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Publications de Yann HERAULT

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

    Arbogast T(1,)(2,)(3,)(4), Ouagazzal AM(1,)(2,)(3,)(4), Chevalier C(1,)(2,)(3,)(4), Kopanitsa M(5), Afinowi N(5), Migliavacca E(6,)(7), Cowling BS(1,)(2,)(3,)(4), Birling MC(8), Champy MF(8), Reymond A(6), Herault Y(1,)(2,)(3,)(4,)(8).

    PLoS Genet 12 février 2016

  • The DNA methyltransferase DNMT3C protects male germ cells from transposon activity.

    Barau J(1), Teissandier A(1,)(2), Zamudio N(1), Roy S(3), Nalesso V(4,)(5,)(6), Herault Y(4,)(5,)(6), Guillou F(3), Bourc'his D(7).

    Science 18 novembre 2016

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

    Hrabe de Angelis M, Nicholson G, Selloum M, White JK, Morgan H, Ramirez-Solis R, Sorg T, Wells S, Fuchs H, Fray M, Adams DJ, Adams NC, Adler T, Aguilar-Pimentel A, Ali-Hadji D, Amann G, AndrE P, Atkins S, Auburtin A, Ayadi A, Becker J, Becker L, Bedu E, Bekeredjian R, Birling MC, Blake A, Bottomley J, Bowl MR, Brault V, Busch DH, Bussell JN, Calzada-Wack J, Cater H, Champy MF, Charles P, Chevalier C, Chiani F, Codner GF, Combe R, Cox R, Dalloneau E, Dierich A, Di Fenza A, Doe B, Duchon A, Eickelberg O, Esapa CT, Fertak LE, Feigel T, Emelyanova I, Estabel J, Favor J, Flenniken A, Gambadoro A, Garrett L, Gates H, Gerdin AK, Gkoutos G, Greenaway S, Glasl L, Goetz P, Da Cruz IG, Gotz A, Graw J, Guimond A, Hans W, Hicks G, Holter SM, Hofler H, Hancock JM, Hoehndorf R, Hough T, Houghton R, Hurt A, Ivandic B, Jacobs H, Jacquot S, Jones N, Karp NA, Katus HA, Kitchen S, Klein-Rodewald T, Klingenspor M, Klopstock T, Lalanne V, Leblanc S, Lengger C, le Marchand E, Ludwig T, Lux A, McKerlie C, Maier H, Mandel JL, Marschall S, Mark M, Melvin DG, Meziane H, Micklich K, Mittelhauser C, Monassier L, Moulaert D, Muller S, Naton B, Neff F, Nolan PM, Nutter LM, Ollert M, Pavlovic G, Pellegata NS, Peter E, Petit-Demouliere B, Pickard A, Podrini C, Potter P, Pouilly L, Puk O, Richardson D, Rousseau S, Quintanilla-Fend L, Quwailid MM, Racz I, Rathkolb B, Riet F, Rossant J, Roux M, Rozman J, Ryder E, Salisbury J, Santos L, Schable KH, Schiller E, Schrewe A, Schulz H, Steinkamp R, Simon M, Stewart M, Stoger C, Stoger T, Sun M, Sunter D, Teboul L, Tilly I, Tocchini-Valentini GP, Tost M, Treise I, Vasseur L, Velot E, Vogt-Weisenhorn D, Wagner C, Walling A, Wattenhofer-Donze M, Weber B, Wendling O, Westerberg H, Willershauser M, Wolf E, Wolter A, Wood J, Wurst W, Yildirim AO, Zeh R, Zimmer A, Zimprich A; EUMODIC Consortium, Holmes C, Steel KP, Herault Y, Gailus-Durner V, Mallon AM, Brown SD.

    Nat Genet Sep 2015

  • Applying the ARRIVE Guidelines to an In Vivo Database.

    Karp NA(1), Meehan TF(2), Morgan H(3), Mason JC(2), Blake A(3), Kurbatova N(2), Smedley D(1), Jacobsen J(1), Mott RF(4), Iyer V(5), Matthews P(5), Melvin DG(1), Wells S(3), Flenniken AM(6), Masuya H(7), Wakana S(7), White JK(8), Lloyd KC(9), Reynolds CL(10), Paylor R(11), West DB(12), Svenson KL(13), Chesler EJ(13), de Angelis MH(14), Tocchini-Valentini GP(15), Sorg T(16), Herault Y(16), Parkinson H(2), Mallon AM(3), Brown SD(3).

    PLoS Biol 20 mai 2015

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

    Dubos A(1), Castells-Nobau A(2), Meziane H(3), Oortveld MA(2), Houbaert X(4), Iacono G(5), Martin C(4), Mittelhaeuser C(3), Lalanne V(3), Kramer JM(2), Bhukel A(6), Quentin C(7), Slabbert J(8), Verstreken P(8), Sigrist SJ(7), Messaddeq N(9), Birling MC(3), Selloum M(3), Stunnenberg HG(5), Humeau Y(4), Schenck A(10), Herault Y(11).

    Hum Mol Genet 1 décembre 2015

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

    Arbogast T(1), Raveau M(1), Chevalier C(1), Nalesso V(1), Dembele D(1), Jacobs H(2), Wendling O(2), Roux M(3), Duchon A(1), Herault Y(4).

    Dis Model Mech Jun 2015

  • Dosage of the Abcg1-U2af1 region modifies locomotor and cognitive deficits observed in the Tc1 mouse model of Down syndrome.

    Marechal D(1), Lopes Pereira P(2), Duchon A(1), Herault Y(3).

    PLoS One 23 février 2015

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

    Hussein MA(1), Shrestha E(1), Ouimet M(2), Barrett TJ(2), Leone S(1), Moore KJ(2), Herault Y(3), Fisher EA(2), Garabedian MJ(1).

    PLoS One 19 août 2015

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