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41 matches for
Evangelou E,
showing the first 20.
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+
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 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+
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
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
and 22 more — show all
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
11 pages
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
and 88 more — show all
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,
Kuusisto J,
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
9 pages
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
and 254 more — show all
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,
Kuusisto J,
Lakka TA,
Langefeld CD,
Langenberg C,
Launer LJ,
Lehne B,
Lemaitre RN,
Li Y,
Liang J,
Liu J,
Liu K,
Loh M,
Louie T,
Mägi R,
Manichaikul AW,
McKenzie CA,
Meitinger T,
Metspalu A,
Milaneschi Y,
Milani L,
Mohlke KL,
Mosley TH,
Mukamal KJ,
Nalls MA,
Nauck M,
Nelson CP,
Sotoodehnia N,
O'Connell JR,
Palmer ND,
Pazoki R,
Pedersen NL,
Peters A,
Peyser PA,
Polasek O,
Poulter N,
Raffel LJ,
Raitakari OT,
Reiner AP,
Rice TK,
Rich SS,
Robino A,
Robinson JG,
Rose LM,
Rudan I,
Schmidt CO,
Schreiner PJ,
Scott WR,
Sever P,
Shi Y,
Sidney S,
Sims M,
Smith BH,
Smith JA,
Snieder H,
Starr JM,
Strauch K,
Tan N,
Taylor KD,
Teo YY,
Tham YC,
Uitterlinden AG,
van Heemst D,
Vuckovic D,
Waldenberger M,
Wang L,
Wang Y,
Wang Z,
Wei WB,
Williams C,
Wilson G,
Wojczynski MK,
Yao J,
Yu B,
Yu C,
Yuan JM,
Zhao W,
Zonderman AB,
Becker DM,
Boehnke M,
Bowden DW,
Chambers JC,
Deary IJ,
Esko T,
Farrall M,
Franks PW,
Freedman BI,
Froguel P,
Gasparini P,
Gieger C,
Horta BL,
Kamatani Y,
Kato N,
Kooner JS,
Laakso M,
Leander K,
Lehtimäki T,
Magnusson PKE,
Penninx B,
Pereira AC,
Rauramaa R,
Samani NJ,
Scott J,
Shu XO,
van der Harst P,
Wagenknecht LE,
Wang YX,
Wareham NJ,
Watkins H,
Weir DR,
Wickremasinghe AR,
Zheng W,
Elliott P,
North KE,
Bouchard C,
Evans MK,
Gudnason V,
Liu CT,
Liu Y,
Psaty BM,
Ridker PM,
van Dam RM,
Kardia SLR,
Zhu X,
Rotimi CN,
Mook-Kanamori DO,
Fornage M,
Kelly TN,
Fox ER,
Hayward C,
van Duijn CM,
Tai ES,
Wong TY,
Liu J,
Rotter JI,
Gauderman WJ,
Province MA,
Munroe PB,
Rice K,
Chasman DI,
Cupples LA,
Rao DC,
Morrison AC
InterAct Consortium · Lifelines Cohort, Groningen, The Netherlands (Lifelines Cohort Study)
American journal of epidemiology · 2019 · PMID 30698716
8 pages
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
and 170 more — show all
Liu CT,
Minster RL,
Moayyeri A,
Vandenput L,
Willner D,
Xiao SM,
Yerges-Armstrong LM,
Zheng HF,
Alonso N,
Eriksson J,
Kammerer CM,
Kaptoge SK,
Leo PJ,
Thorleifsson G,
Wilson SG,
Wilson JF,
Aalto V,
Alen M,
Aragaki AK,
Aspelund T,
Center JR,
Dailiana Z,
Duggan DJ,
Garcia M,
Garcia-Giralt N,
Giroux S,
Hallmans G,
Hocking LJ,
Husted LB,
Jameson KA,
Khusainova R,
Kim GS,
Kooperberg C,
Koromila T,
Kruk M,
Laaksonen M,
Lacroix AZ,
Lee SH,
Leung PC,
Lewis JR,
Masi L,
Mencej-Bedrac S,
Nguyen TV,
Nogues X,
Nogues X,
Patel MS,
Prezelj J,
Rose LM,
Scollen S,
Siggeirsdottir K,
Smith AV,
Svensson O,
Trompet S,
Trummer O,
van Schoor NM,
Woo J,
Zhu K,
Balcells S,
Brandi ML,
Buckley BM,
Cheng S,
Christiansen C,
Cooper C,
Dedoussis G,
Ford I,
Frost M,
Goltzman D,
González-Macías J,
Kähönen M,
Karlsson M,
Khusnutdinova E,
Koh JM,
Kollia P,
Langdahl BL,
Leslie WD,
Lips P,
Ljunggren Ö,
Lorenc RS,
Marc J,
Mellström D,
Obermayer-Pietsch B,
Olmos JM,
Pettersson-Kymmer U,
Reid DM,
Riancho JA,
Ridker PM,
Rousseau F,
Slagboom PE,
Tang NL,
Urreizti R,
Van Hul W,
Viikari J,
Zarrabeitia MT,
Aulchenko YS,
Castano-Betancourt M,
Grundberg E,
Herrera L,
Ingvarsson T,
Johannsdottir H,
Kwan T,
Li R,
Luben R,
Medina-Gómez C,
Palsson ST,
Reppe S,
Rotter JI,
Sigurdsson G,
van Meurs JB,
Verlaan D,
Williams FM,
Wood AR,
Zhou Y,
Gautvik KM,
Pastinen T,
Raychaudhuri S,
Cauley JA,
Chasman DI,
Clark GR,
Cummings SR,
Danoy P,
Dennison EM,
Eastell R,
Eisman JA,
Gudnason V,
Hofman A,
Jackson RD,
Jones G,
Jukema JW,
Khaw KT,
Lehtimäki T,
Liu Y,
Lorentzon M,
McCloskey E,
Mitchell BD,
Nandakumar K,
Nicholson GC,
Oostra BA,
Peacock M,
Pols HA,
Prince RL,
Raitakari O,
Reid IR,
Robbins J,
Sambrook PN,
Sham PC,
Shuldiner AR,
Tylavsky FA,
van Duijn CM,
Wareham NJ,
Cupples LA,
Econs MJ,
Evans DM,
Harris TB,
Kung AW,
Psaty BM,
Reeve J,
Spector TD,
Streeten EA,
Zillikens MC,
Thorsteinsdottir U,
Ohlsson C,
Karasik D,
Richards JB,
Brown MA,
Stefansson K,
Uitterlinden AG,
Ralston SH,
Ioannidis JP,
Kiel DP,
Rivadeneira F
Nature genetics · 2012 · PMID 22504420 · open access
7 pages
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,
Igo RP Jr,
Buitendijk GH
and 144 more — show all
Sim X,
Weeks DE,
Guymer RH,
Merriam JE,
Francis PJ,
Hannum G,
Agarwal A,
Armbrecht AM,
Audo I,
Aung T,
Barile GR,
Benchaboune M,
Bird AC,
Bishop PN,
Branham KE,
Brooks M,
Brucker AJ,
Cade WH,
Cain MS,
Campochiaro PA,
Chan CC,
Cheng CY,
Chew EY,
Chin KA,
Chowers I,
Clayton DG,
Cojocaru R,
Conley YP,
Cornes BK,
Daly MJ,
Dhillon B,
Edwards AO,
Evangelou E,
Fagerness J,
Ferreyra HA,
Friedman JS,
Geirsdottir A,
George RJ,
Gieger C,
Gupta N,
Hagstrom SA,
Harding SP,
Haritoglou C,
Heckenlively JR,
Holz FG,
Hughes G,
Ioannidis JP,
Ishibashi T,
Joseph P,
Jun G,
Kamatani Y,
Katsanis N,
N Keilhauer C,
Khan JC,
Kim IK,
Kiyohara Y,
Klein BE,
Klein R,
Kovach JL,
Kozak I,
Lee CJ,
Lee KE,
Lichtner P,
Lotery AJ,
Meitinger T,
Mitchell P,
Mohand-Saïd S,
Moore AT,
Morgan DJ,
Morrison MA,
Myers CE,
Naj AC,
Nakamura Y,
Okada Y,
Orlin A,
Ortube MC,
Othman MI,
Pappas C,
Park KH,
Pauer GJ,
Peachey NS,
Poch O,
Priya RR,
Reynolds R,
Richardson AJ,
Ripp R,
Rudolph G,
Ryu E,
Sahel JA,
Schaumberg DA,
Scholl HP,
Schwartz SG,
Scott WK,
Shahid H,
Sigurdsson H,
Silvestri G,
Sivakumaran TA,
Smith RT,
Sobrin L,
Souied EH,
Stambolian DE,
Stefansson H,
Sturgill-Short GM,
Takahashi A,
Tosakulwong N,
Truitt BJ,
Tsironi EE,
Uitterlinden AG,
van Duijn CM,
Vijaya L,
Vingerling JR,
Vithana EN,
Webster AR,
Wichmann HE,
Winkler TW,
Wong TY,
Wright AF,
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1 page
Questions about this list
Why is my paper here? I never gave you permission.
Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page
cites your work, and links to the paper on PubMed — which is what a citation is.
Your title and author list come from Europe PMC, the same public record a library
catalogue uses.
Why are all the authors listed instead of "et al."?
Because a study that needed 622 people is a different kind of study from one that
needed four, and "et al." erases that. Twelve names show and the rest are one click
away. Everyone is searchable, including the 187th name on a consortium paper —
that person exists and may be looking for it.
My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
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.