Pierre Billuart

6.2k total citations · 2 hit papers
63 papers, 3.8k citations indexed

About

Pierre Billuart is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Pierre Billuart has authored 63 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 38 papers in Genetics and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in Pierre Billuart's work include Genetics and Neurodevelopmental Disorders (37 papers), Ubiquitin and proteasome pathways (9 papers) and Neuroscience and Neuropharmacology Research (9 papers). Pierre Billuart is often cited by papers focused on Genetics and Neurodevelopmental Disorders (37 papers), Ubiquitin and proteasome pathways (9 papers) and Neuroscience and Neuropharmacology Research (9 papers). Pierre Billuart collaborates with scholars based in France, Italy and United States. Pierre Billuart's co-authors include Chérif Beldjord, Axel Kahn, Jamel Chelly, Béatrice Romagnolo, Monique Fabrè, Jamel Chelly, Claire-Angélique Renard, Olivier Soubrane, Christine Perret and Marie‐Annick Buendia and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Pierre Billuart

63 papers receiving 3.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Somatic mutations of the β-catenin gene are frequent in mouse and human hepatocellular carcinomas

1998 916 citations Pierre Billuart, Chérif Beldjord et al. profile →
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

1998 589 citations Vincent des Portes, Pierre Billuart et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Pierre Billuart France	30	2.4k	1.1k	887	769	473	63	3.8k
Angeliki Louvi United States	31	2.4k 1.0×	1.1k 1.0×	520 0.6×	378 0.5×	507 1.1×	43	4.0k
Chérif Beldjord France	30	2.5k 1.0×	1.3k 1.2×	686 0.8×	698 0.9×	470 1.0×	59	4.3k
G. Giacomo Consalez Italy	35	2.0k 0.9×	667 0.6×	723 0.8×	371 0.5×	454 1.0×	93	3.3k
Fadel Tissir Belgium	36	2.5k 1.1×	763 0.7×	1.7k 1.9×	1.0k 1.4×	1.1k 2.4×	99	4.4k
Matthew R. Sarkisian United States	32	1.7k 0.7×	780 0.7×	1.1k 1.2×	397 0.5×	487 1.0×	63	3.5k
Gonzalo Álvarez‐Bolado Germany	29	2.2k 0.9×	500 0.5×	759 0.9×	337 0.4×	561 1.2×	69	3.2k
Philip M. Smallwood United States	37	5.4k 2.3×	1.1k 1.0×	1.2k 1.4×	879 1.1×	214 0.5×	52	6.5k
Yvan Arsenijévic Switzerland	38	3.3k 1.4×	853 0.8×	1.1k 1.2×	297 0.4×	718 1.5×	101	4.8k
Frédéric Charron Canada	34	4.3k 1.8×	878 0.8×	1.9k 2.1×	801 1.0×	1.0k 2.1×	67	6.0k
Shinji Hirotsune Japan	34	3.9k 1.6×	1.1k 1.0×	924 1.0×	1.6k 2.1×	815 1.7×	60	5.3k

Countries citing papers authored by Pierre Billuart

Since Specialization

Citations

This map shows the geographic impact of Pierre Billuart'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 Pierre Billuart with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pierre Billuart more than expected).

Fields of papers citing papers by Pierre Billuart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pierre Billuart. 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 Pierre Billuart. The network helps show where Pierre Billuart may publish in the future.

Co-authorship network of co-authors of Pierre Billuart

This figure shows the co-authorship network connecting the top 25 collaborators of Pierre Billuart. A scholar is included among the top collaborators of Pierre Billuart 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 Pierre Billuart. Pierre Billuart is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Mariano, Vittoria, Alexandros K. Kanellopoulos, Claudia Ricci, et al.. (2023). Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization. Biological Psychiatry. 95(2). 161–174. 7 indexed citations

Moriceau, Stéphanie, Elena Dossi, Philippe Bun, et al.. (2023). Activation of the PI3K/AKT/mTOR Pathway in Cajal–Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures. International Journal of Molecular Sciences. 24(6). 5376–5376. 4 indexed citations

Cresto, Noémie, Nicolas Lebrun, Florent Dumont, et al.. (2022). Hippocampal Excitatory Synaptic Transmission and Plasticity Are Differentially Altered during Postnatal Development by Loss of the X-Linked Intellectual Disability Protein Oligophrenin-1. Cells. 11(9). 1545–1545. 4 indexed citations

Ribot, Jérôme, Charles‐Félix Calvo, Julien Moulard, et al.. (2021). Astrocytes close the mouse critical period for visual plasticity. Science. 373(6550). 77–81. 74 indexed citations

Grozdanov, Petar N., Vera M. Kalscheuer, Thierry Bienvenu, et al.. (2020). A missense mutation in the CSTF2 gene that impairs the function of the RNA recognition motif and causes defects in 3′ end processing is associated with intellectual disability in humans. Nucleic Acids Research. 48(17). 9804–9821. 12 indexed citations

Cresto, Noémie, Yoann Saillour, Grégory Ghézali, et al.. (2020). The intellectual disability protein Oligophrenin‐1 controls astrocyte morphology and migration. Glia. 68(9). 1729–1742. 6 indexed citations

Montani, Caterina, Mariana Ramos-Brossier, Luisa Ponzoni, et al.. (2017). The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity. Journal of Neuroscience. 37(28). 6606–6627. 34 indexed citations

Zhang, Chun-Lei, Xander Houbaert, Hajer El Oussini, et al.. (2017). Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 Deficiency. Journal of Neuroscience. 37(46). 11114–11126. 7 indexed citations

Compagnucci, Claudia, Sabina Barresi, Stefania Petrini, et al.. (2016). Rho Kinase Inhibition Is Essential During In Vitro Neurogenesis and Promotes Phenotypic Rescue of Human Induced Pluripotent Stem Cell-Derived Neurons With Oligophrenin-1 Loss of Function. Stem Cells Translational Medicine. 5(7). 860–869. 18 indexed citations

10.

Gorreßen, Simone, Nina Sarah Gowert, Pierre Billuart, et al.. (2016). Oligophrenin1 protects mice against myocardial ischemia and reperfusion injury by modulating inflammation and myocardial apoptosis. Cellular Signalling. 28(8). 967–978. 19 indexed citations

11.

Delépine, Chloé, Hamid Méziane, Juliette Nectoux, et al.. (2015). Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes. Human Molecular Genetics. 25(1). 146–157. 50 indexed citations

12.

Delépine, Chloé, Juliette Nectoux, Franck Letourneur, et al.. (2015). Astrocyte Transcriptome from the Mecp2308-Truncated Mouse Model of Rett Syndrome. NeuroMolecular Medicine. 17(4). 353–363. 29 indexed citations

13.

Pavlowsky, Alice, Antonella Gianfelice, Marta Pallotto, et al.. (2010). A Postsynaptic Signaling Pathway that May Account for the Cognitive Defect Due to IL1RAPL1 Mutation. Current Biology. 20(2). 103–115. 94 indexed citations

14.

Houbron, Christophe, Pierre Billuart, Isabelle Brunet, et al.. (2009). Autophosphorylation-independent and -dependent Functions of Focal Adhesion Kinase during Development. Journal of Biological Chemistry. 284(50). 34769–34776. 41 indexed citations

15.

Gambino, Frédéric, Alice Pavlowsky, Henriette Skala, et al.. (2009). IL1RAPL1 controls inhibitory networks during cerebellar development in mice. European Journal of Neuroscience. 30(8). 1476–1486. 30 indexed citations

16.

Khelfaoui, Malik, Cécile V. Denis, Frédéric de Bock, et al.. (2007). Loss of X-Linked Mental Retardation Gene Oligophrenin1 in Mice Impairs Spatial Memory and Leads to Ventricular Enlargement and Dendritic Spine Immaturity. Journal of Neuroscience. 27(35). 9439–9450. 112 indexed citations

17.

Billuart, Pierre, Jamel Chelly, & S Gilgenkrantz. (2005). Retards mentaux liés à l’X. médecine/sciences. 21(11). 947–953. 4 indexed citations

18.

Billuart, Pierre, et al.. (2001). Regulating Axon Branch Stability. Cell. 107(2). 195–207. 178 indexed citations

19.

Portes, Vincent des, Pierre Billuart, Marie Claude Vinet, et al.. (1998). A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome. Cell. 92(1). 51–61. 589 indexed citations breakdown →

20.

Billuart, Pierre, T. Bienvenu, Nathalie Ronce, et al.. (1998). Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardation.. PubMed. 46(9). 678–678. 33 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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