Yann Herault

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Guillaume PavlovicIGBMC- PHENOMIN- ICSAdresse e-mail validée de igbmc.fr
Dierssen MaraCenter for Genomic RegulationAdresse e-mail validée de crg.eu
Duboule DenisProfessor of Genetics, Collège de France, Paris, EPFL Lausanne and University of GenevaAdresse e-mail validée de unige.ch
Stylianos E. AntonarakisProfessor of Genetic Medicine, University of Geneva Medical SchoolAdresse e-mail validée de unige.ch
Andrew J. SharpIcahn School of Medicine at Mount SinaiAdresse e-mail validée de mssm.edu
Victor TybulewiczFrancis Crick InstituteAdresse e-mail validée de crick.ac.uk
José M. Delgado-García (0000-0001-7...Universidad Pablo de Olavide, Seville, SpainAdresse e-mail validée de upo.es
Ferdinando ScavizziCNR, Institute of cell biology and neurobiologyAdresse e-mail validée de cnr.it
Jean RossierProfesseur, Neuroscience Paris Seine, Sorbonne UniversityAdresse e-mail validée de rossier.paris
Xavier Estivill MD PhDqGenomics (Quantitative Genomics Laboratories)Adresse e-mail validée de qgenomics.com
Jozef DulakProfessor of biochemistryAdresse e-mail validée de uj.edu.pl
Latif RachdiAdresse e-mail validée de inserm.fr
Basile TarchiniAssociate professor, The Jackson LaboratoryAdresse e-mail validée de jax.org
George KolliasBSRC 'Alexander Fleming' and Dept Physiology, Medical School, University of AthensAdresse e-mail validée de med.uoa.gr
Jos JonkersSenior Group Leader, Division of Molecular Pathology, Netherlands Cancer Institute, Oncode InstituteAdresse e-mail validée de nki.nl
Nelly FrossardResearch Director at Inserm (french NIH)Adresse e-mail validée de unistra.fr
Christine WhiteHudson Institute of Medical ResearchAdresse e-mail validée de monash.edu
Jean-Jacques PANTHIEREcole Nationale Vétérinaire d'Alfort, Institut Pasteur
Ramiro Ramirez-SolisDirector of Institutional Research Core Laboratories, UT Health San AntonioAdresse e-mail validée de uthscsa.edu
Ewan BirneyDirector, EMBL-EBIAdresse e-mail validée de ebi.ac.uk

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Yann Herault

IGBMC, CELPHEDIA-PHENOMIN-ICS

Adresse e-mail validée de igbmc.fr - Page d'accueil

Genetics and Phenomics


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
Distinct fibroblast lineages determine dermal architecture in skin development and repair RR Driskell, BM Lichtenberger, E Hoste, K Kretzschmar, BD Simons, ... Nature 504 (7479), 277-281, 2013	1164	2013
High-throughput discovery of novel developmental phenotypes ME Dickinson, AM Flenniken, X Ji, L Teboul, MD Wong, JK White, ... Nature 537 (7621), 508-514, 2016	1059	2016
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains MM Simon, S Greenaway, JK White, H Fuchs, V Gailus-Durner, S Wells, ... Genome biology 14, 1-22, 2013	509	2013
The DNA methyltransferase DNMT3C protects male germ cells from transposon activity J Barau, A Teissandier, N Zamudio, S Roy, V Nalesso, Y Hérault, ... Science 354 (6314), 909-912, 2016	368	2016
Epigallocatechin‐3‐gallate, a DYRK1A inhibitor, rescues cognitive deficits in D own syndrome mouse models and in humans R De la Torre, S De Sola, M Pons, A Duchon, MM de Lagran, M Farré, ... Molecular nutrition & food research 58 (2), 278-288, 2014	329	2014
The mammalian gene function resource: the International Knockout Mouse Consortium A Bradley, K Anastassiadis, A Ayadi, JF Battey, C Bell, MC Birling, ... Mammalian genome 23, 580-586, 2012	320	2012
Domains of genome-wide gene expression dysregulation in Down’s syndrome A Letourneau, FA Santoni, X Bonilla, MR Sailani, D Gonzalez, J Kind, ... Nature 508 (7496), 345-350, 2014	298	2014
Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs M Kmita, N Fraudeau, Y Hérault, D Duboule Nature 420 (6912), 145-150, 2002	253	2002
Identification of the translocation breakpoints in the Ts65Dn and Ts1Cje mouse lines: relevance for modeling Down syndrome A Duchon, M Raveau, C Chevalier, V Nalesso, AJ Sharp, Y Herault Mammalian Genome 22, 674-684, 2011	235	2011
Prevalence of sexual dimorphism in mammalian phenotypic traits NA Karp, J Mason, AL Beaudet, Y Benjamini, L Bower, RE Braun, ... Nature communications 8 (1), 15475, 2017	234	2017
Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium TF Meehan, N Conte, DB West, JO Jacobsen, J Mason, J Warren, ... Nature genetics 49 (8), 1231-1238, 2017	225	2017
Engineering chromosomes in mice through targeted meiotic recombination (TAMERE) Y Hérault, M Rassoulzadegan, F Cuzin Nature genetics 20 (4), 381-384, 1998	206	1998
Specific targeting of the GABA-A receptor α5 subtype by a selective inverse agonist restores cognitive deficits in Down syndrome mice J Braudeau, B Delatour, A Duchon, PL Pereira, L Dauphinot, ... Journal of psychopharmacology 25 (8), 1030-1042, 2011	202	2011
Rodent models in Down syndrome research: impact and future opportunities Y Herault, JM Delabar, EMC Fisher, VLJ Tybulewicz, E Yu, V Brault Disease models & mechanisms 10 (10), 1165-1186, 2017	184	2017
Down syndrome: from understanding the neurobiology to therapy K Gardiner, Y Herault, IT Lott, SE Antonarakis, RH Reeves, M Dierssen Journal of Neuroscience 30 (45), 14943-14945, 2010	171	2010
Aneuploidy: from a physiological mechanism of variance to Down syndrome M Dierssen, Y Herault, X Estivill Physiological reviews, 2009	171	2009
Genetics of dark skin in mice KR Fitch, KA McGowan, CD Van Raamsdonk, H Fuchs, D Lee, A Puech, ... Genes & development 17 (2), 214-228, 2003	171	2003
DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome A Duchon, Y Herault Frontiers in behavioral neuroscience 10, 104, 2016	160	2016
DYRK1A: a master regulatory protein controlling brain growth F Guedj, PL Pereira, S Najas, MJ Barallobre, C Chabert, B Souchet, ... Neurobiology of disease 46 (1), 190-203, 2012	159	2012
Ulnaless (Ul), a regulatory mutation inducing both loss-of-function and gain- of-function of posterior Hoxd genes Y Hérault, N Fraudeau, J Zákány, D Duboule Development 124 (18), 3493-3500, 1997	157	1997

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