Joris Andrieux
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Molecular Biology top 5%
- Congenital heart defects research
Papers in
- Genetics 120
- Genomic variations and chromosomal abnormalities 92
- Genetics and Neurodevelopmental Disorders 50
- Genomics and Rare Diseases 30
- Myeloproliferative Neoplasms: Diagnosis and Treatment 14
- Hematology 25
- Acute Myeloid Leukemia Research 18
- Co-authors
- Muriel Holder‐Espinasse (15 shared papers)Cédric Le Caignec (5 shared papers)Bruno Delobel (13 shared papers)Sylvie Manouvrier‐Hanu (14 shared papers)F Bauters (7 shared papers)Stéphane Auvin (2 shared papers)Florence Petit (13 shared papers)Maria Tropeano (3 shared papers)
- Journals
- European Journal of Medical Genetics (26 papers)European Journal of Human Genetics (15 papers)Journal of Medical Genetics (12 papers)Clinical Genetics (7 papers)The American Journal of Human Genetics (5 papers)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Joris Andrieux
161 papers receiving 5.6k citations
Peers
Comparison fields: 5 of 112
- Genetics 3.7k
- Genetics 550
- Molecular Biology 2.6k
- Developmental Biology 80
- Hematology 385
Countries citing papers authored by Joris Andrieux
This map shows the geographic impact of Joris Andrieux'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 Joris Andrieux with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joris Andrieux more than expected).
Fields of papers citing papers by Joris Andrieux
This network shows the impact of papers produced by Joris Andrieux. 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 Joris Andrieux. The network helps show where Joris Andrieux may publish in the future.
Co-authors
The 25 scholars most cited alongside Joris Andrieux, 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 164 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 420 | |
| 2 | 2011 | 372 | |
| 3 | 2012 | 240 | |
| 4 | 2009 | 188 | |
| 5 | 2015 | 188 | |
| 6 | 2016 | 161 | |
| 7 | 2011 | 151 | |
| 8 | 2018 | 133 | |
| 9 | 2017 | 130 | |
| 10 | 2007 | 121 | |
| 11 | 2013 | 117 | |
| 12 | 2012 | 113 | |
| 13 | 2010 | 111 | |
| 14 | 2009 | 109 | |
| 15 | 2015 | 88 | |
| 16 | 2012 | 84 | |
| 17 | 2012 | 82 | |
| 18 | 2016 | 80 | |
| 19 | 2012 | 78 | |
| 20 | 2014 | 78 |
About Joris Andrieux
Joris Andrieux is a scholar working on Genetics, Genetics, Hematology, Molecular Biology and Pediatrics, Perinatology and Child Health, having authored 164 papers that have together received 6.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (92 papers), Genetics and Neurodevelopmental Disorders (50 papers), Congenital heart defects research (34 papers), Genomics and Rare Diseases (30 papers), Acute Myeloid Leukemia Research (18 papers), Prenatal Screening and Diagnostics (17 papers), Chromosomal and Genetic Variations (17 papers) and Myeloproliferative Neoplasms: Diagnosis and Treatment (14 papers). The work is most often cited by research in Genetics (3.7k citations), Genetics (550 citations), Molecular Biology (2.6k citations), Developmental Biology (80 citations) and Hematology (385 citations). Joris Andrieux has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Muriel Holder‐Espinasse, Cédric Le Caignec, Bruno Delobel, Sylvie Manouvrier‐Hanu, F Bauters, Stéphane Auvin, Florence Petit, Maria Tropeano, Frenny J. Sheth and Jean Luc Laı̈. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Journal of Medical Genetics, Clinical Genetics and The American Journal of Human 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.