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143 matches for
Gudnason V,
showing the first 20.
A genome-wide association study of serum proteins reveals shared loci with common diseases
Gudjonsson A,
Gudmundsdottir V,
Axelsson GT,
Gudmundsson EF,
Jonsson BG,
Launer LJ,
Lamb JR,
Jennings LL,
Aspelund T,
Emilsson V,
Gudnason V
Nature communications · 2022 · PMID 35078996 · open access
12 pages+
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss
Trpchevska N,
Freidin MB,
Broer L,
Oosterloo BC,
Yao S,
Zhou Y,
Vona B,
Bishop C,
Bizaki-Vallaskangas A,
Canlon B,
Castellana F,
Chasman DI
and 54 more — show all
Cherny S,
Christensen K,
Concas MP,
Correa A,
Elkon R,
Mengel-From J,
Gao Y,
Giersch ABS,
Girotto G,
Gudjonsson A,
Gudnason V,
Heard-Costa NL,
Hertzano R,
Hjelmborg JVB,
Hjerling-Leffler J,
Hoffman HJ,
Kaprio J,
Kettunen J,
Krebs K,
Kähler AK,
Lallemend F,
Launer LJ,
Lee IM,
Leonard H,
Li CM,
Lowenheim H,
Magnusson PKE,
van Meurs J,
Milani L,
Morton CC,
Mäkitie A,
Nalls MA,
Nardone GG,
Nygaard M,
Palviainen T,
Pratt S,
Quaranta N,
Rämö J,
Saarentaus E,
Sardone R,
Satizabal CL,
Schweinfurth JM,
Seshadri S,
Shiroma E,
Shulman E,
Simonsick E,
Spankovich C,
Tropitzsch A,
Lauschke VM,
Sullivan PF,
Goedegebure A,
Cederroth CR,
Williams FMK,
Nagtegaal AP
Estonian Biobank Research Team
American journal of human genetics · 2022 · PMID 35580588 · open access
12 pages+
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Wang Z,
Emmerich A,
Pillon NJ,
Moore T,
Hemerich D,
Cornelis MC,
Mazzaferro E,
Broos S,
Ahluwalia TS,
Bartz TM,
Bentley AR,
Bielak LF
and 206 more — show all
Chong M,
Chu AY,
Berry D,
Dorajoo R,
Dueker ND,
Kasbohm E,
Feenstra B,
Feitosa MF,
Gieger C,
Graff M,
Hall LM,
Haller T,
Hartwig FP,
Hillis DA,
Huikari V,
Heard-Costa N,
Holzapfel C,
Jackson AU,
Johansson Å,
Jørgensen AM,
Kaakinen MA,
Karlsson R,
Kerr KF,
Kim B,
Koolhaas CM,
Kutalik Z,
Lagou V,
Lind PA,
Lorentzon M,
Lyytikäinen LP,
Mangino M,
Metzendorf C,
Monroe KR,
Pacolet A,
Pérusse L,
Pool R,
Richmond RC,
Rivera NV,
Robiou-du-Pont S,
Schraut KE,
Schulz CA,
Stringham HM,
Tanaka T,
Teumer A,
Turman C,
van der Most PJ,
Vanmunster M,
van Rooij FJA,
van Vliet-Ostaptchouk JV,
Zhang X,
Zhao JH,
Zhao W,
Balkhiyarova Z,
Balslev-Harder MN,
Baumeister SE,
Beilby J,
Blangero J,
Boomsma DI,
Brage S,
Braund PS,
Brody JA,
Bruinenberg M,
Ekelund U,
Liu CT,
Cole JW,
Collins FS,
Cupples LA,
Esko T,
Enroth S,
Faul JD,
Fernandez-Rhodes L,
Fohner AE,
Franco OH,
Galesloot TE,
Gordon SD,
Grarup N,
Hartman CA,
Heiss G,
Hui J,
Illig T,
Jago R,
James A,
Joshi PK,
Jung T,
Kähönen M,
Kilpeläinen TO,
Koh WP,
Kolcic I,
Kraft PP,
Kuusisto J,
Launer LJ,
Li A,
Linneberg A,
Luan J,
Vidal PM,
Medland SE,
Milaneschi Y,
Moscati A,
Musk B,
Nelson CP,
Nolte IM,
Pedersen NL,
Peters A,
Peyser PA,
Power C,
Raitakari OT,
Reedik M,
Reiner AP,
Ridker PM,
Rudan I,
Ryan K,
Sarzynski MA,
Scott LJ,
Scott RA,
Sidney S,
Siggeirsdottir K,
Smith AV,
Smith JA,
Sonestedt E,
Strøm M,
Tai ES,
Teo KK,
Thorand B,
Tönjes A,
Tremblay A,
Uitterlinden AG,
Vangipurapu J,
van Schoor N,
Völker U,
Willemsen G,
Williams K,
Wong Q,
Xu H,
Young KL,
Yuan JM,
Zillikens MC,
Zonderman AB,
Ameur A,
Bandinelli S,
Bis JC,
Boehnke M,
Bouchard C,
Chasman DI,
Smith GD,
de Geus EJC,
Deldicque L,
Dörr M,
Evans MK,
Ferrucci L,
Fornage M,
Fox C,
Garland T Jr,
Gudnason V,
Gyllensten U,
Hansen T,
Hayward C,
Horta BL,
Hyppönen E,
Jarvelin MR,
Johnson WC,
Kardia SLR,
Kiemeney LA,
Laakso M,
Langenberg C,
Lehtimäki T,
Marchand LL,
Magnusson PKE,
Martin NG,
Melbye M,
Metspalu A,
Meyre D,
North KE,
Ohlsson C,
Oldehinkel AJ,
Orho-Melander M,
Pare G,
Park T,
Pedersen O,
Penninx BWJH,
Pers TH,
Polasek O,
Prokopenko I,
Rotimi CN,
Samani NJ,
Sim X,
Snieder H,
Sørensen TIA,
Spector TD,
Timpson NJ,
van Dam RM,
van der Velde N,
van Duijn CM,
Vollenweider P,
Völzke H,
Voortman T,
Waeber G,
Wareham NJ,
Weir DR,
Wichmann HE,
Wilson JF,
Hevener AL,
Krook A,
Zierath JR,
Thomis MAI,
Loos RJF,
Hoed MD
Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
12 pages+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
and 610 more — show all
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
Rüeger S,
Sim X,
Vrieze S,
Ahluwalia TS,
Akiyama M,
Allison MA,
Alvarez M,
Andersen MK,
Ani A,
Appadurai V,
Arbeeva L,
Bhaskar S,
Bielak LF,
Bollepalli S,
Bonnycastle LL,
Bork-Jensen J,
Bradfield JP,
Bradford Y,
Braund PS,
Brody JA,
Burgdorf KS,
Cade BE,
Cai H,
Cai Q,
Campbell A,
Cañadas-Garre M,
Catamo E,
Chai JF,
Chai X,
Chang LC,
Chang YC,
Chen CH,
Chesi A,
Choi SH,
Chung RH,
Cocca M,
Concas MP,
Couture C,
Cuellar-Partida G,
Danning R,
Daw EW,
Degenhard F,
Delgado GE,
Delitala A,
Demirkan A,
Deng X,
Devineni P,
Dietl A,
Dimitriou M,
Dimitrov L,
Dorajoo R,
Ekici AB,
Engmann JE,
Fairhurst-Hunter Z,
Farmaki AE,
Faul JD,
Fernandez-Lopez JC,
Forer L,
Francescatto M,
Freitag-Wolf S,
Fuchsberger C,
Galesloot TE,
Gao Y,
Gao Z,
Geller F,
Giannakopoulou O,
Giulianini F,
Gjesing AP,
Goel A,
Gordon SD,
Gorski M,
Grove J,
Guo X,
Gustafsson S,
Haessler J,
Hansen TF,
Havulinna AS,
Haworth SJ,
He J,
Heard-Costa N,
Hebbar P,
Hindy G,
Ho YA,
Hofer E,
Holliday E,
Horn K,
Hornsby WE,
Hottenga JJ,
Huang H,
Huang J,
Huerta-Chagoya A,
Huffman JE,
Hung YJ,
Huo S,
Hwang MY,
Iha H,
Ikeda DD,
Isono M,
Jackson AU,
Jäger S,
Jansen IE,
Johansson I,
Jonas JB,
Jonsson A,
Jørgensen T,
Kalafati IP,
Kanai M,
Kanoni S,
Kårhus LL,
Kasturiratne A,
Katsuya T,
Kawaguchi T,
Kember RL,
Kentistou KA,
Kim HN,
Kim YJ,
Kleber ME,
Knol MJ,
Kurbasic A,
Lauzon M,
Le P,
Lea R,
Lee JY,
Leonard HL,
Li SA,
Li X,
Li X,
Liang J,
Lin H,
Lin SY,
Liu J,
Liu X,
Lo KS,
Long J,
Lores-Motta L,
Luan J,
Lyssenko V,
Lyytikäinen LP,
Mahajan A,
Mamakou V,
Mangino M,
Manichaikul A,
Marten J,
Mattheisen M,
Mavarani L,
McDaid AF,
Meidtner K,
Melendez TL,
Mercader JM,
Milaneschi Y,
Miller JE,
Millwood IY,
Mishra PP,
Mitchell RE,
Møllehave LT,
Morgan A,
Mucha S,
Munz M,
Nakatochi M,
Nelson CP,
Nethander M,
Nho CW,
Nielsen AA,
Nolte IM,
Nongmaithem SS,
Noordam R,
Ntalla I,
Nutile T,
Pandit A,
Christofidou P,
Pärna K,
Pauper M,
Petersen ERB,
Petersen LV,
Pitkänen N,
Polašek O,
Poveda A,
Preuss MH,
Pyarajan S,
Raffield LM,
Rakugi H,
Ramirez J,
Rasheed A,
Raven D,
Rayner NW,
Riveros C,
Rohde R,
Ruggiero D,
Ruotsalainen SE,
Ryan KA,
Sabater-Lleal M,
Saxena R,
Scholz M,
Sendamarai A,
Shen B,
Shi J,
Shin JH,
Sidore C,
Sitlani CM,
Slieker RC,
Smit RAJ,
Smith AV,
Smith JA,
Smyth LJ,
Southam L,
Steinthorsdottir V,
Sun L,
Takeuchi F,
Tallapragada DSP,
Taylor KD,
Tayo BO,
Tcheandjieu C,
Terzikhan N,
Tesolin P,
Teumer A,
Theusch E,
Thompson DJ,
Thorleifsson G,
Timmers PRHJ,
Trompet S,
Turman C,
Vaccargiu S,
van der Laan SW,
van der Most PJ,
van Klinken JB,
van Setten J,
Verma SS,
Verweij N,
Veturi Y,
Wang CA,
Wang C,
Wang L,
Wang Z,
Warren HR,
Bin Wei W,
Wickremasinghe AR,
Wielscher M,
Wiggins KL,
Winsvold BS,
Wong A,
Wu Y,
Wuttke M,
Xia R,
Xie T,
Yamamoto K,
Yang J,
Yao J,
Young H,
Yousri NA,
Yu L,
Zeng L,
Zhang W,
Zhang X,
Zhao JH,
Zhao W,
Zhou W,
Zimmermann ME,
Zoledziewska M,
Adair LS,
Adams HHH,
Aguilar-Salinas CA,
Al-Mulla F,
Arnett DK,
Asselbergs FW,
Åsvold BO,
Attia J,
Banas B,
Bandinelli S,
Bennett DA,
Bergler T,
Bharadwaj D,
Biino G,
Bisgaard H,
Boerwinkle E,
Böger CA,
Bønnelykke K,
Boomsma DI,
Børglum AD,
Borja JB,
Bouchard C,
Bowden DW,
Brandslund I,
Brumpton B,
Buring JE,
Caulfield MJ,
Chambers JC,
Chandak GR,
Chanock SJ,
Chaturvedi N,
Chen YI,
Chen Z,
Cheng CY,
Christophersen IE,
Ciullo M,
Cole JW,
Collins FS,
Cooper RS,
Cruz M,
Cucca F,
Cupples LA,
Cutler MJ,
Damrauer SM,
Dantoft TM,
de Borst GJ,
de Groot LCPGM,
De Jager PL,
de Kleijn DPV,
Janaka de Silva H,
Dedoussis GV,
den Hollander AI,
Du S,
Easton DF,
Elders PJM,
Eliassen AH,
Ellinor PT,
Elmståhl S,
Erdmann J,
Evans MK,
Fatkin D,
Feenstra B,
Feitosa MF,
Ferrucci L,
Ford I,
Fornage M,
Franke A,
Franks PW,
Freedman BI,
Gasparini P,
Gieger C,
Girotto G,
Goddard ME,
Golightly YM,
Gonzalez-Villalpando C,
Gordon-Larsen P,
Grallert H,
Grant SFA,
Grarup N,
Griffiths L,
Gudnason V,
Haiman C,
Hakonarson H,
Hansen T,
Hartman CA,
Hattersley AT,
Hayward C,
Heckbert SR,
Heng CK,
Hengstenberg C,
Hewitt AW,
Hishigaki H,
Hoyng CB,
Huang PL,
Huang W,
Hunt SC,
Hveem K,
Hyppönen E,
Iacono WG,
Ichihara S,
Ikram MA,
Isasi CR,
Jackson RD,
Jarvelin MR,
Jin ZB,
Jöckel KH,
Joshi PK,
Jousilahti P,
Jukema JW,
Kähönen M,
Kamatani Y,
Kang KD,
Kaprio J,
Kardia SLR,
Karpe F,
Kato N,
Kee F,
Kessler T,
Khera AV,
Khor CC,
Kiemeney LALM,
Kim BJ,
Kim EK,
Kim HL,
Kirchhof P,
Kivimaki M,
Koh WP,
Koistinen HA,
Kolovou GD,
Kooner JS,
Kooperberg C,
Köttgen A,
Kovacs P,
Kraaijeveld A,
Kraft P,
Krauss RM,
Kumari M,
Kutalik Z,
Laakso M,
Lange LA,
Langenberg C,
Launer LJ,
Le Marchand L,
Lee H,
Lee NR,
Lehtimäki T,
Li H,
Li L,
Lieb W,
Lin X,
Lind L,
Linneberg A,
Liu CT,
Liu J,
Loeffler M,
London B,
Lubitz SA,
Lye SJ,
Mackey DA,
Mägi R,
Magnusson PKE,
Marcus GM,
Vidal PM,
Martin NG,
März W,
Matsuda F,
McGarrah RW,
McGue M,
McKnight AJ,
Medland SE,
Mellström D,
Metspalu A,
Mitchell BD,
Mitchell P,
Mook-Kanamori DO,
Morris AD,
Mucci LA,
Munroe PB,
Nalls MA,
Nazarian S,
Nelson AE,
Neville MJ,
Newton-Cheh C,
Nielsen CS,
Nöthen MM,
Ohlsson C,
Oldehinkel AJ,
Orozco L,
Pahkala K,
Pajukanta P,
Palmer CNA,
Parra EJ,
Pattaro C,
Pedersen O,
Pennell CE,
Penninx BWJH,
Perusse L,
Peters A,
Peyser PA,
Porteous DJ,
Posthuma D,
Power C,
Pramstaller PP,
Province MA,
Qi Q,
Qu J,
Rader DJ,
Raitakari OT,
Ralhan S,
Rallidis LS,
Rao DC,
Redline S,
Reilly DF,
Reiner AP,
Rhee SY,
Ridker PM,
Rienstra M,
Ripatti S,
Ritchie MD,
Roden DM,
Rosendaal FR,
Rotter JI,
Rudan I,
Rutters F,
Sabanayagam C,
Saleheen D,
Salomaa V,
Samani NJ,
Sanghera DK,
Sattar N,
Schmidt B,
Schmidt H,
Schmidt R,
Schulze MB,
Schunkert H,
Scott LJ,
Scott RJ,
Sever P,
Shiroma EJ,
Shoemaker MB,
Shu XO,
Simonsick EM,
Sims M,
Singh JR,
Singleton AB,
Sinner MF,
Smith JG,
Snieder H,
Spector TD,
Stampfer MJ,
Stark KJ,
Strachan DP,
't Hart LM,
Tabara Y,
Tang H,
Tardif JC,
Thanaraj TA,
Timpson NJ,
Tönjes A,
Tremblay A,
Tuomi T,
Tuomilehto J,
Tusié-Luna MT,
Uitterlinden AG,
van Dam RM,
van der Harst P,
Van der Velde N,
van Duijn CM,
van Schoor NM,
Vitart V,
Völker U,
Vollenweider P,
Völzke H,
Wacher-Rodarte NH,
Walker M,
Wang YX,
Wareham NJ,
Watanabe RM,
Watkins H,
Weir DR,
Werge TM,
Widen E,
Wilkens LR,
Willemsen G,
Willett WC,
Wilson JF,
Wong TY,
Woo JT,
Wright AF,
Wu JY,
Xu H,
Yajnik CS,
Yokota M,
Yuan JM,
Zeggini E,
Zemel BS,
Zheng W,
Zhu X,
Zmuda JM,
Zonderman AB,
Zwart JA,
Chasman DI,
Cho YS,
Heid IM,
McCarthy MI,
Ng MCY,
O'Donnell CJ,
Rivadeneira F,
Thorsteinsdottir U,
Sun YV,
Tai ES,
Boehnke M,
Deloukas P,
Justice AE,
Lindgren CM,
Loos RJF,
Mohlke KL,
North KE,
Stefansson K,
Walters RG,
Winkler TW,
Young KL,
Loh PR,
Yang J,
Esko T,
Assimes TL,
Auton A,
Abecasis GR,
Willer CJ,
Locke AE,
Berndt SI,
Lettre G,
Frayling TM,
Okada Y,
Wood AR,
Visscher PM,
Hirschhorn JN
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
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
and 135 more — show all
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 and 2 more consortia
Nature genetics · 2024 · PMID 38689001 · open access
12 pages+
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases
Roselli C,
Surakka I,
Olesen MS,
Sveinbjornsson G,
Marston NA,
Choi SH,
Holm H,
Chaffin M,
Gudbjartsson D,
Hill MC,
Aegisdottir H,
Albert CM
and 145 more — show all
Alonso A,
Anderson CD,
Arking DE,
Arnar DO,
Barnard J,
Benjamin EJ,
Braunwald E,
Brumpton B,
Campbell A,
Chami N,
Chasman DI,
Cho K,
Choi EK,
Christophersen IE,
Chung MK,
Conen D,
Crijns HJ,
Cutler MJ,
Czuba T,
Damrauer SM,
Dichgans M,
Dörr M,
Dudink E,
Duong T,
Erikstrup C,
Esko T,
Fatkin D,
Faul JD,
Ferreira M,
Freitag DF,
Ganesh SK,
Gaziano JM,
Geelhoed B,
Ghouse J,
Gieger C,
Giulianini F,
Graham SE,
Gudnason V,
Guo X,
Haggerty C,
Hayward C,
Heckbert SR,
Hveem K,
Ito K,
Johnson R,
Jukema JW,
Jurgens SJ,
Kääb S,
Kane JP,
Kany S,
Kardia SLR,
Kavousi M,
Khurshid S,
Kamanu FK,
Kirchhof P,
Kleber ME,
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