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Author Details

Yann Herault
Institut Clinique de la Souris (ICS), Universite de Strasbourg, CNRS, INSERM
1991
175
43
PMIDPaper TitleJournal TitlePublished Year
36658491Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion.BMC Neurosci2023
37308929Development of HPV16 mouse and dog models for more accurate prediction of human vaccine efficacy.Lab Anim Res2023
37074246The Impact of Mmu17 Non-Hsa21 Orthologous Genes in the Ts65Dn Mouse Model of Down Syndrome: The Gold Standard Refuted.Biol Psychiatry2023
37465586Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders.Front Neurosci2023
37294348Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice.Mamm Genome2023
37225732Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.NPJ Genom Med2023
36995673CRISMERE Chromosome Engineering in Mouse and Rat.Methods Mol Biol2023
36833328Increased On-Target Rate and Risk of Concatemerization after CRISPR-Enhanced Targeting in ES Cells.Genes (Basel)2023
36672706Timeline of Developmental Defects Generated upon Genetic Inhibition of the Retinoic Acid Receptor Signaling Pathway.Biomedicines2023
36703114Gdaphen, R pipeline to identify the most important qualitative and quantitative predictor variables from phenotypic data.BMC Bioinformatics2023
34328547INFRAFRONTIER quality principles in systemic phenotyping.Mamm Genome2022
35769334The Human <i>SCN9A</i> <sup><i>R</i>185<i>H</i></sup> Point Mutation Induces Pain Hypersensitivity and Spontaneous Pain in Mice.Front Mol Neurosci2022
35715439Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts.NPJ Genom Med2022
36551904Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.Biomedicines2022
36374158Ts66Yah, a mouse model of Down syndrome with improved construct and face validity.Dis Model Mech2022
35914814Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.Life Sci Alliance2022
35042677Overproduction of hydrogen sulfide, generated by cystathionine β-synthase, disrupts brain wave patterns and contributes to neurobehavioral dysfunction in a rat model of down syndrome.Redox Biol2022
35195951Behavioral Testing Design for Evaluation of Cognitive Disabilities.Curr Protoc2022
32721466Reliable and robust droplet digital PCR (ddPCR) and RT-ddPCR protocols for mouse studies.Methods2021
33838271Droplet digital PCR or quantitative PCR for in-depth genomic and functional validation of genetically altered rodents.Methods2021
33693642Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models.Hum Mol Genet2021
33775738Pain behavior in SCN9A (Nav1.7) and SCN10A (Nav1.8) mutant rodent models.Neurosci Lett2021
33660221Specific Susceptibility to COVID-19 in Adults with Down Syndrome.Neuromolecular Med2021
34925037The Human SCN10A<sup>G1662S</sup> Point Mutation Established in Mice Impacts on Mechanical, Heat, and Cool Sensitivity.Front Pharmacol2021
34862403ProMetIS, deep phenotyping of mouse models by combined proteomics and metabolomics analysis.Sci Data2021
34587162Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome.PLoS Genet2021
34582789HDAC inhibitor ameliorates behavioral deficits in Mecp2<sup>308/y</sup> mouse model of Rett syndrome.Brain Res2021
34602984Delta Opioid Receptor in Astrocytes Contributes to Neuropathic Cold Pain and Analgesic Tolerance in Female Mice.Front Cell Neurosci2021
34421499Building the Future Therapies for Down Syndrome: The Third International Conference of the T21 Research Society.Mol Syndromol2021
34797469Correction to: Specific Susceptibility to COVID-19 in Adults with Down Syndrome.Neuromolecular Med2021
34248930Immune Dysregulation and the Increased Risk of Complications and Mortality Following Respiratory Tract Infections in Adults With Down Syndrome.Front Immunol2021
34292972The effects of Cstb duplication on APP/amyloid-β pathology and cathepsin B activity in a mouse model.PLoS One2021
34203310Pathogenesis of Anorectal Malformations in Retinoic Acid Receptor Knockout Mice Studied by HREM.Biomedicines2021
33948879Correction to: Specific Susceptibility to COVID-19 in Adults with Down Syndrome.Neuromolecular Med2021
34356832High Resolution Episcopic Microscopy for Qualitative and Quantitative Data in Phenotyping Altered Embryos and Adult Mice Using the New "Histo3D" System.Biomedicines2021
33436060Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models.Mol Autism2021
33476328Identifying causative mechanisms linking early-life stress to psycho-cardio-metabolic multi-morbidity: The EarlyCause project.PLoS One2021
31591642Soft windowing application to improve analysis of high-throughput phenotyping data.Bioinformatics2020
32088735PATHBIO: an international training program for precision mouse phenotyping.Mamm Genome2020
32057313Modeling Down syndrome in animals from the early stage to the 4.0 models and next.Prog Brain Res2020
31929527High-throughput discovery of genetic determinants of circadian misalignment.PLoS Genet2020
31980673A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology Treatment.Sci Rep2020
31652355Long-lasting correction of in vivo LTP and cognitive deficits of mice modelling Down syndrome with an α5-selective GABA<sub>A</sub> inverse agonist.Br J Pharmacol2020
33370286Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.PLoS Genet2020
33035509Mechanism of cystathionine-β-synthase inhibition by disulfiram: The role of bis(N,N-diethyldithiocarbamate)-copper(II).Biochem Pharmacol2020
32620926Author Correction: A Small Compound Targeting Prohibitin with Potential Interest for Cognitive Deficit Rescue in Aging mice and Tau Pathology Treatment.Sci Rep2020
32643117Introduction to Mammalian Genome Special Issue: Epigenetics.Mamm Genome2020
32243835Variability in Genome Editing Outcomes: Challenges for Research Reproducibility and Clinical Safety.Mol Ther2020
32407325BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice.PLoS One2020
31431136Genetic quality assurance and genetic monitoring of laboratory mice and rats: FELASA Working Group Report.Lab Anim2020
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Collaborators

Universite de Strasbourg, CNRS, INSERM, Institut de La Clinique de La Souris
Co-authored papers 27
CNRS, INSERM, Universite de Strasbourg, PHENOMIN-Institut Clinique de la Souris (ICS)
Co-authored papers 26
German Center for Diabetes Research (DZD e.V.)
Co-authored papers 24
Mary Lyon Centre Harwell Science and Innovation Campus Oxfordshire UK.
Co-authored papers 17
The Turing Institute
Co-authored papers 16
The Hospital for Sick Children
Co-authored papers 15
Mary Lyon Centre at Medical Research Council
Co-authored papers 15
Wellcome Trust Sanger Institute
Co-authored papers 14
Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Co-authored papers 14
University of California davis
Co-authored papers 14
Monterotondo Mouse Clinic (MMC), Italian National Research Council (CNR)
Co-authored papers 12
European Bioinformatics Institute
Co-authored papers 11
Co-authored papers 11
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 11
European Bioinformatics Institute
Co-authored papers 11
European Molecular Biology Laboratory - European Bioinformatics Institute
Co-authored papers 11
Institute of Developmental Genetics, German Research Center for Environmental Health
Co-authored papers 10
Institute of Experimental Genetics, German Mouse Clinic
Co-authored papers 10
The Hospital for Sick Children
Co-authored papers 10
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 9
Nanjing Biomedical Research Institute, Nanjing University
Co-authored papers 9
University of Maine
Co-authored papers 9
Wellcome Sanger Institute
Co-authored papers 9
University of California davis
Co-authored papers 9
Translational and Clinical Research Institute, Newcastle University
Co-authored papers 9
Co-authored papers 9
Columbia University.
Co-authored papers 8
Baylor College of Medicine
Co-authored papers 8
European Bioinformatics Institute
Co-authored papers 8
Wellcome Sanger Institute
Co-authored papers 8