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Publications du CNG

Publié le 4 décembre 2015
  
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
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
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
"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
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
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
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
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
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
Engineering of the epigenome: synthetic biology to define functional causality and develop innovative therapies.
Tost J
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
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
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
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
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