Julie Bouron
Impact in
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- Craniofacial Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Ocular Disorders and Treatments
- Cleft Lip and Palate Research
- Virus-based gene therapy research
Papers in
- Genetics 6
- Genomic variations and chromosomal abnormalities 4
- Congenital Ear and Nasal Anomalies 2
- Ocular Disorders and Treatments 2
- Dermatological and Skeletal Disorders 1
- Connective tissue disorders research 1
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- CRISPR and Genetic Engineering 2
- Wnt/β-catenin signaling in development and cancer 1
- Co-authors
- Caroline Rooryck (7 shared papers)Dorothée Cailley (4 shared papers)Benoı̂t Arveiler (5 shared papers)Jérôme Toutain (5 shared papers)Cyril Goizet (3 shared papers)Didier Lacombe (5 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)European Journal of Human Genetics (1 paper)American Journal of Medical Genetics Part A (1 paper)Clinical Dysmorphology (1 paper)
- Partner nations
- FranceMartinique
In The Last Decade
Julie Bouron
8 papers receiving 155 citations
Peers
Comparison fields: 5 of 34
- Genetics 104
- Business and International Management 4
- Pediatrics, Perinatology and Child Health 38
- Genetics 20
- Developmental Biology 4
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 | 50 | |
| 2 | 2010 | 44 | |
| 3 | 2013 | 24 | |
| 4 | 2011 | 20 | |
| 5 | 2023 | 16 | |
| 6 | 2012 | 4 | |
| 7 | 2018 | 3 | |
| 8 | 2017 | 1 |
About Julie Bouron
Julie Bouron is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Developmental Biology, having authored 8 papers that have together received 162 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Congenital Ear and Nasal Anomalies (2 papers), CRISPR and Genetic Engineering (2 papers), Ocular Disorders and Treatments (2 papers), Innovation and Socioeconomic Development (1 paper), Dermatological and Skeletal Disorders (1 paper), Connective tissue disorders research (1 paper) and Wnt/β-catenin signaling in development and cancer (1 paper). The work is most often cited by research in Genetics (104 citations), Business and International Management (4 citations), Pediatrics, Perinatology and Child Health (38 citations), Genetics (20 citations) and Developmental Biology (4 citations). Julie Bouron has collaborated with scholars based in France and Martinique. Frequent co-authors include Caroline Rooryck, Dorothée Cailley, Benoı̂t Arveiler, Jérôme Toutain, Cyril Goizet, Didier Lacombe, Marie‐Ange Delrue, Sandrine Marlin, Perrine Pennamen and Élodie Richard. Their work appears in journals such as European Journal of Medical Genetics, Nature Communications, European Journal of Human Genetics, American Journal of Medical Genetics Part A and Clinical Dysmorphology.
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.