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성함이나 학술지명, PMID로 찾아보십시오.
Van Duijn CM에 대해
171건, 그중 20건 표시.
Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology
Spracklen CN,
Karaderi T,
Yaghootkar H,
Schurmann C,
Fine RS,
Kutalik Z,
Preuss MH,
Lu Y,
Wittemans LBL,
Adair LS,
Allison M,
Amin N
외 92명 — 모두 보기
Auer PL,
Bartz TM,
Blüher M,
Boehnke M,
Borja JB,
Bork-Jensen J,
Broer L,
Chasman DI,
Chen YI,
Chirstofidou P,
Demirkan A,
van Duijn CM,
Feitosa MF,
Garcia ME,
Graff M,
Grallert H,
Grarup N,
Guo X,
Haesser J,
Hansen T,
Harris TB,
Highland HM,
Hong J,
Ikram MA,
Ingelsson E,
Jackson R,
Jousilahti P,
Kähönen M,
Kizer JR,
Kovacs P,
Kriebel J,
Laakso M,
Lange LA,
Lehtimäki T,
Li J,
Li-Gao R,
Lind L,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mackey DA,
Mahajan A,
Mangino M,
Männistö S,
McCarthy MI,
McKnight B,
Medina-Gomez C,
Meigs JB,
Molnos S,
Mook-Kanamori D,
Morris AP,
de Mutsert R,
Nalls MA,
Nedeljkovic I,
North KE,
Pennell CE,
Pradhan AD,
Province MA,
Raitakari OT,
Raulerson CK,
Reiner AP,
Ridker PM,
Ripatti S,
Roberston N,
Rotter JI,
Salomaa V,
Sandoval-Zárate AA,
Sitlani CM,
Spector TD,
Strauch K,
Stumvoll M,
Taylor KD,
Thuesen B,
Tönjes A,
Uitterlinden AG,
Venturini C,
Walker M,
Wang CA,
Wang S,
Wareham NJ,
Willems SM,
Willems van Dijk K,
Wilson JG,
Wu Y,
Yao J,
Young KL,
Langenberg C,
Frayling TM,
Kilpeläinen TO,
Lindgren CM,
Loos RJF,
Mohlke KL
American journal of human genetics · 2019 · PMID 31178129
페이지 2개
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
Armstrong NJ,
Mather KA,
Sargurupremraj M,
Knol MJ,
Malik R,
Satizabal CL,
Yanek LR,
Wen W,
Gudnason VG,
Dueker ND,
Elliott LT,
Hofer E
외 74명 — 모두 보기
Bis J,
Jahanshad N,
Li S,
Logue MA,
Luciano M,
Scholz M,
Smith AV,
Trompet S,
Vojinovic D,
Xia R,
Alfaro-Almagro F,
Ames D,
Amin N,
Amouyel P,
Beiser AS,
Brodaty H,
Deary IJ,
Fennema-Notestine C,
Gampawar PG,
Gottesman R,
Griffanti L,
Jack CR Jr,
Jenkinson M,
Jiang J,
Kral BG,
Kwok JB,
Lampe L,
C M Liewald D,
Maillard P,
Marchini J,
Bastin ME,
Mazoyer B,
Pirpamer L,
Rafael Romero J,
Roshchupkin GV,
Schofield PR,
Schroeter ML,
Stott DJ,
Thalamuthu A,
Trollor J,
Tzourio C,
van der Grond J,
Vernooij MW,
Witte VA,
Wright MJ,
Yang Q,
Morris Z,
Siggurdsson S,
Psaty B,
Villringer A,
Schmidt H,
Haberg AK,
van Duijn CM,
Jukema JW,
Dichgans M,
Sacco RL,
Wright CB,
Kremen WS,
Becker LC,
Thompson PM,
Mosley TH,
Wardlaw JM,
Ikram MA,
Adams HHH,
Seshadri S,
Sachdev PS,
Smith SM,
Launer L,
Longstreth W,
DeCarli C,
Schmidt R,
Fornage M,
Debette S,
Nyquist PA
Stroke · 2020 · PMID 32517579
페이지 2개
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study
Jones E,
Hummerich H,
Viré E,
Uphill J,
Dimitriadis A,
Speedy H,
Campbell T,
Norsworthy P,
Quinn L,
Whitfield J,
Linehan J,
Jaunmuktane Z
외 53명 — 모두 보기
Brandner S,
Jat P,
Nihat A,
How Mok T,
Ahmed P,
Collins S,
Stehmann C,
Sarros S,
Kovacs GG,
Geschwind MD,
Golubjatnikov A,
Frontzek K,
Budka H,
Aguzzi A,
Karamujić-Čomić H,
van der Lee SJ,
Ibrahim-Verbaas CA,
van Duijn CM,
Sikorska B,
Golanska E,
Liberski PP,
Calero M,
Calero O,
Sanchez-Juan P,
Salas A,
Martinón-Torres F,
Bouaziz-Amar E,
Haïk S,
Laplanche JL,
Brandel JP,
Amouyel P,
Lambert JC,
Parchi P,
Bartoletti-Stella A,
Capellari S,
Poleggi A,
Ladogana A,
Pocchiari M,
Aneli S,
Matullo G,
Knight R,
Zafar S,
Zerr I,
Booth S,
Coulthart MB,
Jansen GH,
Glisic K,
Blevins J,
Gambetti P,
Safar J,
Appleby B,
Collinge J,
Mead S
The Lancet. Neurology · 2020 · PMID 32949544
페이지 2개
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Willer CJ,
Speliotes EK,
Loos RJ,
Li S,
Lindgren CM,
Heid IM,
Berndt SI,
Elliott AL,
Jackson AU,
Lamina C,
Lettre G,
Lim N
외 133명 — 모두 보기
Lyon HN,
McCarroll SA,
Papadakis K,
Qi L,
Randall JC,
Roccasecca RM,
Sanna S,
Scheet P,
Weedon MN,
Wheeler E,
Zhao JH,
Jacobs LC,
Prokopenko I,
Soranzo N,
Tanaka T,
Timpson NJ,
Almgren P,
Bennett A,
Bergman RN,
Bingham SA,
Bonnycastle LL,
Brown M,
Burtt NP,
Chines P,
Coin L,
Collins FS,
Connell JM,
Cooper C,
Smith GD,
Dennison EM,
Deodhar P,
Elliott P,
Erdos MR,
Estrada K,
Evans DM,
Gianniny L,
Gieger C,
Gillson CJ,
Guiducci C,
Hackett R,
Hadley D,
Hall AS,
Havulinna AS,
Hebebrand J,
Hofman A,
Isomaa B,
Jacobs KB,
Johnson T,
Jousilahti P,
Jovanovic Z,
Khaw KT,
Kraft P,
Kuokkanen M,
Kuusisto J,
Laitinen J,
Lakatta EG,
Luan J,
Luben RN,
Mangino M,
McArdle WL,
Meitinger T,
Mulas A,
Munroe PB,
Narisu N,
Ness AR,
Northstone K,
O'Rahilly S,
Purmann C,
Rees MG,
Ridderstråle M,
Ring SM,
Rivadeneira F,
Ruokonen A,
Sandhu MS,
Saramies J,
Scott LJ,
Scuteri A,
Silander K,
Sims MA,
Song K,
Stephens J,
Stevens S,
Stringham HM,
Tung YC,
Valle TT,
Van Duijn CM,
Vimaleswaran KS,
Vollenweider P,
Waeber G,
Wallace C,
Watanabe RM,
Waterworth DM,
Watkins N,
Witteman JC,
Zeggini E,
Zhai G,
Zillikens MC,
Altshuler D,
Caulfield MJ,
Chanock SJ,
Farooqi IS,
Ferrucci L,
Guralnik JM,
Hattersley AT,
Hu FB,
Jarvelin MR,
Laakso M,
Mooser V,
Ong KK,
Ouwehand WH,
Salomaa V,
Samani NJ,
Spector TD,
Tuomi T,
Tuomilehto J,
Uda M,
Uitterlinden AG,
Wareham NJ,
Deloukas P,
Frayling TM,
Groop LC,
Hayes RB,
Hunter DJ,
Mohlke KL,
Peltonen L,
Schlessinger D,
Strachan DP,
Wichmann HE,
McCarthy MI,
Boehnke M,
Barroso I,
Abecasis GR,
Hirschhorn JN
Wellcome Trust Case Control Consortium · Genetic Investigation of ANthropometric Traits Consortium
Nature genetics · 2009 · PMID 19079261
페이지 1개
Genome-wide association meta-analysis for total serum bilirubin levels
Johnson AD,
Kavousi M,
Smith AV,
Chen MH,
Dehghan A,
Aspelund T,
Lin JP,
van Duijn CM,
Harris TB,
Cupples LA,
Uitterlinden AG,
Launer L
외 7명 — 모두 보기
Human molecular genetics · 2009 · PMID 19414484
페이지 1개
Multiple loci associated with indices of renal function and chronic kidney disease
Köttgen A,
Glazer NL,
Dehghan A,
Hwang SJ,
Katz R,
Li M,
Yang Q,
Gudnason V,
Launer LJ,
Harris TB,
Smith AV,
Arking DE
외 27명 — 모두 보기
Astor BC,
Boerwinkle E,
Ehret GB,
Ruczinski I,
Scharpf RB,
Chen YD,
de Boer IH,
Haritunians T,
Lumley T,
Sarnak M,
Siscovick D,
Benjamin EJ,
Levy D,
Upadhyay A,
Aulchenko YS,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
van Duijn CM,
Chasman DI,
Paré G,
Ridker PM,
Kao WH,
Witteman JC,
Coresh J,
Shlipak MG,
Fox CS
Nature genetics · 2009 · PMID 19430482
페이지 1개
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium
Heard-Costa NL,
Zillikens MC,
Monda KL,
Johansson A,
Harris TB,
Fu M,
Haritunians T,
Feitosa MF,
Aspelund T,
Eiriksdottir G,
Garcia M,
Launer LJ
외 49명 — 모두 보기
Smith AV,
Mitchell BD,
McArdle PF,
Shuldiner AR,
Bielinski SJ,
Boerwinkle E,
Brancati F,
Demerath EW,
Pankow JS,
Arnold AM,
Chen YD,
Glazer NL,
McKnight B,
Psaty BM,
Rotter JI,
Amin N,
Campbell H,
Gyllensten U,
Pattaro C,
Pramstaller PP,
Rudan I,
Struchalin M,
Vitart V,
Gao X,
Kraja A,
Province MA,
Zhang Q,
Atwood LD,
Dupuis J,
Hirschhorn JN,
Jaquish CE,
O'Donnell CJ,
Vasan RS,
White CC,
Aulchenko YS,
Estrada K,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Witteman JC,
Oostra BA,
Kaplan RC,
Gudnason V,
O'Connell JR,
Borecki IB,
van Duijn CM,
Cupples LA,
Fox CS,
North KE
PLoS genetics · 2009 · PMID 19557197 · open access
페이지 1개
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Benjamin EJ,
Rice KM,
Arking DE,
Pfeufer A,
van Noord C,
Smith AV,
Schnabel RB,
Bis JC,
Boerwinkle E,
Sinner MF,
Dehghan A,
Lubitz SA
외 44명 — 모두 보기
D'Agostino RB Sr,
Lumley T,
Ehret GB,
Heeringa J,
Aspelund T,
Newton-Cheh C,
Larson MG,
Marciante KD,
Soliman EZ,
Rivadeneira F,
Wang TJ,
Eiríksdottir G,
Levy D,
Psaty BM,
Li M,
Chamberlain AM,
Hofman A,
Vasan RS,
Harris TB,
Rotter JI,
Kao WH,
Agarwal SK,
Stricker BH,
Wang K,
Launer LJ,
Smith NL,
Chakravarti A,
Uitterlinden AG,
Wolf PA,
Sotoodehnia N,
Köttgen A,
van Duijn CM,
Meitinger T,
Mueller M,
Perz S,
Steinbeck G,
Wichmann HE,
Lunetta KL,
Heckbert SR,
Gudnason V,
Alonso A,
Kääb S,
Ellinor PT,
Witteman JC
Nature genetics · 2009 · PMID 19597492 · open access
페이지 1개
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts
Dehghan A,
Yang Q,
Peters A,
Basu S,
Bis JC,
Rudnicka AR,
Kavousi M,
Chen MH,
Baumert J,
Lowe GD,
McKnight B,
Tang W
외 29명 — 모두 보기
de Maat M,
Larson MG,
Eyhermendy S,
McArdle WL,
Lumley T,
Pankow JS,
Hofman A,
Massaro JM,
Rivadeneira F,
Kolz M,
Taylor KD,
van Duijn CM,
Kathiresan S,
Illig T,
Aulchenko YS,
Volcik KA,
Johnson AD,
Uitterlinden AG,
Tofler GH,
Gieger C,
Psaty BM,
Couper DJ,
Boerwinkle E,
Koenig W,
O'Donnell CJ,
Witteman JC,
Strachan DP,
Smith NL,
Folsom AR
Wellcome Trust Case Control Consortium
Circulation. Cardiovascular genetics · 2009 · PMID 20031576
페이지 1개
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
외 82명 — 모두 보기
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
Thompson JR,
Aulchenko YS,
Nelis M,
Aben KK,
den Heijer M,
Dirksen A,
Ashraf H,
Soranzo N,
Valdes AM,
Steves C,
Uitterlinden AG,
Hofman A,
Tönjes A,
Kovacs P,
Hottenga JJ,
Willemsen G,
Vogelzangs N,
Döring A,
Dahmen N,
Nitz B,
Pergadia ML,
Saez B,
De Diego V,
Lezcano V,
Garcia-Prats MD,
Ripatti S,
Perola M,
Kettunen J,
Hartikainen AL,
Pouta A,
Laitinen J,
Isohanni M,
Huei-Yi S,
Allen M,
Krestyaninova M,
Hall AS,
Jones GT,
van Rij AM,
Mueller T,
Dieplinger B,
Haltmayer M,
Jonsson S,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Kiemeney LA,
Mayordomo JI,
Lindholt JS,
Pedersen JH,
Franklin WA,
Wolf H,
Montgomery GW,
Heath AC,
Martin NG,
Madden PA,
Giegling I,
Rujescu D,
Järvelin MR,
Salomaa V,
Stumvoll M,
Spector TD,
Wichmann HE,
Metspalu A,
Samani NJ,
Penninx BW,
Oostra BA,
Boomsma DI,
Tiemeier H,
van Duijn CM,
Kaprio J,
Gulcher JR,
McCarthy MI,
Peltonen L,
Thorsteinsdottir U,
Stefansson K
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
페이지 1개
Common genetic variants associate with serum phosphorus concentration
Kestenbaum B,
Glazer NL,
Köttgen A,
Felix JF,
Hwang SJ,
Liu Y,
Lohman K,
Kritchevsky SB,
Hausman DB,
Petersen AK,
Gieger C,
Ried JS
외 27명 — 모두 보기
Meitinger T,
Strom TM,
Wichmann HE,
Campbell H,
Hayward C,
Rudan I,
de Boer IH,
Psaty BM,
Rice KM,
Chen YD,
Li M,
Arking DE,
Boerwinkle E,
Coresh J,
Yang Q,
Levy D,
van Rooij FJ,
Dehghan A,
Rivadeneira F,
Uitterlinden AG,
Hofman A,
van Duijn CM,
Shlipak MG,
Kao WH,
Witteman JC,
Siscovick DS,
Fox CS
Journal of the American Society of Nephrology : JASN · 2010 · PMID 20558539
페이지 1개
Genome-wide association analysis identifies multiple loci related to resting heart rate
Eijgelsheim M,
Newton-Cheh C,
Sotoodehnia N,
de Bakker PI,
Müller M,
Morrison AC,
Smith AV,
Isaacs A,
Sanna S,
Dörr M,
Navarro P,
Fuchsberger C
외 62명 — 모두 보기
Nolte IM,
de Geus EJ,
Estrada K,
Hwang SJ,
Bis JC,
Rückert IM,
Alonso A,
Launer LJ,
Hottenga JJ,
Rivadeneira F,
Noseworthy PA,
Rice KM,
Perz S,
Arking DE,
Spector TD,
Kors JA,
Aulchenko YS,
Tarasov KV,
Homuth G,
Wild SH,
Marroni F,
Gieger C,
Licht CM,
Prineas RJ,
Hofman A,
Rotter JI,
Hicks AA,
Ernst F,
Najjar SS,
Wright AF,
Peters A,
Fox ER,
Oostra BA,
Kroemer HK,
Couper D,
Völzke H,
Campbell H,
Meitinger T,
Uda M,
Witteman JC,
Psaty BM,
Wichmann HE,
Harris TB,
Kääb S,
Siscovick DS,
Jamshidi Y,
Uitterlinden AG,
Folsom AR,
Larson MG,
Wilson JF,
Penninx BW,
Snieder H,
Pramstaller PP,
van Duijn CM,
Lakatta EG,
Felix SB,
Gudnason V,
Pfeufer A,
Heckbert SR,
Stricker BH,
Boerwinkle E,
O'Donnell CJ
Human molecular genetics · 2010 · PMID 20639392
페이지 1개
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium
Fornage M,
Debette S,
Bis JC,
Schmidt H,
Ikram MA,
Dufouil C,
Sigurdsson S,
Lumley T,
DeStefano AL,
Fazekas F,
Vrooman HA,
Shibata DK
외 51명 — 모두 보기
Maillard P,
Zijdenbos A,
Smith AV,
Gudnason H,
de Boer R,
Cushman M,
Mazoyer B,
Heiss G,
Vernooij MW,
Enzinger C,
Glazer NL,
Beiser A,
Knopman DS,
Cavalieri M,
Niessen WJ,
Harris TB,
Petrovic K,
Lopez OL,
Au R,
Lambert JC,
Hofman A,
Gottesman RF,
Garcia M,
Heckbert SR,
Atwood LD,
Catellier DJ,
Uitterlinden AG,
Yang Q,
Smith NL,
Aspelund T,
Romero JR,
Rice K,
Taylor KD,
Nalls MA,
Rotter JI,
Sharrett R,
van Duijn CM,
Amouyel P,
Wolf PA,
Gudnason V,
van der Lugt A,
Boerwinkle E,
Psaty BM,
Seshadri S,
Tzourio C,
Breteler MM,
Mosley TH,
Schmidt R,
Longstreth WT,
DeCarli C,
Launer LJ
Annals of neurology · 2011 · PMID 21681796
페이지 1개
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
외 379명 — 모두 보기
Ferrara A,
Lu L,
Ziegler JT,
Sale MM,
Divers J,
Shriner D,
Adeyemo A,
Rotimi CN,
Ng MC,
Langefeld CD,
Freedman BI,
Bowden DW,
Voight BF,
Scott LJ,
Steinthorsdottir V,
Morris AP,
Dina C,
Welch RP,
Zeggini E,
Huth C,
Aulchenko YS,
Thorleifsson G,
McCulloch LJ,
Ferreira T,
Grallert H,
Amin N,
Wu G,
Willer CJ,
Raychaudhuri S,
McCarroll SA,
Langenberg C,
Hofmann OM,
Dupuis J,
Qi L,
Segrè AV,
van Hoek M,
Navarro P,
Ardlie K,
Balkau B,
Benediktsson R,
Bennett AJ,
Blagieva R,
Boerwinkle E,
Bonnycastle LL,
Boström KB,
Bravenboer B,
Bumpstead S,
Burtt NP,
Charpentier G,
Chines PS,
Cornelis M,
Couper DJ,
Crawford G,
Doney AS,
Elliott KS,
Elliott AL,
Erdos MR,
Fox CS,
Franklin CS,
Ganser M,
Gieger C,
Grarup N,
Green T,
Griffin S,
Groves CJ,
Guiducci C,
Hadjadj S,
Hassanali N,
Herder C,
Isomaa B,
Jackson AU,
Johnson PR,
Jørgensen T,
Kao WH,
Klopp N,
Kong A,
Kraft P,
Kuusisto J,
Lauritzen T,
Li M,
Lieverse A,
Lindgren CM,
Lyssenko V,
Marre M,
Meitinger T,
Midthjell K,
Morken MA,
Narisu N,
Nilsson P,
Owen KR,
Payne F,
Perry JR,
Petersen AK,
Platou C,
Proença C,
Prokopenko I,
Rathmann W,
Rayner NW,
Robertson NR,
Rocheleau G,
Roden M,
Sampson MJ,
Saxena R,
Shields BM,
Shrader P,
Sigurdsson G,
Sparsø T,
Strassburger K,
Stringham HM,
Sun Q,
Swift AJ,
Thorand B,
Tichet J,
Tuomi T,
van Dam RM,
van Haeften TW,
van Herpt T,
van Vliet-Ostaptchouk JV,
Walters GB,
Weedon MN,
Wijmenga C,
Witteman J,
Bergman RN,
Cauchi S,
Collins FS,
Gloyn AL,
Gyllensten U,
Hansen T,
Hide WA,
Hitman GA,
Hofman A,
Hunter DJ,
Hveem K,
Laakso M,
Mohlke KL,
Morris AD,
Palmer CN,
Pramstaller PP,
Rudan I,
Sijbrands E,
Stein LD,
Tuomilehto J,
Uitterlinden A,
Walker M,
Wareham NJ,
Watanabe RM,
Abecasis GR,
Boehm BO,
Campbell H,
Daly MJ,
Hattersley AT,
Hu FB,
Meigs JB,
Pankow JS,
Pedersen O,
Wichmann HE,
Barroso I,
Florez JC,
Frayling TM,
Groop L,
Sladek R,
Thorsteinsdottir U,
Wilson JF,
Illig T,
Froguel P,
van Duijn CM,
Stefansson K,
Altshuler D,
Boehnke M,
McCarthy MI,
Soranzo N,
Wheeler E,
Glazer NL,
Bouatia-Naji N,
Mägi R,
Randall J,
Johnson T,
Elliott P,
Rybin D,
Henneman P,
Dehghan A,
Hottenga JJ,
Song K,
Goel A,
Egan JM,
Lajunen T,
Doney A,
Kanoni S,
Cavalcanti-Proença C,
Kumari M,
Timpson NJ,
Zabena C,
Ingelsson E,
An P,
O'Connell J,
Luan J,
Elliott A,
McCarroll SA,
Roccasecca RM,
Pattou F,
Sethupathy P,
Ariyurek Y,
Barter P,
Beilby JP,
Ben-Shlomo Y,
Bergmann S,
Bochud M,
Bonnefond A,
Borch-Johnsen K,
Böttcher Y,
Brunner E,
Bumpstead SJ,
Chen YD,
Chines P,
Clarke R,
Coin LJ,
Cooper MN,
Crisponi L,
Day IN,
de Geus EJ,
Delplanque J,
Fedson AC,
Fischer-Rosinsky A,
Forouhi NG,
Frants R,
Franzosi MG,
Galan P,
Goodarzi MO,
Graessler J,
Grundy S,
Gwilliam R,
Hallmans G,
Hammond N,
Han X,
Hartikainen AL,
Hayward C,
Heath SC,
Hercberg S,
Hicks AA,
Hillman DR,
Hingorani AD,
Hui J,
Hung J,
Jula A,
Kaakinen M,
Kaprio J,
Kesaniemi YA,
Kivimaki M,
Knight B,
Koskinen S,
Kovacs P,
Kyvik KO,
Lathrop GM,
Lawlor DA,
Le Bacquer O,
Lecoeur C,
Li Y,
Mahley R,
Mangino M,
Manning AK,
Martínez-Larrad MT,
McAteer JB,
McPherson R,
Meisinger C,
Melzer D,
Meyre D,
Mitchell BD,
Mukherjee S,
Naitza S,
Neville MJ,
Oostra BA,
Orrù M,
Pakyz R,
Paolisso G,
Pattaro C,
Pearson D,
Peden JF,
Pedersen NL,
Perola M,
Pfeiffer AF,
Pichler I,
Polasek O,
Posthuma D,
Potter SC,
Pouta A,
Province MA,
Psaty BM,
Rayner NW,
Rice K,
Ripatti S,
Rivadeneira F,
Rolandsson O,
Sandbaek A,
Sandhu M,
Sanna S,
Sayer AA,
Scheet P,
Seedorf U,
Sharp SJ,
Shields B,
Sijbrands EJ,
Silveira A,
Simpson L,
Singleton A,
Smith NL,
Sovio U,
Swift A,
Syddall H,
Syvänen AC,
Tanaka T,
Tönjes A,
Uitterlinden AG,
van Dijk KW,
Varma D,
Visvikis-Siest S,
Vitart V,
Vogelzangs N,
Waeber G,
Wagner PJ,
Walley A,
Ward KL,
Watkins H,
Wild SH,
Willemsen G,
Willemsen G,
Witteman JC,
Yarnell JW,
Zelenika D,
Zethelius B,
Zhai G,
Zhao JH,
Zillikens MC,
Borecki IB,
Loos RJ,
Meneton P,
Magnusson PK,
Nathan DM,
Williams GH,
Silander K,
Salomaa V,
Smith GD,
Bornstein SR,
Schwarz P,
Spranger J,
Karpe F,
Shuldiner AR,
Cooper C,
Dedoussis GV,
Serrano-Ríos M,
Lind L,
Palmer LJ,
Franks PW,
Ebrahim S,
Marmot M,
Kao WH,
Pramstaller PP,
Wright AF,
Stumvoll M,
Hamsten A,
Buchanan TA,
Valle TT,
Rotter JI,
Siscovick DS,
Penninx BW,
Boomsma DI,
Deloukas P,
Spector TD,
Ferrucci L,
Cao A,
Scuteri A,
Schlessinger D,
Uda M,
Ruokonen A,
Jarvelin MR,
Waterworth DM,
Vollenweider P,
Peltonen L,
Mooser V,
Sladek R
DIAGRAM Consortium · MAGIC Investigators
PloS one · 2012 · PMID 22238593 · open access
페이지 1개
Common variants at 6q22 and 17q21 are associated with intracranial volume
Ikram MA,
Fornage M,
Smith AV,
Seshadri S,
Schmidt R,
Debette S,
Vrooman HA,
Sigurdsson S,
Ropele S,
Taal HR,
Mook-Kanamori DO,
Coker LH
외 44명 — 모두 보기
Longstreth WT Jr,
Niessen WJ,
DeStefano AL,
Beiser A,
Zijdenbos AP,
Struchalin M,
Jack CR Jr,
Rivadeneira F,
Uitterlinden AG,
Knopman DS,
Hartikainen AL,
Pennell CE,
Thiering E,
Steegers EA,
Hakonarson H,
Heinrich J,
Palmer LJ,
Jarvelin MR,
McCarthy MI,
Grant SF,
St Pourcain B,
Timpson NJ,
Smith GD,
Sovio U,
Nalls MA,
Au R,
Hofman A,
Gudnason H,
van der Lugt A,
Harris TB,
Meeks WM,
Vernooij MW,
van Buchem MA,
Catellier D,
Jaddoe VW,
Gudnason V,
Windham BG,
Wolf PA,
van Duijn CM,
Mosley TH Jr,
Schmidt H,
Launer LJ,
Breteler MM,
DeCarli C
Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
페이지 1개
Common variants at 12q15 and 12q24 are associated with infant head circumference
Taal HR,
Pourcain BS,
Thiering E,
Das S,
Mook-Kanamori DO,
Warrington NM,
Kaakinen M,
Kreiner-Møller E,
Bradfield JP,
Freathy RM,
Geller F,
Guxens M
외 74명 — 모두 보기
Cousminer DL,
Kerkhof M,
Timpson NJ,
Ikram MA,
Beilin LJ,
Bønnelykke K,
Buxton JL,
Charoen P,
Chawes BLK,
Eriksson J,
Evans DM,
Hofman A,
Kemp JP,
Kim CE,
Klopp N,
Lahti J,
Lye SJ,
McMahon G,
Mentch FD,
Müller M,
O'Reilly PF,
Prokopenko I,
Rivadeneira F,
Steegers EAP,
Sunyer J,
Tiesler C,
Yaghootkar H,
Breteler MMB,
Debette S,
Fornage M,
Gudnason V,
Launer LJ,
van der Lugt A,
Mosley TH,
Seshadri S,
Smith AV,
Vernooij MW,
Blakemore AI,
Chiavacci RM,
Feenstra B,
Fernandez-Benet J,
Grant SFA,
Hartikainen AL,
van der Heijden AJ,
Iñiguez C,
Lathrop M,
McArdle WL,
Mølgaard A,
Newnham JP,
Palmer LJ,
Palotie A,
Palotie A,
Pouta A,
Ring SM,
Sovio U,
Standl M,
Uitterlinden AG,
Wichmann HE,
Vissing NH,
DeCarli C,
van Duijn CM,
McCarthy MI,
Koppelman GH,
Estivill X,
Hattersley AT,
Melbye M,
Bisgaard H,
Pennell CE,
Widen E,
Hakonarson H,
Smith GD,
Heinrich J,
Jarvelin MR,
Jaddoe VWV
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium 외 컨소시엄 1곳
Nature genetics · 2012 · PMID 22504419
페이지 1개
FTO genotype is associated with phenotypic variability of body mass index
Yang J,
Loos RJ,
Powell JE,
Medland SE,
Speliotes EK,
Chasman DI,
Rose LM,
Thorleifsson G,
Steinthorsdottir V,
Mägi R,
Waite L,
Smith AV
외 160명 — 모두 보기
Yerges-Armstrong LM,
Monda KL,
Hadley D,
Mahajan A,
Li G,
Kapur K,
Vitart V,
Huffman JE,
Wang SR,
Palmer C,
Esko T,
Fischer K,
Zhao JH,
Demirkan A,
Isaacs A,
Feitosa MF,
Luan J,
Heard-Costa NL,
White C,
Jackson AU,
Preuss M,
Ziegler A,
Eriksson J,
Kutalik Z,
Frau F,
Nolte IM,
Van Vliet-Ostaptchouk JV,
Hottenga JJ,
Jacobs KB,
Verweij N,
Goel A,
Medina-Gomez C,
Estrada K,
Bragg-Gresham JL,
Sanna S,
Sidore C,
Tyrer J,
Teumer A,
Prokopenko I,
Mangino M,
Lindgren CM,
Assimes TL,
Shuldiner AR,
Hui J,
Beilby JP,
McArdle WL,
Hall P,
Haritunians T,
Zgaga L,
Kolcic I,
Polasek O,
Zemunik T,
Oostra BA,
Junttila MJ,
Grönberg H,
Schreiber S,
Peters A,
Hicks AA,
Stephens J,
Foad NS,
Laitinen J,
Pouta A,
Kaakinen M,
Willemsen G,
Vink JM,
Wild SH,
Navis G,
Asselbergs FW,
Homuth G,
John U,
Iribarren C,
Harris T,
Launer L,
Gudnason V,
O'Connell JR,
Boerwinkle E,
Cadby G,
Palmer LJ,
James AL,
Musk AW,
Ingelsson E,
Psaty BM,
Beckmann JS,
Waeber G,
Vollenweider P,
Hayward C,
Wright AF,
Rudan I,
Groop LC,
Metspalu A,
Khaw KT,
van Duijn CM,
Borecki IB,
Province MA,
Wareham NJ,
Tardif JC,
Huikuri HV,
Cupples LA,
Atwood LD,
Fox CS,
Boehnke M,
Collins FS,
Mohlke KL,
Erdmann J,
Schunkert H,
Hengstenberg C,
Stark K,
Lorentzon M,
Ohlsson C,
Cusi D,
Staessen JA,
Van der Klauw MM,
Pramstaller PP,
Kathiresan S,
Jolley JD,
Ripatti S,
Jarvelin MR,
de Geus EJ,
Boomsma DI,
Penninx B,
Wilson JF,
Campbell H,
Chanock SJ,
van der Harst P,
Hamsten A,
Watkins H,
Hofman A,
Witteman JC,
Zillikens MC,
Uitterlinden AG,
Rivadeneira F,
Zillikens MC,
Kiemeney LA,
Vermeulen SH,
Abecasis GR,
Schlessinger D,
Schipf S,
Stumvoll M,
Tönjes A,
Spector TD,
North KE,
Lettre G,
McCarthy MI,
Berndt SI,
Heath AC,
Madden PA,
Nyholt DR,
Montgomery GW,
Martin NG,
McKnight B,
Strachan DP,
Hill WG,
Snieder H,
Ridker PM,
Thorsteinsdottir U,
Stefansson K,
Frayling TM,
Hirschhorn JN,
Goddard ME,
Visscher PM
Nature · 2012 · PMID 22982992
페이지 1개
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course
Graff M,
Ngwa JS,
Workalemahu T,
Homuth G,
Schipf S,
Teumer A,
Völzke H,
Wallaschofski H,
Abecasis GR,
Edward L,
Francesco C,
Sanna S
외 37명 — 모두 보기
Scheet P,
Schlessinger D,
Sidore C,
Xiao X,
Wang Z,
Chanock SJ,
Jacobs KB,
Hayes RB,
Hu F,
Van Dam RM,
Crout RJ,
Marazita ML,
Shaffer JR,
Atwood LD,
Fox CS,
Heard-Costa NL,
White C,
Choh AC,
Czerwinski SA,
Demerath EW,
Dyer TD,
Towne B,
Amin N,
Oostra BA,
Van Duijn CM,
Zillikens MC,
Esko T,
Nelis M,
Nikopensius T,
Metspalu A,
Strachan DP,
Monda K,
Qi L,
North KE,
Cupples LA,
Gordon-Larsen P,
Berndt SI
GIANT Consortium
Human molecular genetics · 2013 · PMID 23669352
페이지 1개
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,
DeStafano AL,
Bis JC,
Beecham GW,
Grenier-Boley B,
Russo G,
Thorton-Wells TA
외 160명 — 모두 보기
Jones N,
Smith AV,
Chouraki V,
Thomas C,
Ikram MA,
Zelenika D,
Vardarajan BN,
Kamatani Y,
Lin CF,
Gerrish A,
Gerrish A,
Schmidt H,
Kunkle B,
Dunstan ML,
Ruiz A,
Bihoreau MT,
Choi SH,
Reitz C,
Pasquier F,
Cruchaga C,
Craig D,
Amin N,
Berr C,
Lopez OL,
De Jager PL,
Deramecourt V,
Johnston JA,
Evans D,
Lovestone S,
Letenneur L,
Morón FJ,
Rubinsztein DC,
Eiriksdottir G,
Sleegers K,
Goate AM,
Fiévet N,
Huentelman MW,
Gill M,
Brown K,
Kamboh MI,
Keller L,
Barberger-Gateau P,
McGuiness 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,
Bossù P,
Spalletta G,
Proitsi P,
Collinge J,
Sorbi S,
Sanchez-Garcia F,
Fox NC,
Hardy J,
Deniz Naranjo MC,
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,
Lannefelt L,
Hakonarson H,
Pichler S,
Carrasquillo MM,
Ingelsson M,
Beekly D,
Alvarez V,
Zou F,
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 Jr,
Bennett DA,
Harris TB,
Fratiglioni L,
Holmes C,
de Bruijn RF,
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 JS,
Boerwinkle E,
Riemenschneider M,
Boada M,
Hiltuenen M,
Martin ER,
Schmidt R,
Rujescu D,
Wang LS,
Dartigues JF,
Mayeux R,
Tzourio C,
Hofman A,
Nöthen 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
European Alzheimer's Disease Initiative (EADI) · Genetic and Environmental Risk in Alzheimer's Disease 외 컨소시엄 2곳
Nature genetics · 2013 · PMID 24162737
페이지 1개
Modulation of genetic associations with serum urate levels by body-mass-index in humans
Huffman JE,
Albrecht E,
Teumer A,
Mangino M,
Kapur K,
Johnson T,
Kutalik Z,
Pirastu N,
Pistis G,
Lopez LM,
Haller T,
Salo P
외 108명 — 모두 보기
Goel A,
Li M,
Tanaka T,
Dehghan A,
Ruggiero D,
Malerba G,
Smith AV,
Nolte IM,
Portas L,
Phipps-Green A,
Boteva L,
Navarro P,
Johansson A,
Hicks AA,
Polasek O,
Esko T,
Peden JF,
Harris SE,
Murgia F,
Wild SH,
Tenesa A,
Tin A,
Mihailov E,
Grotevendt A,
Gislason GK,
Coresh J,
D'Adamo P,
Ulivi S,
Vollenweider P,
Waeber G,
Campbell S,
Kolcic I,
Fisher K,
Viigimaa M,
Metter JE,
Masciullo C,
Trabetti E,
Bombieri C,
Sorice R,
Döring A,
Reischl E,
Strauch K,
Hofman A,
Uitterlinden AG,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Dalbeth N,
Stamp L,
Smit JH,
Kirin M,
Nagaraja R,
Nauck M,
Schurmann C,
Budde K,
Farrington SM,
Theodoratou E,
Jula A,
Salomaa V,
Sala C,
Hengstenberg C,
Burnier M,
Mägi R,
Klopp N,
Kloiber S,
Schipf S,
Ripatti S,
Cabras S,
Soranzo N,
Homuth G,
Nutile T,
Munroe PB,
Hastie N,
Campbell H,
Rudan I,
Cabrera C,
Haley C,
Franco OH,
Merriman TR,
Gudnason V,
Pirastu M,
Penninx BW,
Snieder H,
Metspalu A,
Ciullo M,
Pramstaller PP,
van Duijn CM,
Ferrucci L,
Gambaro G,
Deary IJ,
Dunlop MG,
Wilson JF,
Gasparini P,
Gyllensten U,
Spector TD,
Wright AF,
Hayward C,
Watkins H,
Perola M,
Bochud M,
Kao WH,
Caulfield M,
Toniolo D,
Völzke H,
Gieger C,
Köttgen A,
Vitart V
PloS one · 2015 · PMID 25811787 · open access
페이지 1개
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