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성함이나 학술지명, PMID로 찾아보십시오.
Van Duijn CM에 대해
171건, 그중 20건 표시.
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels
Richards JB,
Waterworth D,
O'Rahilly S,
Hivert MF,
Loos RJ,
Perry JR,
Tanaka T,
Timpson NJ,
Semple RK,
Soranzo N,
Song K,
Rocha N
외 54명 — 모두 보기
Grundberg E,
Dupuis J,
Florez JC,
Langenberg C,
Prokopenko I,
Saxena R,
Sladek R,
Aulchenko Y,
Evans D,
Waeber G,
Erdmann J,
Burnett MS,
Sattar N,
Devaney J,
Willenborg C,
Hingorani A,
Witteman JC,
Vollenweider P,
Glaser B,
Hengstenberg C,
Ferrucci L,
Melzer D,
Stark K,
Deanfield J,
Winogradow J,
Grassl M,
Hall AS,
Egan JM,
Thompson JR,
Ricketts SL,
König IR,
Reinhard W,
Grundy S,
Wichmann HE,
Barter P,
Mahley R,
Kesaniemi YA,
Rader DJ,
Reilly MP,
Epstein SE,
Stewart AF,
Van Duijn CM,
Schunkert H,
Burling K,
Deloukas P,
Pastinen T,
Samani NJ,
McPherson R,
Davey Smith G,
Frayling TM,
Wareham NJ,
Meigs JB,
Mooser V,
Spector TD
GIANT Consortium
PLoS genetics · 2009 · PMID 20011104 · open access
페이지 2개
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals
Heid IM,
Henneman P,
Hicks A,
Coassin S,
Winkler T,
Aulchenko YS,
Fuchsberger C,
Song K,
Hivert MF,
Waterworth DM,
Timpson NJ,
Richards JB
외 30명 — 모두 보기
Perry JR,
Tanaka T,
Amin N,
Kollerits B,
Pichler I,
Oostra BA,
Thorand B,
Frants RR,
Illig T,
Dupuis J,
Glaser B,
Spector T,
Guralnik J,
Egan JM,
Florez JC,
Evans DM,
Soranzo N,
Bandinelli S,
Carlson OD,
Frayling TM,
Burling K,
Smith GD,
Mooser V,
Ferrucci L,
Meigs JB,
Vollenweider P,
Dijk KW,
Pramstaller P,
Kronenberg F,
van Duijn CM
Atherosclerosis · 2010 · PMID 20018283
페이지 2개
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25
Hysi PG,
Young TL,
Mackey DA,
Andrew T,
Fernández-Medarde A,
Solouki AM,
Hewitt AW,
Macgregor S,
Vingerling JR,
Li YJ,
Ikram MK,
Fai LY
외 13명 — 모두 보기
Sham PC,
Manyes L,
Porteros A,
Lopes MC,
Carbonaro F,
Fahy SJ,
Martin NG,
van Duijn CM,
Spector TD,
Rahi JS,
Santos E,
Klaver CC,
Hammond CJ
Nature genetics · 2010 · PMID 20835236
페이지 2개
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Solouki AM,
Verhoeven VJ,
van Duijn CM,
Verkerk AJ,
Ikram MK,
Hysi PG,
Despriet DD,
van Koolwijk LM,
Ho L,
Ramdas WD,
Czudowska M,
Kuijpers RW
외 23명 — 모두 보기
Amin N,
Struchalin M,
Aulchenko YS,
van Rij G,
Riemslag FC,
Young TL,
Mackey DA,
Spector TD,
Gorgels TG,
Willemse-Assink JJ,
Isaacs A,
Kramer R,
Swagemakers SM,
Bergen AA,
van Oosterhout AA,
Oostra BA,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
de Jong PT,
Hammond CJ,
Vingerling JR,
Klaver CC
Nature genetics · 2010 · PMID 20835239
페이지 2개
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo
Ikram MK,
Sim X,
Jensen RA,
Cotch MF,
Hewitt AW,
Ikram MA,
Wang JJ,
Klein R,
Klein BE,
Breteler MM,
Cheung N,
Liew G
외 45명 — 모두 보기
Mitchell P,
Uitterlinden AG,
Rivadeneira F,
Hofman A,
de Jong PT,
van Duijn CM,
Kao L,
Cheng CY,
Smith AV,
Glazer NL,
Lumley T,
McKnight B,
Psaty BM,
Jonasson F,
Eiriksdottir G,
Aspelund T,
Harris TB,
Launer LJ,
Taylor KD,
Li X,
Iyengar SK,
Xi Q,
Sivakumaran TA,
Mackey DA,
Macgregor S,
Martin NG,
Young TL,
Bis JC,
Wiggins KL,
Heckbert SR,
Hammond CJ,
Andrew T,
Fahy S,
Attia J,
Holliday EG,
Scott RJ,
Islam FM,
Rotter JI,
McAuley AK,
Boerwinkle E,
Tai ES,
Gudnason V,
Siscovick DS,
Vingerling JR,
Wong TY
Global BPgen Consortium
PLoS genetics · 2010 · PMID 21060863 · open access
페이지 2개
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area
Khor CC,
Ramdas WD,
Vithana EN,
Cornes BK,
Sim X,
Tay WT,
Saw SM,
Zheng Y,
Lavanya R,
Wu R,
Wang JJ,
Mitchell P
외 13명 — 모두 보기
Uitterlinden AG,
Rivadeneira F,
Teo YY,
Chia KS,
Seielstad M,
Hibberd M,
Vingerling JR,
Klaver CC,
Jansonius NM,
Tai ES,
Wong TY,
van Duijn CM,
Aung T
Human molecular genetics · 2011 · PMID 21307088
페이지 2개
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
Schumann G,
Coin LJ,
Lourdusamy A,
Charoen P,
Berger KH,
Stacey D,
Desrivières S,
Aliev FA,
Khan AA,
Amin N,
Aulchenko YS,
Bakalkin G
외 104명 — 모두 보기
Bakker SJ,
Balkau B,
Beulens JW,
Bilbao A,
de Boer RA,
Beury D,
Bots ML,
Breetvelt EJ,
Cauchi S,
Cavalcanti-Proença C,
Chambers JC,
Clarke TK,
Dahmen N,
de Geus EJ,
Dick D,
Ducci F,
Easton A,
Edenberg HJ,
Esko T,
Fernández-Medarde A,
Foroud T,
Freimer NB,
Girault JA,
Grobbee DE,
Guarrera S,
Gudbjartsson DF,
Hartikainen AL,
Heath AC,
Hesselbrock V,
Hofman A,
Hottenga JJ,
Isohanni MK,
Kaprio J,
Khaw KT,
Kuehnel B,
Laitinen J,
Lobbens S,
Luan J,
Mangino M,
Maroteaux M,
Matullo G,
McCarthy MI,
Mueller C,
Navis G,
Numans ME,
Núñez A,
Nyholt DR,
Onland-Moret CN,
Oostra BA,
O'Reilly PF,
Palkovits M,
Penninx BW,
Polidoro S,
Pouta A,
Prokopenko I,
Ricceri F,
Santos E,
Smit JH,
Soranzo N,
Song K,
Sovio U,
Stumvoll M,
Surakk I,
Thorgeirsson TE,
Thorsteinsdottir U,
Troakes C,
Tyrfingsson T,
Tönjes A,
Uiterwaal CS,
Uitterlinden AG,
van der Harst P,
van der Schouw YT,
Staehlin O,
Vogelzangs N,
Vollenweider P,
Waeber G,
Wareham NJ,
Waterworth DM,
Whitfield JB,
Wichmann EH,
Willemsen G,
Witteman JC,
Yuan X,
Zhai G,
Zhao JH,
Zhang W,
Martin NG,
Metspalu A,
Doering A,
Scott J,
Spector TD,
Loos RJ,
Boomsma DI,
Mooser V,
Peltonen L,
Stefansson K,
van Duijn CM,
Vineis P,
Sommer WH,
Kooner JS,
Spanagel R,
Heberlein UA,
Jarvelin MR,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2011 · PMID 21471458
페이지 2개
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
Grallert H,
Dupuis J,
Bis JC,
Dehghan A,
Barbalic M,
Baumert J,
Lu C,
Smith NL,
Uitterlinden AG,
Roberts R,
Khuseyinova N,
Schnabel RB
외 33명 — 모두 보기
Rice KM,
Rivadeneira F,
Hoogeveen RC,
Fontes JD,
Meisinger C,
Keaney JF Jr,
Lemaitre R,
Aulchenko YS,
Vasan RS,
Ellis S,
Hazen SL,
van Duijn CM,
Nelson JJ,
März W,
Schunkert H,
McPherson RM,
Stirnadel-Farrant HA,
Psaty BM,
Gieger C,
Siscovick D,
Hofman A,
Illig T,
Cushman M,
Yamamoto JF,
Rotter JI,
Larson MG,
Stewart AF,
Boerwinkle E,
Witteman JC,
Tracy RP,
Koenig W,
Benjamin EJ,
Ballantyne CM
European heart journal · 2012 · PMID 22003152
페이지 2개
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Bis JC,
DeCarli C,
Smith AV,
van der Lijn F,
Crivello F,
Fornage M,
Debette S,
Shulman JM,
Schmidt H,
Srikanth V,
Schuur M,
Yu L
외 71명 — 모두 보기
Choi SH,
Sigurdsson S,
Verhaaren BF,
DeStefano AL,
Lambert JC,
Jack CR Jr,
Struchalin M,
Stankovich J,
Ibrahim-Verbaas CA,
Fleischman D,
Zijdenbos A,
den Heijer T,
Mazoyer B,
Coker LH,
Enzinger C,
Danoy P,
Amin N,
Arfanakis K,
van Buchem MA,
de Bruijn RF,
Beiser A,
Dufouil C,
Huang J,
Cavalieri M,
Thomson R,
Niessen WJ,
Chibnik LB,
Gislason GK,
Hofman A,
Pikula A,
Pikula A,
Amouyel P,
Freeman KB,
Phan TG,
Oostra BA,
Stein JL,
Medland SE,
Vasquez AA,
Hibar DP,
Wright MJ,
Franke B,
Martin NG,
Thompson PM,
Nalls MA,
Uitterlinden AG,
Au R,
Elbaz A,
Beare RJ,
van Swieten JC,
Lopez OL,
Harris TB,
Chouraki V,
Breteler MM,
De Jager PL,
Becker JT,
Vernooij MW,
Knopman D,
Fazekas F,
Wolf PA,
van der Lugt A,
Gudnason V,
Longstreth WT Jr,
Brown MA,
Bennett DA,
van Duijn CM,
Mosley TH,
Schmidt R,
Tzourio C,
Launer LJ,
Ikram MA,
Seshadri S
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504421 · open access
페이지 2개
Genome-wide association analysis identifies susceptibility loci for migraine without aura
Freilinger T,
Anttila V,
de Vries B,
Malik R,
Kallela M,
Terwindt GM,
Pozo-Rosich P,
Winsvold B,
Nyholt DR,
van Oosterhout WP,
Artto V,
Todt U
외 31명 — 모두 보기
Hämäläinen E,
Fernández-Morales J,
Louter MA,
Kaunisto MA,
Schoenen J,
Raitakari O,
Lehtimäki T,
Vila-Pueyo M,
Göbel H,
Wichmann E,
Sintas C,
Uitterlinden AG,
Hofman A,
Rivadeneira F,
Heinze A,
Tronvik E,
van Duijn CM,
Kaprio J,
Cormand B,
Wessman M,
Frants RR,
Meitinger T,
Müller-Myhsok B,
Zwart JA,
Färkkilä M,
Macaya A,
Ferrari MD,
Kubisch C,
Palotie A,
Dichgans M,
van den Maagdenberg AM
International Headache Genetics Consortium
Nature genetics · 2012 · PMID 22683712
페이지 2개
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes
Sobrin L,
Ripke S,
Yu Y,
Fagerness J,
Bhangale TR,
Tan PL,
Souied EH,
Buitendijk GH,
Merriam JE,
Richardson AJ,
Raychaudhuri S,
Reynolds R
외 22명 — 모두 보기
Chin KA,
Lee AY,
Leveziel N,
Zack DJ,
Campochiaro P,
Smith RT,
Barile GR,
Hogg RE,
Chakravarthy U,
Behrens TW,
Uitterlinden AG,
van Duijn CM,
Vingerling JR,
Brantley MA Jr,
Baird PN,
Klaver CC,
Allikmets R,
Katsanis N,
Graham RR,
Ioannidis JP,
Daly MJ,
Seddon JM
Ophthalmology · 2012 · PMID 22705344
페이지 2개
Genetic variation associated with circulating monocyte count in the eMERGE Network
Crosslin DR,
McDavid A,
Weston N,
Zheng X,
Hart E,
de Andrade M,
Kullo IJ,
McCarty CA,
Doheny KF,
Pugh E,
Kho A,
Hayes MG
외 52명 — 모두 보기
Ritchie MD,
Saip A,
Crawford DC,
Crane PK,
Newton K,
Carrell DS,
Gallego CJ,
Nalls MA,
Li R,
Mirel DB,
Crenshaw A,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Zakai NA,
Yango Q,
Garcia M,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Felix JF,
Dehghan A,
Wilson JG,
Bis JC,
Fox CS,
Glazer NL,
Cupples LA,
Coresh J,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK,
Larson EB,
Carlson CS,
Jarvik GP
CHARGE Hematology Working Group · electronic Medical Records and Genomics (eMERGE) Network
Human molecular genetics · 2013 · PMID 23314186
페이지 2개
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
Cheng CY,
Schache M,
Ikram MK,
Young TL,
Guggenheim JA,
Vitart V,
MacGregor S,
Verhoeven VJ,
Barathi VA,
Liao J,
Hysi PG,
Bailey-Wilson JE
외 96명 — 모두 보기
St Pourcain B,
Kemp JP,
McMahon G,
Timpson NJ,
Evans DM,
Montgomery GW,
Mishra A,
Wang YX,
Wang JJ,
Rochtchina E,
Polasek O,
Wright AF,
Amin N,
van Leeuwen EM,
Wilson JF,
Pennell CE,
van Duijn CM,
de Jong PT,
Vingerling JR,
Zhou X,
Chen P,
Li R,
Tay WT,
Zheng Y,
Chew M,
Burdon KP,
Craig JE,
Iyengar SK,
Igo RP Jr,
Lass JH Jr,
Chew EY,
Haller T,
Mihailov E,
Metspalu A,
Wedenoja J,
Simpson CL,
Wojciechowski R,
Höhn R,
Mirshahi A,
Zeller T,
Pfeiffer N,
Lackner KJ,
Bettecken T,
Meitinger T,
Oexle K,
Pirastu M,
Portas L,
Nag A,
Williams KM,
Yonova-Doing E,
Klein R,
Klein BE,
Hosseini SM,
Paterson AD,
Makela KM,
Lehtimaki T,
Kahonen M,
Raitakari O,
Yoshimura N,
Matsuda F,
Chen LJ,
Pang CP,
Yip SP,
Yap MK,
Meguro A,
Mizuki N,
Inoko H,
Foster PJ,
Zhao JH,
Vithana E,
Tai ES,
Fan Q,
Xu L,
Campbell H,
Fleck B,
Rudan I,
Aung T,
Hofman A,
Uitterlinden AG,
Bencic G,
Khor CC,
Forward H,
Pärssinen O,
Mitchell P,
Rivadeneira F,
Hewitt AW,
Williams C,
Oostra BA,
Teo YY,
Hammond CJ,
Stambolian D,
Mackey DA,
Klaver CC,
Wong TY,
Saw SM,
Baird PN
Consortium for Refractive Error and Myopia · Fuchs' Genetics Multi-Center Study Group 외 컨소시엄 2곳
American journal of human genetics · 2013 · PMID 24144296
페이지 2개
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age
Deelen J,
Beekman M,
Uh HW,
Broer L,
Ayers KL,
Tan Q,
Kamatani Y,
Bennet AM,
Tamm R,
Trompet S,
Guðbjartsson DF,
Flachsbart F
외 75명 — 모두 보기
Rose G,
Viktorin A,
Fischer K,
Nygaard M,
Cordell HJ,
Crocco P,
van den Akker EB,
Böhringer S,
Helmer Q,
Nelson CP,
Saunders GI,
Alver M,
Andersen-Ranberg K,
Breen ME,
van der Breggen R,
Caliebe A,
Capri M,
Cevenini E,
Collerton JC,
Dato S,
Davies K,
Ford I,
Gampe J,
Garagnani P,
de Geus EJ,
Harrow J,
van Heemst D,
Heijmans BT,
Heinsen FA,
Hottenga JJ,
Hofman A,
Jeune B,
Jonsson PV,
Lathrop M,
Lechner D,
Martin-Ruiz C,
Mcnerlan SE,
Mihailov E,
Montesanto A,
Mooijaart SP,
Murphy A,
Nohr EA,
Paternoster L,
Postmus I,
Rivadeneira F,
Ross OA,
Salvioli S,
Sattar N,
Schreiber S,
Stefánsson H,
Stott DJ,
Tiemeier H,
Uitterlinden AG,
Westendorp RG,
Willemsen G,
Samani NJ,
Galan P,
Sørensen TI,
Boomsma DI,
Jukema JW,
Rea IM,
Passarino G,
de Craen AJ,
Christensen K,
Nebel A,
Stefánsson K,
Metspalu A,
Magnusson P,
Blanché H,
Christiansen L,
Kirkwood TB,
van Duijn CM,
Franceschi C,
Houwing-Duistermaat JJ,
Slagboom PE
Human molecular genetics · 2014 · PMID 24688116 · open access
페이지 2개
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Springelkamp H,
Höhn R,
Mishra A,
Hysi PG,
Khor CC,
Loomis SJ,
Bailey JN,
Gibson J,
Thorleifsson G,
Janssen SF,
Luo X,
Ramdas WD
외 66명 — 모두 보기
Vithana E,
Nongpiur ME,
Montgomery GW,
Xu L,
Mountain JE,
Gharahkhani P,
Lu Y,
Amin N,
Karssen LC,
Sim KS,
van Leeuwen EM,
Iglesias AI,
Verhoeven VJ,
Hauser MA,
Loon SC,
Despriet DD,
Nag A,
Venturini C,
Sanfilippo PG,
Schillert A,
Kang JH,
Landers J,
Jonasson F,
Cree AJ,
van Koolwijk LM,
Rivadeneira F,
Souzeau E,
Jonsson V,
Menon G,
Weinreb RN,
de Jong PT,
Oostra BA,
Uitterlinden AG,
Hofman A,
Ennis S,
Thorsteinsdottir U,
Burdon KP,
Spector TD,
Mirshahi A,
Saw SM,
Vingerling JR,
Teo YY,
Haines JL,
Wolfs RC,
Lemij HG,
Tai ES,
Jansonius NM,
Jonas JB,
Cheng CY,
Aung T,
Viswanathan AC,
Klaver CC,
Craig JE,
Macgregor S,
Mackey DA,
Lotery AJ,
Stefansson K,
Bergen AA,
Young TL,
Wiggs JL,
Pfeiffer N,
Wong TY,
Pasquale LR,
Hewitt AW,
van Duijn CM,
Hammond CJ
Blue Mountains Eye Study—GWAS group · NEIGHBORHOOD Consortium 외 컨소시엄 1곳
Nature communications · 2014 · PMID 25241763 · open access
페이지 2개
A novel common variant in DCST2 is associated with length in early life and height in adulthood
van der Valk RJ,
Kreiner-Møller E,
Kooijman MN,
Guxens M,
Stergiakouli E,
Sääf A,
Bradfield JP,
Geller F,
Hayes MG,
Cousminer DL,
Körner A,
Thiering E
외 105명 — 모두 보기
Curtin JA,
Myhre R,
Huikari V,
Joro R,
Kerkhof M,
Warrington NM,
Pitkänen N,
Ntalla I,
Horikoshi M,
Veijola R,
Freathy RM,
Teo YY,
Barton SJ,
Evans DM,
Kemp JP,
St Pourcain B,
Ring SM,
Davey Smith G,
Bergström A,
Kull I,
Hakonarson H,
Mentch FD,
Bisgaard H,
Chawes B,
Stokholm J,
Waage J,
Eriksen P,
Sevelsted A,
Melbye M,
van Duijn CM,
Medina-Gomez C,
Hofman A,
de Jongste JC,
Taal HR,
Uitterlinden AG,
Armstrong LL,
Eriksson J,
Palotie A,
Bustamante M,
Estivill X,
Gonzalez JR,
Llop S,
Kiess W,
Mahajan A,
Flexeder C,
Tiesler CM,
Murray CS,
Simpson A,
Magnus P,
Sengpiel V,
Hartikainen AL,
Keinanen-Kiukaanniemi S,
Lewin A,
Da Silva Couto Alves A,
Blakemore AI,
Buxton JL,
Kaakinen M,
Rodriguez A,
Sebert S,
Vaarasmaki M,
Lakka T,
Lindi V,
Gehring U,
Postma DS,
Ang W,
Newnham JP,
Lyytikäinen LP,
Pahkala K,
Raitakari OT,
Panoutsopoulou K,
Zeggini E,
Boomsma DI,
Groen-Blokhuis M,
Ilonen J,
Franke L,
Hirschhorn JN,
Pers TH,
Liang L,
Huang J,
Hocher B,
Knip M,
Saw SM,
Holloway JW,
Melén E,
Grant SF,
Feenstra B,
Lowe WL,
Widén E,
Sergeyev E,
Grallert H,
Custovic A,
Jacobsson B,
Jarvelin MR,
Atalay M,
Koppelman GH,
Pennell CE,
Niinikoski H,
Dedoussis GV,
Mccarthy MI,
Frayling TM,
Sunyer J,
Timpson NJ,
Rivadeneira F,
Bønnelykke K,
Jaddoe VW
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium 외 컨소시엄 1곳
Human molecular genetics · 2015 · PMID 25281659 · open access
페이지 2개
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Cornelis MC,
Byrne EM,
Esko T,
Nalls MA,
Ganna A,
Paynter N,
Monda KL,
Amin N,
Fischer K,
Renstrom F,
Ngwa JS,
Huikari V
외 142명 — 모두 보기
Cavadino A,
Nolte IM,
Teumer A,
Yu K,
Marques-Vidal P,
Rawal R,
Manichaikul A,
Wojczynski MK,
Vink JM,
Zhao JH,
Burlutsky G,
Lahti J,
Mikkilä V,
Lemaitre RN,
Eriksson J,
Musani SK,
Tanaka T,
Geller F,
Luan J,
Hui J,
Mägi R,
Dimitriou M,
Garcia ME,
Ho WK,
Wright MJ,
Rose LM,
Magnusson PK,
Pedersen NL,
Couper D,
Oostra BA,
Hofman A,
Ikram MA,
Tiemeier HW,
Uitterlinden AG,
van Rooij FJ,
Barroso I,
Johansson I,
Xue L,
Kaakinen M,
Milani L,
Power C,
Snieder H,
Stolk RP,
Baumeister SE,
Biffar R,
Gu F,
Bastardot F,
Kutalik Z,
Jacobs DR Jr,
Forouhi NG,
Mihailov E,
Lind L,
Lindgren C,
Michaëlsson K,
Morris A,
Jensen M,
Khaw KT,
Luben RN,
Wang JJ,
Männistö S,
Perälä MM,
Kähönen M,
Lehtimäki T,
Viikari J,
Mozaffarian D,
Mukamal K,
Psaty BM,
Döring A,
Heath AC,
Montgomery GW,
Dahmen N,
Carithers T,
Tucker KL,
Ferrucci L,
Boyd HA,
Melbye M,
Treur JL,
Mellström D,
Hottenga JJ,
Prokopenko I,
Tönjes A,
Deloukas P,
Kanoni S,
Lorentzon M,
Houston DK,
Liu Y,
Danesh J,
Rasheed A,
Mason MA,
Zonderman AB,
Franke L,
Kristal BS,
Karjalainen J,
Reed DR,
Westra HJ,
Evans MK,
Saleheen D,
Harris TB,
Dedoussis G,
Curhan G,
Stumvoll M,
Beilby J,
Pasquale LR,
Feenstra B,
Bandinelli S,
Ordovas JM,
Chan AT,
Peters U,
Ohlsson C,
Gieger C,
Martin NG,
Waldenberger M,
Siscovick DS,
Raitakari O,
Eriksson JG,
Mitchell P,
Hunter DJ,
Kraft P,
Rimm EB,
Boomsma DI,
Borecki IB,
Loos RJ,
Wareham NJ,
Vollenweider P,
Caporaso N,
Grabe HJ,
Neuhouser ML,
Wolffenbuttel BH,
Hu FB,
Hyppönen E,
Järvelin MR,
Cupples LA,
Franks PW,
Ridker PM,
van Duijn CM,
Heiss G,
Metspalu A,
North KE,
Ingelsson E,
Nettleton JA,
van Dam RM,
Chasman DI
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) 외 컨소시엄 2곳
Molecular psychiatry · 2015 · PMID 25288136
페이지 2개
Genetic studies of body mass index yield new insights for obesity biology
Locke AE,
Kahali B,
Berndt SI,
Justice AE,
Pers TH,
Day FR,
Powell C,
Vedantam S,
Buchkovich ML,
Yang J,
Croteau-Chonka DC,
Esko T
외 470명 — 모두 보기
Fall T,
Ferreira T,
Gustafsson S,
Kutalik Z,
Luan J,
Mägi R,
Randall JC,
Winkler TW,
Wood AR,
Workalemahu T,
Faul JD,
Smith JA,
Zhao JH,
Zhao W,
Chen J,
Fehrmann R,
Hedman ÅK,
Karjalainen J,
Schmidt EM,
Absher D,
Amin N,
Anderson D,
Beekman M,
Bolton JL,
Bragg-Gresham JL,
Buyske S,
Demirkan A,
Deng G,
Ehret GB,
Feenstra B,
Feitosa MF,
Fischer K,
Goel A,
Gong J,
Jackson AU,
Kanoni S,
Kleber ME,
Kristiansson K,
Lim U,
Lotay V,
Mangino M,
Leach IM,
Medina-Gomez C,
Medland SE,
Nalls MA,
Palmer CD,
Pasko D,
Pechlivanis S,
Peters MJ,
Prokopenko I,
Shungin D,
Stančáková A,
Strawbridge RJ,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van Setten J,
Van Vliet-Ostaptchouk JV,
Wang Z,
Yengo L,
Zhang W,
Isaacs A,
Albrecht E,
Ärnlöv J,
Arscott GM,
Attwood AP,
Bandinelli S,
Barrett A,
Bas IN,
Bellis C,
Bennett AJ,
Berne C,
Blagieva R,
Blüher M,
Böhringer S,
Bonnycastle LL,
Böttcher Y,
Boyd HA,
Bruinenberg M,
Caspersen IH,
Chen YI,
Clarke R,
Daw EW,
de Craen AJM,
Delgado G,
Dimitriou M,
Doney ASF,
Eklund N,
Estrada K,
Eury E,
Folkersen L,
Fraser RM,
Garcia ME,
Geller F,
Giedraitis V,
Gigante B,
Go AS,
Golay A,
Goodall AH,
Gordon SD,
Gorski M,
Grabe HJ,
Grallert H,
Grammer TB,
Gräßler J,
Grönberg H,
Groves CJ,
Gusto G,
Haessler J,
Hall P,
Haller T,
Hallmans G,
Hartman CA,
Hassinen M,
Hayward C,
Heard-Costa NL,
Helmer Q,
Hengstenberg C,
Holmen O,
Hottenga JJ,
James AL,
Jeff JM,
Johansson Å,
Jolley J,
Juliusdottir T,
Kinnunen L,
Koenig W,
Koskenvuo M,
Kratzer W,
Laitinen J,
Lamina C,
Leander K,
Lee NR,
Lichtner P,
Lind L,
Lindström J,
Lo KS,
Lobbens S,
Lorbeer R,
Lu Y,
Mach F,
Magnusson PKE,
Mahajan A,
McArdle WL,
McLachlan S,
Menni C,
Merger S,
Mihailov E,
Milani L,
Moayyeri A,
Monda KL,
Morken MA,
Mulas A,
Müller G,
Müller-Nurasyid M,
Musk AW,
Nagaraja R,
Nöthen MM,
Nolte IM,
Pilz S,
Rayner NW,
Renstrom F,
Rettig R,
Ried JS,
Ripke S,
Robertson NR,
Rose LM,
Sanna S,
Scharnagl H,
Scholtens S,
Schumacher FR,
Scott WR,
Seufferlein T,
Shi J,
Smith AV,
Smolonska J,
Stanton AV,
Steinthorsdottir V,
Stirrups K,
Stringham HM,
Sundström J,
Swertz MA,
Swift AJ,
Syvänen AC,
Tan ST,
Tayo BO,
Thorand B,
Thorleifsson G,
Tyrer JP,
Uh HW,
Vandenput L,
Verhulst FC,
Vermeulen SH,
Verweij N,
Vonk JM,
Waite LL,
Warren HR,
Waterworth D,
Weedon MN,
Wilkens LR,
Willenborg C,
Wilsgaard T,
Wojczynski MK,
Wong A,
Wright AF,
Zhang Q,
Brennan EP,
Choi M,
Dastani Z,
Drong AW,
Eriksson P,
Franco-Cereceda A,
Gådin JR,
Gharavi AG,
Goddard ME,
Handsaker RE,
Huang J,
Karpe F,
Kathiresan S,
Keildson S,
Kiryluk K,
Kubo M,
Lee JY,
Liang L,
Lifton RP,
Ma B,
McCarroll SA,
McKnight AJ,
Min JL,
Moffatt MF,
Montgomery GW,
Murabito JM,
Nicholson G,
Nyholt DR,
Okada Y,
Perry JRB,
Dorajoo R,
Reinmaa E,
Salem RM,
Sandholm N,
Scott RA,
Stolk L,
Takahashi A,
Tanaka T,
van 't Hooft FM,
Vinkhuyzen AAE,
Westra HJ,
Zheng W,
Zondervan KT,
Heath AC,
Arveiler D,
Bakker SJL,
Beilby J,
Bergman RN,
Blangero J,
Bovet P,
Campbell H,
Caulfield MJ,
Cesana G,
Chakravarti A,
Chasman DI,
Chines PS,
Collins FS,
Crawford DC,
Cupples LA,
Cusi D,
Danesh J,
de Faire U,
den Ruijter HM,
Dominiczak AF,
Erbel R,
Erdmann J,
Eriksson JG,
Farrall M,
Felix SB,
Ferrannini E,
Ferrières J,
Ford I,
Forouhi NG,
Forrester T,
Franco OH,
Gansevoort RT,
Gejman PV,
Gieger C,
Gottesman O,
Gudnason V,
Gyllensten U,
Hall AS,
Harris TB,
Hattersley AT,
Hicks AA,
Hindorff LA,
Hingorani AD,
Hofman A,
Homuth G,
Hovingh GK,
Humphries SE,
Hunt SC,
Hyppönen E,
Illig T,
Jacobs KB,
Jarvelin MR,
Jöckel KH,
Johansen B,
Jousilahti P,
Jukema JW,
Jula AM,
Kaprio J,
Kastelein JJP,
Keinanen-Kiukaanniemi SM,
Kiemeney LA,
Knekt P,
Kooner JS,
Kooperberg C,
Kovacs P,
Kraja AT,
Kumari M,
Kuusisto J,
Lakka TA,
Langenberg C,
Marchand LL,
Lehtimäki T,
Lyssenko V,
Männistö S,
Marette A,
Matise TC,
McKenzie CA,
McKnight B,
Moll FL,
Morris AD,
Morris AP,
Murray JC,
Nelis M,
Ohlsson C,
Oldehinkel AJ,
Ong KK,
Madden PAF,
Pasterkamp G,
Peden JF,
Peters A,
Postma DS,
Pramstaller PP,
Price JF,
Qi L,
Raitakari OT,
Rankinen T,
Rao DC,
Rice TK,
Ridker PM,
Rioux JD,
Ritchie MD,
Rudan I,
Salomaa V,
Samani NJ,
Saramies J,
Sarzynski MA,
Schunkert H,
Schwarz PEH,
Sever P,
Shuldiner AR,
Sinisalo J,
Stolk RP,
Strauch K,
Tönjes A,
Trégouët DA,
Tremblay A,
Tremoli E,
Virtamo J,
Vohl MC,
Völker U,
Waeber G,
Willemsen G,
Witteman JC,
Zillikens MC,
Adair LS,
Amouyel P,
Asselbergs FW,
Assimes TL,
Bochud M,
Boehm BO,
Boerwinkle E,
Bornstein SR,
Bottinger EP,
Bouchard C,
Cauchi S,
Chambers JC,
Chanock SJ,
Cooper RS,
de Bakker PIW,
Dedoussis G,
Ferrucci L,
Franks PW,
Froguel P,
Groop LC,
Haiman CA,
Hamsten A,
Hui J,
Hunter DJ,
Hveem K,
Kaplan RC,
Kivimaki M,
Kuh D,
Laakso M,
Liu Y,
Martin NG,
März W,
Melbye M,
Metspalu A,
Moebus S,
Munroe PB,
Njølstad I,
Oostra BA,
Palmer CNA,
Pedersen NL,
Perola M,
Pérusse L,
Peters U,
Power C,
Quertermous T,
Rauramaa R,
Rivadeneira F,
Saaristo TE,
Saleheen D,
Sattar N,
Schadt EE,
Schlessinger D,
Slagboom PE,
Snieder H,
Spector TD,
Thorsteinsdottir U,
Stumvoll M,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van der Harst P,
Walker M,
Wallaschofski H,
Wareham NJ,
Watkins H,
Weir DR,
Wichmann HE,
Wilson JF,
Zanen P,
Borecki IB,
Deloukas P,
Fox CS,
Heid IM,
O'Connell JR,
Strachan DP,
Stefansson K,
van Duijn CM,
Abecasis GR,
Franke L,
Frayling TM,
McCarthy MI,
Visscher PM,
Scherag A,
Willer CJ,
Boehnke M,
Mohlke KL,
Lindgren CM,
Beckmann JS,
Barroso I,
North KE,
Ingelsson E,
Hirschhorn JN,
Loos RJF,
Speliotes EK
LifeLines Cohort Study · ADIPOGen Consortium 외 컨소시엄 12곳
Nature · 2015 · PMID 25673413
페이지 2개
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
van Leeuwen EM,
Sabo A,
Bis JC,
Huffman JE,
Manichaikul A,
Smith AV,
Feitosa MF,
Demissie S,
Joshi PK,
Duan Q,
Marten J,
van Klinken JB
외 86명 — 모두 보기
Surakka I,
Nolte IM,
Zhang W,
Mbarek H,
Li-Gao R,
Trompet S,
Verweij N,
Evangelou E,
Lyytikäinen LP,
Tayo BO,
Deelen J,
van der Most PJ,
van der Laan SW,
Arking DE,
Morrison A,
Dehghan A,
Franco OH,
Hofman A,
Rivadeneira F,
Sijbrands EJ,
Uitterlinden AG,
Mychaleckyj JC,
Campbell A,
Hocking LJ,
Padmanabhan S,
Brody JA,
Rice KM,
White CC,
Harris T,
Isaacs A,
Campbell H,
Lange LA,
Rudan I,
Kolcic I,
Navarro P,
Zemunik T,
Salomaa V,
Kooner AS,
Kooner JS,
Lehne B,
Scott WR,
Tan ST,
de Geus EJ,
Milaneschi Y,
Penninx BW,
Willemsen G,
de Mutsert R,
Ford I,
Gansevoort RT,
Segura-Lepe MP,
Raitakari OT,
Viikari JS,
Nikus K,
Forrester T,
McKenzie CA,
de Craen AJ,
de Ruijter HM,
Pasterkamp G,
Snieder H,
Oldehinkel AJ,
Slagboom PE,
Cooper RS,
Kähönen M,
Lehtimäki T,
Elliott P,
van der Harst P,
Jukema JW,
Mook-Kanamori DO,
Boomsma DI,
Chambers JC,
Swertz M,
Ripatti S,
Willems van Dijk K,
Vitart V,
Polasek O,
Hayward C,
Wilson JG,
Wilson JF,
Gudnason V,
Rich SS,
Psaty BM,
Borecki IB,
Boerwinkle E,
Rotter JI,
Cupples LA,
van Duijn CM
LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
페이지 2개
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
Iotchkova V,
Huang J,
Morris JA,
Jain D,
Barbieri C,
Walter K,
Min JL,
Chen L,
Astle W,
Cocca M,
Deelen P,
Elding H
외 55명 — 모두 보기
Farmaki AE,
Franklin CS,
Franberg M,
Gaunt TR,
Hofman A,
Jiang T,
Kleber ME,
Lachance G,
Luan J,
Malerba G,
Matchan A,
Mead D,
Memari Y,
Ntalla I,
Panoutsopoulou K,
Pazoki R,
Perry JRB,
Rivadeneira F,
Sabater-Lleal M,
Sennblad B,
Shin SY,
Southam L,
Traglia M,
van Dijk F,
van Leeuwen EM,
Zaza G,
Zhang W,
Amin N,
Butterworth A,
Chambers JC,
Dedoussis G,
Dehghan A,
Franco OH,
Franke L,
Frontini M,
Gambaro G,
Gasparini P,
Hamsten A,
Issacs A,
Kooner JS,
Kooperberg C,
Langenberg C,
Marz W,
Scott RA,
Swertz MA,
Toniolo D,
Uitterlinden AG,
van Duijn CM,
Watkins H,
Zeggini E,
Maurano MT,
Timpson NJ,
Reiner AP,
Auer PL,
Soranzo N
UK10K Consortium
Nature genetics · 2016 · PMID 27668658
페이지 2개
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