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Publications archive

Publié le 23 mai 2017

  
Common Polymorphisms in the CYP11B1 and CYP11B2 Genes: Evidence for a Digenic Influence on Hypertension
Alvarez-Madrazo S, MacKenzie SM, Davies E, Fraser R, Lee WK, Brown M, Caulfield MJ, Dominiczak AF, Farrall M, Lathrop M, Hedner T, Melander O, Munroe PB, Samani N, Stewart PM, Wahlstrand B, Webster J, Palmer CNA, Padmanabhan S, Connell JM
Individual and combined effects of DNA methylation and copy number alterations on miRNA expression in breast tumors
Aure MR, Leivonen SK, Fleischer T, Zhu Q, Overgaard J, Alsner J, Tramm T, Louhimo R, Alnaes GIG, Perala M, Busato F, Touleimat N, Tost J, Borresen-Dale AL, Hautaniemi S, Troyanskaya OG, Lingjaerde OC, Sahlberg KK, Kristensen VN
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats
Baud A, Hermsen R, Guryev V, Stridh P, Graham D, McBride MW, Foroud T, Calderari S, Diez M, Ockinger J, Beyeen AD, Gillett A, Abdelmagid N, Guerreiro-Cacais AO, Jagodic M, Tuncel J, Norin U, Beattie E, Huynh N, Miller WH, Koller DL, Alam I, Falak S, Osborne-Pellegrin M, Martinez-Membrives E, Canete T, Blazquez G, Vicens-Costa E, Mont-Cardona C, Diaz-Moran S, Tobena A, Hummel O, Zelenika D, Saar K, Patone G, Bauerfeind A, Bihoreau MT, Heinig M, Lee YA, Rintisch C, Schulz H, Wheeler DA, Worley KC, Muzny DM, Gibbs RA, Lathrop M, Lansu N, Toonen P, Ruzius FP, de Bruijn E, Hauser H, Adams DJ, Keane T, Atanur SS, Aitman TJ, Flicek P, Malinauskas T, Jones EY, Ekman D, Lopez-Aumatell R, Dominiczak AF, Johannesson M, Holmdahl R, Olsson T, Gauguier D, Hubner N, Fernandez-Teruel A, Cuppen E, Mott R, Flint J
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, Cotsapas C, Shah TS, Spencer C, Booth D, Goris A, Oturai A, Saarela J, Fontaine B, Hemmer B, Martin C, Zipp F, D'Alfonso S, Martinelli-Boneschi F, Taylor B, Harbo HF, Kockum I, Hillert J, Olsson T, Ban M, Oksenberg JR, Hintzen R, Barcellos LF, Agliardi C, Alfredsson L, Alizadeh M, Anderson C, Andrews R, Sondergaard HB, Baker A, Band G, Baranzini SE, Barizzone N, Barrett J, Bellenguez C, Bergamaschi L, Bernardinelli L, Berthele A, Biberacher V, Binder TMC, Blackburn H, Bomfim IL, Brambilla P, Broadley S, Brochet B, Brundin L, Buck D, Butzkueven H, Caillier SJ, Camu W, Carpentier W, Cavalla P, Celius EG, Coman I, Comi G, Corrado L, Cosemans L, Cournu-Rebeix I, Cree BAC, Cusi D, Damotte V, Defer G, Delgado SR, Deloukas P, di Sapio A, Dilthey AT, Donnelly P, Dubois B, Duddy M, Edkins S, Elovaara I, Esposito F, Evangelou N, Fiddes B, Field J, Franke A, Freeman C, Frohlich IY, Galimberti D, Gieger C, Gourraud PA, Graetz C, Graham A, Grummel V, Guaschino C, Hadjixenofontos A, Hakonarson H, Halfpenny C, Hall G, Hall P, Hamsten A, Harley J, Harrower T, Hawkins C, Hellenthal G, Hillier C, Hobart J, Hoshi M, Hunt SE, Jagodic M, Jelcic I, Jochim A, Kendall B, Kermode A, Kilpatrick T, Koivisto K, Konidari I, Korn T, Kronsbein H, Langford C, Larsson M, Lathrop M, Lebrun-Frenay C, Lechner-Scott J, Lee MH, Leone MA, Leppa V, Liberatore G, Lie BA, Lill CM, Linden M, Link J, Luessi F, Lycke J, Macciardi F, Mannisto S, Manrique CP, Martin R, Martinelli V, Mason D, Mazibrada G, McCabe C, Mero IL, Mescheriakova J, Moutsianas L, Myhr KM, Nagels G, Nicholas R, Nilsson P, Piehl F, Pirinen M, Price SE, Quach H, Reunanen M, Robberecht W, Robertson NP, Rodegher M, Rog D, Salvetti M, Schnetz-Boutaud NC, Sellebjerg F, Selter RC, Schaefer C, Shaunak S, Shen L, Shields S, Siffrin V, Slee M, Sorensen PS, Sorosina M, Sospedra M, Spurkland A, Strange A, Sundqvist E, Thijs V, Thorpe J, Ticca A, Tienari P, van Duijn C, Visser EM, Vucic S, Westerlind H, Wiley JS, Wilkins A, Wilson JF, Winkelmann J, Zajicek J, Zindler E, Haines JL, Pericak-Vance MA, Ivinson AJ, Stewart G, Hafler D, Hauser SL, Compston A, McVean G, De Jager P, Sawcer SJ, McCauley JL
Genome-wide linkage disequilibrium in the Blonde d'Aquitaine cattle breed
Beghain J, Boitard S, Weiss B, Boussaha M, Gut I, Rocha D
CpG Methylation Changes within the IL2RA Promoter in Type 1 Diabetes of Childhood Onset
Belot MP, Fradin D, Mai N, Le Fur S, Zelenika D, Kerr-Conte J, Pattou F, Lucas B, Bougneres P
Improving Breast Cancer Survival Analysis through Competition-Based Multidimensional Modeling
Bilal E, Dutkowski J, Guinney J, Jang IS, Logsdon BA, Pandey G, Sauerwine BA, Shimoni Y, Vollan HKM, Mecham BH, Rueda OM, Tost J, Curtis C, Alvarez MJ, Kristensen VN, Aparicio S, Borresen-Dale AL, Caldas C, Califano A, Friend SH, Ideker T, Schadt EE, Stolovitzky GA, Margolin AA
Inhibition of Comt with tolcapone slows progression of polycystic kidney disease in the more severely affected PKD/Mhm (cy/ plus ) substrain of the Hannover Sprague-Dawley rat
Boehn SNE, Spahn S, Neudecker S, Keppler A, Bihoreau MT, Kranzlin B, Pandey P, Hoffmann SC, Li L, Torres VE, Grone HJ, Gretz N
Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms
Bonaventure A, Rudant J, Goujon-Bellec S, Orsi L, Leverger G, Baruchel A, Bertrand Y, Nelken B, Pasquet M, Michel G, Sirvent N, Bordigoni P, Ducassou S, Rialland X, Zelenika D, Hemon D, Clavel J
Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus
Bouchet S, Servin B, Bertin P, Madur D, Combes V, Dumas F, Brunel D, Laborde J, Charcosset A, Nicolas S
Influence of SNPs in nutrient-sensitive candidate genes and gene-diet interactions on blood lipids: the DiOGenes study
Brahe LK, Angquist L, Larsen LH, Vimaleswaran KS, Hager J, Viguerie N, Loos RJF, Handjieva-Darlenska T, Jebb SA, Hlavaty P, Larsen TM, Martinez JA, Papadaki A, Pfeiffer AFH, van Baak MA, Sorensen TIA, Holst C, Langin D, Astrup A, Saris WHM
Mutations in BCAP31 Cause a Severe X-Linked Phenotype with Deafness, Dystonia, and Central Hypomyelination and Disorganize the Golgi Apparatus
Cacciagli P, Sutera-Sardo J, Borges-Correia A, Roux JC, Dorboz I, Desvignes JP, Badens C, Delepine M, Lathrop M, Cau P, Levy N, Girard N, Sarda P, Boespflug-Tanguy O, Villard L
Whole genome resequencing in tomato reveals variation associated with introgression and breeding events
Causse M, Desplat N, Pascual L, Le Paslier MC, Sauvage C, Bauchet G, Berard A, Bounon R, Tchoumakov M, Brunel D, Bouchet JP
"Development of real-time PCR method for the detection and the quantification of a new endogenous reference gene in sugar beet ""Beta vulgaris L."": GMO application"
Chaouachi M, Alaya A, Ali IB, Ben Hafsa A, Nabi N, Berard A, Romaniuk M, Skhiri F, Said K
Relative quantification in seed GMO analysis: state of art and bottlenecks
Chaouachi M, Berard A, Said K
Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology
Chapuis J, Hansmannel F, Gistelinck M, Mounier A, Van Cauwenberghe C, Kolen KV, Geller F, Sottejeau Y, Harold D, Dourlen P, Grenier-Boley B, Kamatani Y, Delepine B, Demiautte F, Zelenika D, Zommer N, Hamdane M, Bellenguez C, Dartigues JF, Hauw JJ, Letronne F, Ayral AM, Sleegers K, Schellens A, Broeck LV, Engelborghs S, De Deyn PP, Vandenberghe R, O'Donovan M, Owen M, Epelbaum J, Mercken M, Karran E, Bantscheff M, Drewes G, Joberty G, Campion D, Octave JN, Berr C, Lathrop M, Callaerts P, Mann D, Williams J, Buee L, Dewachter I, Van Broeckhoven C, Amouyel P, Moechars D, Dermaut B, Lambert JC
Phospholipase A2 Receptor (PLA2R1) Sequence Variants in Idiopathic Membranous Nephropathy
Coenen MJH, Hofstra JM, Debiec H, Stanescu HC, Medlar AJ, Stengel B, Boland-Auge A, Groothuismink JM, Bockenhauer D, Powis SH, Mathieson PW, Brenchley PE, Kleta R, Wetzels JFM, Ronco P
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
Cordell HJ, Bentham J, Topf A, Zelenika D, Heath S, Mamasoula C, Cosgrove C, Blue G, Granados-Riveron J, Setchfield K, Thornborough C, Breckpot J, Soemedi R, Martin R, Rahman TJ, Hall D, van Engelen K, Moorman AFM, Zwinderman AH, Barnett P, Koopmann TT, Adriaens ME, Varro A, George AL, dos Remedios C, Bishopric NH, Bezzina CR, O'Sullivan J, Gewillig M, Bu'Lock FA, Winlaw D, Bhattacharya S, Devriendt K, Brook JD, Mulder BJM, Mital S, Postma AV, Lathrop GM, Farrall M, Goodship JA, Keavney BD
Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot
Cordell HJ, Topf A, Mamasoula C, Postma AV, Bentham J, Zelenika D, Heath S, Blue G, Cosgrove C, Riveron JG, Darlay R, Soemedi R, Wilson IJ, Ayers KL, Rahman TJ, Hall D, Mulder BJM, Zwinderman AH, van Engelen K, Brook JD, Setchfield K, Bu'Lock FA, Thornborough C, O'Sullivan J, Stuart AG, Parsons J, Bhattacharya S, Winlaw D, Mital S, Gewillig M, Breckpot J, Devriendt K, Moorman AFM, Rauch A, Lathrop GM, Keavney BD, Goodship JA
Large-scale association analysis identifies new risk loci for coronary artery disease
Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, Ingelsson E, Saleheen D, Erdmann J, Goldstein BA, Stirrups K, Konig IR, Cazier JB, Johansson A, Hall AS, Lee JY, Willer CJ, Chambers JC, Esko T, Folkersen L, Goel A, Grundberg E, Havulinna AS, Ho WK, Hopewell JC, Eriksson N, Kleber ME, Kristiansson K, Lundmark P, Lyytikainen LP, Rafelt S, Shungin D, Strawbridge RJ, Thorleifsson G, Tikkanen E, Van Zuydam N, Voight BF, Waite LL, Zhang WH, Ziegler A, Absher D, Altshuler D, Balmforth AJ, Barroso I, Braund PS, Burgdorf C, Claudi-Boehm S, Cox D, Dimitriou M, Do R, Doney ASF, El Mokhtari N, Eriksson P, Fischer K, Fontanillas P, Franco-Cereceda A, Gigante B, Groop L, Gustafsson S, Hager J, Hallmans G, Han BG, Hunt SE, Kang HM, Illig T, Kessler T, Knowles JW, Kolovou G, Kuusisto J, Langenberg C, Langford C, Leander K, Lokki ML, Lundmark A, McCarthy MI, Meisinger C, Melander O, Mihailov E, Maouche S, Morris AD, Muller-Nurasyid M, Nikus K, Peden JF, Rayner NW, Rasheed A, Rosinger S, Rubin D, Rumpf MP, Schafer A, Sivananthan M, Song C, Stewart AFR, Tan ST, Thorgeirsson G, van der Schoot CE, Wagner PJ, Wells GA, Wild PS, Yang TP, Amouyel P, Arveiler D, Basart H, Boehnke M, Boerwinkle E, Brambilla P, Cambien F, Cupples AL, de Faire U, Dehghan A, Diemert P, Epstein SE, Evans A, Ferrario MM, Ferrieres J, Gauguier D, Go AS, Goodall AH, Gudnason V, Hazen SL, Holm H, Iribarren C, Jang Y, Kahonen M, Kee F, Kim HS, Klopp N, Koenig W, Kratzer W, Kuulasmaa K, Laakso M, Laaksonen R, Lee JY, Lind L, Ouwehand WH, Parish S, Park JE, Pedersen NL, Peters A, Quertermous T, Rader DJ, Salomaa V, Schadt E, Shah SH, Sinisalo J, Stark K, Stefansson K, Tregouet DA, Virtamo J, Wallentin L, Wareham N, Zimmermann ME, Nieminen MS, Hengstenberg C, Sandhu MS, Pastinen T, Syvanen AC, Hovingh GK, Dedoussis G, Franks PW, Lehtimaki T, Metspalu A, Zalloua PA, Siegbahn A, Schreiber S, Ripatti S, Blankenberg SS, Perola M, Clarke R, Boehm BO, O'Donnell C, Reilly MP, Marz W, Collins R, Kathiresan S, Hamsten A, Kooner JS, Thorsteinsdottir U, Danesh J, Palmer CNA, Roberts R, Watkins H, Schunkert H, Samani NJ
Genome-wide interval mapping using SNPs identifies new QTL for growth, body composition and several physiological variables in an F-2 intercross between fat and lean chicken lines
Demeure O, Duclos MJ, Bacciu N, Le Mignon G, Filangi O, Pitel F, Boland A, Lagarrigue S, Cogburn LA, Simon J, Le Roy P, Le Bihan-Duval E
Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222
Enciso-Mora V, Hosking FJ, Di Stefano AL, Zelenika D, Shete S, Broderick P, Idbaih A, Delattre JY, Hoang-Xuan K, Marie Y, Labussiere M, Alentorn A, Ciccarino P, Rossetto M, Armstrong G, Liu Y, Gousias K, Schramm J, Lau C, Hepworth SJ, Schoemaker M, Strauch K, Muller-Nurasyid M, Schreiber S, Franke A, Moebus S, Eisele L, Swerdlow A, Simon M, Bondy M, Lathrop M, Sanson M, Houlston RS
Deciphering the 8q24.21 association for glioma
Enciso-Mora V, Hosking FJ, Kinnersley B, Wang YF, Shete S, Zelenika D, Broderick P, Idbaih A, Delattre JY, Hoang-Xuan K, Marie Y, Di Stefano AL, Labussiere M, Dobbins S, Boisselier B, Ciccarino P, Rossetto M, Armstrong G, Liu YH, Gousias K, Schramm J, Lau C, Hepworth SJ, Strauch K, Muller-Nurasyid M, Schreiber S, Franke A, Moebus S, Eisele L, Forsti A, Hemminki K, Tomlinson IP, Swerdlow A, Lathrop M, Simon M, Bondy M, Sanson M, Houlston RS
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity
Esko T, Mezzavilla M, Nelis M, Borel C, Debniak T, Jakkula E, Julia A, Karachanak S, Khrunin A, Kisfali P, Krulisova V, Kucinskiene ZA, Rehnstrom K, Traglia M, Nikitina-Zake L, Zimprich F, Antonarakis SE, Estivill X, Glavac D, Gut I, Klovins J, Krawczak M, Kucinskas V, Lathrop M, Macek M, Marsal S, Meitinger T, Melegh B, Limborska S, Lubinski J, Paolotie A, Schreiber S, Toncheva D, Toniolo D, Wichmann HE, Zimprich A, Metspalu M, Gasparini P, Metspalu A, D'Adamo P
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
Fingerlin TE, Murphy E, Zhang W, Peljto AL, Brown KK, Steele MP, Loyd JE, Cosgrove GP, Lynch D, 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, Cogan JD, Mason WR, 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, Smith K, McKean D, Pedersen BS, Talbert J, Kidd RN, Markin CR, Beckman KB, Lathrop M, Schwarz MI, Schwartz DA
Seven new loci associated with age-related macular degeneration
Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GHS, Sim XL, Weeks DE, Guymer RH, Merriam JE, Francis PJ, Hannum G, Agarwal A, Armbrecht AM, Audo I, Aung T, Barile GR, Benchaboune M, Bird AC, Bishop PN, Branham KE, Brooks M, Brucker AJ, Cade WH, Cain MS, Campochiaroll PA, Chan CC, Cheng CY, Chew EY, Chin KA, Chowers I, Clayton DG, Cojocaru R, Conley YP, Cornes BK, Daly MJ, Dhillon B, Edwards A, Evangelou E, Fagemess J, Ferreyra HA, Friedman JS, Geirsdottir A, George RJ, Gieger C, Gupta N, Hagstrom SA, Harding SP, Haritoglou C, Heckenlively JR, Hoz FG, Hughes G, Ioannidis JPA, Ishibashi T, Joseph P, Jun G, Kamatani Y, Katsanis N, Keilhauer CN, Khan JC, Kim IK, Kiyohara Y, Klein BEK, Klein R, Kovach JL, Kozak I, Lee CJ, Lee KE, Lichtner P, Lotery AJ, Meitinger T, Mitchell P, Mohand-Said S, Moore AT, Morgan DJ, Margaux AM, Myers CE, Naj AC, Nakamura Y, Okada Y, Orlin A, Ortube MC, Othman MI, Pappas C, Park KH, Pauer GJT, Peachey NS, Poch O, Priya RR, Reynolds R, Richardson AJ, Ripp R, Rudolph G, Ryu E, Sahel JA, Schaumberg DA, Scholl HPN, Schwartz SG, Scott WK, Shahid H, Sigurdsson H, Silvestri G, Sivakumaran TA, Smith RT, Sobrin L, Souied EH, Stambolian DE, Stefansson H, Sturgill-Short GM, Takahashi A, Tosakulwong N, Truitt BJ, Tsironi EE, Uitterlinden AG, van Duijn CM, Vijaya L, Vingerling JR, Vithana EN, Webster AR, Wichmann HE, Winkler TW, Wong TY, Wright AF, Zelenika D, Zhang M, Zhao L, Zhang K, Klein ML, Hageman GS, Lathrop GM, Stefansson K, Allikmets R, Baird PN, Gorin MB, Wang JJ, Klaver CCW, Seddon JM, Pericak-Vance MA, Iyengar SK, Yates JRW, Swaroop A, Weber BHF, Kubo M, DeAngelis MM, Leveillard T, Thorsteinsdottir U, Haines JL, Farrer LA, Heid IM, Abecasis GR
Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension
Germain M, Eyries M, Montani D, Poirier O, Girerd B, Dorfmuller P, Coulet F, Nadaud S, Maugenre S, Guignabert C, Carpentier W, Vonk-Noordegraaf A, Levy M, Chaouat A, Lambert JC, Bertrand M, Dupuy AM, Letenneur L, Lathrop M, Amouyel P, de Ravel TJL, Delcroix M, Austin ED, Robbins IM, Hemnes AR, Loyd JE, Berman-Rosenzweig E, Barst RJ, Chung WK, Simonneau G, Tregouet DA, Humbert M, Soubrier F
Age-Dependent Association between Pulmonary Tuberculosis and Common TOX Variants in the 8q12-13 Linkage Region
Grant AV, El Baghdadi J, Sabri A, El Azbaoui S, Alaoui-Tahiri K, Rhorfi IA, Gharbaoui Y, Abid A, Benkirane M, Raharimanga V, Richard V, Orlova M, Boland A, Migaud M, Okada S, Nolan DK, Bustamante J, Barreiro LB, Schurr E, Boisson-Dupuis S, Rasolofo V, Casanova JL, Abel L
A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis
Greliche N, Germain M, Lambert JC, Cohen W, Bertrand M, Dupuis AM, Letenneur L, Lathrop M, Amouyel P, Morange PE, Tregouet DA
Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer
Henrion M, Frampton M, Scelo G, Purdue M, Ye YQ, Broderick P, Ritchie A, Kaplan R, Meade A, McKay J, Johansson M, Lathrop M, Larkin J, Rothman N, Wang ZM, Chow WH, Stevens VL, Diver WR, Gapstur SM, Albanes D, Virtamo J, Wu XF, Brennan P, Chanock S, Eisen T, Houlston RS
Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study
Hopewell JC, Parish S, Offer A, Link E, Clarke R, Lathrop M, Armitage J, Collins R
A variant in FTO shows association with melanoma risk not due to BMI
Iles MM, Law MH, Stacey SN, Han JL, Fang SY, Pfeiffer R, Harland M, MacGregor S, Taylor JC, Aben KK, Akslen LA, Avril MF, Azizi E, Bakker B, Benediktsdottir KR, Bergman W, Scarra GB, Brown KM, Calista D, Chaudru V, Fargnoli MC, Cust AE, Demenais F, de Waal AC, Debniak T, Elder DE, Friedman E, Galan P, Ghiorzo P, Gillanders EM, Goldstein AM, Gruis NA, Hansson J, Helsing P, Hocevar M, Hoiom V, Hopper JL, Ingvar C, Janssen M, Jenkins MA, Kanetsky PA, Kiemeney LA, Lang JL, Lathrop GM, Leachman S, Lee JE, Lubinski J, Mackie RM, Mann GJ, Martin NG, Mayordomo JI, Molven A, Mulder S, Nagore E, Novakovic S, Okamoto I, Olafsson JH, Olsson H, Pehamberger H, Peris K, Grasa MP, Planelles D, Puig S, Puig-Butille JA, Randerson-Moor J, Requena C, Rivoltini L, Rodolfo M, Santinami M, Sigurgeirsson B, Snowden H, Song FJ, Sulem P, Thorisdottir K, Tuominen R, Van Belle P, van der Stoep N, van Rossum MM, Wei QY, Wendt J, Zelenika D, Zhang MF, Landi MT, Thorleifsson G, Bishop DT, Amos CI, Hayward NK, Stefansson K, Bishop JAN, Barrett JH
Organelle and Cellular Abnormalities Associated with Hippocampal Heterotopia in Neonatal Doublecortin Knockout Mice
Khalaf-Nazzal R, Bruel-Jungerman E, Rio JP, Bureau J, Irinopoulou T, Sumia I, Roumegous A, Martin E, Olaso R, Parras C, Cifuentes-Diaz C, Francis F
Sensitive Detection of KRAS Mutations Using Enhanced-ice-COLD-PCR Mutation Enrichment and Direct Sequence Identification
Kit AH, Mazaleyrat N, Daunay A, Nielsen HM, Terris B, Tost J
Quantitative DNA methylation analyses reveal stage dependent DNA methylation and association to clinico-pathological factors in breast tumors
Klajic J, Fleischer T, Dejeux E, Edvardsen H, Warnberg F, Bukholm I, Lonning PE, Solvang H, Borresen-Dale AL, Tost J, Kristensen VN
Genome-wide association of quantitative trait loci with levels of hemostatic factors and thrombin generation in the GIFT study
Koenderman JS, Castoldi E, Tregouet DA, Morange PE, Lathrop M, Vos HL, Bertina RM, Houwing-Duistermaat J, Reitsma PH, De Visser MCH
J. Thromb. Haemost. 11 (), 16-16, 2013
Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease
Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, Alvarez V, Sims R, Gerrish A, Chapman J, Deniz-Naranjo C, Solfrizzi V, Sorbi S, Arosio B, Spalletta G, Siciliano G, Epelbaum J, Hannequin D, Dartigues JF, Tzourio C, Berr C, Schrijvers EMC, Rogers R, Tosto G, Pasquier F, Bettens K, Van Cauwenberghe C, Fratiglioni L, Graff C, Delepine M, Ferri R, Reynolds CA, Lannfelt L, Ingelsson M, Prince JA, Chillotti C, Pilotto A, Seripa D, Boland A, Mancuso M, Bossu P, Annoni G, Nacmias B, Bosco P, Panza F, Sanchez-Garcia F, Del Zompo M, Coto E, Owen M, O'Donovan M, Valdivieso F, Caffara P, Scarpini E, Combarros O, Buee L, Campion D, Soininen H, Breteler M, Riemenschneider M, Van Broeckhoven C, Alperovitch A, Lathrop M, Tregouet DA, Williams J, Amouyel P
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, Jun G, DeStefano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thornton-Wells TA, Jones N, Smith AV, Chouraki V, Thomas C, Ikram MA, Zelenika D, Vardarajan BN, Kamatani Y, Lin CF, Gerrish A, Schmidt H, Kunkle B, Dunstan ML, Ruiz A, Bihoreau MT, Choi SH, Reitz C, Pasquier F, Hollingworth P, Ramirez A, Hanon O, Fitzpatrick AL, Buxbaum JD, Campion D, Crane PK, Baldwin C, Becker T, Gudnason V, Cruchaga C, Craig D, Amin N, Berr C, Lopez OL, De Jager PL, Deramecourt V, Johnston JA, Evans D, Lovestone S, Letenneur L, Moron FJ, Rubinsztein DC, Eiriksdottir G, Sleegers K, Goate AM, Fievet N, Huentelman MJ, Gill M, Brown K, Kamboh MI, Keller L, Barberger-Gateau P, McGuinness B, Larson EB, Green R, Myers AJ, Dufouil C, Todd S, Wallon D, Love S, Rogaeva E, Gallacher J, St George-Hyslop P, Clarimon J, Lleo A, Bayer A, Tsuang DW, Yu L, Tsolaki M, Bossu P, Spalletta G, Proitsi P, Collinge J, Sorbi S, Sanchez-Garcia F, Fox NC, Hardy J, Naranjo MCD, Bosco P, Clarke R, Brayne C, Galimberti D, Mancuso M, Matthews F, Moebus S, Mecocci P, Del Zompo M, Maier W, Hampel H, Pilotto A, Bullido M, Panza F, Caffarra P, Nacmias B, Gilbert JR, Mayhaus M, Lannfelt L, Hakonarson H, Pichler S, Carrasquillo MM, Ingelsson M, Beekly D, Alvarez V, Zou FG, Valladares O, Younkin SG, Coto E, Hamilton-Nelson KL, Gu W, Razquin C, Pastor P, Mateo I, Owen MJ, Faber KM, Jonsson PV, Combarros O, O'Donovan MC, Cantwell LB, Soininen H, Blacker D, Mead S, Mosley TH, Bennett DA, Harris TB, Fratiglioni L, Holmes C, de Bruijn Rfag, Passmore P, Montine TJ, Bettens K, Rotter JI, Brice A, Morgan K, Foroud TM, Kukull WA, Hannequin D, Powell JF, Nalls MA, Ritchie K, Lunetta KL, Kauwe JSK, Boerwinkle E, Riemenschneider M, Boada M, Hiltunen M, Martin ER, Schmidt R, Rujescu D, Wang LS, Dartigues JF, Mayeux R, Tzourio C, Hofman A, Nothen MM, Graff C, Psaty BM, Jones L, Haines JL, Holmans PA, Lathrop M, Pericak-Vance MA, Launer LJ, Farrer LA, van Duijn CM, Van Broeckhoven C, Moskvina V, Seshadri S, Williams J, Schellenberg GD, Amouyel P
Genome-wide association study in breast cancer survivors reveals SNPs associated with gene expression of genes belonging to MHC class I and II
Landmark-Hoyvik H, Dumeaux V, Nebdal D, Lund E, Tost J, Kamatani Y, Renault V, Borresen-Dale AL, Kristensen V, Edvardsen H
Differential selection pressures exerted by host resistance quantitative trait loci on a pathogen population: a case study in an apple Venturia inaequalis pathosystem
Le Van A, Caffier V, Lasserre-Zuber P, Chauveau A, Brunel D, Le Cam B, Durel CE
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, Andreassen OA, Anjorin A, Anney R, Anttila V, Arking DE, Asherson P, Azevedo MH, Backlund L, Badner JA, Bailey AJ, Banaschewski T, Barchas JD, Barnes MR, Barrett TB, Bass N, Battaglia A, Bauer M, Bayes M, Bellivier F, Bergen SE, Berrettini W, Betancur C, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DHR, Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Bruggeman R, Cormican P, Buccola NG, Buitelaar JK, Bunney WE, Buxbaum JD, Byerley WF, Byrne EM, Caesar S, Cahn W, Cantor RM, Casas M, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook EH, Coon H, Cormand B, Corvin A, Coryell WH, Craig DW, Craig IW, Crosbie J, Cuccaro ML, Curtis D, Czamara D, Datta S, Dawson G, Day R, De Geus EJ, Degenhardt F, Djurovic S, Donohoe GJ, Doyle AE, Duan JB, Dudbridge F, Duketis E, Ebstein RP, Edenberg HJ, Elia J, Ennis S, Etain B, Fanous A, Farmer AE, Ferrier IN, Flickinger M, Fombonne E, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer NB, Freitag CM, Friedl M, Frisen L, Gallagher L, Gejman PV, Georgieva L, Gershon ES, Geschwind DH, Giegling I, Gill M, Gordon SD, Gordon-Smith K, Green EK, Greenwood TA, Grice DE, Gross M, Grozeva D, Guan WH, Gurling H, De Haan L, Haines JL, Hakonarson H, Hallmayer J, Hamilton SP, Hamshere ML, Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S, Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hoogendijk WJ, Hottenga JJ, Hultman CM, Hus V, Ingason A, Ising M, Jamain S, Jones EG, Jones I, Jones L, Tzeng JY, Kahler AK, Kahn RS, Kandaswamy R, Keller MC, Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Klauck SM, Klei L, Knowles JA, Kohli MA, Koller DL, Konte B, Korszun A, Krabbendam L, Krasucki R, Kuntsi J, Kwan P, Landen M, Langstrom N, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Ledbetter DH, Lee PH, Lencz T, Lesch KP, Levinson DF, Lewis CM, Li J, Lichtenstein P, Lieberman JA, Lin DY, Linszen DH, Liu CY, Lohoff FW, Loo SK, Lord C, Lowe JK, Lucae S, MacIntyre DJ, Madden PAF, Maestrini E, Magnusson PKE, Mahon PB, Maier W, Malhotra AK, Mane SM, Martin CL, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll SA, McGhee KA, McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McMahon WM, McQuillin A, Medeiros H, Medland SE, Meier S, Melle I, Meng F, Meyer J, Middeldorp CM, Middleton L, Milanova V, Miranda A, Monaco AP, Montgomery GW, Moran JL, Moreno-De-Luca D, Morken G, Morris DW, Morrow EM, Moskvina V, Muglia P, Muhleisen TW, Muir WJ, Muller-Myhsok B, Murtha M, Myers RM, Myin-Germeys I, Neale MC, Nelson SF, Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nothen MM, Nurnberger JI, Nwulia EA, Nyholt DR, O'Dushlaine C, Oades RD, Olincy A, Oliveira G, Olsen L, Ophoff RA, Osby U, Owen MJ, Palotie A, Parr JR, Paterson AD, Pato CN, Pato MT, Penninx BW, Pergadia ML, Pericak-Vance MA, Pickard BS, Pimm J, Piven J, Posthuma D, Potash JB, Poustka F, Propping P, Puri V, Quested DJ, Quinn EM, Ramos-Quiroga JA, Rasmussen HB, Raychaudhuri S, Rehnstrom K, Reif A, Ribases M, Rice JP, Rietschel M, Roeder K, Roeyers H, Rossin L, Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Sanders SJ, Santangelo SL, Sergeant JA, Schachar R, Schalling M, Schatzberg AF, Scheftner WA, Schellenberg GD, Scherer SW, Schork NJ, Schulze TG, Schumacher J, Schwarz M, Scolnick E, Scott LJ, Shi JX, Shilling PD, Shyn SI, Silverman JM, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke EJS, St Clair D, State M, Steffens M, Steinhausen HC, Strauss JS, Strohmaier J, Stroup TS, Sutcliffe JS, Szatmari P, Szelinger S, Thirumalai S, Thompson RC, Todorov AA, Tozzi F, Treutlein J, Uhr M, van den Oord EJCG, Van Grootheest G, Van Os J, Vicente AM, Vieland VJ, Vincent JB, Visscher PM, Walsh CA, Wassink TH, Watson SJ, Weissman MM, Werge T, Wienker TF, Wijsman EM, Willemsen G, Williams N, Willsey AJ, Witt SH, Xu W, Young AH, Yu TW, Zammit S, Zandi PP, Zhang P, Zitman FG, Zollner S, Devlin B, Kelsoe JR, Sklar P, Daly MJ, O'Donovan MC, Craddock N, Sullivan PF, Smoller JW, Kendler KS, Wray NR
A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines
Liang LM, Morar N, Dixon AL, Lathrop GM, Abecasis GR, Moffatt MF, Cookson WOC
Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7697 Cases and 13 125 Controls
Mamasoula C, Prentice RR, Pierscionek T, Pangilinan F, Mills JL, Druschel C, Pass K, Russell MW, Hall D, Topf A, Brown DL, Zelenika D, Bentham J, Cosgrove C, Bhattacharya S, Riveron JG, Setchfield K, Brook JD, Bu'Lock FA, Thornborough C, Rahman TJ, Doza JP, Tan HL, O'Sullivan J, Stuart AG, Blue G, Winlaw D, Postma AV, Mulder BJM, Zwinderman AH, van Engelen K, Moorman AFM, Rauch A, Gewillig M, Breckpot J, Devriendt K, Lathrop GM, Farrall M, Goodship JA, Cordell HJ, Brody LC, Keavney BD
Intrauterine undernutrition alters patterns of DNA methylation in the next generation offspring through the male line
Martinez D, Pentinat T, Davidaud C, Ribo S, Cebria J, Diaz R, Tost J, Jimenez-Chillaron JC
Diabetologia 56 (), S114-S114, 2013
High-Specificity Single-Tube Multiplex Genotyping Using Ribo-PAP PCR, Tag Primers, Alkali Cleavage of RNA/DNA Chimeras and MALDI-TOF MS
Mauger F, Gelfand DH, Gupta A, Bodepudi V, Will SG, Bauer K, Myers TW, Gut IG
Single KTP nanocrystals as second-harmonic generation biolabels in cortical neurons
Mayer L, Slablab A, Dantelle G, Jacques V, Lepagnol-Bestel AM, Perruchas S, Spinicelli P, Thomas A, Chauvat D, Simonneau M, Gacoin T, Roch JF
DNA sequencing - spanning the generations
McGinn S, Gut IG
FTO, obesity and the adolescent brain
Melka MG, Gillis J, Bernard M, Abrahamowicz M, Chakravarty MM, Leonard GT, Perron M, Richer L, Veillette S, Banaschewski T, Barker GJ, Buchel C, Conrod P, Flor H, Heinz A, Garavan H, Bruhl R, Mann K, Artiges E, Lourdusamy A, Lathrop M, Loth E, Schwartz Y, Frouin V, Rietschel M, Smolka MN, Strohle A, Gallinat J, Struve M, Lattka E, Waldenberger M, Schumann G, Pavlidis P, Gaudet D, Paus T, Pausova Z
Farm exposure and time trends in early childhood may influence DNA methylation in genes related to asthma and allergy
Michel S, Busato F, Genuneit J, Pekkanen J, Dalphin JC, Riedler J, Mazaleyrat N, Weber J, Karvonen AM, Hirvonen MR, Braun-Fahrlander C, Lauener R, von Mutius E, Kabesch M, Tost J
DNA methylation associated with polycomb repression in retinoic acid receptor beta silencing
Moison C, Senamaud-Beaufort C, Fourriere L, Champion C, Ceccaldi A, Lacomme S, Daunay A, Tost J, Arimondo PB, Guieysse-Peugeot AL
A Phenotypic Structure and Neural Correlates of Compulsive Behaviors in Adolescents
Montigny C, Castellanos-Ryan N, Whelan R, Banaschewski T, Barker GJ, Buchel C, Gallinat J, Flor H, Mann K, Paillere-Martinot ML, Nees F, Lathrop M, Loth E, Paus T, Pausova Z, Rietschel M, Schumann G, Smolka MN, Struve M, Robbins TW, Garavan H, Conrod PJ
Isolation, characterization and cross-species amplification of polymorphic microsatellite markers for Oxytenanthera abyssinica (A. Rich.) Munro (Poaceae)
Ndiaye A, Rivallan R, Legavre T, Brunel D, Sagna M, Gassama YK, Risterucci AM
Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions
Nelissen ECM, Dumoulin JCM, Daunay A, Evers JLH, Tost J, van Montfoort APA
Germline and somatic genetic variations of TNFAIP3 in lymphoma complicating primary Sjogren's syndrome
Nocturne G, Boudaoud S, Miceli-Richard C, Viengchareun S, Lazure T, Nititham J, Taylor KE, Ma A, Busato F, Melki J, Lessard CJ, Sivils KL, Dubost JJ, Hachulla E, Gottenberg JE, Lombes M, Tost J, Criswell LA, Mariette X
GERMINAL AND SOMATIC GENETIC VARIANTS OF TNFAIP3 PROMOTE LYMPHOMAGENESIS PROCESS COMPLICATING PRIMARY SJOGREN'S SYNDROME
Nocturne G, Boudaoud S, Richard CM, Viengchareun S, Lazure T, Nititham J, Taylor KE, Criswell LA, Ma A, Busato F, Melki J, Dubost JJ, Hachulla E, Gottenberg JE, Lombes M, Tost J, Mariette X
Ann. Rheum. Dis. 72 (), 55-56, 2013
Differences in Transcription Patterns between Induced Pluripotent Stem Cells Produced from the Same Germ Layer Are Erased upon Differentiation
Pirozhkova I, Barat A, Dmitriev P, Kim E, Robert T, Guegan J, Bilhou-Nabera C, Busato F, Tost J, Carnac G, Laoudj-Chenivesse D, Lipinski M, Vassetzky Y
Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice
Prieur X, Dollet L, Takahashi M, Nemani M, Pillot B, Le May C, Mounier C, Takigawa-Imamura H, Zelenika D, Matsuda F, Feve B, Capeau J, Lathrop M, Costet P, Cariou B, Magre J
ERBB2 in Cat Mammary Neoplasias Disclosed a Positive Correlation between RNA and Protein Low Expression Levels: A Model for erbB-2 Negative Human Breast Cancer
Santos S, Baptista CS, Abreu RMV, Bastos E, Amorim I, Gut IG, Gartner F, Chaves R
TFAP2B-Dietary Protein and Glycemic Index Interactions and Weight Maintenance after Weight Loss in the DiOGenes Trial
Stocks T, Angquist L, Hager J, Charon C, Hoist C, Martinez JA, Saris WHM, Astrup A, Sorensen TIA, Larsen LH
A Genome-Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium
Tang WH, Teichert M, Chasman DI, Heit JA, Morange PE, Li G, Pankratz N, Leebeek FW, Pare G, de Andrade M, Tzourio C, Psaty BM, Basu S, Ruiter R, Rose L, Armasu SM, Lumley T, Heckbert SR, Uitterlinden AG, Lathrop M, Rice KM, Cushman M, Hofman A, Lambert JC, Glazer NL, Pankow JS, Witteman JC, Amouyel P, Bis JC, Bovill EG, Kong XX, Tracy RP, Boerwinkle E, Rotter JI, Tregouet DA, Loth DW, Stricker BHC, Ridker PM, Folsom AR, Smith NL
Quantitative Variation in Plasma Angiotensin-I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus
Terao C, Bayoumi N, McKenzie CA, Zelenika D, Muro S, Mishima M, Connell JMC, Vickers MA, Lathrop GM, Farrall M, Matsuda F, Keavney BD
DNA methylation alterations: Promising biomarkers for diagnosis and treatment response in cancer
Tost J
Eur. J. Cancer 49 (), S14-S14, 2013
HIGH-THROUGHPUT DNA METHYLATION ANALYSIS OF CELL SORTED BLOOD CELL POPULATIONS REVEALS WIDESPREAD EPIGENETIC DEREGULATION IN SJOGREN'S SYNDROME
Tost J, Touleimat N, Boudaoud S, Miceli C, Mariette X
Ann. Rheum. Dis. 72 (), 68-68, 2013
Genome-Wide Association Study of Genetic Factors Related to Confectionery Intake: Potential Roles of the ADIPOQ Gene
Wakai K, Matsuo K, Matsuda F, Yamada R, Takahashi M, Kawaguchi T, Yatabe Y, Ito H, Hosono S, Tajima K, Naito M, Morita E, Yin G, Sakamoto T, Takashima N, Suzuki S, Nakahata N, Mikami H, Ohnaka K, Watanabe Y, Arisawa K, Kubo M, Hamajima N, Tanaka H
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis
Weidinger S, Willis-Owen SAG, Kamatani Y, Baurecht H, Morar N, Liang LM, Edser P, Street T, Rodriguez E, O'Regan GM, Beattie P, Folster-Holst R, Franke A, Novak N, Fahy CM, Winge MCG, Kabesch M, Illig T, Heath S, Soderhall C, Melen E, Pershagen G, Kere J, Bradley M, Lieden A, Nordenskjold M, Harper JI, McLean WHI, Brown SJ, Cookson WOC, Lathrop GM, Irvine AD, Moffatt MF
Phenotypic diversity and association mapping for fruit quality traits in cultivated tomato and related species
Xu JX, Ranc N, Munos S, Rolland S, Bouchet JP, Desplat N, Le Paslier MC, Liang Y, Brunel D, Causse M
Discovery and mapping of a new expressed sequence tag-single nucleotide polymorphism and simple sequence repeat panel for large-scale genetic studies and breeding of Theobroma cacao L
Allegre M, Argout X, Boccara M, Fouet O, Roguet Y, Berard A, Thevenin J M, Chauveau A, Rivallan R, Clement D, Courtois B, Gramacho K, Boland-Auge A, Tahi M, Umaharan P, Brunel D, Lanaud C
Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models
Andrews TD, Whittle B, Field MA, Balakishnan B, Zhang Y, Shao Y, Cho V, Kirk M, Singh M, Xia Y, Hager J, Winslade S, Sjollema G, Beutler B, Enders A, Goodnow CC
Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration
Angelakopoulou A, Shah T, Sofat R, Shah S, Berry D J, Cooper J, Palmen J, Tzoulaki I, Wong A, Jefferis B J, Maniatis N, Drenos F, Gigante B, Hardy R, Laxton R C, Leander K, Motterle A, Simpson I A, Smeeth L, Thomson A, Verzilli C, Kuh D, Ireland H, Deanfield J, Caulfield M, Wallace C, Samani N, Munroe P B, Lathrop M, Fowkes F G R, Marmot M, Whincup P H, Whittaker J C, de Faire U, Kivimaki M, Kumari M, Hypponen E, Power C, Humphries S E, Talmud P J, Price J, Morris R W, Ye S, Casas J P, Hingorani A D
Epigenetics
Arimondo PB, Egger G, Tost J
ANALYSIS OF SMARCA2 AND GENES ENCODING INTERACTORS OF SWI/SNF SMARCA2/BRM PROTEIN IN SCHIZOPHRENIA PATIENTS FROM AN ALGERIAN TRIO COHORT
Benmessaoud D, Bestel AML, Delepine M, Hager J, Moalic JM, Gorwood P, Kacha F, Simonneau M
Eur. Psychiat. 27 (), -, 2012
Impact of Common Variation in Bone-Related Genes on Type 2 Diabetes and Related Traits
Billings LK, Hsu YH, Ackerman RJ, Dupuis J, Voight BF, Rasmussen-Torvik LJ, Hercberg S, Lathrop M, Barnes D, Langenberg C, Hui JN, Fu M, Bouatia-Naji N, Lecoeur C, An P, Magnusson PK, Surakka I, Ripatti S, Christiansen L, Dalgard C, Folkersen L, Grundberg E, Eriksson P, Kaprio J, Kyvik KO, Pedersen NL, Borecki IB, Province MA, Balkau B, Froguel P, Shuldiner AR, Palmer LJ, Wareham N, Meneton P, Johnson T, Pankow JS, Karasik D, Meigs JB, Kiel DP, Florez JC
Maternal smoking during pregnancy, genetic polymorphisms of metabolic enzymes, and childhood acute leukemia: the ESCALE Study (SFCE)
Bonaventure A, Goujon-Bellec S, Rudant J, Orsi L, Leverger G, Baruchel A, Bertrand Y, Nelken B, Pasquet M, Michel G, Sirvent N, Bordigoni P, Ducassou S, Rialland X, Zelenika D, Hemon D, Clavel J
An N-Ethyl-N-Nitrosourea (ENU)-Induced Dominant Negative Mutation in the JAK3 Kinase Protects against Cerebral Malaria
Bongfen S E, Rodrigue-Gervais I G, Berghout J, Torre S, Cingolani P, Wiltshire S A, Leiva-Torres G A, Letourneau L, Sladek R, Blanchette M, Lathrop M, Behr M A, Gruenheid S, Vidal S M, Saleh M, Gros P
Specific TGM1 Mutation Profiles in Bathing Suit and Self-Improving Collodion Ichthyoses Phenotypic and Genotypic Data From 9 Patients With Dynamic Phenotypes of Autosomal Recessive Congenital Ichthyosis
Bourrat E, Blanchet-Bardon C, Derbois C, Cure S, Fischer J
Associations between Nitric Oxide Synthase Genes and Exhaled NO-Related Phenotypes according to Asthma Status
Bouzigon E, Monier F, Boussaha M, Le Moual N, Huyvaert H, Matran R, Letort S, Bousquet J, Pin I, Lathrop M, Kauffmann F, Demenais F, Nadif R
Sources of Pre-Analytical Variations in Yield of DNA Extracted from Blood Samples: Analysis of 50,000 DNA Samples in EPIC
Caboux E, Lallemand C, Ferro G, Hemon B, Mendy M, Biessy C, Sims M, Wareham N, Britten A, Boland A, Hutchinson A, Siddiq A, Vineis P, Riboli E, Romieu I, Rinaldi S, Gunter MJ, Peeters PHM, van der Schouw YT, Travis R, Bueno-de-Mesquita HB, Canzian F, Sanchez MJ, Skeie G, Olsen KS, Lund E, Bilbao R, Sala N, Barricarte A, Palli D, Navarro C, Panico S, Redondo ML, Polidoro S, Dossus L, Boutron-Ruault MC, Clavel-Chapelon F, Trichopoulou A, Trichopoulos D, Lagiou P, Boeing H, Fisher E, Tumino R, Agnoli C, Hainaut P
Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure
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 R A, Fellous M
Genomic binding of Pol III transcription machinery and relationship with TFIIS transcription factor distribution in mouse embryonic stem cells
Carriere L, Graziani S, Alibert O, Ghavi-Helm Y, Boussouar F, Humbertclaude H, Jounier S, Aude J C, Keime C, Murvai J, Foglio M, Gut M, Gut I, Lathrop M, Soutourina J, Gerard M, Werner M
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXBFKBPLNOTCH4 region of chromosome 6p21.3
Cipriani V, Leung HT, Plagnol V, Bunce C, Khan JC, Shahid H, Moore AT, Harding SP, Bishop PN, Hayward C, Campbell S, Armbrecht AM, Dhillon B, Deary IJ, Campbell H, Dunlop M, Dominiczak AF, Mann SS, Jenkins SA, Webster AR, Bird AC, Lathrop M, Zelenika D, Souied EH, Sahel JA, Leveillard T, Cree AJ, Gibson J, Ennis S, Lotery AJ, Wright AF, Clayton DG, Yates JRW
Homocysteine and Coronary Heart Disease: Meta-analysis of MTHFR Case-Control Studies, Avoiding Publication Bias
Clarke R, Bennett D A, Parish S, Verhoef P, Dotsch-Klerk M, Lathrop M, Xu P, Nordestgaard B G, Holm H, Hopewell J C, Saleheen D, Tanaka T, Anand S S, Chambers J C, Kleber M E, Ouwehand W H, Yamada Y, Elbers C, Peters B, Stewart A F R, Reilly M M, Thorand B, Yusuf S, Engert J C, Assimes T L, Kooner J, Danesh J, Watkins H, Samani N J, Collins R, Peto R, Mthfr Studies Collaborative Grp
Confirmation of novel type 1 diabetes risk loci in families
Cooper J D, Howson J M M, Smyth D, Walker N M, Stevens H, Yang J H M, She J X, Eisenbarth G S, Rewers M, Todd J A, Akolkar B, Concannon P, Erlich H A, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Rich S S, Type 1 Diabet Genetics Consortium
A TRANSCRIPTOMIC ANALYSIS OF TYPE II AUTOSOMAL DOMINANT OSTEOPETROSIS OSTEOCLASTS: IDENTIFICATION OF NEW DISEASE MARKERS
Coudert AE, Olaso R, Collet C, de Vernejoul MC
Osteoporosis Int. 23 (), S401-S401, 2012
Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals
Dastani Z, Hivert MF, Timpson N, Perry JRB, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikainen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, Beekman M, Coassin S, Lohman K, Qi L, Kanoni S, Pankow JS, Uh HW, Wu Y, Bidulescu A, Rasmussen-Torvik LJ, Greenwood CMT, Ladouceur M, Grimsby J, Manning AK, Liu CT, Kooner J, Mooser VE, Vollenweider P, Kapur KA, Chambers J, Wareham NJ, Langenberg C, Frants R, Willems-vanDijk K, Oostra BA, Willems SM, Lamina C, Winkler TW, Psaty BM, Tracy RP, Brody J, Chen I, Viikari J, Kahonen M, Pramstaller PP, Evans DM, St Pourcain B, Sattar N, Wood AR, Bandinelli S, Carlson OD, Egan JM, Bohringer S, van Heemst D, Kedenko L, Kristiansson K, Nuotio ML, Loo BM, Harris T, Garcia M, Kanaya A, Haun M, Klopp N, Wichmann HE, Deloukas P, Katsareli E, Couper DJ, Duncan BB, Kloppenburg M, Adair LS, Borja JB, Wilson JG, Musani S, Guo XQ, Johnson T, Semple R, Teslovich TM, Allison MA, Redline S, Buxbaum SG, Mohlke KL, Meulenbelt I, Ballantyne CM, Dedoussis GV, Hu FB, Liu YM, Paulweber B, Spector TD, Slagboom PE, Ferrucci L, Jula A, Perola M, Raitakari O, Florez JC, Salomaa V, Eriksson JG, Frayling TM, Hicks AA, Lehtimaki T, Smith GD, Siscovick DS, Kronenberg F, van Duijn C, Loos RJF, Waterworth DM, Meigs JB, Dupuis J, Richards JB
Evidence for genetic heterogeneity of ADRB2 gene according to age at onset in bipolar disorder: a combined positional cloning and candidate gene approach
Dizier MH, Etain B, Lajnef M, Lathrop M, Grozeva D, Craddock N, Henry C, Gard S, Jamain S, Lajnef M, Leboyer M, Bellivier F, Mathieu F
Ann. Hum. Genet. 76 (), 425-425, 2012
Genetic Heterogeneity According to Age at Onset in Bipolar Disorder: A Combined Positional Cloning and Candidate Gene Approach
Dizier MH, Etain B, Lajnef M, Lathrop M, Grozeva D, Craddock N, Henry C, Gard S, Jamain S, Leboyer M, Bellivier F, Mathieu F
The ANO3/MUC15 locus is associated with eczema in families ascertained through asthma
Dizier MH, Margaritte-Jeannin P, Madore AM, Esparza-Gordillo J, Moffatt M, Corda E, Monier F, Guilloud-Bataille M, Franke A, Weidinger S, Annesi-Maesano I, Just J, Pin I, Kauffmann F, Cookson W, Lee YA, Laprise C, Lathrop M, Bouzigon E, Demenais F
The Ano3/Muc15 Locus Is Associated With Eczema In Family Samples Ascertained Through Asthmatics
Dizier Mhmh, Jeannin P P, Madore Amam, Esparza J J, Moffatt M M, Corda E E, Monier F F, Annesi-Maesano II, Just J J, Pin II, Kauffmann F F, Cookson W W, Lee Yaya, Laprise C C, Lathrop M M, Bouzigon E E, Demenais F F
Genetic Epidemiology 36 (2), 161-161, 2012
Serial translocation by means of circular intermediates underlies colour sidedness in cattle
Durkin K, Coppieters W, Drogemuller C, Ahariz N, Cambisano N, Druet T, Fasquelle C, Haile A, Horin P, Huang L S, Kamatani Y, Karim L, Lathrop M, Moser S, Oldenbroek K, Rieder S, Sartelet A, Solkner J, Stalhammar H, Zelenika D, Zhang Z Y, Leeb T, Georges M, Charlier C
Genome-wide Association Study in Breast Cancer Survivors Reveals SNPs Associated with Gene Expression of Genes Belonging to MHC Class I and II (meeting)
Edvardsen H, Landmark-Hoyvik H, Dumeaux V, Nebdal D, Lund E, Tost J, Kamatani Y, Renault V, Borresen-Dale A L, Kristensen V N
European Journal of Cancer 48 (), S160-S160, 2012
Natural history of platelet antibody formation against alpha IIb beta 3 in a French cohort of Glanzmann thrombasthenia patients
Fiore M, Firah N, Pillois X, Nurden P, Heilig R, Nurden A T
DNA Methylation Profiling Identifies Luminal a Breast Tumors With Poor Survival
Fleischer T, Jovanovic J, Edvardsen H, Alnaes GIG, Naume B, Tost J, Borresen-Dale AL, Kristensen VN
Eur. J. Cancer 48 (), S140-S140, 2012
Association of the CpG Methylation Pattern of the Proximal Insulin Gene Promoter with Type 1 Diabetes
Fradin D, Le Fur S, Mille C, Naoui N, Groves C, Zelenika D, McCarthy MI, Lathrop M, Bougneres P
Establishment and Characterization of a Highly Tumourigenic and Cancer Stem Cell Enriched Pancreatic Cancer Cell Line as a Well Defined Model System
Fredebohm J, Boettcher M, Eisen C, Gaida MM, Heller A, Keleg S, Tost J, Greulich-Bode KM, Hotz-Wagenblatt A, Lathrop M, Giese NA, Hoheisel JD
Comparison of SNPs and microsatellites for assessing the genetic structure of chicken populations
Garke C, Ytournel F, Bed'Hom B, Gut I, Lathrop M, Weigend S, Simianer H
Caution in Interpreting Results from Imputation Analysis When Linkage Disequilibrium Extends over a Large Distance: A Case Study on Venous Thrombosi
Germain M, Saut N, Oudot-Mellakh T, Letenneur L, Dupuy AM, Bertrand M, Alessi MC, Lambert JC, Zelenika D, Emmerich J, Tiret L, Cambien F, Lathrop M, Amouyel P, Morange PE, Tregouet DA
Methylation profile of the promoter region of IRF5 in primary Sjogren's syndrome
Gestermann N, Koutero M, Belkhir R, Tost J, Mariette X, Miceli-Richard C
Association study of IL21R gene polymorphisms and type 1 diabetes populations
Ghandii P, Ghadiri A, Julier C
J. Med. Genet. 49 (), S83-S83, 2012
Genetic and environmental influences on total plasma homocysteine and its role in coronary artery disease risk
Ghassibe-Sabbagh M, Platt D E, Youhanna S, Abchee A B, Stewart K, Badro D A, Haber M, Salloum A K, Douaihy B, El Bayeh H, Othman R, Shasha N, Kibbani S, Chammas E, Milane A, Nemr R, Kamatani Y, Hager J, Cazier J B, Gauguier D, Zalloua P A, Fgentcard Consortium
Genome-wide association analysis identifies three new breast cancer susceptibility loci
Ghoussaini M, Fletcher O, Michailidou K, Turnbull C, Schmidt M K, Dicks E, Dennis J, Wang Q, Humphreys M K, Luccarini C, Baynes C, Conroy D, Maranian M, Ahmed S, Driver K, Johnson N, Orr N, Silva I D, Waisfisz Q, Meijers-Heijboer H, Uitterlinden A G, Rivadeneira F, Hall P, Czene K, Irwanto A, Liu J J, Nevanlinna H, Aittomaki K, Blomqvist C, Meindl A, Schmutzler R K, Muller-Myhsok B, Lichtner P, Chang-Claude J, Hein R, Nickels S, Flesch-Janys D, Tsimiklis H, Makalic E, Schmidt D, Bui M, Hopper J L, Apicella C, Park D J, Southey M, Hunter D J, Chanock S J, Broeks A, Verhoef S, Hogervorst F B L, Fasching P A, Lux M P, Beckmann M W, Ekici A B, Sawyer E, Tomlinson I, Kerin M, Marme F, Schneeweiss A, Sohn C, Burwinkel B, Guenal P, Truong T, Cordina-Duverger E, Menegaux F, Bojesen S E, Nordestgaard B G, Nielsen S F, Flyger H, Milne R L, Alonso M R, Gonzalez-Neira A, Benitez J, Anton-Culver H, Ziogas A, Bernstein L, Dur C C, Brenner H, Muller H, Arndt V, Stegmaier C, Justenhoven C, Brauch H, Bruning T, Wang-Gohrke S, Eilber U, Dork T, Schurmann P, Bremer M, Hillemanns P, Bogdanova N V, Antonenkova N N, Rogov Y I, Karstens J H, Bermisheva M, Prokofieva D, Khusnutdinova E, Lindblom A, Margolin S, Mannermaa A, Kataja V, Kosma V M, Hartikainen J M, Lambrechts D, Yesilyurt B T, Floris G, Leunen K, Manoukian S, Bonanni B, Fortuzzi S, Peterlongo P, Couch F J, Wang X S, Stevens K, Lee A, Giles G G, Baglietto L, Severi G, McLean C, Alnaes G G, Kristensen V, Borrensen-Dale A L, John E M, Miron A, Winqvist R, Pylkas K, Jukkola-Vuorinen A, Kauppila S, Andrulis I L, Glendon G, Mulligan A M, Devilee P, van Asperen C J, Tollenaar Raem, Seynaeve C, Figueroa J D, Garcia-Closas M, Brinton L, Lissowska J, Hooning M J, Hollestelle A, Oldenburg R A, van den Ouweland A M W, Cox A, Reed M W R, Shah M, Jakubowska A, Lubinski J, Jaworska K, Durda K, Jones M, Schoemaker M, Ashworth A, Swerdlow A, Beesley J, Chen X Q, Muir K R, Lophatananon A, Rattanamongkongul S, Chaiwerawattana A, Kang D, Yoo K Y, Noh D Y, Shen C Y, Yu J C, Wu P E, Hsiung C N, Perkins A, Swann R, Velentzis L, Eccles D M, Tapper W J, Gerty S M, Graham N J, Ponder B A J, Chenevix-Trench G, Pharoah P D P, Lathrop M, Dunning A M, Rahman N, Peto J, Easton D F, Netherlands Collaborative Grp Here, Fbcs, Gene Environm Interaction Breast C, kConFab Investigators, Australian Ovarian Canc Study Grp
PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans
Grall A, Guaguere E, Planchais S, Grond S, Bourrat E, Hausser I, Hitte C, Le Gallo M, Derbois C, Kim G J, Lagoutte L, Degorce-Rubiales F, Radner F P W, Thomas A, Kury S, Bensignor E, Fontaine J, Pin D, Zimmermann R, Zechner R, Lathrop M, Galibert F, Andre C, Fischer J
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis
Hager J, Kamatani Y, Cazier JB, Youhanna S, Ghassibe-Sabbagh M, Platt DE, Abchee AB, Romanos J, Khazen G, Othman R, Badro DA, Haber M, Salloum AK, Douaihy B, Shasha N, Kabbani S, Sbeite H, Chammas E, El Bayeh H, RousseaU F, Zelenika D, Gut I, Lathrop M, Farrall M, Gauguier D, Zalloua PA
PNPLA1 mutations cause recessive lamellar ichthyosis in humans and dogs: morphological correlations
Hausser I, Grall A, Guaguere E, Planchais S, Grond S, Bourrat E, Hitte C, Le Gallo M, Derbois C, Kim GJ, Lagoutte L, Degorce-Rubiales F, Radner FPW, Thomas A, Kury C, Bensignor E, Fontaine J, Pin D, Zimmermann R, Zechner R, Lathrop M, Galibert F, Andre C, Fischer J
Exp. Dermatol. 21 (9), E3-E3, 2012
Dietary Factors Impact on the Association between CTSS Variants and Obesity Related Traits
Hooton H, Angquist L, Holst C, Hager J, RousseaU F, Hansen RD, Tjonneland A, Roswall N, van der A DL, Overvad K, Jakobsen MU, Boeing H, Meidtner K, Palli D, Masala G, Bouatia-Naji N, Saris WHM, Feskens EJM, Wareham NJ, Vimaleswaran KS, Langin D, Loos RJF, Sorensen TIA, Clement K
Environmental and genetic risk factors for myopathy in Chinese participants from HPS2-THRIVE
Hopewell JC, Offer A, Parish S, Haynes R, Li J, Jiang L, Lathrop M, Armitage J, Collins R
Eur. Heart J. 33 (), 445-445, 2012
DNA methylation based biomarkers: Practical considerations and applications
How Kit A, Nielsen HM, Tost J
MeQA: a pipeline for MeDIP-seq data quality assessment and analysis
Huang J, Renault V, Sengenes J, Touleimat N, Michel S, Lathrop M, Tost J
Genome-wide association study of lung function decline in adults with and without asthma
Imboden M, Bouzigon E, Curjuric I, Ramasamy A, Kumar A, Hancock D B, Wilk J B, Vonk J M, Thun G A, Siroux V, Nadif R, Monier F, Gonzalez J R, Wjst M, Heinrich J, Loehr L R, Franceschini N, North K E, Altmuller J, Koppelman G H, Guerra S, Kronenberg F, Lathrop M, Moffatt M F, O'Connor G T, Strachan D P, Postma D S, London S J, Schindler C, Kogevinas M, Kauffmann F, Jarvis D L, Demenais F, Probst-Hensch N M
A polymorphism in the SOST promoter is associated with SOST expression in human bone and with fracture in osteogenesis imperfecta
Jehan F, Domingues A, Delepine M, Boland A, Zelznika D, Hannouche D, de Vernejoul MC
Using Prior Information from the Medical Literature in GWAS of Oral Cancer Identifies Novel Susceptibility Variant on Chromosome 4-the AdAPT Method
Johansson M, Roberts A, Chen D, Li YY, Delahaye-Sourdeix M, Aswani N, Greenwood MA, Benhamou S, Lagiou P, Holcatova I, Richiardi L, Kjaerheim K, Agudo A, Castellsague X, Macfarlane TV, Barzan L, Canova C, Thakker NS, Conway DI, Znaor A, Healy CM, Ahrens W, Zaridze D, Szeszenia-Dabrowska N, Lissowska J, Fabianova E, Mates IN, Bencko V, Foretova L, Janout V, Curado MP, Koifman S, Menezes A, Wunsch V, Eluf-Neto J, Boffetta P, Franceschi S, Herrero R, Garrote LF, Talamini R, Boccia S, Galan P, Vatten L, Thomson P, Zelenika D, Lathrop M, Byrnes G, Cunningham H, Brennan P, Wakefield J, McKay JD
Lung cancer and DNA repair genes: multilevel association analysis from the International Lung Cancer Consortium
Kazma R, Babron M C, Gaborieau V, Genin E, Brennan P, Hung R J, McLaughlin J R, Krokan H E, Elvestad M B, Skorpen F, Anderssen E, Vooder T, Valk K, Metspalu A, Field J K, Lathrop M, Sarasin A, Benhamou S, Ilcco Consortium
Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis
Kiryluk K, Li YF, Sanna-Cherchi S, Rohanizadegan M, Suzuki H, Eitner F, Snyder HJ, Choi M, Hou P, Scolari F, Izzi C, Gigante M, Gesualdo L, Savoldi S, Amoroso A, Cusi D, Zamboli P, Julian BA, Novak J, Wyatt RJ, Mucha K, Perola M, Kristiansson K, Viktorin A, Magnusson PK, Thorleifsson G, Thorsteinsdottir U, Stefansson K, Boland A, Metzger M, Thibaudin L, Wanner C, Jager KJ, Goto S, Maixnerova D, Karnib HH, Nagy J, Panzer U, Xie JY, Chen N, Tesar V, Narita I, Berthoux F, Floege J, Stengel B, Zhang H, Lifton RP, Gharavi AG
High-throughput Allele-specific Single Cell and Single Molecule DNA Methylation Assays for the Analysis of Multiple Candidate Loci
Kit AH, Krapf M, Maleszweska M, Goodhardt M, Tost J
Eur. J. Cancer 48 (), S146-S146, 2012
Analyses of single nucleotide polymorphisms in selected nutrient-sensitive genes in weight-regain prevention: the DIOGENES study
Larsen L H, Angquist L, Vimaleswaran K S, Hager J, Viguerie N, Loos R J F, Handjieva-Darlenska T, Jebb S A, Kunesova M, Larsen T M, Martinez J A, Papadaki A, Pfeiffer A F H, van Baak M A, Sorensen T I A, Holst C, Langin D, Astrup A, Saris W H M
CHARACTERIZATION OF MOLECULAR PARTNERS OF THE PKD SUSCEPTIBILITY GENE SAMCYSTIN (ANKS6)
Laure D, Estelle R, Zeineb B, Brigitte L, Marie-Therese B, Dominique G
Nephrol. Dial. Transplant. 27 (), 46-46, 2012
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
Leblond C S, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsater H, Nygren G, Gillberg I C, Melke J, Toro R, Regnault B, Fauchereau F, Mercati O, Lemiere N, Skuse D, Poot M, Holt R, Monaco A P, Jarvela I, Kantojarvi K, Vanhala R, Curran S, Collier D A, Bolton P, Chiocchetti A, Klauck S M, Poustka F, Freitag C M, Waltes R, Kopp M, Duketis E, Bacchelli E, Minopoli F, Ruta L, Battaglia A, Mazzone L, Maestrini E, Sequeira A F, Oliveira B, Vicente A, Oliveira G, Pinto D, Scherer S W, Zelenika D, Delepine M, Lathrop M, Bonneau D, Guinchat V, Devillard F, Assouline B, Mouren M C, Leboyer M, Gillberg C, Boeckers T M, Bourgeron T
Sex-Specific Regulation of Mitochondrial DNA Levels: Genome-Wide Linkage Analysis to Identify Quantitative Trait Loci
Lopez S, Buil A, Souto JC, Casademont J, Blangero J, Martinez-Perez A, Fontcuberta J, Lathrop M, Almasy L, Soria JM
Reduction of palmoplantar keratoderma Buschke-Fischer-Brauer locus to only 0.967 Mb
Mamai O, Boussofara L, Adala L, Amara A, Ben Charfeddine I, Ghariani N, Sriha B, Denguezli M, Mili A, Belazreg T, Saada A, Fischer J, Gribaa M
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
Manning A K, Hivert M F, Scott R A, Grimsby J L, Bouatia-Naji N, Chen H, Rybin D, Liu C T, Bielak L F, Prokopenko I, Amin N, Barnes D, Cadby G, Hottenga J J, Ingelsson E, Jackson A U, Johnson T, Kanoni S, Ladenvall C, Lagou V, Lahti J, Lecoeur C, Liu Y M, Martinez-Larrad M T, Montasser M E, Navarro P, Perry J R B, Rasmussen-Torvik L J, Salo P, Sattar N, Shungin D, Strawbridge R J, Tanaka T, van Duijn C M, An P, de Andrade M, Andrews J S, Aspelund T, Atalay M, Aulchenko Y, Balkau B, Bandinelli S, Beckmann J S, Beilby J P, Bellis C, Bergman R N, Blangero J, Boban M, Boehnke M, Boerwinkle E, Bonnycastle L L, Boomsma D I, Borecki I B, Boettcher Y, Bouchard C, Brunner E, Budimir D, Campbell H, Carlson O, Chines P S, Clarke R, Collins F S, Corbaton-Anchuelo A, Couper D, de Faire U, Dedoussis G V, Deloukas P, Dimitriou M, Egan J M, Eiriksdottir G, Erdos M R, Eriksson J G, Eury E, Ferrucci L, Ford I, Forouhi N G, Fox C S, Franzosi M G, Franks P W, Frayling T M, Froguel P, Galan P, de Geus E, Gigante B, Glazer N L, Goel A, Groop L, Gudnason V, Hallmans G, Hamsten A, Hansson O, Harris T B, Hayward C, Heath S, Hercberg S, Hicks A A, Hingorani A, Hofman A, Hui J, Hung J, Jarvelin M R, Jhun M A, Johnson P C D, Jukema J W, Jula A, Kao W H, Kaprio J, Kardia S L R, Keinanen-Kiukaanniemi S, Kivimaki M, Kolcic I, Kovacs P, Kumari M, Kuusisto J, Kyvik K O, Laakso M, Lakka T, Lannfelt L, Lathrop G M, Launer L J, Leander K, Li G, Lind L, Lindstrom J, Lobbens S, Loos R J F, Luan J A, Lyssenko V, Magi R, Magnusson P K E, Marmot M, Meneton P, Mohlke K L, Mooser V, Morken M A, Miljkovic I, Narisu N, O'Connell J, Ong K K, Oostra B A, Palmer L J, Palotie A, Pankow J S, Peden J F, Pedersen N L, Pehlic M, Peltonen L, Penninx B, Pericic M, Perola M, Perusse L, Peyser P A, Polasek O, Pramstaller P P, Province M A, Raikkonen K, Rauramaa R, Rehnberg E, Rice K, Rotter J I, Rudan I, Ruokonen A, Saaristo T, Sabater-Lleal M, Salomaa V, Savage D B, Saxena R, Schwarz P, Seedorf U, Sennblad B, Serrano-Rios M, Shuldiner A R, Sijbrands E J G, Siscovick D S, Smit J H, Small K S, Smith N L, Smith A V, Stancakova A, Stirrups K, Stumvoll M, Sun Y V, Swift A J, Toenjes A, Tuomilehto J, Trompet S, Uitterlinden A G, Uusitupa M, Vikstrom M, Vitart V, Vohl M C, Voight B F, Vollenweider P, Waeber G, Waterworth D M, Watkins H, Wheeler E, Widen E, Wild S H, Willems S M, Willemsen G, Wilson J F, Witteman J C M, Wright A F, Yaghootkar H, Zelenika D, Zemunik T, Zgaga L, Wareham N J, McCarthy M I, Barroso I, Watanabe R M, Florez J C, Dupuis J, Meigs J B, Langenberg C, Diagram Consortium, Muther Consortium
Genetics of affective intensity: A GWAS approach on bipolar disorder
Mathieu F, Etain B, Dizier MH, Lathrop M, Gard S, Leboyer M, Henry C, Bellivier F
Ann. Hum. Genet. 76 (), 428-428, 2012
A trans-ethnic genetic study of rheumatoid arthritis identified FCGR2A as a candidate common risk factor in Japanese and European populations
Meziani R, Yamada R, Takahashi M, Ohigashi K, Morinobu A, Terao C, Hiratani H, Ohmura K, Yamaguchi M, Nomura T, Vasilescu A, Kokubo M, Renault V, Hirosawa K, Ratanajaraya C, Heath S, Mimori T, Sakaguchi S, Lathrop M, Melchers I, Kumagai S, Matsuda F
IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance
Murphy R, Ibanez L, Hattersley A, Tost J
Determinants of Early Alcohol Use In Healthy Adolescents: The Differential Contribution of Neuroimaging and Psychological Factors
Nees F, Tzschoppe J, Patrick C J, Vollstadt-Klein S, Steiner S, Poustka L, Banaschewski T, Barker G J, Buchel C, Conrod P J, Garavan H, Heinz A, Gallinat J, Lathrop M, Mann K, Artiges E, Paus T, Poline J B, Robbins T W, Rietschel M, Smolka M N, Spanagel R, Struve M, Loth E, Schumann G, Flor H, Imagen Consortium
Epigenetic changes in inflammatory and autoimmune diseases
Nielsen HM, Tost J
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
Okada Y, Terao C, Ikari K, Kochi Y, Ohmura K, Suzuki A, Kawaguchi T, Stahl E A, Kurreeman F A S, Nishida N, Ohmiya H, Myouzen K, Takahashi M, Sawada T, Nishioka Y, Yukioka M, Matsubara T, Wakitani S, Teshima R, Tohma S, Takasugi K, Shimada K, Murasawa A, Honjo S, Matsuo K, Tanaka H, Tajima K, Suzuki T, Iwamoto T, Kawamura Y, Tanii H, Okazaki Y, Sasaki T, Gregersen P K, Padyukov L, Worthington J, Siminovitch K A, Lathrop M, Taniguchi A, Takahashi A, Tokunaga K, Kubo M, Nakamura Y, Kamatani N, Mimori T, Plenge R M, Yamanaka H, Momohara S, Yamada R, Matsuda F, Yamamoto K
A reference genetic map of C. clementina hort. ex Tan.. citrus evolution inferences from comparative mapping
Ollitrault P, Terol J, Chen CX, Federici CT, Lotfy S, Hippolyte I, Ollitrault F, Berard A, Chauveau A, Cuenca J, Costantino G, Kacar Y, Mu L, Garcia-Lor A, Froelicher Y, Aleza P, Boland A, Billot C, Navarro L, Luro F, Roose ML, Gmitter FG, Talon M, Brunel D
Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project
Oudot-Mellakh T, Cohen W, Germain M, Saut N, Kallel C, Zelenika D, Lathrop M, Tregouet D A, Morange P E
A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, Lu LY, Ziegler JT, Sale MM, Divers J, Shriner D, Adeyemo A, Rotimi CN, Ng MCY, Langefeld CD, Freedman BI, Bowden DW
GENOME-WIDE ASSOCIATION STUDY IDENTIFIES VARIANTS ASSOCIATED WITH LIVER FIBROSIS PROGRESSION IN HCV-INFECTED PATIENTS
Patin E, Kutalik Z, Guergnon J, Bibert S, Nalpas B, Jouanguy E, Munteanu M, Bousquet L, Argiro L, Halfon P, Boland A, Mullhaupt B, Semela D, Dufour J F, Heim M H, Moradpour D, Cerny A, Malinverni R, Hirsch H, Martinetti G, Suppiah V, Stewart G, Booth D R, George J, Casanova J L, Brechot C, Rice C M, Talal A H, Jacobson I M, Bourliere M, Theodorou I, Poynard T, Negro F, Pol S, Abel L, Bochud P Y, Swiss Hepatitis C Cohort Study, Int Hepatitis C Genetics Consortiu, French Anrs H C E P Genoscan Stud
J Hepatol 56 (), S551-S551, 2012
Genome-Wide Association Study Identifies Variants Associated With Progression of Liver Fibrosis From HCV Infection
Patin E, Kutalik Z, Guergnon J, Bibert S, Nalpas B, Jouanguy E, Munteanu M, Bousquet L, Argiro L, Halfon P, Boland A, Mullhaupt B, Semela D, Dufour JF, Heim MH, Moradpour D, Cerny A, Malinverni R, Hirsch H, Martinetti G, Suppiah V, Stewart G, Booth DR, George J, Casanova JL, Brechot C, Rice CM, Talal AH, Jacobson IM, Bourliere M, Theodorou I, Poynard T, Negro F, Pol S, Bochud PY, Abel L
A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection
Pedergnana V, Gessain A, Tortevoye P, Byun M, Bacq-Daian D, Boland A, Casanova J L, Abel L, Plancoulaine S
Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project
Perroud N, Uher R, Ng M Y M, Guipponi M, Hauser J, Henigsberg N, Maier W, Mors O, Gennarelli M, Rietschel M, Souery D, Dernovsek M Z, Stamp A S, Lathrop M, Farmer A, Breen G, Aitchison K J, Lewis C M, Craig I W, McGuffin P
Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolates
Pimenoff VN, Laval G, Comas D, Palo JU, Gut I, Cann H, Excoffier L, Sajantila A
Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions
Pinel P, Fauchereau F, Moreno A, Barbot A, Lathrop M, Zelenika D, Le Bihan D, Poline J B, Bourgeron T, Dehaene S
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder
Priebe L, Degenhardt F A, Herms S, Haenisch B, Mattheisen M, Nieratschker V, Weingarten M, Witt S, Breuer R, Paul T, Alblas M, Moebus S, Lathrop M, Leboyer M, Schreiber S, Grigoroiu-Serbanescu M, Maier W, Propping P, Rietschel M, Nothen M M, Cichon S, Muhleisen T W
Mice with sepine deficiency are lipoatrophic, insulinoresistant, but hypotriglyceridemic
Prieur X, Takahashi M, Nemani M, Pillot B, Mounier C, Zelenika D, Feve B, Capeau J, Lathrop M, Cariou B, Costet P, Magre J
Diabetes & Metabolism 38 (), A8-A8, 2012
Genome-wide association study of glioma and meta-analysis
Rajaraman P, Melin BS, Wang ZM, McKean-Cowdin R, Michaud DS, Wang SS, Bondy M, Houlston R, Jenkins RB, Wrensch M, Yeager M, Ahlbom A, Albanes D, Andersson U, Freeman LEB, Buring JE, Butler MA, Braganza M, Carreon T, Feychting M, Fleming SJ, Gapstur SM, Gaziano JM, Giles GG, Hallmans G, Henriksson R, Hoffman-Bolton J, Inskip PD, Johansen C, Kitahara CM, Lathrop M, Liu CW, Le Marchand L, Linet MS, Lonn S, Peters U, Purdue MP, Rothman N, Ruder AM, Sanson M, Sesso HD, Severi G, Shu XO, Simon M, Stampfer M, Stevens VL, Visvanathan K, White E, Wolk A, Zeleniuch-Jacquotte A, Zheng W, Decker P, Enciso-Mora V, Fridley B, Gao YT, Kosel M, Lachance DH, Lau C, Rice T, Swerdlow A, Wiemels JL, Wiencke JK, Shete S, Xiang YB, Xiao YY, Hoover RN, Fraumeni JF, Chatterjee N, Hartge P, Chanock SJ
Genome-Wide Association Mapping in Tomato (Solanum lycopersicum) Is Possible Using Genome Admixture of Solanum lycopersicum var. cerasiforme
Ranc N, Munos S, Xu JX, Le Paslier MC, Chauveau A, Bounon R, Rolland S, Bouchet JP, Brunel D, Causse M
Maximizing the Reliability of Genomic Selection by Optimizing the Calibration Set of Reference Individuals: Comparison of Methods in Two Diverse Groups of Maize Inbreds (Zea mays L.)
Rincent R, Laloe D, Nicolas S, Altmann T, Brunel D, Revilla P, Rodriguez VM, Moreno-Gonzalez J, Melchinger A, Bauer E, Schoen CC, Meyer N, Giauffret C, Bauland C, Jamin P, Laborde J, Monod H, Flament P, Charcosset A, Moreau L
Sequence Variants and Haplotype Analysis of Cat ERBB2 Gene: A Survey on Spontaneous Cat Mammary Neoplastic and Non-Neoplastic Lesions
Santos S, Bastos E, Baptista C S, Sa D, Caloustian C, Guedes-Pinto H, Gartner F, Gut I G, Chaves R
Taking Into Account Imprinting And Maternal Genotype Effects Facilitates Detection Of New Genes
Sarnowski C, Malerba G, Laprise C, Rohde K, Moffatt M, Jeannin P, Dizier M H, Pignatti P F, Cookson W O C, Lathrop M, Demenais F, Bouzigon E
Genetic Epidemiology 36 (2), 122-123, 2012
SHANK1 Deletions in Males with Autism Spectrum Disorder
Sato D, Lionel A C, Leblond C S, Prasad A, Pinto D, Walker S, O'Connor I, Russell C, Drmic I E, Hamdan F F, Michaud J L, Endris V, Roeth R, Delorme R, Huguet G, Leboyer M, Rastam M, Gillberg C, Lathrop M, Stavropoulos D J, Anagnostou E, Weksberg R, Fombonne E, Zwaigenbaum L, Fernandez B A, Roberts W, Rappold G A, Marshall C R, Bourgeron T, Szatmari P, Scherer S W
Risk Taking and the Adolescent Reward System: A Potential Common Link to Substance Abuse
Schneider S, Peters J, Bromberg U, Brassen S, Miedl S F, Banaschewski T, Barker G J, Conrod P, Flor H, Garavan H, Heinz A, Ittermann B, Lathrop M, Loth E, Mann K, Martinot J L, Nees F, Paus T, Rietschel M, Robbins T W, Smolka M N, Spanagel R, Strohle A, Struve M, Schumann G, Buchel C, Imagen Consortium
High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly
Servin B, Faraut T, Iannuccelli N, Zelenika D, Milan D
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11
Siddiq A, Couch FJ, Chen GK, Lindstrom S, Eccles D, Millikan RC, Michailidou K, Stram DO, Beckmann L, Rhie SK, Ambrosone CB, Aittomaki K, Amiano P, Apicella C, Baglietto L, Bandera EV, Beckmann MW, Berg CD, Bernstein L, Blomqvist C, Brauch H, Brinton L, Bui QM, Buring JE, Buys SS, Campa D, Carpenter JE, Chasman DI, Chang-Claude J, Chen C, Clavel-Chapelon F, Cox A, Cross SS, Czene K, Deming SL, Diasio RB, Diver WR, Dunning AM, Durcan L, Ekici AB, Fasching PA, Feigelson HS, Fejerman L, Figueroa JD, Fletcher O, Flesch-Janys D, Gaudet MM, Gerty SM, Rodriguez-Gil JL, Giles GG, van Gils CH, Godwin AK, Graham N, Greco D, Hall P, Hankinson SE, Hartmann A, Hein R, Heinz J, Hoover RN, Hopper JL, Hu JJ, Huntsman S, Ingles SA, Irwanto A, Isaacs C, Jacobs KB, John EM, Justenhoven C, Kaaks R, Kolonel LN, Coetzee GA, Lathrop M, Marchand L, Lee AM, Lee IM, Lesnick T, Lichtner P, Liu JJ, Lund E, Makalic E, Martin NG, McLean CA, Meijers-Heijboer H, Meindl A, Miron P, Monroe KR, Montgomery GW, Muller-Myhsok B, Nickels S, Nyante SJ, Olswold C, Overvad K, Palli D, Park DJ, Palmer JR, Pathak H, Peto J, Pharoah P, Rahman N, Rivadeneira F, Schmidt DF, Schmutzler RK, Slager S, Southey MC, Stevens KN, Sinn HP, Press MF, Ross E, Riboli E, Ridker PM, Schumacher FR, Severi G, Silva ID, Stone J, Sund M, Tapper WJ, Thun MJ, Travis RC, Turnbull C, Uitterlinden AG, Waisfisz Q, Wang XS, Wang ZM, Weaver J, Schulz-Wendtland R, Wilkens LR, Van Den Berg D, Zheng W, Ziegler RG, Ziv E, Nevanlinna H, Easton DF, Hunter DJ, Henderson BE, Chanock SJ, Garcia-Closas M, Kraft P, Haiman CA, Vachon CM
Transient receptor potential genes, smoking, occupational exposures and cough in adults
Smit L A M, Kogevinas M, Anto J M, Bouzigon E, Gonzalez J R, Le Moual N, Kromhout H, Carsin A E, Pin I, Jarvis D, Vermeulen R, Janson C, Heinrich J, Gut I, Lathrop M, Valverde M A, Demenais F, Kauffmann F
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls.
Soemedi R, Topf A, Wilson I J, Darlay R, Rahman T, Glen E, Hall D, Huang N, Bentham J, Bhattacharya S, Cosgrove C, Brook J D, Granados-Riveron J, Setchfield K, Bu'Lock F, Thornborough C, Devriendt K, Breckpot J, Hofbeck M, Lathrop M, Rauch A, Blue G M, Winlaw D S, Hurles M, Santibanez-Koref M, Cordell H J, Goodship J A, Keavney B D
Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease
Soemedi R, Wilson IJ, Bentham J, Darlay R, Topf A, Zelenika D, Cosgrove C, Setchfield K, Thornborough C, Granados-Riveron J, Blue GM, Breckpot J, Hellens S, Zwolinkski S, Glen E, Mamasoula C, Rahman TJ, Hall D, Rauch A, Devriendt K, Gewillig M, O' Sullivan J, Winlaw DS, Bu'Lock F, Brook JD, Bhattacharya S, Lathrop M, Santibanez-Koref M, Cordell HJ, Goodship JA, Keavney BD
Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype
Sofat R, Casas J P, Webster A R, Bird A C, Mann S S, Yates J R W, Moore A T, Sepp T, Cipriani V, Bunce C, Khan J C, Shahid H, Swaroop A, Abecasis G, Branham K E H, Zareparsi S, Bergen A A, Klaver C C W, Baas D C, Zhang K, Chen Y H, Gibbs D, Weber B H F, Keilhauer C N, Fritsche L G, Lotery A, Cree A J, Griffiths H L, Bhattacharya S S, Chen L L, Jenkins S A, Peto T, Lathrop M, Leveillard T, Gorin M B, Weeks D E, Ortube M C, Ferrell R E, Jakobsdottir J, Conley Y P, Rahu M, Seland J H, Soubrane G, Topouzis F, Vioque J, Tomazzoli L, Young I, Whittaker J, Chakravarthy U, de Jong Ptvm, Smeeth L, Fletcher A, Hingorani A D
Insight into the Wild Origin, Migration and Domestication History of the Fine Flavour Nacional Theobroma cacao L. Variety from Ecuador
Solorzano RGL, Fouet O, Lemainque A, Pavek S, Boccara M, Argout X, Amores F, Courtois B, Risterucci AM, Lanaud C
RASGRF2 regulates alcohol-induced reinforcement by influencing mesolimbic dopamine neuron activity and dopamine release
Stacey D, Bilbao A, Maroteaux M, Jia TY, Easton AC, Longueville S, Nymberg C, Banaschewski T, Barker GJ, Buchel C, Carvalho F, Conrod PJ, Desrivieres S, Fauth-Buhler M, Fernandez-Medarde A, Flor H, Gallinat J, Garavan H, Bokde ALW, Heinz A, Ittermann B, Lathrop M, Lawrence C, Loth E, Lourdusamy A, Mann KF, Martinot JL, Nees F, Palkovits M, Paus T, Pausova Z, Rietschel M, Ruggeri B, Santos E, Smolka MN, Staehlin O, Jarvelin MR, Elliott P, Sommer WH, Mameli M, Muller CP, Spanagel R, Girault JA, Schumann G
Lentiviral transduction of CD34+cells induces genome-wide epigenetic modifications (meeting)
Stockholm D, Yoshiaki Y, Paietti V, Corre G, Poinsignon C, Touleimat N, Delafoy D, Besse C, Tost J, Galy A, Paldi A
Hum. Gene Ther. 23 (10), A48-A49, 2012
TFAP2B Influences the Effect of Dietary Fat on Weight Loss under Energy Restriction
Stocks T, Angquist L, Banasik K, Harder MN, Taylor MA, Hager J, Arner P, Oppert JM, Martinez JA, Polak J, RousseaU F, Langin D, Rossner S, Holst C, MacDonald IA, Kamatani Y, Pfeiffer AFH, Kunesova M, Saris WHM, Hansen T, Pedersen O, Astrup A, Sorensen TIA
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis
Sun L, Rommens J M, Corvol H, Li W L, Li X, Chiang T A, Lin F, Dorfman R, Busson P F, Parekh R V, Zelenika D, Blackman S M, Corey M, Doshi V K, Henderson L, Naughton K M, O'Neal W K, Pace R G, Stonebraker J R, Wood S D, Wright F A, Zielenski J, Clement A, Drumm M L, Boelle P Y, Cutting G R, Knowles M R, Durie P R, Strug L J
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal H R, St Pourcain B, Thiering E, Das S, Mook-Kanamori D O, Warrington N M, Kaakinen M, Kreiner-Moller E, Bradfield J P, Freathy R M, Geller F, Guxens M, Cousminer D L, Kerkhof M, Timpson N J, Ikram M A, Beilin L J, Bonnelykke K, Buxton J L, Charoen P, Chawes B L K, Eriksson J, Evans D M, Hofman A, Kemp J P, Kim C E, Klopp N, Lahti J, Lye S J, McMahon G, Mentch F D, Muller-Nurasyid M, O'Reilly P F, Prokopenko I, Rivadeneira F, Steegers E A P, Sunyer J, Tiesler C, Yaghootkar H, Breteler M M B, Debette S, Fornage M, Gudnason V, Launer L J, van der Lugt A, Mosley T H, Seshadri S, Smith A V, Vernooij M W, Blakemore A I F, Chiavacci R M, Feenstra B, Fernandez-Banet J, Grant S F A, Hartikainen A L, van der Heijden A J, Iniguez C, Lathrop M, McArdle W L, Molgaard A, Newnham J P, Palmer L J, Palotie A, Pouta A, Ring S M, Sovio U, Standl M, Uitterlinden A G, Wichmann H E, Vissing N H, DeCarli C, van Duijn C M, McCarthy M I, Koppelman G H, Estivill X, Hattersley A T, Melbye M, Bisgaard H, Pennell C E, Widen E, Hakonarson H, Smith G D, Heinrich J, Jarvelin M R, Jaddoe V W V, Adair L S, Ang W, Atalay M, van Beijsterveldt T, Bergen N, Benke K, Berry D, Coin L, Davis O S P, Elliott P, Flexeder C, Frayling T, Gaillard R, Groen-Blokhuis M, Goh L K, Haworth C M A, Hadley D, Hedebrand J, Hinney A, Hirschhorn J N, Holloway J W, Holst C, Hottenga J J, Horikoshi M, Huikari V, Hypponen E, Kilpelainen T O, Kirin M, Kowgier M, Lakka H M, Lange L A, Lawlor D A, Lehtimaki T, Lewin A, Lindgren C, Lindi V, Maggi R, Marsh J, Middeldorp C, Millwood I, Murray J C, Nivard M, Nohr E A, Ntalla I, Oken E, Panoutsopoulou K, Pararajasingham J, Rodriguez A, Salem R M, Sebert S, Siitonen N, Strachan D P, Teo Y Y, Valcarcel B, White S, Willemsen G, Zeggini E, Boomsma D I, Cooper C, Gillman M, Hocher B, Lakka T A, Mohlke K L, Dedoussis G V, Ong K K, Pearson E R, Price T S, Power C, Raitakari O T, Saw S M, Scherag A, Simell O, Sorensen T I A, Wilson J F, Schmidt R, Vrooman H A, Sigurdsson S, Ropele S, Coker L H, Longstreth W T, Niessen W J, DeStefano A L, Beiser A, Zijdenbos A P, Struchalin M, Jack C R, Nalls M A, Au R, Gudnason H, Harris T B, Meeks W M, van Buchem M A, Catellier D, Windham B G, Wolf P A, Schmidt H, Cohorts Heart Aging Res Genetic Ep, Early Genetics Lifecourse Epidemio, Early Growth Genetics E G G Consorti
Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia
Tesson C, Nawara M, Salih MAM, Rossignol R, Zaki MS, Al Balwi M, Schule R, Mignot C, Obre E, Bouhouche A, Santorelli FM, Durand CM, Oteyza AC, El-Hachimi KH, Al Drees A, Bouslam N, Lamari F, Elmalik SA, Kabiraj MM, Seidahmed MZ, Esteves T, Gaussen M, Monin ML, Gyapay G, Lechner D, Gonzalez M, Depienne C, Mochel F, Lavie J, Schols L, Lacombe D, Yahyaoui M, Al Abdulkareem I, Zuchner S, Yamashita A, Benomar A, Goizet C, Durr A, Gleeson JG, Darios F, Brice A, Stevanin G
Complete pipeline for Infinium (R) Human Methylation 450K BeadChip data processing using subset quantile normalization for accurate DNA methylation estimation
Touleimat N, Tost J
Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
Tsoi LC, Spain SL, Knight J, Ellinghaus E, Stuart PE, Capon F, Ding J, Li YM, Tejasvi T, Gudjonsson JE, Kang HM, Allen MH, McManus R, Novelli G, Samuelsson L, Schalkwijk J, Stahle M, Burden AD, Smith CH, Cork MJ, Estivill X, Bowcock AM, Krueger GG, Weger W, Worthington J, Tazi-Ahnini R, Nestle FO, Hayday A, Hoffmann P, Winkelmann J, Wijmenga C, Langford C, Edkins S, Andrews R, Blackburn H, Strange A, Band G, Pearson RD, Vukcevic D, Spencer CCA, Deloukas P, Mrowietz U, Schreiber S, Weidinger S, Koks S, Kingo K, Esko T, Metspalu A, Lim HW, Voorhees JJ, Weichenthal M, Wichmann HE, Chandran V, Rosen CF, Rahman P, Gladman DD, Griffiths CEM, Reis A, Kere J, Nair RP, Franke A, Barker JNWN, Abecasis GR, Elder JT, Trembath RC, Duffin KC, Helms C, Goldgar D, Li Y, Paschall J, Malloy MJ, Pullinger CR, Kane JP, Gardner J, Perlmutter A, Miner A, Feng BJ, Hiremagalore R, Ike RW, Christophers E, Henseler T, Ruether A, Schrodi SJ, Prahalad S, Guthery SL, Fischer J, Liao W, Kwok P, Menter A, Lathrop GM, Wise C, Begovich AB, Onoufriadis A, Weale ME, Hofer A, Salmhofer W, Wolf P, Kainu K, Saarialho-Kere U, Suomela S, Badorf P, Huffmeier U, Kurrat W, Kuster W, Lascorz J, Mossner R, Schurmeier-Horst F, Stander M, Traupe H, Bergboer JGM, den Heijer M, van de Kerkhof PCV, Zeeuwen PLJM, Barnes L, Campbell LE, Cusack C, Coleman C, Conroy J, Ennis S, Fitzgerald O, Gallagher P, Irvine AD, Kirby B, Markham T, McLean WHI, McPartlin J, Rogers SF, Ryan AW, Zawirska A, Giardina E, Lepre T, Perricone C, Martin-Ezquerra G, Pujol RM, Riveira-Munoz E, Inerot A, Naluai AT, Mallbris L, Wolk K, Leman J, Barton A, Warren RB, Young HS, Ricano-Ponce I, Trynka G, Pellett FJ, Henschel A, Aurand M, Bebo B, Gieger C, Illig T, Moebus S, Jockel KH, Erbe R, Donnelly P, Peltonen L, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Craddock N, Duncanson A, Jankowski J, Markus HS, Mathew CG, McCarthy MI, Palmer CNA, Plomin R, Rautanen A, Sawcer SJ, Samani N, Viswanathan AC, Wood NW, Bellenguez C, Freeman C, Hellenthal G, Giannoulatou E, Pirinen M, Su Z, Hunt SE, Gwilliam R, Bumpstead SJ, Dronov S, Gillman M, Gray E, Hammond N, Jayakumar A, McCann OT, Liddle J, Perez ML, Potter SC, Ravindrarajah R, Ricketts M, Waller M, Weston P, Widaa S, Whittaker P
Genome-Wide Association Study of Classical Hodgkin Lymphoma and Epstein-Barr Virus Status-Defined Subgroups
Urayama K Y, Jarrett R F, Hjalgrim H, Diepstra A, Kamatani Y, Chabrier A, Gaborieau V, Boland A, Nieters A, Becker N, Foretova L, Benavente Y, Maynadie M, Staines A, Shield L, Lake A, Montgomery D, Taylor M, Smedby K E, Amini R M, Adami H O, Glimelius B, Feenstra B, Nolte I M, Visser L, van Imhoff G W, Lightfoot T, Cocco P, Kiemeney L, Vermeulen S H, Holcatova I, Vatten L, Macfarlane G J, Thomson P, Conway D I, Benhamou S, Agudo A, Healy C M, Overvad K, Tjonneland A, Melin B, Canzian F, Khaw K T, Travis R C, Peeters P H M, Gonzalez C A, Quiros J R, Sanchez M J, Huerta J M, Ardanaz E, Dorronsoro M, Clavel-Chapelon F, Bueno-De-Mesquita H B, Riboli E, Roman E, Boffetta P, de Sanjose S, Zelenika D, Melbye M, van den Berg A, Lathrop M, Brennan P, McKay J D
Host gene response to endosymbiont and pathogen in the cereal weevil Sitophilus oryzae
Vigneron A, Charif D, Vincent-Monegat C, Vallier A, Gavory F, Wincker P, Heddi A
Determinants of Human Adipose Tissue Gene Expression: Impact of Diet, Sex, Metabolic Status, and Cis Genetic Regulation
Viguerie N, Montastier E, Maoret JJ, Roussel B, Combes M, Valle C, Villa-Vialaneix N, Iacovoni JS, Martinez JA, Holst C, Astrup A, Vidal H, Clement K, Hager J, Saris WHM, Langin D
Adolescent impulsivity phenotypes characterized by distinct brain networks
Whelan R, Conrod P J, Poline J B, Lourdusamy A, Banaschewski T, Barker G J, Bellgrove M A, Buchel C, Byrne M, Cummins T D R, Fauth-Buhler M, Flor H, Gallinat J, Heinz A, Ittermann B, Mann K, Martinot J L, Lalor E C, Lathrop M, Loth E, Nees F, Paus T, Rietschel M, Smolka M N, Spanagel R, Stephens D N, Struve M, Thyreau B, Vollstaedt-Klein S, Robbins T W, Schumann G, Garavan H, Imagen Consortium
A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23
Wu X F, Scelo G, Purdue M P, Rothman N, Johansson M, Ye Y Q, Wang Z M, Zelenika D, Moore L E, Wood C G, Prokhortchouk E, Gaborieau V, Jacobs K B, Chow W H, Toro J R, Zaridze D, Lin J, Lubinski J, Trubicka J, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Mates D, Jinga V, Bencko V, Slamova A, Holcatova I, Navratilova M, Janout V, Boffetta P, Colt J S, Davis F G, Schwartz K L, Banks R E, Selby P J, Harnden P, Berg C D, Hsing A W, Grubb R L, Boeing H, Vineis P, Clavel-Chapelon F, Palli D, Tumino R, Krogh V, Panico S, Duell E J, Quiros J R, Sanchez M J, Navarro C, Ardanaz E, Dorronsoro M, Khaw K T, Allen N E, Bueno-De-Mesquita H B, Peeters P H M, Trichopoulos D, Linseisen J, Ljungberg B, Overvad K, Tjonneland A, Romieu I, Riboli E, Stevens V L, Thun M J, Diver W R, Gapstur S M, Pharoah P D, Easton D F, Albanes D, Virtamo J, Vatten L, Hveem K, Fletcher T, Koppova K, Cussenot O, Cancel-Tassin G, Benhamou S, Hildebrandt M A, Pu X, Foglio M, Lechner D, Hutchinson A, Yeager M, Fraumeni J F, Lathrop M, Skryabin K G, McKay J D, Gu J, Brennan P, Chanock S J
Lentiviral Transduction of CD34(+) Cells Induces Genome-Wide Epigenetic Modifications
Yamagata Y, Parietti V, Stockholm D, Corre G, Poinsignon C, Touleimat N, Delafoy D, Besse C, Tost J, Galy A, Paldi A
Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinoma
Zhang M F, Liang L M, Morar N, Dixon A L, Lathrop G M, Ding J, Moffatt M F, Cookson W O C, Kraft P, Qureshi A A, Han J L
The EvA study: aims and strategy
Ziegler-Heitbrock L, Frankenberger M, Heimbeck I, Burggraf D, Wjst M, Haussinger K, Brightling C, Gupta S, Parr D, Subramanian D, Singh D, Kolsum U, Boschetto P, Potena A, Gorecka D, Nowinski A, Barta I, Dome B, Strausz J, Greulich T, Vogelmeier C, Bals R, Hohlfeld JM, Welte T, Venge P, Gut I, Boland A, Olaso R, Hager J, Hiemstra P, Rabe KF, Unmuessig M, Muller-Ouernhelm J, Prasse A
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels
Antoni G, Oudot-Mellakh T, Dimitromanolakis A, Germain M, Cohen W, Wells P, Lathrop M, Gagnon F, Morange P E, Tregouet D A
The genome of Theobroma cacao
Argout X, Salse J, Aury J M, Guiltinan M J, Droc G, Gouzy J, Allegre M, Chaparro C, Legavre T, Maximova S N, Abrouk M, Murat F, Fouet O, Poulain J, Ruiz M, Roguet Y, Rodier-Goud M, Barbosa-Neto J F, Sabot F, Kudrna D, Ammiraju J S S, Schuster S C, Carlson J E, Sallet E, Schiex T, Dievart A, Kramer M, Gelley L, Shi Z, Berard A, Viot C, Boccara M, Risterucci A M, Guignon V, Sabau X, Axtell M J, Ma Z R, Zhang Y F, Brown S, Bourge M, Golser W, Song X A, Clement D, Rivallan R, Tahi M, Akaza J M, Pitollat B, Gramacho K, D'Hont A, Brunel D, Infante D, Kebe I, Costet P, Wing R, McCombie W R, Guiderdoni E, Quetier F, Panaud O, Wincker P, Bocs S, Lanaud C
Transcriptomic analysis of the interaction between Helianthus annuus and its obligate parasite Plasmopara halstedii shows single nucleotide polymorphisms in CRN sequences
As-sadi F, Carrere S, Gascuel Q, Hourlier T, Rengel D, Le Paslier M C, Bordat A, Boniface M C, Brunel D, Gouzy J, Godiard L, Vincourt P
A Genome-Wide Association Study of the Protein C Anticoagulant Pathway
Athanasiadis G, Buil A, Souto J C, Borrell M, Lopez S, Martinez-Perez A, Lathrop M, Fontcuberta J, Almasy L, Soria J M
Genome-wide association study identifies three new melanoma susceptibility loci
Barrett J H, Iles M M, Harland M, Taylor J C, Aitken J F, Andresen P A, Akslen L A, Armstrong B K, Avril M F, Azizi E, Bakker B, Bergman W, Bianchi-Scarra G, Bressac-de Paillerets B, Calista D, Cannon-Albright L A, Corda E, Cust A E, Debniak T, Duffy D, Dunning A M, Easton D F, Friedman E, Galan P, Ghiorzo P, Giles G G, Hansson J, Hocevar M, Hoiom V, Hopper J L, Ingvar C, Janssen B, Jenkins M A, Jonsson G, Kefford R F, Landi G, Landi M T, Lang J, Lubinski J, Mackie R, Malvehy J, Martin N G, Molven A, Montgomery G W, van Nieuwpoort F A, Novakovic S, Olsson H, Pastorino L, Puig S, Puig-Butille J A, Randerson-Moor J, Snowden H, Tuominen R, VanBelle P, van der Stoep N, Whiteman D C, Zelenika D, Han J L, Fang S Y, Lee J E, Wei Q Y, Lathrop G M, Gillanders E M, Brown K M, Goldstein A M, Kanetsky P A, Mann G J, MacGregor S, Elder D E, Amos C I, Hayward N K, Gruis N A, Demenais F, Bishop J A N, Bishop D T, Geno M E L Consortium
A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma
Bertolotto C, Lesueur F, Giuliano S, Strub T, de Lichy M, Bille K, Dessen P, d'Hayer B, Mohamdi H, Remenieras A, Maubec E, de la Fouchardiere A, Molinie V, Vabres P, Dalle S, Poulalhon N, Martin-Denavit T, Thomas L, Andry-Benzaquen P, Dupin N, Boitier F, Rossi A, Perrot J L, Labeille B, Robert C, Escudier B, Caron O, Brugieres L, Saule S, Gardie B, Gad S, Richard S, Couturier J, Teh B T, Ghiorzo P, Pastorino L, Puig S, Badenas C, Olsson H, Ingvar C, Rouleau E, Lidereau R, Bahadoran P, Vielh P, Corda E, Blanche H, Zelenika D, Galan P, Chaudru V, Lenoir G M, Lathrop M, Davidson I, Avril M F, Demenais F, Ballotti R, Bressac-de Paillerets B, French Familial Melanoma Study Grp
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
Bonnet C, Grati M, Marlin S, Levilliers J, Hardelin J P, Parodi M, Niasme-Grare M, Zelenika D, Delepine M, Feldmann D, Jonard L, El-Amraoui A, Weil D, Delobel B, Vincent C, Dollfus H, Eliot M M, David A, Calais C, Vigneron J, Montaut-Verient B, Bonneau D, Dubin J, Thauvin C, Duvillard A, Francannet C, Mom T, Lacombe D, Duriez F, Drouin-Garraud V, Thuillier-Obstoy M F, Sigaudy S, Frances A M, Collignon P, Challe G, Couderc R, Lathrop M, Sahel J A, Weissenbach J, Petit C, Denoyelle F
Genetic and functional evaluation of MITF as a candidate gene for cutaneous melanoma predisposition in pigs
Bourneuf E, Du Z Q, Estelle J, Gilbert H, Crechet F, Piton G, Milan D, Geffrotin C, Lathrop M, Demenais F, Rogel-Gaillard C, Vincent-Naulleau S
Epigenetic regulation in murine offspring as a novel mechanism for transmaternal asthma protection induced by microbes
Brand S, Teich R, Dicke T, Harb H, Yildirim A O, Tost J, Schneider-Stock R, Waterland R A, Bauer U M, von Mutius E, Garn H, Pfefferle P I, Renz H
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease
Bustamante J, Arias A A, Vogt G, Picard C, Galicia L B, Prando C, Grant A V, Marchal C C, Hubeau M, Chapgier A, de Beaucoudrey L, Puel A, Feinberg J, Valinetz E, Janniere L, Besse C, Boland A, Brisseau J M, Blanche S, Lortholary O, Fieschi C, Emile J F, Boisson-Dupuis S, Al-Muhsen S, Woda B, Newburger P E, Condino-Neto A, Dinauer M C, Abel L, Casanova J L
Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease
Butterworth A S, Braund P S, Farrall M, Hardwick R J, Saleheen D, Peden J F, Soranzo N, Chambers J C, Sivapalaratnam S, Kleber M E, Keating B, Qasim A, Klopp N, Erdmann J, Assimes T L, Ball S G, Balmforth A J, Barnes T A, Basart H, Baumert J, Bezzina C R, Boerwinkle E, Boehm B O, Brocheton J, Bugert P, Cambien F, Clarke R, Codd V, Collins R, Couper D, Cupples L A, de Jong J S, Diemert P, Ejebe K, Elbers C C, Elliott P, Fornage M, Franzosi M G, Frossard P, Garner S, Goel A, Goodall A H, Hengstenberg C, Hunt S E, Kastelein J J P, Klungel O H, Kluter H, Koch K, Konig I R, Kooner A S, Laaksonen R, Lathrop M, Li M Y, Liu K, McPherson R, Musameh M D, Musani S, Nelson C P, O'Donnell C J, Ongen H, Papanicolaou G, Peters A, Peters B J M, Potter S, Psaty B M, Qu L M, Rader D J, Rasheed A, Rice C, Scott J, Seedorf U, Sehmi J S, Sotoodehnia N, Stark K, Stephens J, van der Schoot C E, van der Schouw Y T, Thorsteinsdottir U, Tomaszewski M, van der Harst P, Vasan R S, Wilde A A M, Willenborg C, Winkelmann B R, Zaidi M, Zhang W H, Ziegler A, de Bakker P I W, Koenig W, Marz W, Trip M D, Reilly M P, Kathiresan S, Schunkert H, Hamsten A, Hall A S, Kooner J S, Thompson S G, Thompson J R, Deloukas P, Ouwehand W H, Watkins H, Danesh J, Samani N J, Ibc K Cad Consortium
Converging Evidence for an Association of ATP2B2 Allelic Variants with Autism in Male Subjects
Carayol J, Sacco R, Tores F, RousseaU F, Lewin P, Hager J, Persico A M
Two families confirm Schopf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum
Castori M, Castiglia D, Brancati F, Foglio M, Heath S, Floriddia G, Madonna S, Fischer J, Zambruno G
C5-DNA Methyltransferase Inhibitors: From Screening to Effects on Zebrafish Embryo Development
Ceccaldi A, Rajavelu A, Champion C, Rampon C, Jurkowska R, Jankevicius G, Senamaud-Beaufort C, Ponger L, Gagey N, Ali H D, Tost J, Vriz S, Ros S, Dauzonne D, Jeltsch A, Guianvarc'h D, Arimondo P B
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
Chambers J C, Zhang W H, Sehmi J, Li X Z, Wass M N, van der Harst P, Holm H, Sanna S, Kavousi M, Baumeister S E, Coin L J, Deng G H, Gieger C, Heard-Costa N L, Hottenga J J, Kuhnel B, Kumar V, Lagou V, Liang L M, Luan J A, Vidal P M, Leach I M, O'Reilly P F, Peden J F, Rahmioglu N, Soininen P, Speliotes E K, Yuan X, Thorleifsson G, Alizadeh B Z, Atwood L D, Borecki I B, Brown M J, Charoen P, Cucca F, Das D, de Geus E J C, Dixon A L, Doering A, Ehret G, Eyjolfsson G I, Farrall M, Forouhi N G, Friedrich N, Goessling W, Gudbjartsson D F, Harris T B, Hartikainen A L, Heath S, Hirschfield G M, Hofman A, Homuth G, Hypponen E, Janssen H L A, Johnson T, Kangas A J, Kema I P, Kuhn J P, Lai S, Lathrop M, Lerch M M, Li Y, Liang T J, Lin J P, Loos R J F, Martin N G, Moffatt M F, Montgomery G W, Munroe P B, Musunuru K, Nakamura Y, O'Donnell C J, Olafsson I, Penninx B W, Pouta A, Prins B P, Prokopenko I, Puls R, Ruokonen A, Savolainen M J, Schlessinger D, Schouten J N L, Seedorf U, Sen-Chowdhry S, Siminovitch K A, Smit J H, Spector T D, Tan W T, Teslovich T M, Tukiainen T, Uitterlinden A G, van der Klauw M M, Vasan R S, Wallace C, Wallaschofski H, Wichmann H E, Willemsen G, Wurtz P, Xu C, Yerges-Armstrong L M, Abecasis G R, Ahmadi K R, Boomsma D I, Caulfield M, Cookson W O, van Duijn C M, Froguel P, Matsuda K, McCarthy M I, Meisinger C, Mooser V, Pietilainen K H, Schumann G, Snieder H, Sternberg M J E, Stolk R P, Thomas H C, Thorsteinsdottir U, Uda M, Waeber G, Wareham N J, Waterworth D M, Watkins H, Whitfield J B, Witteman J C M, Wolffenbuttel B H R, Fox C S, Ala-Korpela M, Stefansson K, Vollenweider P, Volzke H, Schadt E E, Scott J, Jarvelin M R, Elliott P, Kooner J S, Alcohol Genome-wide Assoc AlcGen, Diabet Genetics Replication, Genetic Invest Anthropometric, Global Lipids Genetics Consortium, Genetics Liver Dis Gold Consortium, Int Consortium Blood Pressure Icbp, Meta-Anal Glucose Insulin-Related
Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine
Chancerel E, Lepoittevin C, Le Provost G, Lin Y C, Jaramillo-Correa J P, Eckert A J, Wegrzyn J L, Zelenika D, Boland A, Frigerio J M, Chaumeil P, Garnier-Gere P, Boury C, Grivet D, Gonzalez-Martinez S C, Rouze P, Van de Peer Y, Neale D B, Cervera M T, Kremer A, Plomion C
Histone H3 trimethylation at lysine 36 is associated with constitutive and facultative heterochromatin
Chantalat S, Depaux A, Hery P, Barral S, Thuret JY, Dimitrov S, Gerard M
Combination of promoter hypomethylation and PDX1 overexpression leads to TBX15 decrease in vascular IUGR placentas
Chelbi S T, Doridot L, Mondon F, Dussour C, Rebourcet R, Busato F, Gascoin-Lachambre G, Barbaux S, Rigourd V, Mignot T M, Tost J, Vaiman D
Genome-wide association study of HPV seropositivity
Chen D, McKay J D, Clifford G, Gaborieau V, Chabrier A, Waterboer T, Zaridze D, Lissowska J, Rudnai P, Fabianova E, Bencko V, Janout V, Foretova L, Mates I N, Szeszenia-Dabrowska N, Curado M P, Koifman S, Menezes A, Wunsch V, Eluf-Neto J, Garrote L F, Matos E, Zelenika D, Boland A, Boffetta P, Pawlita M, Lathrop M, Brennan P
Tumour necrosis factor haplotypes associated with sensory neuropathy in Asian and Caucasian human immunodeficiency virus patients
Chew C S, Cherry C L, Imran D, Yunihastuti E, Kamarulzaman A, Varna S, Ismail R, Phipps M, Aghafar Z, Gut I, Price P
Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region
Chureau C, Chantalat S, Romito A, Galvani A, Duret L, Avner P, Rougeulle C
Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder (vol 88, pg 372, 2011)
Cichon S, Muehleisen T W, Degenhardt F A, Mattheisen M, Miro X, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Alexander M, Vollmer J, Breuer R, Schmal C, Tessmann P, Moebus S, Wichmann H E, Schreiber S, Muller-Myhsok B, Lucae S, Jamain S, Leboyer M, Bellivier F, Etain B, Henry C, Kahn J P, Heath S, Hamshere M, O'Donovan M C, Owen M J, Craddock N, Schwarz M, Vedder H, Kammerer-Ciernioch J, Reif A, Sasse J, Bauer M, Hautzinger M, Wright A, Mitchell P B, Schofield P R, Montgomery G W, Medland S E, Gordon S D, Martin N G, Gustafsson O, Andreassen O, Djurovic S, Sigurdsson E, Steinberg S, Stefansson H, Stefansson K, Kapur-Pojskic L, Oruc L, Rivas F, Mayoral F, Chuchalin A, Babadjanova G, Tiganov A S, Pantelejeva G, Abramova L I, Grigoroiu-Serbanescu M, Diaconu C C, Czerski P M, Hauser J, Zimmer A, Lathrop M, Schulze T G, Wienker T F, Schumacher J, Maier W, Propping P, Rietschel M, Nothen M M, Bipolar Disorder Genome Study Bi G S
Genome-wide Association Study Identifies Genetic Variation in Neurocan as a Susceptibility Factor for Bipolar Disorder
Cichon S, Muhleisen T W, Degenhardt F A, Mattheisen M, Miro X, Strohmaier J, Steffens M, Meesters C, Herms S, Weingarten M, Priebe L, Haenisch B, Aexander M, Vollmer J, Breuer R, Schmal C, Tessmann P, Moebus S, Wichmann H E, Schreiber S, Muller-Myhsok B, Lucae S, Jamain S, Leboyer M, Bellivier F, Etain B, Henry C, Kahn J P, Heath S, Hamshere M, O'Donovan M C, Owen M J, Craddock N, Schwarz M, Vedder H, Kammerer-Ciernioch J, Reif A, Sasse J, Bauer M, Hautzinger M, Wright A, Mitchell P B, Schofield P R, Montgomery G W, Medland S E, Gordon S D, Martin N G, Gustafsson O, Andreassen O, Djurovic S, Sigurdsson E, Steinberg S, Stefansson H, Stefansson K, Kapur-Pojskic L, Oruc L, Rivas F, Mayoral F, Chuchalin A, Babadjanova G, Tiganov A S, Pantelejeva G, Abramova L I, Grigoroiu-Serbanescu M, Diaconu C C, Czerski P M, Hauser J, Zimmer A, Lathrop M, Schulze T G, Wienker T F, Schumacher J, Maier W, Propping P, Rietschel M, Nothen M M, Bipolar Disorder Genome Study Bi G S
KCNJ6 is Associated with Adult Alcohol Dependence and Involved in Gene x Early Life Stress Interactions in Adolescent Alcohol Drinking
Clarke T K, Laucht M, Ridinger M, Wodarz N, Rietschel M, Maier W, Lathrop M, Lourdusamy A, Zimmermann U S, Desrivieres S, Schumann G
Detection of CNVs throughout the genome of a porcine melanoma model
Corominas J, Estelle J, Ramayo-Caldas Y, Lathrop M, Demenais F, Rogel-Gaillard C, Vincent-Naulleau S, Folch J M, Bourneuf E
PIGMENT CELL & MELANOMA RESEARCH 24 (4), 850-851, 2011
Family-Based Association Study of SPA3, a New Susceptibility Locus for Spondyloarthritis on 6p11-q11
Costantino F, Izac B, Chiocchia G, Said-Nahal R, Leboime A, Zinovieva E, Zelenika D, Breban M A, Garchon H J
Arthritis Rheum 63 (10), S524-S524, 2011
A transcriptomic analysis of type II autosomal dominant osteopetrosis osteoclasts
Coudert A E, Olaso R, Collet C, de Vernejoul M C
Possible conformational change within the desolvated and cationized sBBI/trypsin non-covalent complex during the collision-induced dissociation process
Darii E, Saravanamuthu G, Afonso C, Alves S, Gut I, Tabet J C
Sex-Specific Role for Adenylyl Cyclase Type 7 in Alcohol Dependence
Desrivieres S, Pronko S P, Lourdusamy A, Ducci F, Hoffman P L, Wodarz N, Ridinger M, Rietschel M, Zelenika D, Lathrop M, Schumann G, Tabakoff B
Unusual Regulation of a STAT Protein by an SLC6 Family Transporter in C. elegans Epidermal Innate Immunity
Dierking K, Polanowska J, Omi S, Engelmann I, Gut M, Lembo F, Ewbank J J, Pujol N
Effects of the Circadian Rhythm Gene Period 1 (Per1) on Psychosocial Stress-Induced Alcohol Drinking
Dong L, Bilbao A, Laucht M, Henriksson R, Yakovleva T, Ridinger M, Desrivieres S, Clarke T K, Lourdusamy A, Smolka M N, Cichon S, Blomeyer D, Treutlein J, Perreau-Lenz S, Witt S, Leonardi-Essmann F, Wodarz N, Zill P, Soyka M, Albrecht U, Rietschel M, Lathrop M, Bakalkin G, Spanagel R, Schumann G
Gene-environment interaction for childhood asthma and exposure to farming in Central Europe
Ege M J, Strachan D P, Cookson Wocm, Moffatt M F, Gut I, Lathrop M, Kabesch M, Genuneit J, Buchele G, Sozanska B, Boznanski A, Cullinan P, Horak E, Bieli C, Braun-Fahrlander C, Heederik D, von Mutius E, Gabriela Study Grp
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Ehret G B, Munroe P B, Rice K M, Bochud M, Johnson A D, Chasman D I, Smith A V, Tobin M D, Verwoert G C, Hwang S J, Pihur V, Vollenweider P, O'Reilly P F, Amin N, Bragg-Gresham J L, Teumer A, Glazer N L, Launer L, Zhao J H, Aulchenko Y, Heath S, Sober S, Parsa A, Luan J A, Arora P, Dehghan A, Zhang F, Lucas G, Hicks A A, Jackson A U, Peden J F, Tanaka T, Wild S H, Rudan I, Igl W, Milaneschi Y, Parker A N, Fava C, Chambers J C, Fox E R, Kumari M, Go M J, van der Harst P, Kao W H L, Sjogren M, Vinay D G, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup P H, Liu Y M, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen K D H, Lehtimaki T, Matullo G, Wu Y, Gaunt T R, Onland-Moret N C, Cooper M N, Platou C G P, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund P S, Kuznetsova T, Uiterwaal Cspm, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer N D, Aspelund T, Garcia M, Chang Y P C, O'Connell J R, Steinle N I, Grobbee D E, Arking D E, Kardia S L, Morrison A C, Hernandez D, Najjar S, McArdle W L, Hadley D, Brown M J, Connell J M, Hingorani A D, Day I N M, Lawlor D A, Beilby J P, Lawrence R W, Clarke R, Hopewell J C, Ongen H, Dreisbach A W, Li Y L, Young J H, Bis J C, Kahonen M, Viikari J, Adair L S, Lee N R, Chen M H, Olden M, Pattaro C, Bolton J A H, Kottgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling T M, Islam M, Jafar T H, Erdmann J, Kulkarni S R, Bornstein S R, Grassler J, Groop L, Voight B F, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I S, Khaw K T, Weder A B, Hunt S C, Sun Y V, Bergman R N, Collins F S, Bonnycastle L L, Scott L J, Stringham H M, Peltonen L, Perola M, Vartiainen E, Brand S M, Staessen J A, Wang T J, Burton P R, Artigas M S, Dong Y B, Snieder H, Wang X L, Zhu H D, Lohman K K, Rudock M E, Heckbert S R, Smith N L, Wiggins K L, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld C D, Rosengren A, Thelle D S, Corsi A M, Singleton A, Forrester T, Hilton G, McKenzie C A, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann H E, Cho Y S, Kim H L, Lee J Y, Scott J, Sehmi J S, Zhang W H, Hedblad B, Nilsson P, Smith G D, Wong A, Narisu N, Stancakova A, Raffel L J, Yao J, Kathiresan S, O'Donnell C J, Schwartz S M, Ikram M A, Longstreth W T, Mosley T H, Seshadri S, Shrine N R G, Wain L V, Morken M A, Swift A J, Laitinen J, Prokopenko I, Zitting P, Cooper J A, Humphries S E, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker S J L, van Gilst W H, Janipalli C S, Mani K R, Yajnik C S, Hofman A, Mattace-Raso F U S, Oostra B A, Demirkan A, Isaacs A, Rivadeneira F, Lakatta E G, Orru M, Scuteri A, Ala-Korpela M, Kangas A J, Lyytikainen L P, Soininen P, Tukiainen T, Wurtz P, Ong R T H, Dorr M, Kroemer H K, Volker U, Volzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector T D, Zhai G J, Meschia J F, Nalls M A, Sharma P, Terzic J, Kumar M V K, Denniff M, Zukowska-Szczechowska E, Wagenknecht L E, Fowkes F G R, Charchar F J, Schwarz P E H, Hayward C, Guo X Q, Rotimi C, Bots M L, Brand E, Samani N J, Polasek O, Talmud P J, Nyberg F, Kuh D, Laan M, Hveem K, Palmer L J, van der Schouw Y T, Casas J P, Mohlke K L, Vineis P, Raitakari O, Ganesh S K, Wong T Y, Tai E S, Cooper R S, Laakso M, Rao D C, Harris T B, Morris R W, Dominiczak A F, Kivimaki M, Marmot M G, Miki T, Saleheen D, Chandak G R, Coresh J, Navis G, Salomaa V, Han B G, Zhu X F, Kooner J S, Melander O, Ridker P M, Bandinelli S, Gyllensten U B, Wright A F, Wilson J F, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller P P, Elosua R, Soranzo N, Sijbrands E J G, Altshuler D, Loos R J F, Shuldiner A R, Gieger C, Meneton P, Uitterlinden A G, Wareham N J, Gudnason V, Rotter J I, Rettig R, Uda M, Strachan D P, Witteman J C M, Hartikainen A L, Beckmann J S, Boerwinkle E, Vasan R S, Boehnke M, Larson M G, Jarvelin M R, Psaty B M, Abecasis G R, Chakravarti A, Elliott P, van Duijn C M, Newton-Cheh C, Levy D, Caulfield M J, Johnson T, Int Consortium Blood Pressure Geno, C ARDIoGRAM Consortium, C KDGen Consortium, KidneyGen Consortium, EchoGen Consortium, Charge-Hf Consortium
Luminal A Breast Tumours Divided in Two Clusters by DNA Methylation
Fleischer T, Jovanovic J, Edvardsen H, Alnaes G I G, Naume B, Borresen-Dale A L, Tost J, Kristensen V N
European Journal of Cancer 47 (), S97-S97, 2011
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