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  • High Throughput Platform - Genotyping
    P Ikram MK Jensen RA Jørgensen ME Jørgensen T Karaleftheri M Khor CC Kirkpatrick A Kraja AT Kuusisto J Lange EM Lee IT Lee WJ Leong A Liao J Liu C Liu Y Lindgren CM Linneberg A Malerba G Mamakou V Marouli E Maruthur NM Matchan A McKean Cowdin R McLeod O Metcalf GA Mohlke KL Muzny DM Ntalla I Palmer ND Pasko D Peter A Rayner NW Renström F Rice K Sala CF Sennblad B Serafetinidis I Smith JA Soranzo N Speliotes EK Stahl EA Stirrups K Tentolouris N Thanopoulou A Torres M Traglia M Tsafantakis E Javad S Yanek LR Zengini E Becker DM Bis JC Brown JB Adrienne Cupples L Hansen T Ingelsson E Karter AJ Lorenzo C Mathias RA Norris JM Peloso GM Sheu WH Toniolo D Vaidya D Varma R Wagenknecht LE Boeing H Bottinger EP Dedoussis G Deloukas P Ferrannini E Franco OH Franks PW Gibbs RA Gudnason V Hamsten A Harris TB Hattersley AT Hayward C Hofman A Jansson JH Langenberg C Launer LJ Levy D Oostra BA O Donnell CJ O Rahilly S Padmanabhan S Pankow JS Polasek O Province MA Rich SS Ridker PM Rudan I Schulze MB Smith BH Uitterlinden AG Walker M Watkins H Wong TY Zeggini E EPIC InterAct Consortium Laakso M Borecki IB Chasman DI Pedersen O Psaty BM Shyong Tai E van Duijn CM Wareham NJ Waterworth DM Boerwinkle E Linda Kao WH Florez JC Loos RJ Wilson JG Frayling TM Siscovick DS Dupuis J Rotter JI Meigs JB Scott RA Goodarzi MO EPIC InterAct Consortium Low frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility Nat Commun 2015 6 p 5897 Caburet S Zavadakova P Ben Neriah Z Bouhali K Dipietromaria A Charon C Besse C Laissue P Chalifa Caspi V Christin Maitre S Vaiman D Levi G Veitia RA Fellous M Genome wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non syndromic familial Premature Ovarian Failure PLoS One 2012 7 3 p e33412 Yamagata Y Parietti V Stockholm D Corre G Poinsignon C Touleimat N Delafoy D Besse C Tost J Galy A Paldi A Lentiviral transduction of CD34 cells induces genome wide epigenetic modifications PLoS One 2012 7 11 p e48943 Bustamante J Arias AA Vogt G Picard C Galicia LB Prando C Grant AV Marchal CC Hubeau M Chapgier A de Beaucoudrey L Puel A Feinberg J Valinetz E Jannière L Besse C Boland A Brisseau JM Blanche S Lortholary O Fieschi C Emile JF Boisson Dupuis S Al Muhsen S Woda B Newburger PE Condino Neto A Dinauer MC Abel L Casanova JL Germline CYBB mutations that selectively affect macrophages in kindreds with X linked predisposition to tuberculous mycobacterial disease Nat Immunol 2011 12 3 p 213 221 Lagresle Peyrou C Six EM Picard C Rieux Laucat F Michel V Ditadi A Demerens de Chappedelaine C Morillon E Valensi F Simon Stoos KL Mullikin JC Noroski LM Besse

    Original URL path: http://www.cng.fr/en/organisation/laboratories/haut_debit/genotyping/besse_publ.html (2016-01-29)
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  • High Throughput Platform - Sequencing
    Organisation High Throughput Platform Sequencing ORGANISATION DIRECTION LABORATORIES HIGH THROUGHPUT PLATFORM GENOTYPING SEQUENCING Doris Lechner Profile Publications Doris Lechner is graduate engineer in biotechnology She studied at the University of Applied Sciences in Berlin After her diploma she joined Ivo Gut in 1997 at the Max Planck Institute of Molecular Genetics in Berlin Between 1999 and 2004 she established SNP genotyping by mass spectrometry at the CNG In April 2004

    Original URL path: http://www.cng.fr/en/organisation/laboratories/haut_debit/sequencing/lechner_cv_en.html (2016-01-29)
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  • High Throughput Platform - Sequencing
    Romkes M Buch S Nukui T Zhong S Lacko M Manni JJ Peters WH Hung RJ McLaughlin J Vatten L Njølstad I Goodman GE Field JK Liloglou T Vineis P Clavel Chapelon F Palli D Tumino R Krogh V Panico S González CA Quirós JR Martínez C Navarro C Ardanaz E Larrañaga N Khaw KT Key T Bueno de Mesquita HB Peeters PH Trichopoulou A Linseisen J Boeing H Hallmans G Overvad K Tjønneland A Kumle M Riboli E Välk K Voodern T Metspalu A Zelenika D Boland A Delépine M Foglio M Lechner D Blanché H Gut IG Galan P Heath S Hashibe M Hayes RB Boffetta P Lathrop M Brennan P A genome wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium PLoS Genet 2011 7 3 p e1001333 Purdue MP Johansson M Zelenika D Toro JR Scelo G Moore LE Prokhortchouk E Wu X Kiemeney LA Gaborieau V Jacobs KB Chow WH Zaridze D Matveev V Lubinski J Trubicka J Szeszenia Dabrowska N Lissowska J Rudnai P Fabianova E Bucur A Bencko V Foretova L Janout V Boffetta P Colt JS Davis FG Schwartz KL Banks RE Selby PJ Harnden P Berg CD Hsing AW Grubb RL 3rd Boeing H Vineis P Clavel Chapelon F Palli D Tumino R Krogh V Panico S Duell EJ Quirós JR Sanchez MJ Navarro C Ardanaz E Dorronsoro M Khaw KT Allen NE Bueno de Mesquita HB Peeters PH Trichopoulos D Linseisen J Ljungberg B Overvad K Tjønneland A Romieu I Riboli E Mukeria A Shangina O Stevens VL Thun MJ Diver WR Gapstur SM Pharoah PD Easton DF Albanes D Weinstein SJ Virtamo J Vatten L Hveem K Njølstad I Tell GS Stoltenberg C Kumar R Koppova K Cussenot O Benhamou S Oosterwijk E Vermeulen SH Aben KK van der Marel SL Ye Y Wood CG Pu X Mazur AM Boulygina ES Chekanov NN Foglio M Lechner D Gut I Heath S Blanche H Hutchinson A Thomas G Wang Z Yeager M Fraumeni JF Jr Skryabin KG McKay JD Rothman N Chanock SJ Lathrop M Brennan P Genome wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13 3 Nat Genet 2011 43 1 p 60 65 Sanson M Hosking FJ Shete S Zelenika D Dobbins SE Ma Y Enciso Mora V Idbaih A Delattre JY Hoang Xuan K Marie Y Boisselier B Carpentier C Wang XW Di Stefano AL Labussière M Gousias K Schramm J Boland A Lechner D Gut I Armstrong G Liu Y Yu R Lau C Di Bernardo MC Robertson LB Muir K Hepworth S Swerdlow A Schoemaker MJ Wichmann HE Müller M Schreiber S Franke A Moebus S Eisele L Försti A Hemminki K Lathrop M Bondy M Houlston RS Simon M Chromosome 7p11 2 EGFR variation influences glioma risk Hum Mol Genet 2011 20 14 p 2897 2904 Druet T Fritz S Boussaha M Ben Jemaa S Guillaume F Derbala D Zelenika D Lechner D

    Original URL path: http://www.cng.fr/en/organisation/laboratories/haut_debit/sequencing/lechner_publ.html (2016-01-29)
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  • Atelier CNG
    B Cookson 12 05 Session 3 Comparative Genomics 12 05 12 35 Molecular dissection of QTLs in rodents and humans D Gauguier 12 35 13 05 Dissection of immune related traits using ENU R Cornall Lunch 14 15 14 45 Selective sweeps and positional identification of trait loci in chicken L Andersson 14 45 15 15 QTLs in cattle A Eggen 15 15 16 15 Perspectives on genomics in the mouse P Avner Coffee 16 45 17 15 Polymorphic miRNA target interactions a novel source of phenotypic variation M Georges 17 15 Session 4 Study design and data interpretation I 17 15 17 45 Quantitative trait analysis M Farrall 17 45 18 15 Genome wide association mapping in bacteria D Falush Day 2 September 26 2006 8 45 Session 5 Copy number variation 8 45 9 05 Clinical applications A Verloes 9 05 9 25 Mental retardation L Colleaux 9 25 9 40 Comparison of methodologies M Lathrop 9 40 10 00 Initiatives for research on rare disorders discussion E Tournier Lasserve 10 00 Session 6 Disease applications II 10 00 10 30 Genetics of neuropsychiatric disease T Bourgeron Coffee 10 50 11 20 Genetics of autism J Hager 11

    Original URL path: http://www.cng.fr/atelier2006/program.html (2016-01-29)
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  • Atelier CNG
    Rory Collins Clinical Trial Service Unit Epidemiological Studies Universite d Oxford William Cookson Imperial College London Richard Cornall Université d Oxford Oxford André Eggen INRA Daniel Falush Université d Oxford Oxford Martin Farrall Université d Oxford Oxford Dominique Gauguier Université d Oxford Oxford Michel Georges Faculte de Medecine Veterinaire Liege Belgique Xavier Gidrol CEA Evry Ivo Gut CNG Evry Jörg Hager Integragen Evry Cecilé Julier Institut Pasteur Paris Ulf Landegren

    Original URL path: http://www.cng.fr/atelier2006/speakers.html (2016-01-29)
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  • Atelier CNG
    COMPLETER EN LETTRES CAPITALES 1 FICHE PAR INSCRIT E INSCRIT E Nom Prénom Titre Pr Dr M Mme Sexe Masculin Féminin Qualification Employeur Adresse postale Pays Téléphone Poste Fax E mail Renseignements complémentaires Bref résumé de votre profil dans le domaine de la recherche des Sciences du Vivant en particulier niveau actuel et expérience en méthodologie et statistique ainsi que 5 publications Nom Résumé Signature Date LE NOMBRE DE PLACES

    Original URL path: http://www.cng.fr/atelier2006/fiche_inscription.html (2016-01-29)
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  • Atelier CNG
    APPLICANT DETAILS Family Name First name Title Prof Dr Mr Ms Sex Male Female Job Title Organisation Postal Address Country Telephone Ext Fax E mail In addition to the above please provide Biosketch of applicant A short statement of research interests outlining your current level of knowledge and experience in methodology statistical methods and up to 5 publications Name Biosketch Signature Date WE ANTICIPATE HIGH DEMAND AND GIVEN THE LIMITED

    Original URL path: http://www.cng.fr/atelier2006/application_form.html (2016-01-29)
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  • Atelier CNG
    Chimie 28 rue Saint Dominique 75007 Paris France Nearest RER train station INVALIDES RER line C Nearest metro underground subway INVALIDES line 8 and line 13 Site map Detailed street map for Maison de la Chimie and surrounding area Detailed

    Original URL path: http://www.cng.fr/atelier2006/directions.html (2016-01-29)
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