı̂t Arveiler (7 shared papers)Dorothée Cailley (5 shared papers)Jérôme Toutain (5 shared papers)Cyril Goizet (4 shared papers)Didier Lacombe (8 shared papers)Marie‐Ange Delrue (1 shared paper)Sandrine Marlin (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Nature Communications (2 papers)Pigment Cell & Melanoma Research (1 paper)European Journal of Paediatric Neurology (1 paper)Clinical Genetics (1 paper)
- Partner nations
- FranceMartinique
In The Last Decade
Julie Bouron
14 papers receiving 321 citations
Peers
Comparison fields: 5 of 52
- Genetics 151
- Cellular and Molecular Neuroscience 53
- Neurology 21
- Genetics 25
- Pediatrics, Perinatology and Child Health 42
Countries citing papers authored by Julie Bouron
This map shows the geographic impact of Julie Bouron'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 Julie Bouron with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julie Bouron more than expected).
Fields of papers citing papers by Julie Bouron
This network shows the impact of papers produced by Julie Bouron. 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 Julie Bouron. The network helps show where Julie Bouron may publish in the future.
Co-authors
The 25 scholars most cited alongside Julie Bouron, 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 | 2021 | 60 | |
| 2 | 2015 | 57 | |
| 3 | 2010 | 52 | |
| 4 | 2014 | 48 | |
| 5 | 2013 | 28 | |
| 6 | 2011 | 22 | |
| 7 | 2016 | 21 | |
| 8 | 2023 | 17 | |
| 9 | 2014 | 9 | |
| 10 | 2012 | 7 | |
| 11 | 2015 | 3 | |
| 12 | 2017 | 3 | |
| 13 | 2018 | 3 | |
| 14 | 2017 | 1 |
About Julie Bouron
Julie Bouron is a scholar working on Genetics, Molecular Biology, Genetics, Cell Biology and Cellular and Molecular Neuroscience, having authored 14 papers that have together received 331 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), CRISPR and Genetic Engineering (2 papers), Connective tissue disorders research (2 papers), Congenital Ear and Nasal Anomalies (2 papers), RNA regulation and disease (2 papers), Genetic Neurodegenerative Diseases (2 papers), Ocular Disorders and Treatments (2 papers) and Innovation and Socioeconomic Development (1 paper). The work is most often cited by research in Genetics (151 citations), Cellular and Molecular Neuroscience (53 citations), Neurology (21 citations), Genetics (25 citations) and Pediatrics, Perinatology and Child Health (42 citations). Julie Bouron has collaborated with scholars based in France and Martinique. Frequent co-authors include Caroline Rooryck, Benoı̂t Arveiler, Dorothée Cailley, Jérôme Toutain, Cyril Goizet, Didier Lacombe, Marie‐Ange Delrue, Sandrine Marlin, Grégoire Cullot and Perrine Pennamen. Their work appears in journals such as European Journal of Medical Genetics, Nature Communications, Pigment Cell & Melanoma Research, European Journal of Paediatric Neurology and Clinical 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.