C. Chevalier

发表

Domains of genome-wide gene expression dysregulation in Down’s syndrome

Stylianos E. Antonarakis, Laurent Farinelli, Richard S. Sandstrom, 2014, Nature.

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

B. D. de Vries, Y. Hérault, T. Sorg, 2017, PLoS genetics.

Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition

B. D. de Vries, Y. Hérault, T. Sorg, 2017, PLoS genetics.

IGF2 Promotes Growth of Adrenocortical Carcinoma Cells, but Its Overexpression Does Not Modify Phenotypic and Molecular Features of Adrenocortical Carcinoma

E. Baudin, J. Bertherat, X. Bertagna, 2014, PloS one.

Systematic screening for PRKAR1A gene rearrangement in Carney complex: identification and functional characterization of a new in-frame deletion.

J. Bertherat, C. Stratakis, A. Horvath, 2014, European journal of endocrinology.

Missense Mutation in the Second RNA Binding Domain Reveals a Role for Prkra (PACT/RAX) during Skull Development

Y. Hérault, C. Chevalier, C. White, 2011, PloS one.

DMM017814 623..634

Y. Hérault, D. Dembélé, A. Duchon, 2015 .

A 16p11.2 deletion mouse model displays quantitatively and qualitatively different behaviours in sociability and social novelty over short- and long-term observation

Y. Hérault, F. de Chaumont, V. Brault, 2022, bioRxiv.

Ts66Yah, a mouse model of Down syndrome with improved construct and face validity

Y. Hérault, M. Potier, A. Duchon, 2022, bioRxiv.

Ts 66 Yah , a refined Ts 65 Dn DS mouse model , unravels genetic 1 interaction between regions homologous to Human chromosome 21 2 and the Scaf 8-Pde 10 a genetic interval

Y. Hérault, M. Potier, A. Duchon, 2022 .

Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models

Y. Hérault, J. Delabar, N. Janel, 2019, Scientific Reports.

Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes

A. Reymond, Y. Hérault, M. Champy, 2016, PLoS genetics.

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

Y. Hérault, D. Dembélé, A. Duchon, 2015, Disease Models & Mechanisms.

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

Henrik Westerberg, John M. Hancock, Oliver Eickelberg, 2015, Nature Genetics.

Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models

Y. Hérault, H. Meziane, J. Armspach, 2021, Human molecular genetics.

Multi-influential interactions alters behaviour and cognition through six main biological cascades in Down syndrome mouse models

Y. Hérault, H. Meziane, J. Armspach, 2020, bioRxiv.

Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models

Y. Hérault, C. Chevalier, M. Birling, 2020, bioRxiv.

Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development

J. Sebat, C. Deutsch, C. Corsello, 2019, bioRxiv.

WD40-repeat 47, a microtubule-associated protein, is essential for brain development and autophagy

Y. Hérault, R. Borgatti, B. Yalcin, 2017, Proceedings of the National Academy of Sciences.

Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome

Y. Hérault, A. Sharp, A. Duchon, 2011, Mammalian Genome.

The Mz variety of the St(a+) phenotype--a variant of glycophorin A exhibiting a deletion.

K. Beyreuther, C. Chevalier, J. Cartron, 1990, Biological chemistry Hoppe-Seyler.

Prenatal treatment with EGCG enriched green tea extract rescues GAD67 related developmental and cognitive defects in Down syndrome mouse models

Y. Hérault, J. Delabar, N. Janel, 2019, Scientific Reports.

Chaetozone corona (Polychaeta, Cirratulidae) in the Bay of Biscay: a new alien species for the North-east Atlantic waters?

C. Chevalier, J. Grall, J. Blake, 2016, Journal of the Marine Biological Association of the United Kingdom.

BIN1 genetic risk factor for Alzheimer is sufficient to induce early structural tract alterations in entorhinal cortex-dentate gyrus pathway and related hippocampal multi-scale impairments

Y. Hérault, P. Dutar, D. Le Bihan, 2018, bioRxiv.

The use of the relationships between environmental factors and benthic macrofaunal distribution in the establishment of a baseline for coastal management

C. Chevalier, Mickaël Dutertre, Claire Chevalier, 2013 .

Ts66Yah, a mouse model of Down syndrome with improved construct and face validity

Y. Hérault, M. Potier, A. Duchon, 2022, Disease Models & Mechanisms.

Day-to-day spontaneous social behaviours is quantitatively and qualitatively affected in a 16p11.2 deletion mouse model

Y. Hérault, V. Brault, C. Chevalier, 2023, bioRxiv.