Karine Poirier
- Developmental Neuroscience top 2%
- Cell Biology top 2%
- Microtubule and mitosis dynamics 11
- Cellular transport and secretion 7
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders 25
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 4
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- Fetal and Pediatric Neurological Disorders 7
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- Congenital heart defects research 9
- Co-authors
- Jamel ChellyYoann SaillourNadia Bahi‐BuissonNathalie BoddaertChérif BeldjordNicolas LebrunThierry BienvenuFiona Francis
- Partner nations
- FranceUnited KingdomItaly
In The Last Decade
Karine Poirier
45 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 88
- Developmental Neuroscience 229
- Cell Biology 698
- Genetics 778
- Cellular and Molecular Neuroscience 414
- Pediatrics, Perinatology and Child Health 370
Countries citing papers authored by Karine Poirier
This map shows the geographic impact of Karine Poirier'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 Karine Poirier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karine Poirier more than expected).
Fields of papers citing papers by Karine Poirier
This network shows the impact of papers produced by Karine Poirier. 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 Karine Poirier. The network helps show where Karine Poirier may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Karine Poirier, 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 | 2024 | 0 | |
| 2 | 2023 | 16 | |
| 3 | 2022 | 4 | |
| 4 | 2022 | 2 | |
| 5 | 2018 | 17 | |
| 6 | 2017 | 23 | |
| 7 | Les ratios infirmière/résidents en CHSLD. Pénurie de soins ou pénurie d'infirmières? | 2016 | 0 |
| 8 | 2014 | 190 | |
| 9 | 2013 | 74 | |
| 10 | 2012 | 50 | |
| 11 | 2012 | 11 | |
| 12 | 2010 | 102 | |
| 13 | 2010 | 39 | |
| 14 | 2008 | 26 | |
| 15 | 2007 | 322 | |
| 16 | 2006 | 29 | |
| 17 | 2005 | 32 | |
| 18 | 2004 | 74 | |
| 19 | 2003 | 27 | |
| 20 | 2001 | 8 |
About Karine Poirier
Karine Poirier is a scholar working on Genetics, Developmental Neuroscience and Cell Biology, having authored 48 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (25 papers), Microtubule and mitosis dynamics (11 papers), Congenital heart defects research (9 papers), Cellular transport and secretion (7 papers), Fetal and Pediatric Neurological Disorders (7 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Developmental Neuroscience (229 citations), Cell Biology (698 citations) and Genetics (778 citations). Karine Poirier has collaborated with scholars based in France, United Kingdom and Italy. Frequent co-authors include Jamel Chelly, Yoann Saillour, Nadia Bahi‐Buisson, Jamel Chelly, Nathalie Boddaert, Chérif Beldjord, Nicolas Lebrun, Thierry Bienvenu, Fiona Francis and Isabelle Souville. Their work appears in journals such as Cell, Journal of Clinical Investigation and Nature Communications.
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.