Yann HERAULT

Publications

• 2015

  • Pharmacological correction of excitation/inhibition imbalance in Down syndrome mouse models

    • Benoit Souchet
    • Fayçal Guedj
    • Zsuza Penke-Verdier
    • Fabrice Daubigney
    • Arnaud Duchon
    • Yann Herault
    • Jean-Charles Bizot
    • Nathalie Janel
    • Nicole Créau
    • Benoit Delatour
    • Jean M. Delabar

    Frontiers in Behavioral Neuroscience ; Volume: 9 ; Page: 267

    HAL DOI

  • Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics

    • Martin Hrabě de Angelis
    • George Nicholson
    • Mohammed Selloum
    • Jacqueline White
    • Hugh Morgan
    • Ramiro Ramirez-Solis
    • Tania Sorg
    • Sara Wells
    • Helmut Fuchs
    • Martin Fray
    • David Adams
    • Niels Adams
    • Thure Adler
    • Antonio Aguilar-Pimentel
    • Dalila Ali-Hadji
    • Gregory Amann
    • Philippe André
    • Sarah Atkins
    • Aurelie Auburtin
    • Abdel Ayadi
    • ...

    Nature Genetics ; Volume: 47 ; Page: 969-978

    HAL DOI

  • Dosage of the Abcg1-U2af1 Region Modifies Locomotor and Cognitive Deficits Observed in the Tc1 Mouse Model of Down Syndrome

    • Damien Marechal
    • Patricia Lopes Pereira
    • Arnaud Duchon
    • Yann Herault

    PLoS ONE ; Volume: 10 ; Page: e0115302

    HAL DOI

  • Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration

    • Aline Dubos
    • Anna Castells-Nobau
    • Hamid Meziane
    • Merel A.W. Oortveld
    • Xander Houbaert
    • Giovanni Iacono
    • Christelle Martin
    • Christophe Mittelhaeuser
    • Valérie Lalanne
    • Jamie M. Kramer
    • Anuradha Bhukel
    • Christine Quentin
    • Jan Slabbert
    • Patrik Verstreken
    • Stefan J. Sigrist
    • Nadia Messaddeq
    • Marie-Christine Birling
    • Mohammed Selloum
    • Henk G. Stunnenberg
    • Yann Humeau
    • ...

    Human Molecular Genetics ; Volume: 24 ; Page: 6736--6755

    HAL DOI

  • Applying the ARRIVE Guidelines to an In Vivo Database

    • Natasha A. Karp
    • Terry F. Meehan
    • Hugh Morgan
    • Jeremy C. Mason
    • Andrew Blake
    • Natalja Kurbatova
    • Damian Smedley
    • Julius Jacobsen
    • Richard F. Mott
    • Vivek Iyer
    • Peter Matthews
    • David G. Melvin
    • Sara Wells
    • Ann M. Flenniken
    • Hiroshi Masuya
    • Shigeharu Wakana
    • Jacqueline K. White
    • K. C. Kent Lloyd
    • Corey L. Reynolds
    • Richard Paylor
    • ...

    PLoS Biology ; Volume: 13 ; Page: e1002151

    HAL DOI

  • Opposite Phenotypes of Muscle Strength and Locomotor Function in Mouse Models of Partial Trisomy and Monosomy 21 for the Proximal Hspa13-App Region

    • Véronique Brault
    • Arnaud Duchon
    • Caroline Romestaing
    • Ignasi Sahún
    • Stéphanie Pothion
    • Mona Karout
    • Christelle Borel
    • Doulaye Dembele
    • Jean-Charles Bizot
    • Nadia Messaddeq
    • Andrew J. Sharp
    • Damien Roussel
    • Stylianos E Antonarakis
    • Mara Dierssen
    • Yann Herault

    PLoS Genetics ; Volume: 11 : e1005062. ; Page: 1-27

    HAL DOI

  • LXR-Mediated ABCA1 Expression and Function Are Modulated by High Glucose and PRMT2

    • Maryem A. Hussein
    • Elina Shrestha
    • Mireille Ouimet
    • Tessa J. Barrett
    • Sarah Leone
    • Kathryn J. Moore
    • Yann Herault
    • Edward A. Fisher
    • Michael J. Garabedian

    PLoS ONE ; Volume: 10 ; Page: e0135218

    HAL DOI

  • La révolution de la génomique fonctionnelle

    • Guillaume Pavlovic
    • Tania Sorg
    • Ali Ayadi
    • Marie-Christine Birling
    • Isabelle Goncalves
    • C Fremont
    • B Malissen
    • Yann Hérault

    Biofutur ; Volume: 34 ; Page: 47-53

    HAL

  • Deletion of the App-Runx1 region in mice models human partial monosomy 21

    • Thomas Arbogast
    • Matthieu Raveau
    • Claire Chevalier
    • Valérie Nalesso
    • Doulaye Dembele
    • Hugues Jacobs
    • Olivia Wendling
    • Michel J. Roux
    • Arnaud Duchon
    • Yann Hérault

    Disease Models & Mechanisms ; Volume: 8 ; Page: 623-634

    HAL DOI

• 2014

  • Heterozygous deletion of the Williams–Beuren syndrome critical interval in mice recapitulates most features of the human disorder

    • Maria Segura-Puimedon
    • Ignasi Sahún
    • Emilie Velot
    • Pierre Dubus
    • Cristina Borralleras
    • Ana Rodrigues
    • Maria Adela Valero
    • Olga Valverde
    • Nuno Sousa
    • Yann Hérault
    • Mara Dierssen
    • Luis Pérez-Jurado
    • Victoria Campuzano

    Human Molecular Genetics ; Volume: 23 ; Page: 6481-6494

    HAL DOI