Publications by authors named "Alice Poisson"

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Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).
Eléonore Viora-Dupont, Françoise Robert, Aline Chassagne, Aurore Pélissier, Stéphanie Staraci, Alice Poisson

Eur J Hum Genet· September 2024

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Task-independent neural bases of peer presence effect on cognition in children and adults.
Leslie Tricoche, Denis Pélisson, Léa Longo, Eric Koun, Alice Poisson

Neuroimage· August 2023

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Noradrenaline and Movement Initiation Disorders in Parkinson's Disease: A Pharmacological Functional MRI Study with Clonidine.
Marion Criaud, Chloé Laurencin, Alice Poisson, Elise Metereau, Jérôme Redouté

Cells· August 2022

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Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy.
Claire Bar, Delphine Breuillard, Mathieu Kuchenbuch, Mélanie Jennesson, Gwenaël Le Guyader, Alice Poisson

Epilepsy Behav· January 2022

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Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review.
Christophe Gauld, Alice Poisson, Julie Reversat, Elodie Peyroux, Françoise Houdayer-Robert

BMC Psychiatry· July 2021

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Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
Holly K Harris, Tojo Nakayama, Jenny Lai, Boxun Zhao, Nikoleta Argyrou, Alice Poisson

Genet Med· June 2021

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Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome.
Claire Bar, Mathieu Kuchenbuch, Giulia Barcia, Amy Schneider, Mélanie Jennesson, Alice Poisson

Epilepsia· November 2020

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Neural representations of transitive relations predict current and future math calculation skills in children.
Flora Schwartz, Justine Epinat-Duclos, Jessica Léone, Alice Poisson, Jérôme Prado

Neuropsychologia· April 2020

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Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.
Ash Zawerton, Cyril Mignot, Ashley Sigafoos, Patrick R Blackburn, Abdul Haseeb, Alice Poisson

Genet Med· March 2020

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Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.
Claire Bar, Giulia Barcia, Mélanie Jennesson, Gwenaël Le Guyader, Amy Schneider, Alice Poisson

Hum Mutat· January 2020

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Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.
Alice Poisson, Nicolas Chatron, Audrey Labalme, Pierre Fourneret, Dorothée Ville

BMC Med Genet· January 2020

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Corpus callosum metrics predict severity of visuospatial and neuromotor dysfunctions in ARID1B mutations with Coffin-Siris syndrome.
Caroline Demily, Charlyne Duwime, Clémence Lopez, Cherhazad Hemimou, Alice Poisson

Psychiatr Genet· December 2019

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12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome.
Alice Poisson, Gaetan Lesca, Nicolas Chatron, Emilie Favre, Vincent Cottin

Eur J Med Genet· November 2019

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Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder.
Alice Poisson, Alain Nicolas, Idriss Bousquet, Véronique Raverot, Claude Gronfier

Int J Mol Sci· July 2019

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Subthreshold social cognitive deficits may be a key to distinguish 22q11.2DS from schizophrenia.
Elodie Peyroux, Caroline Rigard, Guillaume Saucourt, Alice Poisson, Julien Plasse

Early Interv Psychiatry· April 2019

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Regressive Autism Spectrum Disorder Expands the Phenotype of BSCL2/Seipin-Associated Neurodegeneration.
Alice Poisson, Nicolas Chatron, Audrey Labalme, Marianne Till, Emmanuel Broussolle

Biol Psychiatry· February 2019

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Impaired neural processing of transitive relations in children with math learning difficulty.
Flora Schwartz, Justine Epinat-Duclos, Jessica Léone, Alice Poisson, Jérôme Prado

Neuroimage Clin· February 2019

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Additive Effect of Variably Penetrant 22q11.2 Duplication and Pathogenic Mutations in Autism Spectrum Disorder: To Which Extent Does the Tree Hide the Forest?
Caroline Demily, Gaétan Lesca, Alice Poisson, Marianne Till, Giulia Barcia

J Autism Dev Disord· August 2018

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Somatic mosaicism for SLC1A1 mutation supports threshold effect and familial aggregation in schizophrenia spectrum disorders.
Caroline Demily, Laurence Hubert, Nicolas Franck, Alice Poisson, Arnold Munnich

Schizophr Res· July 2018

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Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI» study protocol for a randomized controlled trial.
Emilie Favre, Elodie Peyroux, Marie-Noelle Babinet, Alice Poisson, Caroline Demily

BMC Psychiatry· July 2018

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Weight loss induced by quetiapine in a 22q11.2DS patient.
Caroline Demily, Alice Poisson, Florence Thibaut, Nicolas Franck

Mol Genet Metab Rep· December 2017

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Evidence for dopaminergic denervation in classical galactosemia.
Alice Poisson, Emmanuel Roze, Caroline Demily, Stéphane Thobois

Mov Disord· June 2017

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Low dose clozapine controls adult-onset psychosis associated with the neurogenic ataxia-retinitis pigmentosa (NARP) mutation.
Caroline Demily, Charlyne Duwime, Alice Poisson, Nathalie Boddaert, Arnold Munnich

Mol Genet Metab Rep· March 2017

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Authors' reply - Clozapine for mitochondrial psychosis.
Caroline Demily, Charlyne Duwime, Alice Poisson, Nathalie Boddaert, Arnold Munnich

Mol Genet Metab Rep· March 2017

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Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.
Caroline Demily, Alice Poisson, Elodie Peyroux, Valérie Gatellier, Alain Nicolas

BMC Med Genet· January 2017

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