Publications by authors named "Pierre Billuart"

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Intellectual Disability and Behavioral Deficits Linked to CYFIP1 Missense Variants Disrupting Actin Polymerization.
Vittoria Mariano, Alexandros K Kanellopoulos, Carlotta Ricci, Daniele Di Marino, Sarah C Borrie, Pierre Billuart

Biol Psychiatry· January 2024

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Activation of the PI3K/AKT/mTOR Pathway in Cajal-Retzius Cells Leads to Their Survival and Increases Susceptibility to Kainate-Induced Seizures.
Nasim Ramezanidoraki, Driss El Ouardi, Margaux Le, Stéphanie Moriceau, Mahboubeh Ahmadi, Pierre Billuart

Int J Mol Sci· March 2023

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Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.
Hamid Meziane, Marie-Christine Birling, Olivia Wendling, Sophie Leblanc, Aline Dubos, Pierre Billuart

Biomedicines· December 2022

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Hippocampal Excitatory Synaptic Transmission and Plasticity Are Differentially Altered during Postnatal Development by Loss of the X-Linked Intellectual Disability Protein Oligophrenin-1.
Noemie Cresto, Nicolas Lebrun, Florent Dumont, Franck Letourneur, Pierre Billuart

Cells· May 2022

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Astrocytes close the mouse critical period for visual plasticity.
Jérôme Ribot, Rachel Breton, Charles-Félix Calvo, Julien Moulard, Pascal Ezan, Pierre Billuart

Science· July 2021

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[A role for astrocytes in intellectual disabilities?].
Noémie Cresto, Pierre Billuart, Nathalie Rouach

Med Sci (Paris)· October 2020

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The intellectual disability protein Oligophrenin-1 controls astrocyte morphology and migration.
Laure-Elise Pillet, Noémie Cresto, Yoann Saillour, Grégory Ghézali, Alexis-Pierre Bemelmans, Pierre Billuart

Glia· September 2020

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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.
Petar N Grozdanov, Elahe Masoumzadeh, Vera M Kalscheuer, Thierry Bienvenu, Pierre Billuart

Nucleic Acids Res· September 2020

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ROCK/PKA Inhibition Rescues Hippocampal Hyperexcitability and GABAergic Neuron Alterations in a Oligophrenin-1 Knock-Out Mouse Model of X-Linked Intellectual Disability.
Irene Busti, Manuela Allegra, Cristina Spalletti, Chiara Panzi, Laura Restani, Pierre Billuart

J Neurosci· March 2020

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Do Astrocytes Play a Role in Intellectual Disabilities?
Noémie Cresto, Laure-Elise Pillet, Pierre Billuart, Nathalie Rouach

Trends Neurosci· August 2019

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IL-38 Ameliorates Skin Inflammation and Limits IL-17 Production from γδ T Cells.
Yingying Han, Javier Mora, Arnaud Huard, Priscila da Silva, Svenja Wiechmann, Pierre Billuart

Cell Rep· April 2019

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Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences.
Nicolas Lebrun, Claire Mehler-Jacob, Karine Poirier, Cecile Zordan, Didier Lacombe, Pierre Billuart

Gene· December 2018

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RNA Sequencing and Pathway Analysis Identify Important Pathways Involved in Hypertrichosis and Intellectual Disability in Patients with Wiedemann-Steiner Syndrome.
Léo Mietton, Nicolas Lebrun, Irina Giurgea, Alice Goldenberg, Benjamin Saintpierre, Pierre Billuart

Neuromolecular Med· September 2018

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Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome.
Nicolas Lebrun, Irina Giurgea, Alice Goldenberg, Anne Dieux, Alexandra Afenjar, Pierre Billuart

Eur J Hum Genet· January 2018

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Protein Kinase A Deregulation in the Medial Prefrontal Cortex Impairs Working Memory in Murine Oligophrenin-1 Deficiency.
Chun-Lei Zhang, Mattia Aime, Emilie Laheranne, Xander Houbaert, Hajer El Oussini, Pierre Billuart

J Neurosci· November 2017

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CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy.
Karine Poirier, Laurence Hubert, Géraldine Viot, Marlène Rio, Pierre Billuart

Hum Mutat· August 2017

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The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity.
Caterina Montani, Mariana Ramos-Brossier, Luisa Ponzoni, Laura Gritti, Andrzej W Cwetsch, Pierre Billuart

J Neurosci· July 2017

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Loss of Function of KCNC1 is associated with intellectual disability without seizures.
Karine Poirier, Géraldine Viot, Laura Lombardi, Clémence Jauny, Pierre Billuart

Eur J Hum Genet· May 2017

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Pharmacological rescue of adult hippocampal neurogenesis in a mouse model of X-linked intellectual disability.
Manuela Allegra, Cristina Spalletti, Beatrice Vignoli, Stefano Azzimondi, Irene Busti, Pierre Billuart

Neurobiol Dis· April 2017

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Oligophrenin-1 regulates number, morphology and synaptic properties of adult-born inhibitory interneurons in the olfactory bulb.
Nelly Redolfi, Luisa Galla, Andrea Maset, Luca Murru, Eleonora Savoia, Pierre Billuart

Hum Mol Genet· December 2016

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Oligophrenin1 protects mice against myocardial ischemia and reperfusion injury by modulating inflammation and myocardial apoptosis.
Christina Niermann, Simone Gorressen, Meike Klier, Nina S Gowert, Pierre Billuart

Cell Signal· August 2016

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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.
Claudia Compagnucci, Sabina Barresi, Stefania Petrini, Pierre Billuart, Giorgia Piccini

Stem Cells Transl Med· July 2016

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Fasudil treatment in adult reverses behavioural changes and brain ventricular enlargement in Oligophrenin-1 mouse model of intellectual disability.
Hamid Meziane, Malik Khelfaoui, Noemi Morello, Bassem Hiba, Eleonora Calcagno, Pierre Billuart

Hum Mol Genet· June 2016

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Altered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.
Chloé Delépine, Hamid Meziane, Juliette Nectoux, Matthieu Opitz, Amos B Smith, Pierre Billuart

Hum Mol Genet· January 2016

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Early-onset encephalopathy with epilepsy associated with a novel splice site mutation in SMC1A.
Nicolas Lebrun, Sébastien Lebon, Pierre-Yves Jeannet, Sébastien Jacquemont, Pierre Billuart

Am J Med Genet A· December 2015

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