Juliette Nectoux
Impact in
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Developmental Neuroscience top 10%
Papers in
-
- Muscle Physiology and Disorders 9
- Epigenetics and DNA Methylation 7
- Chromatin Remodeling and Cancer 7
- Genetics 28
- Genetics and Neurodevelopmental Disorders 23
- Genomic variations and chromosomal abnormalities 11
- Co-authors
- Thierry Bienvenu (35 shared papers)Jamel Chelly (15 shared papers)Nadia Bahi‐Buisson (14 shared papers)Yann Fichou (9 shared papers)Benôıt Girard (5 shared papers)Nathalie Boddaert (4 shared papers)Chloé Delépine (7 shared papers)Haydeé Rosas‐Vargas (4 shared papers)
- Journals
- Neuromuscular Disorders (7 papers)Neurogenetics (3 papers)Prenatal Diagnosis (2 papers)Journal of Molecular Diagnostics (2 papers)PLoS ONE (2 papers)
- Partner nations
- FranceUnited StatesBelgium
In The Last Decade
Juliette Nectoux
57 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 75
- Genetics 722
- Developmental Neuroscience 52
- Cognitive Neuroscience 177
- Molecular Biology 533
- Pediatrics, Perinatology and Child Health 130
Countries citing papers authored by Juliette Nectoux
This map shows the geographic impact of Juliette Nectoux'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 Juliette Nectoux with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Juliette Nectoux more than expected).
Fields of papers citing papers by Juliette Nectoux
This network shows the impact of papers produced by Juliette Nectoux. 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 Juliette Nectoux. The network helps show where Juliette Nectoux may publish in the future.
Co-authors
The 25 scholars most cited alongside Juliette Nectoux, 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 61 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 209 | |
| 2 | 2007 | 96 | |
| 3 | 2009 | 74 | |
| 4 | 2003 | 66 | |
| 5 | 2009 | 57 | |
| 6 | 2018 | 52 | |
| 7 | 2015 | 50 | |
| 8 | 2016 | 42 | |
| 9 | 2016 | 39 | |
| 10 | 2008 | 39 | |
| 11 | 2015 | 38 | |
| 12 | 2010 | 35 | |
| 13 | 2006 | 30 | |
| 14 | 2010 | 30 | |
| 15 | 2015 | 30 | |
| 16 | 2018 | 29 | |
| 17 | 2010 | 28 | |
| 18 | 2012 | 28 | |
| 19 | 2010 | 27 | |
| 20 | 2008 | 24 |
About Juliette Nectoux
Juliette Nectoux is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cardiology and Cardiovascular Medicine and Plant Science, having authored 61 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (23 papers), Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (11 papers), Muscle Physiology and Disorders (9 papers), Epigenetics and DNA Methylation (7 papers), Chromatin Remodeling and Cancer (7 papers), Cardiomyopathy and Myosin Studies (5 papers) and Autism Spectrum Disorder Research (4 papers). The work is most often cited by research in Genetics (722 citations), Developmental Neuroscience (52 citations), Cognitive Neuroscience (177 citations), Molecular Biology (533 citations) and Pediatrics, Perinatology and Child Health (130 citations). Juliette Nectoux has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Thierry Bienvenu, Jamel Chelly, Nadia Bahi‐Buisson, Yann Fichou, Benôıt Girard, Nathalie Boddaert, Chloé Delépine, Haydeé Rosas‐Vargas, Marlène Rio and France Leturcq. Their work appears in journals such as Neuromuscular Disorders, Neurogenetics, Prenatal Diagnosis, Journal of Molecular Diagnostics and PLoS ONE.
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.