Yann Herault mainly investigates Genetics, Gene, Trisomy, Neuroscience and Phenotype. His study involves Gene duplication, Retrotransposon, DNMT1, DNA methylation and DNA methyltransferase, a branch of Genetics. All of his Gene and Locus, Transposable element, Epigenetics, Transcriptome and DNMT3B investigations are sub-components of the entire Gene study.
His Trisomy research incorporates themes from Down syndrome and Chromosomal translocation. When carried out as part of a general Neuroscience research project, his work on Morris water navigation task and Neuron is frequently linked to work in Brain size and Gap-43 protein, therefore connecting diverse disciplines of study. Yann Herault interconnects Mutation, Mutant, Gene knockout, Induced pluripotent stem cell and Functional validation in the investigation of issues within Phenotype.
His primary areas of study are Genetics, Gene, Phenotype, Down syndrome and Neuroscience. His Gene duplication, Mutant, Copy-number variation, Trisomy and Locus study are his primary interests in Genetics. His Gene duplication study combines topics in areas such as Gene rearrangement and HOXD13.
His Copy-number variation research is multidisciplinary, incorporating elements of Gene dosage and Regulation of gene expression. The study of Gene is intertwined with the study of Computational biology in a number of ways. The study incorporates disciplines such as Endocrinology, Recognition memory, Cognition and Internal medicine in addition to Down syndrome.
Yann Herault spends much of his time researching Gene, Genetics, Phenotype, Computational biology and Gene duplication. Gene is frequently linked to Kinase in his study. His Genetics study is mostly concerned with Copy-number variation, Mutant and Genome-wide association study.
His study in Phenotype is interdisciplinary in nature, drawing from both DYRK1A, Down syndrome, Locus, Neuroscience and RHOA. The various areas that Yann Herault examines in his Computational biology study include Genome editing, Genome, CRISPR and Disease. His research investigates the connection between Gene duplication and topics such as Serum iron that intersect with problems in Red blood cell and Iron-deficiency anemia.
His main research concerns Gene, Computational biology, Genetics, Phenotype and Gene duplication. Yann Herault performs multidisciplinary study in Gene and Actin cytoskeleton in his work. The various areas that Yann Herault examines in his Computational biology study include Genome editing, Disease, Inbred strain and Developmental disorder.
The Genetics study combines topics in areas such as Hemoglobin and Red blood cell. He has researched Phenotype in several fields, including Recognition memory, Zebrafish, Craniofacial and Copy-number variation. His Gene duplication research includes themes of Iron-deficiency anemia, Anemia, Microcytosis, Iron deficiency and Serum iron.
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Distinct fibroblast lineages determine dermal architecture in skin development and repair
Ryan R. Driskell;Ryan R. Driskell;Beate M. Lichtenberger;Beate M. Lichtenberger;Esther Hoste;Kai Kretzschmar;Kai Kretzschmar.
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson;Ann M. Flenniken;Xiao Ji;Lydia Teboul.
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
Michelle M Simon;Simon Greenaway;Jacqueline K White;Helmut Fuchs.
Genome Biology (2013)
Epigallocatechin-3-gallate, a DYRK1A inhibitor, rescues cognitive deficits in Down syndrome mouse models and in humans
Rafael De la Torre;Susana De Sola;Meritxell Pons;Arnaud Duchon.
Molecular Nutrition & Food Research (2014)
The mammalian gene function resource: the international knockout mouse consortium
Allan Bradley;Konstantinos Anastassiadis;Abdelkader Ayadi;James F. Battey.
Mammalian Genome (2012)
The DNA methyltransferase DNMT3C protects male germ cells from transposon activity.
Joan Barau;Aurélie Teissandier;Aurélie Teissandier;Natasha Zamudio;Stéphanie Roy.
Domains of genome-wide gene expression dysregulation in Down/'s syndrome
Audrey Letourneau;Federico A. Santoni;Ximena Bonilla;M. Reza Sailani.
Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs
Marie Kmita;Nadine Fraudeau;Yann Hérault;Yann Hérault;Denis Duboule.
Engineering chromosomes in mice through targeted meiotic recombination (TAMERE).
Yann Hérault;Minoo Rassoulzadegan;François Cuzin;Denis Duboule..
Nature Genetics (1998)
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling down syndrome
Arnaud Duchon;Matthieu Raveau;Claire Chevalier;Valérie Nalesso.
Mammalian Genome (2011)
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