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43 matches for
Cucca F,
showing the first 20.
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Young WJ,
Lahrouchi N,
Isaacs A,
Duong T,
Foco L,
Ahmed F,
Brody JA,
Salman R,
Noordam R,
Benjamins JW,
Haessler J,
Lyytikäinen LP
and 154 more — show all
Repetto L,
Concas MP,
van den Berg ME,
Weiss S,
Baldassari AR,
Bartz TM,
Cook JP,
Evans DS,
Freudling R,
Hines O,
Isaksen JL,
Lin H,
Mei H,
Moscati A,
Müller-Nurasyid M,
Nursyifa C,
Qian Y,
Richmond A,
Roselli C,
Ryan KA,
Tarazona-Santos E,
Thériault S,
van Duijvenboden S,
Warren HR,
Yao J,
Raza D,
Aeschbacher S,
Ahlberg G,
Alonso A,
Andreasen L,
Bis JC,
Boerwinkle E,
Campbell A,
Catamo E,
Cocca M,
Cutler MJ,
Darbar D,
De Grandi A,
De Luca A,
Ding J,
Ellervik C,
Ellinor PT,
Felix SB,
Froguel P,
Fuchsberger C,
Gögele M,
Graff C,
Graff M,
Guo X,
Hansen T,
Heckbert SR,
Huang PL,
Huikuri HV,
Hutri-Kähönen N,
Ikram MA,
Jackson RD,
Junttila J,
Kavousi M,
Kors JA,
Leal TP,
Lemaitre RN,
Lin HJ,
Lind L,
Linneberg A,
Liu S,
MacFarlane PW,
Mangino M,
Meitinger T,
Mezzavilla M,
Mishra PP,
Mitchell RN,
Mononen N,
Montasser ME,
Morrison AC,
Nauck M,
Nauffal V,
Navarro P,
Nikus K,
Pare G,
Patton KK,
Pelliccione G,
Pittman A,
Porteous DJ,
Pramstaller PP,
Preuss MH,
Raitakari OT,
Reiner AP,
Ribeiro ALP,
Rice KM,
Risch L,
Schlessinger D,
Schotten U,
Schurmann C,
Shen X,
Shoemaker MB,
Sinagra G,
Sinner MF,
Soliman EZ,
Stoll M,
Strauch K,
Tarasov K,
Taylor KD,
Tinker A,
Trompet S,
Uitterlinden A,
Völker U,
Völzke H,
Waldenberger M,
Weng LC,
Whitsel EA,
Wilson JG,
Avery CL,
Conen D,
Correa A,
Cucca F,
Dörr M,
Gharib SA,
Girotto G,
Grarup N,
Hayward C,
Jamshidi Y,
Järvelin MR,
Jukema JW,
Kääb S,
Kähönen M,
Kanters JK,
Kooperberg C,
Lehtimäki T,
Lima-Costa MF,
Liu Y,
Loos RJF,
Lubitz SA,
Mook-Kanamori DO,
Morris AP,
O'Connell JR,
Olesen MS,
Orini M,
Padmanabhan S,
Pattaro C,
Peters A,
Psaty BM,
Rotter JI,
Stricker B,
van der Harst P,
van Duijn CM,
Verweij N,
Wilson JF,
Arking DE,
Ramirez J,
Lambiase PD,
Sotoodehnia N,
Mifsud B,
Newton-Cheh C,
Munroe PB
Nature communications · 2022 · PMID 36050321 · 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+
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
Akiyama M
and 205 more — show all
Albert CM,
Aliev F,
Alonso A,
Arnett DK,
Ashley-Koch AE,
Ashrani AA,
Barnes KC,
Barr RG,
Bartz TM,
Becker DM,
Bielak LF,
Benjamin EJ,
Bis JC,
Bjornsdottir G,
Blangero J,
Bleecker ER,
Boardman JD,
Boerwinkle E,
Boomsma DI,
Boorgula MP,
Bowden DW,
Brody JA,
Cade BE,
Chasman DI,
Chavan S,
Chen YI,
Chen Z,
Cheng I,
Cho MH,
Choquet H,
Cole JW,
Cornelis MC,
Cucca F,
Curran JE,
de Andrade M,
Dick DM,
Docherty AR,
Duggirala R,
Eaton CB,
Ehringer MA,
Esko T,
Faul JD,
Fernandes Silva L,
Fiorillo E,
Fornage M,
Freedman BI,
Gabrielsen ME,
Garrett ME,
Gharib SA,
Gieger C,
Gillespie N,
Glahn DC,
Gordon SD,
Gu CC,
Gu D,
Gudbjartsson DF,
Guo X,
Haessler J,
Hall ME,
Haller T,
Harris KM,
He J,
Herd P,
Hewitt JK,
Hickie I,
Hidalgo B,
Hokanson JE,
Hopfer C,
Hottenga J,
Hou L,
Huang H,
Hung YJ,
Hunter DJ,
Hveem K,
Hwang SJ,
Hwu CM,
Iacono W,
Irvin MR,
Jee YH,
Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
Kaprio J,
Kardia SLR,
Keller MC,
Kelly TN,
Kooperberg C,
Korhonen T,
Kraft P,
Krauter K,
Kuusisto J,
Laakso M,
Lasky-Su J,
Lee WJ,
Lee JJ,
Levy D,
Li L,
Li K,
Li Y,
Lin K,
Lind PA,
Liu C,
Lloyd-Jones DM,
Lutz SM,
Ma J,
Mägi R,
Manichaikul A,
Martin NG,
Mathur R,
Matoba N,
McArdle PF,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Meyers DA,
Millwood IY,
Mitchell BD,
Mohlke KL,
Moll M,
Montasser ME,
Morrison AC,
Mulas A,
Nielsen JB,
North KE,
Oelsner EC,
Okada Y,
Orrù V,
Palmer ND,
Palviainen T,
Pandit A,
Park SL,
Peters U,
Peters A,
Peyser PA,
Polderman TJC,
Rafaels N,
Redline S,
Reed RM,
Reiner AP,
Rice JP,
Rich SS,
Richmond NE,
Roan C,
Rotter JI,
Rueschman MN,
Runarsdottir V,
Saccone NL,
Schwartz DA,
Shadyab AH,
Shi J,
Shringarpure SS,
Sicinski K,
Skogholt AH,
Smith JA,
Smith NL,
Sotoodehnia N,
Stallings MC,
Stefansson H,
Stefansson K,
Stitzel JA,
Sun X,
Syed M,
Tal-Singer R,
Taylor AE,
Taylor KD,
Telen MJ,
Thai KK,
Tiwari H,
Turman C,
Tyrfingsson T,
Wall TL,
Walters RG,
Weir DR,
Weiss ST,
White WB,
Whitfield JB,
Wiggins KL,
Willemsen G,
Willer CJ,
Winsvold BS,
Xu H,
Yanek LR,
Yin J,
Young KL,
Young KA,
Yu B,
Zhao W,
Zhou W,
Zöllner S,
Zuccolo L,
Batini C,
Bergen AW,
Bierut LJ,
David SP,
Gagliano Taliun SA,
Hancock DB,
Jiang B,
Munafò MR,
Thorgeirsson TE,
Liu DJ,
Vrieze S
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · 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+
Exome-wide association study of plasma lipids in >300,000 individuals
Liu DJ,
Peloso GM,
Yu H,
Butterworth AS,
Wang X,
Mahajan A,
Saleheen D,
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inconsistent across databases; where two people share a form of a name we cannot
separate them, and we would rather be corrected than guess.
My paper is not here. Does that mean you rejected it?
No. This catalogue is assembled from what a small team could read, and it is
thinnest outside European-ancestry cohorts. A paper is absent because nobody has got
to it, not because it was assessed and turned down.
Which pages rest on a paper?
Each row lists them, up to six, and links to each one. The count beside a row is
how many pages cite it in total.
How often does this change?
It is rebuilt from the pages every hour. A paper appears the moment a page starts
resting on it and disappears if that page stops — there is no separate list to
keep in step, because the citation lives on the page that makes the claim.