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Published on 11 April 2017

  
Parental vitamin D deficiency during pregnancy is associated with increased blood pressure in offspring via Panx1 hypermethylation
Meems LMG, Mahmud H, Buikema H, Tost J, Michel S, Takens J, Verkaik-Schakel RN, Vreeswijk-Baudoin I, Mateo-Leach IV, van der Harst P, Plosch T, de Boer RA
GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients
Cox DG, Curtit E, Romieu G, Fumoleau P, Rios M, Bonnefoi H, Bachelot T, Soulie P, Jouannaud C, Bourgeois H, Petit T, Tennevet I, Assouline D, Mathieu MC, Jacquin JP, Lavau-Denes S, Darut-Jouve A, Ferrero JM, Tarpin C, Levy C, Delecroix V, Trillet-Lenoir V, Cojocarasu O, Meunier J, Pierga JY, Faure-Mercier C, Blanche H, Sahbatou M, Boland A, Bacq D, Besse C, Deleuze JF, Pauporte I, Thomas G, Pivot X
Unique epigenetic modulation by EPIT compared to OIT in a model of peanut sensitized mice: sustainable GATA-3 hypermethylation and Foxp3 hypomethylation
Mondoulet L, Plaquet C, Ligouis M, Dhelft V, Puteaux E, Sampson H, Benhamou PH, Dupont C, Tost J
Allergy 71 (), 3-4, 2016
Substantial and robust changes in microRNA transcriptome support postnatal development of the hypothalamus in rat
Doubi-Kadmiri S, Benoit C, Benigni X, Beaumont G, Vacher CM, Taouis M, Baroin-Tourancheau A, Amar L
Overlap between differentially methylated DNA regions in blood B lymphocytes and genetic at-risk loci in primary Sjogren's syndrome
Miceli-Richard C, Wang-Renault SF, Boudaoud S, Busato F, Lallemand C, Bethune K, Belkhir R, Nocturne G, Mariette X, Tost J
Quantitative comparison of DNA methylation assays for biomarker development and clinical applications
Bock C, Halbritter F, Carmona FJ, Tierling S, Datlinger P, Assenov Y, Berdasco M, Bergmann AK, Booher K, Busato F, Campan M, Dahl C, Dahmcke CM, Diep D, Fernandez AF, Gerhauser C, Haake A, Heilmann K, Holcomb T, Hussmann D, Ito M, Klaver R, Kreutz M, Kulis M, Lopez V, Nair SS, Paul DS, Plongthongkum N, Qu WJ, Queiros AC, Reinicke F, Sauter G, Schlomm T, Statham A, Stirzaker C, Strogantsev R, Urdinguio RG, Walter K, Weichenhan D, Weisenberger DJ, Beck S, Clark SJ, Esteller M, Ferguson-Smith AC, Fraga MF, Guldberg P, Hansen LL, Laird PW, Martin-Subero JI, Nygren AOH, Peist R, Plass C, Shames DS, Siebert R, Sun XG, Tost J, Walter J, Zhang K
Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia
Broix L, Jagline H, Ivanova EL, Schmucker S, Drouot N, Clayton-Smith J, Pagnamenta AT, Metcalfe KA, Isidor B, Louvier UW, Poduri A, Taylor JC, Tilly P, Poirier K, Saillour Y, Lebrun N, Stemmelen T, Rudolf G, Muraca G, Saintpierre B, Elmorjani A, Moise M, Weirauch NB, Guerrini R, Boland A, Olaso R, Masson C, Tripathy R, Keays D, Beldjord C, Nguyen L, Godin J, Kini U, Nischke P, Deleuze JF, Bahi-Buisson N, Sumara I, Hinckelmann MV, Chelly J
Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing
David S, Ferreira J, Quenez O, Rovelet-Lecrux A, Richard AC, Verin M, Jurici S, Le Ber I, Boland A, Deleuze JF, Frebourg T, de Oliveira JRM, Hannequin D, Campion D, Nicolas G
Rapid identification of causal mutations in tomato EMS populations via mapping-by-sequencing
Garcia V, Bres C, Just D, Fernandez L, Tai FWJ, Mauxion JP, Le Paslier MC, Berard A, Brunel D, Aoki K, Alseekh S, Fernie AR, Fraser PD, Rothan C
Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 Deficiency
Salle-Teyssieres L, Auclair M, Terro F, Nemani M, Elsayed SM, Elsobky E, Lathrop M, Delepine M, Lascols O, Capeau J, Magre J, Vigouroux C
The clinical potential of Enhanced-ice-COLD-PCR
Tost J
Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells
de Dieuleveult M, Yen KY, Hmitou I, Depaux A, Oussouar FB, Dargham DB, Jounier S, Humbertclaude H, Ibierre FR, Baulard C, Farrell NP, Park B, Keime C, Carriere L, Erlivet SB, Gut M, Gut I, Werner M, Deleuze JF, Olaso R, Aude JC, Chantalat S, Pugh BFR, Gerard M
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Fritsche LG, Igl W, Bailey JNC, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HPN, Bala E, Lee KE, Hunter DJ, Sardell RJ, Mitchell P, Merriam JE, Cipriani V, Hoffman JD, Schick T, Lechanteur YTE, Guymer RH, Johnson MP, Jiang YD, Stanton CM, Buitendijk GHS, Zhan XW, Kwong AM, Boleda A, Brooks M, Gieser L, Ratnapriya R, Branham KE, Foerster JR, Heckenlively JR, Othman MI, Vote BJ, Liang HH, Souzeau E, McAllister IL, Isaacs T, Hall J, Lake S, Mackey DA, Constable IJ, Craig JE, Kitchner TE, Yang ZL, Su ZG, Luo HR, Chen D, Hong OY, Flagg K, Lin D, Mao GP, Ferreyra H, Starke K, von Strachwitz CN, Wolf A, Brandl C, Rudolph G, Olden M, Morrison MA, Morgan DJ, Schu M, Ahn J, Silvestri G, Tsironi EE, Park KH, Farrer LA, Orlin A, Brucker A, Li MY, Curcio CA, Mohand-Said S, Sahel JM, Audo I, Benchaboune M, Cree AJ, Rennie CA, Goverdhan SV, Grunin M, Hagbi-Levi S, Campochiaro P, Katsanis N, Holz FG, Blond F, Blanche H, Deleuze JF, Igo RP, Truitt B, Peachey NS, Meuer SM, Myers CE, Moore EL, Klein R, Hauser MA, Poste EA, Courtenay MD, Schwartz SG, Kovach JL, Scott WK, Liew G, Tan AG, Gopinath B, Merriam JC, Smith RT, Khan JC, Shahid H, Moore AT, McGrath JA, Laux R, Brantley MA, Agarwal A, Ersoy L, Caramoy A, Langmann T, Saksens NTM, de Jong EK, Hoyng CB, Cain MS, Richardson AJ, Martin TM, Blangero J, Weeks DE, Dhillon B, van Duijn CM, Doheny KF, Romm J, Klaver CCW, Hayward C, Gorin MB, Klein ML, Baird PN, den Hollander AI, Fauser S, Yates JRW, Allikmets R, Wang JJ, Schaumberg DA, Klein BEK, Hagstrom SA, Chowers I, Lotery AJ, Leveillard T, Zhang K, Brilliant MH, Hewitt AW, Swaroop A, Chew EY, Pericak-Vance MA, DeAngelis M, Stambolian D, Haines JL, Iyengar SK, Weber BHF, Abecasis GR, Heid IM
A FAMILY-BASED GENOME-WIDE ASSOCIATION STUDY REVEALS AN ASSOCIATION OF SPONDYLOARTHRITIS WITH MAPK14 (Meeting Abstract)
Costantino F, Talpin A, Said-Nahal R, Leboime A, Zinovieva E, Zelenika D, Gut I, Charon C, Izac B, Weissman M, Chiocchia G, Reveille J, Breban M, Garchon HJ
Clin. Exp. Rheumatol. 34 (4), 732-732, 2016
Identification of differentially methylated genes in purified disease relevant blood cell populations in patients with spondyloarthritis (Meeting abstract 1)
Miceli-Richard C, Tingaard AB, Wang-Renault SF, Busato F, Dougados M, Tost J
Eur. J. Immunol. 46 (), 287-287, 2016
Deregulated expression of MiRNas in purified disease relevant blood cell populations in patients with spondyloarthritis (Meeting Abstract 1)
Miceli-Richard C, Tingaard AB, Wang-Renault SF, Busato F, Dougados M, Tost J
Eur. J. Immunol. 46 (), 509-509, 2016
Identification of differentially methylated genes in purified disease relevant blood cell populations in patients with spondyloarthritis (Meeting abstract 2)
Miceli-Richard C, Tingaard AB, Wang-Renault SF, Busato F, Dougados M, Tost J
Eur. J. Immunol. 46 (), 287-287, 2016
Deregulated expression of MiRNas in purified disease relevant blood cell populations in patients with spondyloarthritis (Meeting Abstract 2)
Miceli-Richard C, Tingaard AB, Wang-Renault SF, Busato F, Dougados M, Tost J
Eur. J. Immunol. 46 (), 509-509, 2016
Characterization of the Poplar Pan-Genome by Genome-Wide Identification of Structural Variation
Pinosio S, Giacomello S, Faivre-Rampant P, Taylor G, Jorge V, Le Paslier MC, Zaina G, Bastien C, Cattonaro F, Marroni F, Morgante M
Systemic epigenetic response to recombinant lentiviral vectors independent of proviral integration
Aranyi T, Stockholm D, Yao R, Poinsignon C, Wiart T, Corre G, Touleimat N, Tost J, Galy A, Paldi A
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