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121 matches for
Morris A,
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+
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Shrine N,
Izquierdo AG,
Chen J,
Packer R,
Hall RJ,
Guyatt AL,
Batini C,
Thompson RJ,
Pavuluri C,
Malik V,
Hobbs BD,
Moll M
and 136 more — show all
Kim W,
Tal-Singer R,
Bakke P,
Fawcett KA,
John C,
Coley K,
Piga NN,
Pozarickij A,
Lin K,
Millwood IY,
Chen Z,
Li L,
Wijnant SRA,
Lahousse L,
Brusselle G,
Uitterlinden AG,
Manichaikul A,
Oelsner EC,
Rich SS,
Barr RG,
Kerr SM,
Vitart V,
Brown MR,
Wielscher M,
Imboden M,
Jeong A,
Bartz TM,
Gharib SA,
Flexeder C,
Karrasch S,
Gieger C,
Peters A,
Stubbe B,
Hu X,
Ortega VE,
Meyers DA,
Bleecker ER,
Gabriel SB,
Gupta N,
Smith AV,
Luan J,
Zhao JH,
Hansen AF,
Langhammer A,
Willer C,
Bhatta L,
Porteous D,
Smith BH,
Campbell A,
Sofer T,
Lee J,
Daviglus ML,
Yu B,
Lim E,
Xu H,
O'Connor GT,
Thareja G,
Albagha OME,
Suhre K,
Granell R,
Faquih TO,
Hiemstra PS,
Slats AM,
Mullin BH,
Hui J,
James A,
Beilby J,
Patasova K,
Hysi P,
Koskela JT,
Wyss AB,
Jin J,
Sikdar S,
Lee M,
May-Wilson S,
Pirastu N,
Kentistou KA,
Joshi PK,
Timmers PRHJ,
Williams AT,
Free RC,
Wang X,
Morrison JL,
Gilliland FD,
Chen Z,
Wang CA,
Foong RE,
Harris SE,
Taylor A,
Redmond P,
Cook JP,
Mahajan A,
Lind L,
Palviainen T,
Lehtimäki T,
Raitakari OT,
Kaprio J,
Rantanen T,
Pietiläinen KH,
Cox SR,
Pennell CE,
Hall GL,
Gauderman WJ,
Brightling C,
Wilson JF,
Vasankari T,
Laitinen T,
Salomaa V,
Mook-Kanamori DO,
Timpson NJ,
Zeggini E,
Dupuis J,
Hayward C,
Brumpton B,
Langenberg C,
Weiss S,
Homuth G,
Schmidt CO,
Probst-Hensch N,
Jarvelin MR,
Morrison AC,
Polasek O,
Rudan I,
Lee JH,
Sayers I,
Rawlins EL,
Dudbridge F,
Silverman EK,
Strachan DP,
Walters RG,
Morris AP,
London SJ,
Cho MH,
Wain LV,
Hall IP,
Tobin MD
China Kadoorie Biobank Collaborative Group · Qatar Genome Program Research (QGPR) Consortium
Nature genetics · 2023 · PMID 36914875 · open access
12 pages+
Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry
Kamiza AB,
Touré SM,
Zhou F,
Soremekun O,
Cissé C,
Wélé M,
Touré AM,
Nashiru O,
Corpas M,
Nyirenda M,
Crampin A,
Shaffer J
and 6 more — show all
Nature communications · 2023 · PMID 37669986 · open access
12 pages+
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Suzuki K,
Hatzikotoulas K,
Southam L,
Taylor HJ,
Yin X,
Lorenz KM,
Mandla R,
Huerta-Chagoya A,
Melloni GEM,
Kanoni S,
Rayner NW,
Bocher O
and 351 more — show all
Arruda AL,
Sonehara K,
Namba S,
Lee SSK,
Preuss MH,
Petty LE,
Schroeder P,
Vanderwerff B,
Kals M,
Bragg F,
Lin K,
Guo X,
Zhang W,
Yao J,
Kim YJ,
Graff M,
Takeuchi F,
Nano J,
Lamri A,
Nakatochi M,
Moon S,
Scott RA,
Cook JP,
Lee JJ,
Pan I,
Taliun D,
Parra EJ,
Chai JF,
Bielak LF,
Tabara Y,
Hai Y,
Thorleifsson G,
Grarup N,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Kwak SH,
Long J,
Sun M,
Tong L,
Chen WM,
Nongmaithem SS,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Brody JA,
Kabagambe E,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Broadaway KA,
Williamson A,
Kamali Z,
Cui J,
Thangam M,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Ahluwalia TS,
Anand SS,
Bertoni A,
Bork-Jensen J,
Brandslund I,
Buchanan TA,
Burant CF,
Butterworth AS,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Danesh J,
Das SK,
de Silva HJ,
Dedoussis G,
Dimitrov L,
Doumatey AP,
Du S,
Duan Q,
Eckardt KU,
Emery LS,
Evans DS,
Evans MK,
Fischer K,
Floyd JS,
Ford I,
Franco OH,
Frayling TM,
Freedman BI,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Gordon-Larsen P,
Gross M,
Guare LA,
Hackinger S,
Hakaste L,
Han S,
Hattersley AT,
Herder C,
Horikoshi M,
Howard AG,
Hsueh W,
Huang M,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Ikram MA,
Ingelsson M,
Islam MT,
Isono M,
Jang HM,
Jasmine F,
Jiang G,
Jonas JB,
Jørgensen T,
Kamanu FK,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee KM,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lynch JA,
Lyssenko V,
Maeda S,
Mamakou V,
Mansuri SR,
Matsuda K,
Meitinger T,
Melander O,
Metspalu A,
Mo H,
Morris AD,
Moura FA,
Nadler JL,
Nalls MA,
Nayak U,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Patil S,
Pei P,
Pereira MA,
Peters A,
Pirie FJ,
Polikowsky HG,
Porneala B,
Prasad G,
Rasmussen-Torvik LJ,
Reiner AP,
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DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium · Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and 3 more consortia
Nature genetics · 2014 · PMID 24509480 · open access
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MAGIC investigators · GIANT Consortium
Nature genetics · 2010 · PMID 20581827
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Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
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UK BiLEVE
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SUMMIT Consortium · BioBank Japan Project
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DBDS Genomic Consortium · FinnGen Study and 3 more consortia
Nature genetics · 2023 · PMID 36914876
8 pages
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