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Publications 2016

Publié le 12 avril 2017

  
Biomass traits and candidate genes for bioenergy revealed through association genetics in coppiced European Populus nigra (L.)
Allwright MR, Payne A, Emiliani G, Milner S, Viger M, Rouse F, Keurentjes JJB, Berard A, Wildhagen H, Faivre-Rampant P, Polle A, Morgante M, Taylor G
"De novo construction of a ""Gene-space"" for diploid plant genome rich in repetitive sequences by an iterative Process of Extraction and Assembly of NGS reads (iPEA protocol) with limited computing resources."
Aluome C, Aubert G, Alves Carvalho S, Le Paslier M C, Burstin J, Brunel D
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
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea.
Bauche S, O'Regan S, Azuma Y, Laffargue F, McMacken G, Sternberg D, Brochier G, Buon C, Bouzidi N, Topf A, Lacene E, Remerand G, Beaufrere A M, Pebrel-Richard C, Thevenon J, El Chehadeh-Djebbar S, Faivre L, Duffourd Y, Ricci F, Mongini T, Fiorillo C, Astrea G, Burloiu C M, Butoianu N, Sandu C, Servais L, Bonne G, Nelson I, Desguerre I, Nougues M C, Boeuf B, Romero N, Laporte J, Boland A, Lechner D, Deleuze J F, Fontaine B, Strochlic L, Lochmuller H, Eymard B, Mayer M, Nicole S
Genome-wide DNA methylation analyses in lung adenocarcinomas: Association with EGFR, KRAS and TP53 mutation status, gene expression and prognosis
Bjaanaes MM, Fleischer T, Halvorsen AR, Daunay A, Busato F, Solberg S, Jorgensen L, Kure E, Edvardsen H, Borresen-Dale AL, Brustugun OT, Tost J, Kristensen V, Helland A
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
Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels
Bonilla C, Lewis SJ, Rowlands MA, Gaunt TR, Smith GD, Gunnell D, Palmer T, Donovan JL, Hamdy FC, Neal DE, Eeles R, Easton D, Kote-Jarai Z, Al Olama AA, Benlloch S, Muir K, Giles GG, Wiklund F, Gronberg H, Haiman CA, Schleutker J, Nordestgaard BG, Travis RC, Pashayan N, Khaw KT, Stanford JL, Blot WJ, Thibodeau S, Maier C, Kibel AS, Cybulski C, Cannon-Albright L, Brenner H, Park J, Kaneva R, Batra J, Teixeira MR, Pandha H, Lathrop M, Martin RM, Holly JMP
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
Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis.
Bruel A L, Masurel-Paulet A, Riviere J B, Duffourd Y, Lehalle D, Bensignor C, Huet F, Borgnon J, Roucher F, Kuentz P, Deleuze J F, Thauvin-Robinet C, Faivre L, Thevenon J
Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13
Costantino F, Chaplais E, Leturcq T, Said-Nahal R, Leboime A, Zinovieva E, Zelenika D, Gut I, Charon C, Chiocchia G, Breban M, Garchon HJ
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
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
Severe axial muscular involvement in Laing distal myopathy with a thumbprint finding on MRI
Dabaj I, Moreno CAM, Neto OA, Bertini E, Castiglioni C, Guimaraes JB, Reed UC, Mesrob L, Lechner D, Fiorillo C, Malfati E, Boland A, Deleuze J, Bonnemann C, Laporte J, Romero N, Gomez D, Quijano-Roy S, Carlier R, Zanoteli E
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
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
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
GFRA3 promoter methylation may be associated with decreased postoperative survival in gastric cancer.
Eftang L L, Klajic J, Kristensen V N, Tost J, Esbensen Q Y, Blom G P, Bukholm I R, Bukholm G
New resources for genetic studies in Populus nigra: genome wide SNP discovery and development of a 12k Infinium array.
Faivre-Rampant P, Zaina G, Jorge V, Giacomello S, Segura V, Scalabrin S, Guerin V, De Paoli E, Aluome C, Viger M, Cattonaro F, Payne A, PaulStephenRaj P, Le Paslier M, Berard A, Allwright M R, Villar M, Taylor G, Bastien C, Morgante M
Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia
Fingerlin TE, Zhang W, Yang IV, Ainsworth HC, Russell PH, Blumhagen RZ, Schwarz MI, Brown KK, Steele MP, Loyd JE, Cosgrove GP, Lynch DA, Groshong S, Collard HR, Wolters PJ, Bradford WZ, Kossen K, Seiwert SD, du Bois RM, Garcia CK, Devine MS, Gudmundsson G, Isaksson HJ, Kaminski N, Zhang Y, Gibson KF, Lancaster LH, Maher TM, Molyneaux PL, Wells AU, Moffatt MF, Selman M, Pardo A, Kim DS, Crapo JD, Make BJ, Regan EA, Walek DS, Daniel JJ, Kamatani Y, Zelenika D, Murphy E, Smith K, McKean D, Pedersen BS, Talbert J, Powers J, Markin CR, Beckman KB, Lathrop M, Freed B, Langefeld CD, Schwartz DA
Immunochip analysis identifies association of the RAD50/IL13 region with human longevity.
Flachsbart F, Ellinghaus D, Gentschew L, Heinsen F A, Caliebe A, Christiansen L, Nygaard M, Christensen K, Blanche H, Deleuze J F, Derbois C, Galan P, Buning C, Brand S, Peters A, Strauch K, Muller-Nurasyid M, Hoffmann P, Nothen M M, Lieb W, Franke A, Schreiber S, Nebel A
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
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
EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome
Gargaun E, Seferian AM, Cardas R, Le Moing AG, Delanoe C, Nectoux J, Nelson I, Bonne G, Bihoreau MT, Deleuze JF, Boland A, Masson C, Servais L, Gidaro T
A genome-wide association study of pulmonary tuberculosis in Morocco
Grant AV, Sabri A, Abid A, Rhorfi IA, Benkirane M, Souhi H, Amrani HN, Alaoui-Tahiri K, Gharbaoui Y, Lazrak F, Sentissi I, Manessouri M, Belkheiri S, Zaid S, Bouraqadi A, El Amraoui N, Hakam M, Belkadi A, Orlova M, Boland A, Deswarte C, Amar L, Bustamante J, Boisson-Dupuis S, Casanova JL, Schurr E, El Baghdadi J, Abel L
Major Loci on Chromosomes 8q and 3q Control Interferon gamma Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations.
Jabot-Hanin F, Cobat A, Feinberg J, Grange G, Remus N, Poirier C, Boland-Auge A, Besse C, Bustamante J, Boisson-Dupuis S, Casanova J L, Schurr E, Alcais A, Hoal E G, Delacourt C, Abel L
DNA Methylation in Newborns and Maternal Smoking in Pregnancy: Genome-wide Consortium Meta-analysis.
Joubert B R, Felix J F, Yousefi P, Bakulski K M, Just A C, Breton C, Reese S E, Markunas C A, Richmond R C, Xu C J, Kupers L K, Oh S S, Hoyo C, Gruzieva O, Soderhall C, Salas L A, Baiz N, Zhang H, Lepeule J, Ruiz C, Ligthart S, Wang T, Taylor J A, Duijts L, Sharp G C, Jankipersadsing S A, Nilsen R M, Vaez A, Fallin M D, Hu D, Litonjua A A, Fuemmeler B F, Huen K, Kere J, Kull I, Munthe-Kaas M C, Gehring U, Bustamante M, Saurel-Coubizolles M J, Quraishi B M, Ren J, Tost J, Gonzalez J R, Peters M J, Haberg S E, Xu Z, van Meurs J B, Gaunt T R, Kerkhof M, Corpeleijn E, Feinberg A P, Eng C, Baccarelli A A, Benjamin Neelon S E, Bradman A, Merid S K, Bergstrom A, Herceg Z, Hernandez-Vargas H, Brunekreef B, Pinart M, Heude B, Ewart S, Yao J, Lemonnier N, Franco O H, Wu M C, Hofman A, McArdle W, Van der Vlies P, Falahi F, Gillman M W, Barcellos L F, Kumar A, Wickman M, Guerra S, Charles M A, Holloway J, Auffray C, Tiemeier H W, Smith G D, Postma D, Hivert M F, Eskenazi B, Vrijheid M, Arshad H, Anto J M, Dehghan A, Karmaus W, Annesi-Maesano I, Sunyer J, Ghantous A, Pershagen G, Holland N, Murphy S K, DeMeo D L, Burchard E G, Ladd-Acosta C, Snieder H, Nystad W, Koppelman G H, Relton C L, Jaddoe V W, Wilcox A, Melen E, London S J
A novel Alzheimer disease locus located near the gene encoding tau protein
Jun G, Ibrahim-Verbaas CA, Vronskaya M, Lambert JC, Chung J, Naj A, Kunkle BW, Wang LS, Bis JC, Bellenguez C, Harold D, Lunetta KL, DeStefano AL, Grenier-Boley B, Sims R, Beecham GW, Smith AV, Chouraki V, Hamilton-Nelson KL, Ikram MA, Fievet N, Denning N, Martin ER, Schmidt H, Kamatani Y, Dunstan ML, Valladares O, Laza AR, Zelenika D, Ramirez A, Foroud TM, Choi SH, Boland A, Becker T, Kukull WA, van der Lee SJ, Pasquier F, Cruchaga C, Beekly D, Fitzpatrick AL, Hanon O, Gill M, Barber R, Gudnason V, Campion D, Love S, Bennett DA, Amin N, Berr C, Tsolaki M, Buxbaum JD, Lopez OL, Deramecourt V, Fox NC, Cantwell LB, Tarraga L, Dufouil C, Hardy J, Crane PK, Eiriksdottir G, Hannequin D, Clarke R, Evans D, Mosley TH, Letenneur L, Brayne C, Maier W, De Jager P, Emilsson V, Dartigues JF, Hampel H, Kamboh MI, de Bruijn Rfag, Tzourio C, Pastor P, Larson EB, Rotter JI, O'Donovan MC, Montine TJ, Nalls MA, Mead S, Reiman EM, Jonsson PV, Holmes C, St George-Hyslop PH, Boada M, Passmore P, Wendland JR, Schmidt R, Morgan K, Winslow AR, Powell JF, Carasquillo M, Younkin SG, Jakobsdottir J, Kauwe JSK, Wilhelmsen KC, Rujescu D, Nothen MM, Hofman A, Jones L, Haines JL, Psaty BM, Van Broeckhoven C, Holmans P, Launer LJ, Mayeux R, Lathrop M, Goate AM, Escott-Price V, Seshadri S, Pericak-Vance MA, Amouyel P, Williams J, van Duijn CM, Schellenberg GD, Farrer LA
Analysis with the exome array identifies multiple new independent variants in lipid loci.
Kanoni S, Masca N G, Stirrups K E, Varga T V, Warren H R, Scott R A, Southam L, Zhang W, Yaghootkar H, Muller-Nurasyid M, Couto Alves A, Strawbridge R J, Lataniotis L, An Hashim N, Besse C, Boland A, Braund P S, Connell J M, Dominiczak A, Farmaki A E, Franks S, Grallert H, Jansson J H, Karaleftheri M, Keinanen-Kiukaanniemi S, Matchan A, Pasko D, Peters A, Poulter N, Rayner N W, Renstrom F, Rolandsson O, Sabater-Lleal M, Sennblad B, Sever P, Shields D, Silveira A, Stanton A V, Strauch K, Tomaszewski M, Tsafantakis E, Waldenberger M, Blakemore A I, Dedoussis G, Escher S A, Kooner J S, McCarthy M I, Palmer C N, Hamsten A, Caulfield M J, Frayling T M, Tobin M D, Jarvelin M R, Zeggini E, Gieger C, Chambers J C, Wareham N J, Munroe P B, Franks P W, Samani N J, Deloukas P
Genome Sequences of Populus tremula Chloroplast and Mitochondrion: Implications for Holistic Poplar Breeding.
Kersten B, Faivre Rampant P, Mader M, Le Paslier M C, Bounon R, Berard A, Vettori C, Schroeder H, Leple J C, Fladung M
ABCA7 rare variants and Alzheimer disease risk.
Le Guennec K, Nicolas G, Quenez O, Charbonnier C, Wallon D, Bellenguez C, Grenier-Boley B, Rousseau S, Richard A C, Rovelet-Lecrux A, Bacq D, Garnier J G, Olaso R, Boland A, Meyer V, Deleuze J F, Amouyel P, Munter H M, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues J F, Pasquier F, Rollin-Sillaire A, Genin E, Lambert J C, Hannequin D, Campion D
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Lesage S, Drouet V, Majounie E, Deramecourt V, Jacoupy M, Nicolas A, Cormier-Dequaire F, Hassoun S M, Pujol C, Ciura S, Erpapazoglou Z, Usenko T, Maurage C A, Sahbatou M, Liebau S, Ding J, Bilgic B, Emre M, Erginel-Unaltuna N, Guven G, Tison F, Tranchant C, Vidailhet M, Corvol J C, Krack P, Leutenegger A L, Nalls M A, Hernandez D G, Heutink P, Gibbs J R, Hardy J, Wood N W, Gasser T, Durr A, Deleuze J F, Tazir M, Destee A, Lohmann E, Kabashi E, Singleton A, Corti O, Brice A
Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Lesage S, Drouet V, Majounie E, Deramecourt V, Jacoupy M, Nicolas A, Cormier-Dequaire F, Hassoun SM, Pujol C, Ciura S, Erpapazoglou Z, Usenko T, Maurage CA, Sahbatou M, Liebau S, Ding JH, Bilgic B, Emre M, Erginel-Unaltuna N, Guven G, Tison F, Tranchant C, Vidailhet M, Corvol JC, Krack P, Leutenegger AL, Nalls MA, Hernandez DG, Heutink P, Gibbs JR, Hardy J, Wood NW, Gasser T, Durr A, Deleuze JF, Tazir M, Destee A, Lohmann E, Kabashi E, Singleton A, Corti O, Brice A
Variations of SOST mRNA expression in human bone are associated with DNA polymorphism and DNA methylation in the SOST gene.
Lhaneche L, Hald J D, Domingues A, Hannouche D, Delepine M, Zelenika D, Boland A, Ostertag A, Cohen-Solal M, Langdahl B L, Harslof T, de Vernejoul M C, Geoffroy V, Jehan F
Multiplexing of E-ice-COLD-PCR Assays for Mutation Detection and Identification.
Mauger F, Daunay A, Deleuze J F, Tost J, How-Kit A
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
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders.
Mercati O, Huguet G, Danckaert A, Andre-Leroux G, Maruani A, Bellinzoni M, Rolland T, Gouder L, Mathieu A, Buratti J, Amsellem F, Benabou M, Van-Gils J, Beggiato A, Konyukh M, Bourgeois J P, Gazzellone M J, Yuen R K, Walker S, Delepine M, Boland A, Regnault B, Francois M, Van Den Abbeele T, Mosca-Boidron A L, Faivre L, Shimoda Y, Watanabe K, Bonneau D, Rastam M, Leboyer M, Scherer S W, Gillberg C, Delorme R, Cloez-Tayarani I, Bourgeron T
Mutation allele burden remains unchanged in chronic myelomonocytic leukaemia responding to hypomethylating agents
Merlevede J, Droin N, Qin TT, Meldi K, Yoshida K, Morabito M, Chautard E, Auboeuf D, Fenaux P, Braun T, Itzykson R, de Botton S, Quesnel B, Commes T, Jourdan E, Vainchenker W, Bernard O, Pata-Merci N, Solier S, Gayevskiy V, Dinger ME, Cowley MJ, Selimoglu-Buet D, Meyer V, Artiguenave F, Deleuze JF, Preudhomme C, Stratton MR, Alexandrov LB, Padron E, Ogawa S, Koscielny S, Figueroa M, Solary E
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
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
The Arabidopsis hnRNP-Q Protein LIF2 and the PRC1 Subunit LHP1 Function in Concert to Regulate the Transcription of Stress-Responsive Genes
Molitor AM, Latrasse D, Zytnicki M, Andrey P, Houba-Herin N, Hachet M, Battail C, Del Prete S, Alberti A, Quesneville E, Gaudin V
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
Recurrent NRAS mutations in pulmonary Langerhans cell histiocytosis.
Mourah S, How-Kit A, Meignin V, Gossot D, Lorillon G, Bugnet E, Mauger F, Lebbe C, Chevret S, Tost J, Tazi A
Back to the Future of Soil Metagenomics
Nesme J, Achouak W, Agathos SN, Bailey M, Baldrian P, Brunel D, Frostegard A, Heulin T, Jansson JK, Jurkevitch E, Kruus KL, Kowalchuk GA, Lagares A, Lappin-Scott HM, Lemanceau P, Le Paslier D, Mandic-Mulec I, Murrell JC, Myrold DD, Nalin R, Nannipieri P, Neufeld JD, O'Gara F, Parnell JJ, Puhler A, Pylro V, Ramos JL, Roesch LFW, Schloter M, Schleper C, Sczyrba A, Sessitsch A, Sjoling S, Sorensen J, Sorensen SJ, Tebbe CC, Topp E, Tsiamis G, van Elsas JD, van Keulen G, Widmer F, Wagner M, Zhang T, Zhang XJ, Zhao LP, Zhu YG, Vogel TM, Simonet P
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease.
Nicolas G, Charbonnier C, Wallon D, Quenez O, Bellenguez C, Grenier-Boley B, Rousseau S, Richard A C, Rovelet-Lecrux A, Le Guennec K, Bacq D, Garnier J G, Olaso R, Boland A, Meyer V, Deleuze J F, Amouyel P
Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons
Nicolas G, Wallon D, Charbonnier C, Quenez O, Rousseau S, Richard AC, Rovelet-Lecrux A, Coutant S, Le Guennec K, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, Deleuze JF, Munter HM, Bourque G, Auld D, Montpetit A, Lathrop M, Guyant-Marechal L, Martinaud O, Pariente J, Rollin-Sillaire A, Pasquier F, Le Ber I, Sarazin M, Croisile B, Boutoleau-Bretonniere C, Thomas-Anterion C, Paquet C, Sauvee M, Moreaud O, Gabelle A, Sellal F, Ceccaldi M, Chamard L, Blanc F, Frebourg T, Campion D, Hannequin D
Genetic diversity, linkage disequilibrium and power of a large grapevine (Vitis vinifera L) diversity panel newly designed for association studies
Nicolas SD, Peros JP, Lacombe T, Launay A, Le Paslier MC, Berard A, Mangin B, Valiere S, Martins F, Le Cunff L, Laucou V, Bacilieri R, Dereeper A, Chatelet P, This P, Doligez A
Toxoplasma gondii exposure may modulate the influence of TLR2 genetic variation on bipolar disorder: a gene-environment interaction study.
Oliveira J, Kazma R, Le Floch E, Bennabi M, Hamdani N, Bengoufa D, Dahoun M, Manier C, Bellivier F, Krishnamoorthy R, Deleuze J F, Yolken R, Leboyer M, Tamouza R
Dissecting quantitative trait variation in the resequencing era: complementarity of bi-parental, multi-parental and association panels
Pascual L, Albert E, Sauvage C, Duangjit J, Bouchet JP, Bitton F, Desplat N, Brunel D, Le Paslier MC, Ranc N, Bruguier L, Chauchard B, Verschave P, Causse M
Role of the Polymerase is an element of sub-unit DPB2 in DNA replication, cell cycle regulation and DNA damage response in Arabidopsis
Pedroza-Garcia JA, Domenichini S, Mazubert C, Bourge M, White C, Hudik E, Bounon R, Tariq Z, Delannoy E, del Olmo I, Pineiro M, Jarillo JA, Bergounioux C, Benhamed M, Raynaud C
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
Genetic Adaptation and Neandertal Admixture Shaped the Immune System of Human Populations
Quach H, Rotival M, Pothlichet J, Loh YHE, Dannemann M, Zidane N, Laval G, Patin E, Harmant C, Lopez M, Deschamps M, Naffakh N, Duffy D, Coen A, Leroux-Roels G, Clement F, Boland A, Deleuze JF, Kelso J, Albert ML, Quintana-Murci L
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
OCT4 Acts as an Integrator of Pluripotency and Signal-Induced Differentiation
Simandi Z, Horvath A, Wright LC, Cuaranta-Monroy I, De Luca I, Karolyi K, Sauer S, Deleuze JF, Gudas LJ, Cowley SM, Nagy L
The clinical potential of Enhanced-ice-COLD-PCR
Tost J
Engineering of the epigenome: synthetic biology to define functional causality and develop innovative therapies.
Tost J
Follow the trace of death: methylation analysis of cell-free DNA for clinical applications in non-cancerous diseases
Tost J
Is there still room for additional common susceptibility alleles for venous thromboembolism?.
Tregouet D A, Delluc A, Roche A, Derbois C, Olaso R, Germain M, de Andrade M, Tang W, Chasman D I, van Hylckama Vlieg A, Reitsma P H, Kabrhel C, Smith N, Morange P E
Aristolochic acid exposure in Romania and implications for renal cell carcinoma
Turesky RJ, Yun BH, Brennan P, Mates D, Jinga V, Harnden P, Banks RE, Blanche H, Bihoreau MT, Chopard P, Letourneau L, Lathrop GM, Scelo G
Mosaic parental germline mutations causing recurrent forms of malformations of cortical development
Zillhardt JL, Poirier K, Broix L, Lebrun N, Elmorjani A, Martinovic J, Saillour Y, Muraca G, Nectoux J, Bessieres B, Fallet-Bianco C, Lyonnet S, Dulac O, Odent S, Rejeb I, Jemaa LB, Rivier F, Pinson L, Geneviève D, Musizzano Y, Bigi N, Leboucq N, Giuliano F, Philip N, Vilain C, Van Bogaert P, Maurey H, Beldjord C, Artiguenave F, Boland A, Olaso R, Masson C, Nitschké P, Deleuze JF, Bahi-Buisson N, Chelly J