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Evangelou E에 대해
41건, 그중 20건 표시.
Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes
Pazoki R,
Vujkovic M,
Elliott J,
Evangelou E,
Gill D,
Ghanbari M,
van der Most PJ,
Pinto RC,
Wielscher M,
Farlik M,
Zuber V,
de Knegt RJ
외 23명 — 모두 보기
Snieder H,
Uitterlinden AG,
Lynch JA,
Jiang X,
Said S,
Kaplan DE,
Lee KM,
Serper M,
Carr RM,
Tsao PS,
Atkinson SR,
Dehghan A,
Tzoulaki I,
Ikram MA,
Herzig KH,
Järvelin MR,
Alizadeh BZ,
O'Donnell CJ,
Saleheen D,
Voight BF,
Chang KM,
Thursz MR,
Elliott P
Lifelines Cohort Study · VA Million Veteran Program
Nature communications · 2021 · PMID 33972514 · open access
페이지 12개+
Genetic analysis of over half a million people characterises C-reactive protein loci
Said S,
Pazoki R,
Karhunen V,
Võsa U,
Ligthart S,
Bodinier B,
Koskeridis F,
Welsh P,
Alizadeh BZ,
Chasman DI,
Sattar N,
Chadeau-Hyam M
외 5명 — 모두 보기
Nature communications · 2022 · PMID 35459240 · open access
페이지 12개+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
외 135명 — 모두 보기
Giri A,
Zheng Z,
Zeng J,
Chasman DI,
Morris AP,
Caulfield MJ,
Hwang SJ,
Kooner JS,
Conen D,
Attia JR,
Morrison AC,
Loos RJF,
Kristiansson K,
Schmidt R,
Hicks AA,
Pramstaller PP,
Nelson CP,
Samani NJ,
Risch L,
Gyllensten U,
Melander O,
Riese H,
Wilson JF,
Campbell H,
Rich SS,
Psaty BM,
Lu Y,
Rotter JI,
Guo X,
Rice KM,
Vollenweider P,
Sundström J,
Langenberg C,
Tobin MD,
Giedraitis V,
Luan J,
Tuomilehto J,
Kutalik Z,
Ripatti S,
Salomaa V,
Girotto G,
Trompet S,
Jukema JW,
van der Harst P,
Ridker PM,
Giulianini F,
Vitart V,
Goel A,
Watkins H,
Harris SE,
Deary IJ,
van der Most PJ,
Oldehinkel AJ,
Keavney BD,
Hayward C,
Campbell A,
Boehnke M,
Scott LJ,
Boutin T,
Mamasoula C,
Järvelin MR,
Peters A,
Gieger C,
Lakatta EG,
Cucca F,
Hui J,
Knekt P,
Enroth S,
De Borst MH,
Polašek O,
Concas MP,
Catamo E,
Cocca M,
Li-Gao R,
Hofer E,
Schmidt H,
Spedicati B,
Waldenberger M,
Strachan DP,
Laan M,
Teumer A,
Dörr M,
Gudnason V,
Cook JP,
Ruggiero D,
Kolcic I,
Boerwinkle E,
Traglia M,
Lehtimäki T,
Raitakari OT,
Johnson AD,
Newton-Cheh C,
Brown MJ,
Dominiczak AF,
Sever PJ,
Poulter N,
Chambers JC,
Elosua R,
Siscovick D,
Esko T,
Metspalu A,
Strawbridge RJ,
Laakso M,
Hamsten A,
Hottenga JJ,
de Geus E,
Morris AD,
Palmer CNA,
Nolte IM,
Milaneschi Y,
Marten J,
Wright A,
Zeggini E,
Howson JMM,
O'Donnell CJ,
Spector T,
Nalls MA,
Simonsick EM,
Liu Y,
van Duijn CM,
Butterworth AS,
Danesh JN,
Menni C,
Wareham NJ,
Khaw KT,
Sun YV,
Wilson PWF,
Cho K,
Visscher PM,
Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study 외 컨소시엄 2곳
Nature genetics · 2024 · PMID 38689001 · open access
페이지 12개+
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
Sim X,
Barnes DR,
Witkowska K,
Staley JR,
Tragante V
외 198명 — 모두 보기
Tukiainen T,
Yaghootkar H,
Masca N,
Freitag DF,
Ferreira T,
Giannakopoulou O,
Tinker A,
Harakalova M,
Mihailov E,
Liu C,
Kraja AT,
Fallgaard Nielsen S,
Rasheed A,
Samuel M,
Zhao W,
Bonnycastle LL,
Jackson AU,
Narisu N,
Swift AJ,
Southam L,
Marten J,
Huyghe JR,
Stančáková A,
Fava C,
Ohlsson T,
Matchan A,
Stirrups KE,
Bork-Jensen J,
Gjesing AP,
Kontto J,
Perola M,
Shaw-Hawkins S,
Havulinna AS,
Zhang H,
Donnelly LA,
Groves CJ,
Rayner NW,
Neville MJ,
Robertson NR,
Yiorkas AM,
Herzig KH,
Kajantie E,
Zhang W,
Willems SM,
Lannfelt L,
Malerba G,
Soranzo N,
Trabetti E,
Verweij N,
Evangelou E,
Moayyeri A,
Vergnaud AC,
Nelson CP,
Poveda A,
Varga TV,
Caslake M,
de Craen AJ,
Trompet S,
Luan J,
Scott RA,
Harris SE,
Liewald DC,
Marioni R,
Menni C,
Farmaki AE,
Hallmans G,
Renström F,
Huffman JE,
Hassinen M,
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Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
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Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
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Komulainen P,
Lakka TA,
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Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
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Männistö S,
Deary IJ,
Starr JM,
Langenberg C,
Wareham NJ,
Brown MJ,
Dominiczak AF,
Connell JM,
Jukema JW,
Sattar N,
Ford I,
Packard CJ,
Esko T,
Mägi R,
Metspalu A,
de Boer RA,
van der Meer P,
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Gambaro G,
Ingelsson E,
Lind L,
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Numans ME,
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Christensen C,
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Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
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Linneberg A,
Skaaby T,
Thuesen B,
Karpe F,
Tuomilehto J,
Doney AS,
Morris AD,
Palmer CN,
Holmen OL,
Hveem K,
Willer CJ,
Tuomi T,
Groop L,
Käräjämäki A,
Palotie A,
Ripatti S,
Salomaa V,
Alam DS,
Shafi Majumder AA,
Di Angelantonio E,
Chowdhury R,
McCarthy MI,
Poulter N,
Stanton AV,
Sever P,
Amouyel P,
Arveiler D,
Blankenberg S,
Ferrières J,
Kee F,
Kuulasmaa K,
Müller-Nurasyid M,
Veronesi G,
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Deloukas P,
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Zeggini E,
Kathiresan S,
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Stringham HM,
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Newton-Cheh C,
Tobin MD,
Nordestgaard BG,
Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
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Asselbergs FW,
Lindgren CM,
Danesh J,
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Howson JM,
Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium 외 컨소시엄 12곳
Nature genetics · 2016 · PMID 27618447 · open access
페이지 11개
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Medina-Gomez C,
Kemp JP,
Dimou NL,
Kreiner E,
Chesi A,
Zemel BS,
Bønnelykke K,
Boer CG,
Ahluwalia TS,
Bisgaard H,
Evangelou E,
Heppe DHM
외 22명 — 모두 보기
Bonewald LF,
Gorski JP,
Ghanbari M,
Demissie S,
Duque G,
Maurano MT,
Kiel DP,
Hsu YH,
C J van der Eerden B,
Ackert-Bicknell C,
Reppe S,
Gautvik KM,
Raastad T,
Karasik D,
van de Peppel J,
Jaddoe VWV,
Uitterlinden AG,
Tobias JH,
Grant SFA,
Bagos PG,
Evans DM,
Rivadeneira F
Nature communications · 2017 · PMID 28743860 · open access
페이지 11개
New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders
Evangelou E,
Gao H,
Chu C,
Ntritsos G,
Ntritsos G,
Blakeley P,
Butts AR,
Pazoki R,
Suzuki H,
Koskeridis F,
Yiorkas AM,
Karaman I
외 88명 — 모두 보기
Elliott J,
Luo Q,
Aeschbacher S,
Bartz TM,
Baumeister SE,
Braund PS,
Brown MR,
Brody JA,
Clarke TK,
Dimou N,
Faul JD,
Homuth G,
Jackson AU,
Kentistou KA,
Joshi PK,
Lemaitre RN,
Lind PA,
Lyytikäinen LP,
Mangino M,
Milaneschi Y,
Nelson CP,
Nolte IM,
Perälä MM,
Polasek O,
Porteous D,
Ratliff SM,
Smith JA,
Stančáková A,
Teumer A,
Tuominen S,
Thériault S,
Vangipurapu J,
Whitfield JB,
Wood A,
Yao J,
Yu B,
Zhao W,
Zhao W,
Arking DE,
Auvinen J,
Liu C,
Männikkö M,
Risch L,
Rotter JI,
Snieder H,
Veijola J,
Blakemore AI,
Boehnke M,
Campbell H,
Conen D,
Eriksson JG,
Grabe HJ,
Guo X,
van der Harst P,
Hartman CA,
Hayward C,
Heath AC,
Jarvelin MR,
Kähönen M,
Kardia SLR,
Kühne M,
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Laakso M,
Lahti J,
Lehtimäki T,
McIntosh AM,
Mohlke KL,
Morrison AC,
Martin NG,
Oldehinkel AJ,
Penninx BWJH,
Psaty BM,
Raitakari OT,
Rudan I,
Samani NJ,
Scott LJ,
Spector TD,
Verweij N,
Weir DR,
Wilson JF,
Levy D,
Tzoulaki I,
Bell JD,
Matthews PM,
Rothenfluh A,
Desrivières S,
Schumann G,
Elliott P
Nature human behaviour · 2019 · PMID 31358974
페이지 9개
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions
de Vries PS,
Brown MR,
Bentley AR,
Sung YJ,
Winkler TW,
Ntalla I,
Schwander K,
Kraja AT,
Guo X,
Franceschini N,
Cheng CY,
Sim X
외 254명 — 모두 보기
Vojinovic D,
Huffman JE,
Musani SK,
Li C,
Feitosa MF,
Richard MA,
Noordam R,
Aschard H,
Bartz TM,
Bielak LF,
Deng X,
Dorajoo R,
Lohman KK,
Manning AK,
Rankinen T,
Smith AV,
Tajuddin SM,
Evangelou E,
Graff M,
Alver M,
Boissel M,
Chai JF,
Chen X,
Divers J,
Gandin I,
Gao C,
Goel A,
Hagemeijer Y,
Harris SE,
Hartwig FP,
He M,
Horimoto ARVR,
Hsu FC,
Jackson AU,
Kasturiratne A,
Komulainen P,
Kühnel B,
Laguzzi F,
Lee JH,
Luan J,
Lyytikäinen LP,
Matoba N,
Nolte IM,
Pietzner M,
Riaz M,
Said MA,
Scott RA,
Sofer T,
Stančáková A,
Takeuchi F,
Tayo BO,
van der Most PJ,
Varga TV,
Wang Y,
Ware EB,
Wen W,
Yanek LR,
Zhang W,
Zhao JH,
Afaq S,
Amin N,
Amini M,
Arking DE,
Aung T,
Ballantyne C,
Boerwinkle E,
Broeckel U,
Campbell A,
Canouil M,
Charumathi S,
Chen YI,
Connell JM,
de Faire U,
de las Fuentes L,
de Mutsert R,
de Silva HJ,
Ding J,
Dominiczak AF,
Duan Q,
Eaton CB,
Eppinga RN,
Faul JD,
Fisher V,
Forrester T,
Franco OH,
Friedlander Y,
Ghanbari M,
Giulianini F,
Grabe HJ,
Grove ML,
Gu CC,
Harris TB,
Heikkinen S,
Heng CK,
Hirata M,
Hixson JE,
Howard BV,
Ikram MA,
Jacobs DR,
Johnson C,
Jonas JB,
Kammerer CM,
Katsuya T,
Khor CC,
Kilpeläinen TO,
Koh WP,
Koistinen HA,
Kolcic I,
Kooperberg C,
Krieger JE,
Kritchevsky SB,
Kubo M,
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Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lemaitre RN,
Li Y,
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Liu J,
Liu K,
Loh M,
Louie T,
Mägi R,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
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Nalls MA,
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Nelson CP,
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Pazoki R,
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Wang L,
Wang Y,
Wang Z,
Wei WB,
Williams C,
Wilson G,
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Yao J,
Yu B,
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Zhao W,
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Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
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Kamatani Y,
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Laakso M,
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Lehtimäki T,
Magnusson PKE,
Penninx B,
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Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
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InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
페이지 8개
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Estrada K,
Styrkarsdottir U,
Evangelou E,
Hsu YH,
Duncan EL,
Ntzani EE,
Oei L,
Albagha OM,
Amin N,
Kemp JP,
Koller DL,
Li G
외 170명 — 모두 보기
Liu CT,
Minster RL,
Moayyeri A,
Vandenput L,
Willner D,
Xiao SM,
Yerges-Armstrong LM,
Zheng HF,
Alonso N,
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Kammerer CM,
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Khusainova R,
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Kooperberg C,
Koromila T,
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Lacroix AZ,
Lee SH,
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Nogues X,
Nogues X,
Patel MS,
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Nature genetics · 2012 · PMID 22504420 · open access
페이지 7개
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,
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외 144명 — 모두 보기
Sim X,
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Hannum G,
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페이지 7개
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
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페이지 7개
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
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외 164명 — 모두 보기
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Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium
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페이지 7개
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis
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외 25명 — 모두 보기
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페이지 4개
Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci
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외 211명 — 모두 보기
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Lifelines Cohort Study
Molecular psychiatry · 2021 · PMID 32372009 · open access
페이지 4개
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
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외 54명 — 모두 보기
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페이지 3개
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
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외 115명 — 모두 보기
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페이지 3개
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels
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외 86명 — 모두 보기
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LifeLines Cohort Study · CHARGE Lipids Working Group
Journal of medical genetics · 2016 · PMID 27036123 · open access
페이지 2개
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
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외 64명 — 모두 보기
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arcOGEN Consortium · arcOGEN Collaborators
Lancet (London, England) · 2012 · PMID 22763110 · open access
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