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성함이나 학술지명, PMID로 찾아보십시오.
Launer L에 대해
113건, 그중 20건 표시.
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function
Hancock DB,
Soler Artigas M,
Gharib SA,
Henry A,
Manichaikul A,
Ramasamy A,
Loth DW,
Imboden M,
Koch B,
McArdle WL,
Smith AV,
Smolonska J
외 78명 — 모두 보기
Sood A,
Tang W,
Wilk JB,
Zhai G,
Zhao JH,
Aschard H,
Burkart KM,
Curjuric I,
Eijgelsheim M,
Elliott P,
Gu X,
Harris TB,
Janson C,
Homuth G,
Hysi PG,
Liu JZ,
Loehr LR,
Lohman K,
Loos RJ,
Manning AK,
Marciante KD,
Obeidat M,
Postma DS,
Aldrich MC,
Brusselle GG,
Chen TH,
Eiriksdottir G,
Franceschini N,
Heinrich J,
Rotter JI,
Wijmenga C,
Williams OD,
Bentley AR,
Hofman A,
Laurie CC,
Lumley T,
Morrison AC,
Joubert BR,
Rivadeneira F,
Couper DJ,
Kritchevsky SB,
Liu Y,
Wjst M,
Wain LV,
Vonk JM,
Uitterlinden AG,
Rochat T,
Rich SS,
Psaty BM,
O'Connor GT,
North KE,
Mirel DB,
Meibohm B,
Launer LJ,
Khaw KT,
Hartikainen AL,
Hammond CJ,
Gläser S,
Marchini J,
Kraft P,
Wareham NJ,
Völzke H,
Stricker BH,
Spector TD,
Probst-Hensch NM,
Jarvis D,
Jarvelin MR,
Heckbert SR,
Gudnason V,
Boezen HM,
Barr RG,
Cassano PA,
Strachan DP,
Fornage M,
Hall IP,
Dupuis J,
Tobin MD,
London SJ
PLoS genetics · 2012 · PMID 23284291 · open access
페이지 2개
A genome-wide association study of early menopause and the combined impact of identified variants
Perry JR,
Corre T,
Esko T,
Chasman DI,
Fischer K,
Franceschini N,
He C,
Kutalik Z,
Mangino M,
Rose LM,
Vernon Smith A,
Stolk L
외 54명 — 모두 보기
Sulem P,
Weedon MN,
Zhuang WV,
Arnold A,
Ashworth A,
Bergmann S,
Buring JE,
Burri A,
Chen C,
Cornelis MC,
Couper DJ,
Goodarzi MO,
Gudnason V,
Harris T,
Hofman A,
Jones M,
Kraft P,
Launer L,
Laven JS,
Li G,
McKnight B,
Masciullo C,
Milani L,
Orr N,
Psaty BM,
Ridker PM,
Rivadeneira F,
Sala C,
Salumets A,
Schoemaker M,
Traglia M,
Waeber G,
Chanock SJ,
Demerath EW,
Garcia M,
Hankinson SE,
Hu FB,
Hunter DJ,
Lunetta KL,
Metspalu A,
Montgomery GW,
Murabito JM,
Newman AB,
Ong KK,
Spector TD,
Stefansson K,
Swerdlow AJ,
Thorsteinsdottir U,
Van Dam RM,
Uitterlinden AG,
Visser JA,
Vollenweider P,
Toniolo D,
Murray A
ReproGen Consortium
Human molecular genetics · 2013 · PMID 23307926 · open access
페이지 2개
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations
O'Seaghdha CM,
Wu H,
Yang Q,
Kapur K,
Guessous I,
Zuber AM,
Köttgen A,
Stoudmann C,
Teumer A,
Kutalik Z,
Mangino M,
Dehghan A
외 97명 — 모두 보기
Zhang W,
Eiriksdottir G,
Li G,
Tanaka T,
Portas L,
Lopez LM,
Hayward C,
Lohman K,
Matsuda K,
Padmanabhan S,
Firsov D,
Sorice R,
Ulivi S,
Brockhaus AC,
Kleber ME,
Mahajan A,
Ernst FD,
Gudnason V,
Launer LJ,
Mace A,
Boerwinckle E,
Arking DE,
Tanikawa C,
Nakamura Y,
Brown MJ,
Gaspoz JM,
Theler JM,
Siscovick DS,
Psaty BM,
Bergmann S,
Vollenweider P,
Vitart V,
Wright AF,
Zemunik T,
Boban M,
Kolcic I,
Navarro P,
Brown EM,
Estrada K,
Ding J,
Harris TB,
Bandinelli S,
Hernandez D,
Singleton AB,
Girotto G,
Ruggiero D,
d'Adamo AP,
Robino A,
Meitinger T,
Meisinger C,
Davies G,
Starr JM,
Chambers JC,
Boehm BO,
Winkelmann BR,
Huang J,
Murgia F,
Wild SH,
Campbell H,
Morris AP,
Franco OH,
Hofman A,
Uitterlinden AG,
Rivadeneira F,
Völker U,
Hannemann A,
Biffar R,
Hoffmann W,
Shin SY,
Lescuyer P,
Henry H,
Schurmann C,
Munroe PB,
Gasparini P,
Pirastu N,
Ciullo M,
Gieger C,
März W,
Lind L,
Spector TD,
Smith AV,
Rudan I,
Wilson JF,
Polasek O,
Deary IJ,
Pirastu M,
Ferrucci L,
Liu Y,
Kestenbaum B,
Kooner JS,
Witteman JC,
Nauck M,
Kao WH,
Wallaschofski H,
Bonny O,
Fox CS,
Bochud M
SUNLIGHT Consortium · GEFOS Consortium
PLoS genetics · 2013 · PMID 24068962 · open access
페이지 2개
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium
Dehghan A,
Bis JC,
White CC,
Smith AV,
Morrison AC,
Cupples LA,
Trompet S,
Chasman DI,
Lumley T,
Völker U,
Buckley BM,
Ding J
외 55명 — 모두 보기
Jensen MK,
Folsom AR,
Kritchevsky SB,
Girman CJ,
Ford I,
Dörr M,
Salomaa V,
Uitterlinden AG,
Eiriksdottir G,
Vasan RS,
Franceschini N,
Carty CL,
Virtamo J,
Demissie S,
Amouyel P,
Arveiler D,
Heckbert SR,
Ferrières J,
Ducimetière P,
Smith NL,
Wang YA,
Siscovick DS,
Rice KM,
Wiklund PG,
Taylor KD,
Evans A,
Kee F,
Rotter JI,
Karvanen J,
Kuulasmaa K,
Heiss G,
Kraft P,
Launer LJ,
Hofman A,
Markus MR,
Rose LM,
Silander K,
Wagner P,
Benjamin EJ,
Lohman K,
Stott DJ,
Rivadeneira F,
Harris TB,
Levy D,
Liu Y,
Rimm EB,
Jukema JW,
Völzke H,
Ridker PM,
Blankenberg S,
Franco OH,
Gudnason V,
Psaty BM,
Boerwinkle E,
O'Donnell CJ
PloS one · 2016 · PMID 26950853 · open access
페이지 2개
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins
Postmus I,
Warren HR,
Trompet S,
Arsenault BJ,
Avery CL,
Bis JC,
Chasman DI,
de Keyser CE,
Deshmukh HA,
Evans DS,
Feng Q,
Li X
외 76명 — 모두 보기
Smit RA,
Smith AV,
Sun F,
Taylor KD,
Arnold AM,
Barnes MR,
Barratt BJ,
Betteridge J,
Boekholdt SM,
Boerwinkle E,
Buckley BM,
Chen YI,
de Craen AJ,
Cummings SR,
Denny JC,
Dubé MP,
Durrington PN,
Eiriksdottir G,
Ford I,
Guo X,
Harris TB,
Heckbert SR,
Hofman A,
Hovingh GK,
Kastelein JJ,
Launer LJ,
Liu CT,
Liu Y,
Lumley T,
McKeigue PM,
Munroe PB,
Neil A,
Nickerson DA,
Nyberg F,
O'Brien E,
O'Donnell CJ,
Post W,
Poulter N,
Vasan RS,
Rice K,
Rich SS,
Rivadeneira F,
Sattar N,
Sever P,
Shaw-Hawkins S,
Shields DC,
Slagboom PE,
Smith NL,
Smith JD,
Sotoodehnia N,
Stanton A,
Stott DJ,
Stricker BH,
Stürmer T,
Uitterlinden AG,
Wei WQ,
Westendorp RG,
Whitsel EA,
Wiggins KL,
Wilke RA,
Ballantyne CM,
Colhoun HM,
Cupples LA,
Franco OH,
Gudnason V,
Hitman G,
Palmer CN,
Psaty BM,
Ridker PM,
Stafford JM,
Stein CM,
Tardif JC,
Caulfield MJ,
Jukema JW,
Rotter JI,
Krauss RM
Journal of medical genetics · 2016 · PMID 27587472
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
Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification
Kavousi M,
Bos MM,
Barnes HJ,
Lino Cardenas CL,
Wong D,
Lu H,
Hodonsky CJ,
Landsmeer LPL,
Turner AW,
Kho M,
Hasbani NR,
de Vries PS
외 77명 — 모두 보기
Bowden DW,
Chopade S,
Deelen J,
Benavente ED,
Guo X,
Hofer E,
Hwang SJ,
Lutz SM,
Lyytikäinen LP,
Slenders L,
Smith AV,
Stanislawski MA,
van Setten J,
Wong Q,
Yanek LR,
Becker DM,
Beekman M,
Budoff MJ,
Feitosa MF,
Finan C,
Hilliard AT,
Kardia SLR,
Kovacic JC,
Kral BG,
Langefeld CD,
Launer LJ,
Malik S,
Hoesein FAAM,
Mokry M,
Schmidt R,
Smith JA,
Taylor KD,
Terry JG,
van der Grond J,
van Meurs J,
Vliegenthart R,
Xu J,
Young KA,
Zilhão NR,
Zweiker R,
Assimes TL,
Becker LC,
Bos D,
Carr JJ,
Cupples LA,
de Kleijn DPV,
de Winther M,
den Ruijter HM,
Fornage M,
Freedman BI,
Gudnason V,
Hingorani AD,
Hokanson JE,
Ikram MA,
Išgum I,
Jacobs DR Jr,
Kähönen M,
Lange LA,
Lehtimäki T,
Pasterkamp G,
Raitakari OT,
Schmidt H,
Slagboom PE,
Uitterlinden AG,
Vernooij MW,
Bis JC,
Franceschini N,
Psaty BM,
Post WS,
Rotter JI,
Björkegren JLM,
O'Donnell CJ,
Bielak LF,
Peyser PA,
Malhotra R,
van der Laan SW,
Miller CL
Nature genetics · 2023 · PMID 37770635
페이지 2개
Large-scale blood pressure GWAS accounting for gene-depression interactions in 564,680 individuals from diverse populations
Lee S,
Miller CL,
Bentley AR,
Brown MR,
Nagarajan P,
Noordam R,
Morrison JL,
Schwander K,
Westerman K,
Kho M,
Kraja AT,
de Vries PS
외 137명 — 모두 보기
Ammous F,
Aschard H,
Bartz TM,
Do A,
Dupont CT,
Feitosa MF,
Gudmundsdottir V,
Guo X,
Harris SE,
Hikino K,
Huang Z,
Lefevre C,
Lyytikäinen LP,
Milaneschi Y,
Nardone GG,
Santin A,
Schmidt H,
Shen B,
Sofer T,
Sun Q,
Tan YA,
Tang J,
Thériault S,
van der Most PJ,
Ware EB,
Weiss S,
Xing WY,
Yu C,
Zhao W,
Ansari MAY,
Anugu P,
Attia JR,
Bazzano LA,
Bis JC,
Breyer M,
Cade B,
Chen G,
Collins S,
Corley J,
Davies G,
Dörr M,
Du J,
Edwards TL,
Faquih T,
Faul JD,
Fohner AE,
Fretts AM,
Gangireddy S,
Gepner A,
Graff M,
Hofer E,
Homuth G,
Hood MM,
Jie X,
Kähönen M,
Kardia SLR,
Karvonen-Gutierrez CA,
Launer LJ,
Levy D,
Maheshwari M,
Martin LW,
Matsuda K,
McNeil JJ,
Nolte IM,
Okochi T,
Raffield LM,
Raitakari OT,
Risch L,
Risch M,
Roux AD,
Ruiz-Narvaez EA,
Russ TC,
Saito T,
Schreiner PJ,
Scott RJ,
Shikany J,
Smith JA,
Snieder H,
Spedicati B,
Tai ES,
Taylor AM,
Taylor KD,
Tesolin P,
van Dam RM,
Wang R,
Wenbin W,
Xie T,
Yao J,
Young KL,
Zhang R,
Zonderman AB,
Concas MP,
Conen D,
Cox SR,
Evans MK,
Fox ER,
de Las Fuentes L,
Giri A,
Girotto G,
Grabe HJ,
Gu C,
Gudnason V,
Harlow SD,
Holliday E,
Jost JB,
Lacaze P,
Lee S,
Lehtimäki T,
Li C,
Liu CT,
Morrison AC,
North KE,
Penninx BWJH,
Peyser PA,
Province MM,
Psaty BM,
Redline S,
Rosendaal FR,
Rotimi CN,
Rotter JI,
Schmidt R,
Sim X,
Terao C,
Weir DR,
Zhu X,
Franceschini N,
O'Connell JR,
Jaquish CE,
Wang H,
Manning A,
Munroe PB,
Rao DC,
Chen H,
Gauderman WJ,
Bierut LJ,
Winkler TW,
Fornage M
Biobank Japan Project · Lifelines Cohort Study,
HGG advances · 2026 · PMID 41520179 · open access
페이지 2개
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
Common variants in KCNN3 are associated with lone atrial fibrillation
Ellinor PT,
Lunetta KL,
Glazer NL,
Pfeufer A,
Alonso A,
Chung MK,
Sinner MF,
de Bakker PI,
Mueller M,
Lubitz SA,
Fox E,
Darbar D
외 50명 — 모두 보기
Smith NL,
Smith JD,
Schnabel RB,
Soliman EZ,
Rice KM,
Van Wagoner DR,
Beckmann BM,
van Noord C,
Wang K,
Ehret GB,
Rotter JI,
Hazen SL,
Steinbeck G,
Smith AV,
Launer LJ,
Harris TB,
Makino S,
Nelis M,
Milan DJ,
Perz S,
Esko T,
Köttgen A,
Moebus S,
Newton-Cheh C,
Li M,
Möhlenkamp S,
Wang TJ,
Kao WH,
Vasan RS,
Nöthen MM,
MacRae CA,
Stricker BH,
Hofman A,
Uitterlinden AG,
Levy D,
Boerwinkle E,
Metspalu A,
Topol EJ,
Chakravarti A,
Gudnason V,
Psaty BM,
Roden DM,
Meitinger T,
Wichmann HE,
Witteman JC,
Barnard J,
Arking DE,
Benjamin EJ,
Heckbert SR,
Kääb S
Nature genetics · 2010 · PMID 20173747 · open access
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,
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CUBN is a gene locus for albuminuria
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외 103명 — 모두 보기
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외 51명 — 모두 보기
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페이지 1개
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외 190명 — 모두 보기
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Alzheimer's Disease Neuroimaging Initiative · EPIGEN Consortium 외 컨소시엄 4곳
Nature genetics · 2012 · PMID 22504417
페이지 1개
Common variants at 6q22 and 17q21 are associated with intracranial volume
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외 44명 — 모두 보기
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Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
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페이지 1개
Common variants at 12q15 and 12q24 are associated with infant head circumference
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외 74명 — 모두 보기
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Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium 외 컨소시엄 1곳
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페이지 1개
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction
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