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71 matches for
Elliott P,
showing the first 20.
Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials
Gill D,
Cameron AC,
Burgess S,
Li X,
Doherty DJ,
Karhunen V,
Abdul-Rahim AH,
Taylor-Rowan M,
Zuber V,
Tsao PS,
Klarin D,
Evangelou E
and 7 more — show all
VA Million Veteran Program
Hypertension (Dallas, Tex. : 1979) · 2021 · PMID 33356394 · open access
12 pages+
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
and 23 more — show all
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
12 pages+
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging
McCartney DL,
Min JL,
Richmond RC,
Lu AT,
Sobczyk MK,
Davies G,
Broer L,
Guo X,
Jeong A,
Jung J,
Kasela S,
Katrinli S
and 97 more — show all
Kuo PL,
Matias-Garcia PR,
Mishra PP,
Nygaard M,
Palviainen T,
Patki A,
Raffield LM,
Ratliff SM,
Richardson TG,
Robinson O,
Soerensen M,
Sun D,
Tsai PC,
van der Zee MD,
Walker RM,
Wang X,
Wang Y,
Xia R,
Xu Z,
Yao J,
Zhao W,
Correa A,
Boerwinkle E,
Dugué PA,
Durda P,
Elliott HR,
Gieger C,
de Geus EJC,
Harris SE,
Hemani G,
Imboden M,
Kähönen M,
Kardia SLR,
Kresovich JK,
Li S,
Lunetta KL,
Mangino M,
Mason D,
McIntosh AM,
Mengel-From J,
Moore AZ,
Murabito JM,
Ollikainen M,
Pankow JS,
Pedersen NL,
Peters A,
Polidoro S,
Porteous DJ,
Raitakari O,
Rich SS,
Sandler DP,
Sillanpää E,
Smith AK,
Southey MC,
Strauch K,
Tiwari H,
Tanaka T,
Tillin T,
Uitterlinden AG,
Van Den Berg DJ,
van Dongen J,
Wilson JG,
Wright J,
Yet I,
Arnett D,
Bandinelli S,
Bell JT,
Binder AM,
Boomsma DI,
Chen W,
Christensen K,
Conneely KN,
Elliott P,
Ferrucci L,
Fornage M,
Hägg S,
Hayward C,
Irvin M,
Kaprio J,
Lawlor DA,
Lehtimäki T,
Lohoff FW,
Milani L,
Milne RL,
Probst-Hensch N,
Reiner AP,
Ritz B,
Rotter JI,
Smith JA,
Taylor JA,
van Meurs JBJ,
Vineis P,
Waldenberger M,
Deary IJ,
Relton CL,
Horvath S,
Marioni RE
Genetics of DNA Methylation Consortium · NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium
Genome biology · 2021 · PMID 34187551 · open access
12 pages+
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
and 5 more — show all
Nature communications · 2022 · PMID 35459240 · open access
12 pages+
Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities
Francis CM,
Futschik ME,
Huang J,
Bai W,
Sargurupremraj M,
Teumer A,
Breteler MMB,
Petretto E,
Ho ASR,
Amouyel P,
Engelter ST,
Bülow R
and 11 more — show all
Völker U,
Völzke H,
Dörr M,
Imtiaz MA,
Aziz NA,
Lohner V,
Ware JS,
Debette S,
Elliott P,
Dehghan A,
Matthews PM
Nature communications · 2022 · PMID 35922433 · open access
12 pages+
GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
Lagou V,
Jiang L,
Ulrich A,
Zudina L,
González KSG,
Balkhiyarova Z,
Faggian A,
Maina JG,
Chen S,
Todorov PV,
Sharapov S,
David A
and 84 more — show all
Marullo L,
Mägi R,
Rujan RM,
Ahlqvist E,
Thorleifsson G,
Gao Η,
Εvangelou Ε,
Benyamin B,
Scott RA,
Isaacs A,
Zhao JH,
Willems SM,
Johnson T,
Gieger C,
Grallert H,
Meisinger C,
Müller-Nurasyid M,
Strawbridge RJ,
Goel A,
Rybin D,
Albrecht E,
Jackson AU,
Stringham HM,
Corrêa IR Jr,
Farber-Eger E,
Steinthorsdottir V,
Uitterlinden AG,
Munroe PB,
Brown MJ,
Schmidberger J,
Holmen O,
Thorand B,
Hveem K,
Wilsgaard T,
Mohlke KL,
Wang Z,
Shmeliov A,
den Hoed M,
Loos RJF,
Kratzer W,
Haenle M,
Koenig W,
Boehm BO,
Tan TM,
Tomas A,
Salem V,
Barroso I,
Tuomilehto J,
Boehnke M,
Florez JC,
Hamsten A,
Watkins H,
Njølstad I,
Wichmann HE,
Caulfield MJ,
Khaw KT,
van Duijn CM,
Hofman A,
Wareham NJ,
Langenberg C,
Whitfield JB,
Martin NG,
Montgomery G,
Scapoli C,
Tzoulaki I,
Elliott P,
Thorsteinsdottir U,
Stefansson K,
Brittain EL,
McCarthy MI,
Froguel P,
Sexton PM,
Wootten D,
Groop L,
Dupuis J,
Meigs JB,
Deganutti G,
Demirkan A,
Pers TH,
Reynolds CA,
Aulchenko YS,
Kaakinen MA,
Jones B,
Prokopenko I
GWA-PA Consortium · Meta-Analysis of Glucose and Insulin-Related Traits Consortium (MAGIC)
Nature genetics · 2023 · PMID 37679419 · open access
12 pages+
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
Speliotes EK,
Willer CJ,
Berndt SI,
Monda KL,
Thorleifsson G,
Jackson AU,
Lango Allen H,
Lindgren CM,
Luan J,
Mägi R,
Randall JC,
Vedantam S
and 366 more — show all
Winkler TW,
Qi L,
Workalemahu T,
Heid IM,
Steinthorsdottir V,
Stringham HM,
Weedon MN,
Wheeler E,
Wood AR,
Ferreira T,
Weyant RJ,
Segrè AV,
Estrada K,
Liang L,
Nemesh J,
Park JH,
Gustafsson S,
Kilpeläinen TO,
Yang J,
Bouatia-Naji N,
Esko T,
Feitosa MF,
Kutalik Z,
Mangino M,
Raychaudhuri S,
Scherag A,
Smith AV,
Welch R,
Zhao JH,
Aben KK,
Absher DM,
Amin N,
Dixon AL,
Fisher E,
Glazer NL,
Goddard ME,
Heard-Costa NL,
Hoesel V,
Hottenga JJ,
Johansson A,
Johnson T,
Ketkar S,
Lamina C,
Li S,
Moffatt MF,
Myers RH,
Narisu N,
Perry JR,
Peters MJ,
Preuss M,
Ripatti S,
Rivadeneira F,
Sandholt C,
Scott LJ,
Timpson NJ,
Tyrer JP,
van Wingerden S,
Watanabe RM,
White CC,
Wiklund F,
Barlassina C,
Chasman DI,
Cooper MN,
Jansson JO,
Lawrence RW,
Pellikka N,
Prokopenko I,
Shi J,
Thiering E,
Alavere H,
Alibrandi MT,
Almgren P,
Arnold AM,
Aspelund T,
Atwood LD,
Balkau B,
Balmforth AJ,
Bennett AJ,
Ben-Shlomo Y,
Bergman RN,
Bergmann S,
Biebermann H,
Blakemore AI,
Boes T,
Bonnycastle LL,
Bornstein SR,
Brown MJ,
Buchanan TA,
Busonero F,
Campbell H,
Cappuccio FP,
Cavalcanti-Proença C,
Chen YD,
Chen CM,
Chines PS,
Clarke R,
Coin L,
Connell J,
Day IN,
den Heijer M,
Duan J,
Ebrahim S,
Elliott P,
Elliott P,
Elosua R,
Eiriksdottir G,
Erdos MR,
Eriksson JG,
Facheris MF,
Felix SB,
Fischer-Posovszky P,
Folsom AR,
Friedrich N,
Freimer NB,
Fu M,
Gaget S,
Gejman PV,
Geus EJ,
Gieger C,
Gjesing AP,
Goel A,
Goyette P,
Grallert H,
Grässler J,
Greenawalt DM,
Groves CJ,
Gudnason V,
Guiducci C,
Hartikainen AL,
Hassanali N,
Hall AS,
Havulinna AS,
Hayward C,
Heath AC,
Hengstenberg C,
Hicks AA,
Hinney A,
Hofman A,
Homuth G,
Hui J,
Igl W,
Iribarren C,
Isomaa B,
Jacobs KB,
Jarick I,
Jewell E,
John U,
Jørgensen T,
Jousilahti P,
Jula A,
Kaakinen M,
Kajantie E,
Kaplan LM,
Kathiresan S,
Kettunen J,
Kinnunen L,
Knowles JW,
Kolcic I,
König IR,
Koskinen S,
Kovacs P,
Kuusisto J,
Kraft P,
Kvaløy K,
Laitinen J,
Lantieri O,
Lanzani C,
Launer LJ,
Lecoeur C,
Lehtimäki T,
Lettre G,
Liu J,
Lokki ML,
Lorentzon M,
Luben RN,
Ludwig B,
Manunta P,
Marek D,
Marre M,
Martin NG,
McArdle WL,
McCarthy A,
McKnight B,
Meitinger T,
Melander O,
Meyre D,
Midthjell K,
Montgomery GW,
Morken MA,
Morris AP,
Mulic R,
Ngwa JS,
Nelis M,
Neville MJ,
Nyholt DR,
O'Donnell CJ,
O'Rahilly S,
Ong KK,
Oostra B,
Paré G,
Parker AN,
Perola M,
Pichler I,
Pietiläinen KH,
Platou CG,
Polasek O,
Pouta A,
Rafelt S,
Raitakari O,
Rayner NW,
Ridderstråle M,
Rief W,
Ruokonen A,
Robertson NR,
Rzehak P,
Salomaa V,
Sanders AR,
Sandhu MS,
Sanna S,
Saramies J,
Savolainen MJ,
Scherag S,
Schipf S,
Schreiber S,
Schunkert H,
Silander K,
Sinisalo J,
Siscovick DS,
Smit JH,
Soranzo N,
Sovio U,
Stephens J,
Surakka I,
Swift AJ,
Tammesoo ML,
Tardif JC,
Teder-Laving M,
Teslovich TM,
Thompson JR,
Thomson B,
Tönjes A,
Tuomi T,
van Meurs JB,
van Ommen GJ,
Vatin V,
Viikari J,
Visvikis-Siest S,
Vitart V,
Vogel CI,
Voight BF,
Waite LL,
Wallaschofski H,
Walters GB,
Widen E,
Wiegand S,
Wild SH,
Willemsen G,
Witte DR,
Witteman JC,
Xu J,
Zhang Q,
Zgaga L,
Ziegler A,
Zitting P,
Beilby JP,
Farooqi IS,
Hebebrand J,
Huikuri HV,
James AL,
James AL,
Kähönen M,
Levinson DF,
Macciardi F,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Ridker PM,
Stumvoll M,
Beckmann JS,
Boeing H,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Chanock SJ,
Collins FS,
Cupples LA,
Smith GD,
Erdmann J,
Froguel P,
Grönberg H,
Gyllensten U,
Hall P,
Hansen T,
Harris TB,
Hattersley AT,
Hayes RB,
Heinrich J,
Hu FB,
Hveem K,
Illig T,
Jarvelin MR,
Kaprio J,
Karpe F,
Khaw KT,
Kiemeney LA,
Krude H,
Laakso M,
Lawlor DA,
Metspalu A,
Munroe PB,
Ouwehand WH,
Pedersen O,
Penninx BW,
Peters A,
Pramstaller PP,
Quertermous T,
Reinehr T,
Rissanen A,
Rudan I,
Samani NJ,
Schwarz PE,
Schwarz PE,
Shuldiner AR,
Spector TD,
Tuomilehto J,
Uda M,
Uitterlinden A,
Valle TT,
Wabitsch M,
Waeber G,
Wareham NJ,
Watkins H,
Wilson JF,
Wright AF,
Zillikens MC,
Chatterjee N,
McCarroll SA,
Purcell S,
Schadt EE,
Visscher PM,
Assimes TL,
Borecki IB,
Deloukas P,
Fox CS,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
Mohlke KL,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
van Duijn CM,
Wichmann HE,
Frayling TM,
Thorsteinsdottir U,
Abecasis GR,
Barroso I,
Boehnke M,
Stefansson K,
North KE,
McCarthy MI,
Hirschhorn JN,
Ingelsson E,
Loos RJ
MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
11 pages
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
and 198 more — show all
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,
Burgess S,
Vasan RS,
Felix JF,
Uria-Nickelsen M,
Malarstig A,
Reily DF,
Hoek M,
Vogt T,
Lin H,
Lieb W,
Traylor M,
Markus HF,
Highland HM,
Justice AE,
Marouli E,
Lindström J,
Uusitupa M,
Komulainen P,
Lakka TA,
Rauramaa R,
Polasek O,
Rudan I,
Rolandsson O,
Franks PW,
Dedoussis G,
Spector TD,
Jousilahti P,
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,
van der Harst P,
Gambaro G,
Ingelsson E,
Lind L,
de Bakker PI,
Numans ME,
Brandslund I,
Christensen C,
Petersen ER,
Korpi-Hyövälti E,
Oksa H,
Chambers JC,
Kooner JS,
Blakemore AI,
Franks S,
Jarvelin MR,
Husemoen LL,
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,
Virtamo J,
Deloukas P,
Elliott P,
Zeggini E,
Kathiresan S,
Melander O,
Kuusisto J,
Laakso M,
Padmanabhan S,
Porteous D,
Hayward C,
Scotland G,
Collins FS,
Mohlke KL,
Hansen T,
Pedersen O,
Boehnke M,
Stringham HM,
Frossard P,
Newton-Cheh C,
Tobin MD,
Nordestgaard BG,
Caulfield MJ,
Mahajan A,
Morris AP,
Tomaszewski M,
Samani NJ,
Saleheen D,
Asselbergs FW,
Lindgren CM,
Danesh J,
Wain LV,
Butterworth AS,
Howson JM,
Munroe PB
CHARGE-Heart Failure Consortium · EchoGen Consortium and 12 more consortia
Nature genetics · 2016 · PMID 27618447 · open access
11 pages
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
Tadros R,
Francis C,
Xu X,
Vermeer AMC,
Harper AR,
Huurman R,
Kelu Bisabu K,
Walsh R,
Hoorntje ET,
Te Rijdt WP,
Buchan RJ,
van Velzen HG
and 58 more — show all
van Slegtenhorst MA,
Vermeulen JM,
Offerhaus JA,
Bai W,
de Marvao A,
Lahrouchi N,
Beekman L,
Karper JC,
Veldink JH,
Kayvanpour E,
Pantazis A,
Baksi AJ,
Whiffin N,
Mazzarotto F,
Sloane G,
Suzuki H,
Schneider-Luftman D,
Elliott P,
Richard P,
Ader F,
Villard E,
Lichtner P,
Meitinger T,
Tanck MWT,
van Tintelen JP,
Thain A,
McCarty D,
Hegele RA,
Roberts JD,
Amyot J,
Dubé MP,
Cadrin-Tourigny J,
Giraldeau G,
L'Allier PL,
Garceau P,
Tardif JC,
Boekholdt SM,
Lumbers RT,
Asselbergs FW,
Barton PJR,
Cook SA,
Prasad SK,
O'Regan DP,
van der Velden J,
Verweij KJH,
Talajic M,
Lettre G,
Pinto YM,
Meder B,
Charron P,
de Boer RA,
Christiaans I,
Michels M,
Wilde AAM,
Watkins H,
Matthews PM,
Ware JS,
Bezzina CR
Nature genetics · 2021 · PMID 33495596 · open access
10 pages
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth
Beaumont RN,
Flatley C,
Vaudel M,
Wu X,
Chen J,
Moen GH,
Skotte L,
Helgeland Ø,
Solé-Navais P,
Banasik K,
Albiñana C,
Ronkainen J
and 76 more — show all
Fadista J,
Stinson SE,
Trajanoska K,
Wang CA,
Westergaard D,
Srinivasan S,
Sánchez-Soriano C,
Bilbao JR,
Allard C,
Groleau M,
Kuulasmaa T,
Leirer DJ,
White F,
Jacques PÉ,
Cheng H,
Hao K,
Andreassen OA,
Åsvold BO,
Atalay M,
Bhatta L,
Bouchard L,
Brumpton BM,
Brunak S,
Bybjerg-Grauholm J,
Ebbing C,
Elliott P,
Engelbrechtsen L,
Erikstrup C,
Estarlich M,
Franks S,
Gaillard R,
Geller F,
Grove J,
Hougaard DM,
Kajantie E,
Morgen CS,
Nohr EA,
Nyegaard M,
Palmer CNA,
Pedersen OB,
Rivadeneira F,
Sebert S,
Shields BM,
Stoltenberg C,
Surakka I,
Thørner LW,
Ullum H,
Vaarasmaki M,
Vilhjalmsson BJ,
Willer CJ,
Lakka TA,
Gybel-Brask D,
Bustamante M,
Hansen T,
Pearson ER,
Reynolds RM,
Ostrowski SR,
Pennell CE,
Jaddoe VWV,
Felix JF,
Hattersley AT,
Melbye M,
Lawlor DA,
Hveem K,
Werge T,
Nielsen HS,
Magnus P,
Evans DM,
Jacobsson B,
Järvelin MR,
Zhang G,
Hivert MF,
Johansson S,
Freathy RM,
Feenstra B,
Njølstad PR
Early Growth Genetics (EGG) Consortium
Nature genetics · 2023 · PMID 37798380 · open access
10 pages
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels
Dehghan A,
Dupuis J,
Barbalic M,
Bis JC,
Eiriksdottir G,
Lu C,
Pellikka N,
Wallaschofski H,
Kettunen J,
Henneman P,
Baumert J,
Strachan DP
and 102 more — show all
Fuchsberger C,
Vitart V,
Wilson JF,
Paré G,
Naitza S,
Rudock ME,
Surakka I,
de Geus EJ,
Alizadeh BZ,
Guralnik J,
Shuldiner A,
Tanaka T,
Zee RY,
Schnabel RB,
Nambi V,
Kavousi M,
Ripatti S,
Nauck M,
Smith NL,
Smith AV,
Sundvall J,
Scheet P,
Liu Y,
Ruokonen A,
Rose LM,
Larson MG,
Hoogeveen RC,
Freimer NB,
Teumer A,
Tracy RP,
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