Karine Poirier

5.8k total citations
48 papers, 2.1k citations indexed

About

Karine Poirier is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Karine Poirier has authored 48 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 26 papers in Molecular Biology and 15 papers in Cell Biology. Recurrent topics in Karine Poirier's work include Genetics and Neurodevelopmental Disorders (25 papers), Microtubule and mitosis dynamics (11 papers) and Congenital heart defects research (9 papers). Karine Poirier is often cited by papers focused on Genetics and Neurodevelopmental Disorders (25 papers), Microtubule and mitosis dynamics (11 papers) and Congenital heart defects research (9 papers). Karine Poirier collaborates with scholars based in France, United Kingdom and Italy. Karine Poirier's 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 and has published in prestigious journals such as Cell, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Karine Poirier

45 papers receiving 2.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Karine Poirier France 23 1.2k 778 698 414 370 48 2.1k
Yoann Saillour France 22 849 0.7× 509 0.7× 539 0.8× 380 0.9× 229 0.6× 35 1.5k
Adria Bodell United States 19 1.2k 1.0× 733 0.9× 379 0.5× 729 1.8× 586 1.6× 21 2.3k
Carlos Cardoso France 24 1.2k 1.0× 871 1.1× 286 0.4× 302 0.7× 282 0.8× 37 2.0k
Kristina M. Allen United States 10 917 0.8× 554 0.7× 354 0.5× 408 1.0× 194 0.5× 13 1.5k
Teruyuki Tanaka Japan 20 1.0k 0.9× 450 0.6× 663 0.9× 634 1.5× 196 0.5× 35 2.1k
R. Sean Hill United States 13 956 0.8× 624 0.8× 199 0.3× 286 0.7× 267 0.7× 17 1.7k
Christopher A. Walsh United States 21 659 0.6× 534 0.7× 268 0.4× 676 1.6× 755 2.0× 31 1.8k
Elena Parrini Italy 22 899 0.8× 1.0k 1.3× 227 0.3× 549 1.3× 596 1.6× 61 2.2k
Pascale Saugier-Véber France 28 1.1k 1.0× 672 0.9× 156 0.2× 437 1.1× 267 0.7× 82 2.3k
Marie Claude Vinet France 8 663 0.6× 457 0.6× 290 0.4× 315 0.8× 150 0.4× 14 1.2k

Countries citing papers authored by Karine Poirier

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Karine Poirier

This figure shows the co-authorship network connecting the top 25 collaborators of Karine Poirier. A scholar is included among the top collaborators of Karine Poirier based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Karine Poirier. Karine Poirier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Barcia, Giulia, Marlène Rio, Cyril Gitiaux, et al.. (2024). Exploring the clinical spectrum of CNTNAP2-related neurodevelopmental disorders: A case series and a literature appraisal. European Journal of Medical Genetics. 72. 104979–104979.
2.
Wang, Huilun, Xiaoqiong Wei, Gerarda Cappuccio, et al.. (2023). Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disorders. Journal of Clinical Investigation. 134(2). 16 indexed citations
3.
Turcotte, Véronique, et al.. (2022). Experience and Appreciation of Health Care Teams Regarding a New Model of Pharmaceutical Care in Long-Term Care Settings. Canadian Journal on Aging / La Revue canadienne du vieillissement. 41(3). 421–430. 2 indexed citations
4.
Poirier, Karine, Richard Belvindrah, Imane Moutkine, et al.. (2022). Novel role of the synaptic scaffold protein Dlgap4 in ventricular surface integrity and neuronal migration during cortical development. Nature Communications. 13(1). 2746–2746. 4 indexed citations
5.
Voyer, Philippe, et al.. (2016). Les ratios infirmière/résidents en CHSLD. Pénurie de soins ou pénurie d'infirmières?. 13(3). 45–50.
6.
Saillour, Yoann, Loïc Broix, Elodie Bruel‐Jungerman, et al.. (2013). Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown. Human Molecular Genetics. 23(6). 1516–1526. 39 indexed citations
7.
Poirier, Karine, Yoann Saillour, Franck J. Fourniol, et al.. (2012). Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria. European Journal of Human Genetics. 21(4). 381–385. 50 indexed citations
8.
Bahi‐Buisson, Nadia, Karine Poirier, Nathalie Boddaert, et al.. (2010). GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex. Brain. 133(11). 3194–3209. 102 indexed citations
9.
Lecourtois, Magalie, Karine Poirier, Gaëlle Friocourt, et al.. (2010). Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype. Acta Neuropathologica. 119(6). 779–789. 39 indexed citations
10.
Zanni, Ginevra, Hilde Van Esch, Yoann Saillour, et al.. (2009). A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation. Neurogenetics. 11(2). 251–255. 43 indexed citations
11.
Bahi‐Buisson, Nadia, Benôıt Girard, Agnès Gautier, et al.. (2009). Epileptic encephalopathy in a girl with an interstitial deletion of Xp22 comprising promoter and exon 1 of the CDKL5 gene. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 202–207. 20 indexed citations
12.
Saillour, Yoann, Mireille Cossée, France Leturcq, et al.. (2008). Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method. Human Mutation. 29(9). 1083–1090. 37 indexed citations
13.
Keays, David A., Guoling Tian, Karine Poirier, et al.. (2007). Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans. Cell. 128(1). 45–57. 322 indexed citations
14.
Nawara, Magdalena, Krzysztof Szczałuba, Karine Poirier, et al.. (2006). The ARX mutations: A frequent cause of X‐linked mental retardation. American Journal of Medical Genetics Part A. 140A(7). 727–732. 29 indexed citations
15.
Friocourt, Gaëlle, Karine Poirier, Sonja Rakić, John G. Parnavelas, & Jamel Chelly. (2006). The role of ARX in cortical development. European Journal of Neuroscience. 23(4). 869–876. 71 indexed citations
16.
Poirier, Karine, Didier Lacombe, Brigitte Gilbert‐Dussardier, et al.. (2005). Screening of ARX in mental retardation families: consequences for the strategy of molecular diagnosis. Neurogenetics. 7(1). 39–46. 32 indexed citations
17.
Poirier, Karine, Isabelle Souville, Cécile Laroche-Raynaud, et al.. (2005). Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation. Human Genetics. 118(1). 45–48. 19 indexed citations
18.
Friocourt, Gaëlle, Caroline Kappeler, Yoann Saillour, et al.. (2004). Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes. Molecular and Cellular Neuroscience. 28(1). 153–164. 33 indexed citations
19.
Poirier, Karine, Céline Chalas, Frédérique Tissier, et al.. (2003). Loss of parental‐specific methylation at the IGF2 locus in human hepatocellular carcinoma. The Journal of Pathology. 201(3). 473–479. 27 indexed citations
20.
Bienvenu, Thierry, Isabelle Souville, Karine Poirier, et al.. (2001). Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy. Human Mutation. 18(3). 251–252. 8 indexed citations

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.

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