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173 matches for
Hofman A,
showing the first 20.
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
Traylor M,
Farrall M,
Holliday EG,
Sudlow C,
Hopewell JC,
Cheng YC,
Fornage M,
Ikram MA,
Malik R,
Bevan S,
Thorsteinsdottir U,
Nalls MA
and 70 more — show all
Longstreth W,
Wiggins KL,
Yadav S,
Parati EA,
Destefano AL,
Worrall BB,
Kittner SJ,
Khan MS,
Reiner AP,
Helgadottir A,
Achterberg S,
Fernandez-Cadenas I,
Abboud S,
Schmidt R,
Walters M,
Chen WM,
Ringelstein EB,
O'Donnell M,
Ho WK,
Pera J,
Lemmens R,
Norrving B,
Higgins P,
Benn M,
Sale M,
Kuhlenbäumer G,
Doney AS,
Vicente AM,
Delavaran H,
Algra A,
Davies G,
Oliveira SA,
Palmer CN,
Deary I,
Schmidt H,
Pandolfo M,
Montaner J,
Carty C,
de Bakker PI,
Kostulas K,
Ferro JM,
van Zuydam NR,
Valdimarsson E,
Nordestgaard BG,
Lindgren A,
Thijs V,
Slowik A,
Saleheen D,
Paré G,
Berger K,
Thorleifsson G,
Hofman A,
Mosley TH,
Mitchell BD,
Furie K,
Clarke R,
Levi C,
Seshadri S,
Gschwendtner A,
Boncoraglio GB,
Sharma P,
Bis JC,
Gretarsdottir S,
Psaty BM,
Rothwell PM,
Rosand J,
Meschia JF,
Stefansson K,
Dichgans M,
Markus HS
Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) · International Stroke Genetics Consortium
The Lancet. Neurology · 2012 · PMID 23041239 · open access
4 pages
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium
Moayyeri A,
Hsu YH,
Karasik D,
Estrada K,
Xiao SM,
Nielson C,
Srikanth P,
Giroux S,
Wilson SG,
Zheng HF,
Smith AV,
Pye SR
and 118 more — show all
Leo PJ,
Teumer A,
Hwang JY,
Ohlsson C,
McGuigan F,
Minster RL,
Hayward C,
Olmos JM,
Lyytikäinen LP,
Lewis JR,
Swart KM,
Masi L,
Oldmeadow C,
Holliday EG,
Cheng S,
van Schoor NM,
Harvey NC,
Kruk M,
del Greco M F,
Igl W,
Trummer O,
Grigoriou E,
Luben R,
Liu CT,
Zhou Y,
Oei L,
Medina-Gomez C,
Zmuda J,
Tranah G,
Brown SJ,
Williams FM,
Soranzo N,
Jakobsdottir J,
Siggeirsdottir K,
Holliday KL,
Hannemann A,
Go MJ,
Garcia M,
Polasek O,
Laaksonen M,
Zhu K,
Enneman AW,
McEvoy M,
Peel R,
Sham PC,
Jaworski M,
Johansson Å,
Hicks AA,
Pludowski P,
Scott R,
Dhonukshe-Rutten RA,
van der Velde N,
Kähönen M,
Viikari JS,
Sievänen H,
Raitakari OT,
González-Macías J,
Hernández JL,
Mellström D,
Ljunggren O,
Cho YS,
Völker U,
Nauck M,
Homuth G,
Völzke H,
Haring R,
Brown MA,
McCloskey E,
Nicholson GC,
Eastell R,
Eisman JA,
Jones G,
Reid IR,
Dennison EM,
Wark J,
Boonen S,
Vanderschueren D,
Wu FC,
Aspelund T,
Richards JB,
Bauer D,
Hofman A,
Khaw KT,
Dedoussis G,
Obermayer-Pietsch B,
Gyllensten U,
Pramstaller PP,
Lorenc RS,
Cooper C,
Kung AW,
Lips P,
Alen M,
Attia J,
Brandi ML,
de Groot LC,
Lehtimäki T,
Riancho JA,
Campbell H,
Liu Y,
Harris TB,
Akesson K,
Karlsson M,
Lee JY,
Wallaschofski H,
Duncan EL,
O'Neill TW,
Gudnason V,
Spector TD,
Rousseau F,
Orwoll E,
Cummings SR,
Wareham NJ,
Rivadeneira F,
Uitterlinden AG,
Prince RL,
Kiel DP,
Reeve J,
Kaptoge SK
Human molecular genetics · 2014 · PMID 24430505
4 pages
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Loth DW,
Soler Artigas M,
Gharib SA,
Wain LV,
Franceschini N,
Koch B,
Pottinger TD,
Smith AV,
Duan Q,
Oldmeadow C,
Lee MK,
Strachan DP
and 148 more — show all
James AL,
Huffman JE,
Vitart V,
Ramasamy A,
Wareham NJ,
Kaprio J,
Wang XQ,
Trochet H,
Kähönen M,
Flexeder C,
Albrecht E,
Lopez LM,
de Jong K,
Thyagarajan B,
Alves AC,
Enroth S,
Omenaas E,
Joshi PK,
Fall T,
Viñuela A,
Launer LJ,
Loehr LR,
Fornage M,
Li G,
Wilk JB,
Tang W,
Manichaikul A,
Lahousse L,
Harris TB,
North KE,
Rudnicka AR,
Hui J,
Gu X,
Lumley T,
Wright AF,
Hastie ND,
Campbell S,
Kumar R,
Pin I,
Scott RA,
Pietiläinen KH,
Surakka I,
Liu Y,
Holliday EG,
Schulz H,
Heinrich J,
Davies G,
Vonk JM,
Wojczynski M,
Pouta A,
Johansson A,
Wild SH,
Ingelsson E,
Rivadeneira F,
Völzke H,
Hysi PG,
Eiriksdottir G,
Morrison AC,
Rotter JI,
Gao W,
Postma DS,
White WB,
Rich SS,
Hofman A,
Aspelund T,
Couper D,
Smith LJ,
Psaty BM,
Lohman K,
Burchard EG,
Uitterlinden AG,
Garcia M,
Joubert BR,
McArdle WL,
Musk AB,
Hansel N,
Heckbert SR,
Zgaga L,
van Meurs JB,
Navarro P,
Rudan I,
Oh YM,
Redline S,
Jarvis DL,
Zhao JH,
Rantanen T,
O'Connor GT,
Ripatti S,
Scott RJ,
Karrasch S,
Grallert H,
Gaddis NC,
Starr JM,
Wijmenga C,
Minster RL,
Lederer DJ,
Pekkanen J,
Gyllensten U,
Campbell H,
Morris AP,
Gläser S,
Hammond CJ,
Burkart KM,
Beilby J,
Kritchevsky SB,
Gudnason V,
Hancock DB,
Williams OD,
Polasek O,
Zemunik T,
Kolcic I,
Petrini MF,
Wjst M,
Kim WJ,
Porteous DJ,
Scotland G,
Smith BH,
Viljanen A,
Heliövaara M,
Attia JR,
Sayers I,
Hampel R,
Gieger C,
Deary IJ,
Boezen HM,
Newman A,
Jarvelin MR,
Wilson JF,
Lind L,
Stricker BH,
Teumer A,
Spector TD,
Melén E,
Peters MJ,
Lange LA,
Barr RG,
Bracke KR,
Verhamme FM,
Sung J,
Hiemstra PS,
Cassano PA,
Sood A,
Hayward C,
Dupuis J,
Hall IP,
Brusselle GG,
Tobin MD,
London SJ
Nature genetics · 2014 · PMID 24929828
4 pages
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
Hysi PG,
Cheng CY,
Springelkamp H,
Macgregor S,
Bailey JNC,
Wojciechowski R,
Vitart V,
Nag A,
Hewitt AW,
Höhn R,
Venturini C,
Mirshahi A
and 79 more — show all
Ramdas WD,
Thorleifsson G,
Vithana E,
Khor CC,
Stefansson AB,
Liao J,
Haines JL,
Amin N,
Wang YX,
Wild PS,
Ozel AB,
Li JZ,
Fleck BW,
Zeller T,
Staffieri SE,
Teo YY,
Cuellar-Partida G,
Luo X,
Allingham RR,
Richards JE,
Senft A,
Karssen LC,
Zheng Y,
Bellenguez C,
Xu L,
Iglesias AI,
Wilson JF,
Kang JH,
van Leeuwen EM,
Jonsson V,
Thorsteinsdottir U,
Despriet DDG,
Ennis S,
Moroi SE,
Martin NG,
Jansonius NM,
Yazar S,
Tai ES,
Amouyel P,
Kirwan J,
van Koolwijk LME,
Hauser MA,
Jonasson F,
Leo P,
Loomis SJ,
Fogarty R,
Rivadeneira F,
Kearns L,
Lackner KJ,
de Jong PTVM,
Simpson CL,
Pennell CE,
Oostra BA,
Uitterlinden AG,
Saw SM,
Lotery AJ,
Bailey-Wilson JE,
Hofman A,
Vingerling JR,
Maubaret C,
Pfeiffer N,
Wolfs RCW,
Lemij HG,
Young TL,
Pasquale LR,
Delcourt C,
Spector TD,
Klaver CCW,
Small KS,
Burdon KP,
Stefansson K,
Wong TY,
Viswanathan A,
Mackey DA,
Craig JE,
Wiggs JL,
van Duijn CM,
Hammond CJ,
Aung T
BMES GWAS Group · NEIGHBORHOOD Consortium and 1 more consortia
Nature genetics · 2014 · PMID 25173106 · open access
4 pages
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI
Verhaaren BF,
Debette S,
Bis JC,
Smith JA,
Ikram MK,
Adams HH,
Beecham AH,
Rajan KB,
Lopez LM,
Barral S,
van Buchem MA,
van der Grond J
and 90 more — show all
Smith AV,
Hegenscheid K,
Aggarwal NT,
de Andrade M,
Atkinson EJ,
Beekman M,
Beiser AS,
Blanton SH,
Boerwinkle E,
Brickman AM,
Bryan RN,
Chauhan G,
Chen CP,
Chouraki V,
de Craen AJ,
Crivello F,
Deary IJ,
Deelen J,
De Jager PL,
Dufouil C,
Elkind MS,
Evans DA,
Freudenberger P,
Gottesman RF,
Guðnason V,
Habes M,
Heckbert SR,
Heiss G,
Hilal S,
Hofer E,
Hofman A,
Ibrahim-Verbaas CA,
Knopman DS,
Lewis CE,
Liao J,
Liewald DC,
Luciano M,
van der Lugt A,
Martinez OO,
Mayeux R,
Mazoyer B,
Nalls M,
Nauck M,
Niessen WJ,
Oostra BA,
Psaty BM,
Rice KM,
Rotter JI,
von Sarnowski B,
Schmidt H,
Schreiner PJ,
Schuur M,
Sidney SS,
Sigurdsson S,
Slagboom PE,
Stott DJ,
van Swieten JC,
Teumer A,
Töglhofer AM,
Traylor M,
Trompet S,
Turner ST,
Tzourio C,
Uh HW,
Uitterlinden AG,
Vernooij MW,
Wang JJ,
Wong TY,
Wardlaw JM,
Windham BG,
Wittfeld K,
Wolf C,
Wright CB,
Yang Q,
Zhao W,
Zijdenbos A,
Jukema JW,
Sacco RL,
Kardia SL,
Amouyel P,
Mosley TH,
Longstreth WT Jr,
DeCarli CC,
van Duijn CM,
Schmidt R,
Launer LJ,
Grabe HJ,
Seshadri SS,
Ikram MA,
Fornage M
Circulation. Cardiovascular genetics · 2015 · PMID 25663218
4 pages
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis
Castaño-Betancourt MC,
Evans DS,
Ramos YF,
Boer CG,
Metrustry S,
Liu Y,
den Hollander W,
van Rooij J,
Kraus VB,
Yau MS,
Mitchell BD,
Muir K
and 25 more — show all
Hofman A,
Doherty M,
Doherty S,
Zhang W,
Kraaij R,
Rivadeneira F,
Barrett-Connor E,
Maciewicz RA,
Arden N,
Nelissen RG,
Kloppenburg M,
Jordan JM,
Nevitt MC,
Slagboom EP,
Hart DJ,
Lafeber F,
Styrkarsdottir U,
Zeggini E,
Evangelou E,
Spector TD,
Uitterlinden AG,
Lane NE,
Meulenbelt I,
Valdes AM,
van Meurs JB
PLoS genetics · 2016 · PMID 27701424 · open access
4 pages
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
Barban N,
Jansen R,
de Vlaming R,
Vaez A,
Mandemakers JJ,
Tropf FC,
Shen X,
Wilson JF,
Chasman DI,
Nolte IM,
Tragante V,
van der Laan SW
and 241 more — show all
Perry JR,
Kong A,
Ahluwalia TS,
Albrecht E,
Yerges-Armstrong L,
Atzmon G,
Auro K,
Ayers K,
Bakshi A,
Ben-Avraham D,
Berger K,
Bergman A,
Bertram L,
Bielak LF,
Bjornsdottir G,
Bonder MJ,
Broer L,
Bui M,
Barbieri C,
Cavadino A,
Chavarro JE,
Turman C,
Concas MP,
Cordell HJ,
Davies G,
Eibich P,
Eriksson N,
Esko T,
Eriksson J,
Falahi F,
Felix JF,
Fontana MA,
Franke L,
Gandin I,
Gaskins AJ,
Gieger C,
Gunderson EP,
Guo X,
Hayward C,
He C,
Hofer E,
Huang H,
Joshi PK,
Kanoni S,
Karlsson R,
Kiechl S,
Kifley A,
Kluttig A,
Kraft P,
Lagou V,
Lecoeur C,
Lahti J,
Li-Gao R,
Lind PA,
Liu T,
Makalic E,
Mamasoula C,
Matteson L,
Mbarek H,
McArdle PF,
McMahon G,
Meddens SF,
Mihailov E,
Miller M,
Missmer SA,
Monnereau C,
van der Most PJ,
Myhre R,
Nalls MA,
Nutile T,
Kalafati IP,
Porcu E,
Prokopenko I,
Rajan KB,
Rich-Edwards J,
Rietveld CA,
Robino A,
Rose LM,
Rueedi R,
Ryan KA,
Saba Y,
Schmidt D,
Smith JA,
Stolk L,
Streeten E,
Tönjes A,
Thorleifsson G,
Ulivi S,
Wedenoja J,
Wellmann J,
Willeit P,
Yao J,
Yengo L,
Zhao JH,
Zhao W,
Zhernakova DV,
Amin N,
Andrews H,
Balkau B,
Barzilai N,
Bergmann S,
Biino G,
Bisgaard H,
Bønnelykke K,
Boomsma DI,
Buring JE,
Campbell H,
Cappellani S,
Ciullo M,
Cox SR,
Cucca F,
Toniolo D,
Davey-Smith G,
Deary IJ,
Dedoussis G,
Deloukas P,
van Duijn CM,
de Geus EJ,
Eriksson JG,
Evans DA,
Faul JD,
Sala CF,
Froguel P,
Gasparini P,
Girotto G,
Grabe HJ,
Greiser KH,
Groenen PJ,
de Haan HG,
Haerting J,
Harris TB,
Heath AC,
Heikkilä K,
Hofman A,
Homuth G,
Holliday EG,
Hopper J,
Hyppönen E,
Jacobsson B,
Jaddoe VW,
Johannesson M,
Jugessur A,
Kähönen M,
Kajantie E,
Kardia SL,
Keavney B,
Kolcic I,
Koponen P,
Kovacs P,
Kronenberg F,
Kutalik Z,
La Bianca M,
Lachance G,
Iacono WG,
Lai S,
Lehtimäki T,
Liewald DC,
Lindgren CM,
Liu Y,
Luben R,
Lucht M,
Luoto R,
Magnus P,
Magnusson PK,
Martin NG,
McGue M,
McQuillan R,
Medland SE,
Meisinger C,
Mellström D,
Metspalu A,
Traglia M,
Milani L,
Mitchell P,
Montgomery GW,
Mook-Kanamori D,
de Mutsert R,
Nohr EA,
Ohlsson C,
Olsen J,
Ong KK,
Paternoster L,
Pattie A,
Penninx BW,
Perola M,
Peyser PA,
Pirastu M,
Polasek O,
Power C,
Kaprio J,
Raffel LJ,
Räikkönen K,
Raitakari O,
Ridker PM,
Ring SM,
Roll K,
Rudan I,
Ruggiero D,
Rujescu D,
Salomaa V,
Schlessinger D,
Schmidt H,
Schmidt R,
Schupf N,
Smit J,
Sorice R,
Spector TD,
Starr JM,
Stöckl D,
Strauch K,
Stumvoll M,
Swertz MA,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tung JY,
Uitterlinden AG,
Vaccargiu S,
Viikari J,
Vitart V,
Völzke H,
Vollenweider P,
Vuckovic D,
Waage J,
Wagner GG,
Wang JJ,
Wareham NJ,
Weir DR,
Willemsen G,
Willeit J,
Wright AF,
Zondervan KT,
Stefansson K,
Krueger RF,
Lee JJ,
Benjamin DJ,
Cesarini D,
Koellinger PD,
den Hoed M,
Snieder H,
Mills MC
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
Meta-analysis of genome-wide association studies on the intolerance of angiotensin-converting enzyme inhibitors
Mahmoudpour SH,
Veluchamy A,
Siddiqui MK,
Asselbergs FW,
Souverein PC,
de Keyser CE,
Hofman A,
Lang CC,
Doney AS,
Stricker BH,
de Boer A,
Maitland-van der Zee AH
and 1 more — show all
PREDICTION-ADR consortium
Pharmacogenetics and genomics · 2017 · PMID 28030426
4 pages
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
Gorski M,
van der Most PJ,
Teumer A,
Chu AY,
Li M,
Mijatovic V,
Nolte IM,
Cocca M,
Taliun D,
Gomez F,
Li Y,
Tayo B
and 114 more — show all
Tin A,
Feitosa MF,
Aspelund T,
Attia J,
Biffar R,
Bochud M,
Boerwinkle E,
Borecki I,
Bottinger EP,
Chen MH,
Chouraki V,
Ciullo M,
Coresh J,
Cornelis MC,
Curhan GC,
d'Adamo AP,
Dehghan A,
Dengler L,
Ding J,
Eiriksdottir G,
Endlich K,
Enroth S,
Esko T,
Franco OH,
Gasparini P,
Gieger C,
Girotto G,
Gottesman O,
Gudnason V,
Gyllensten U,
Hancock SJ,
Harris TB,
Helmer C,
Höllerer S,
Hofer E,
Hofman A,
Holliday EG,
Homuth G,
Hu FB,
Huth C,
Hutri-Kähönen N,
Hwang SJ,
Imboden M,
Johansson Å,
Kähönen M,
König W,
Kramer H,
Krämer BK,
Kumar A,
Kutalik Z,
Lambert JC,
Launer LJ,
Lehtimäki T,
de Borst M,
Navis G,
Swertz M,
Liu Y,
Lohman K,
Loos RJF,
Lu Y,
Lyytikäinen LP,
McEvoy MA,
Meisinger C,
Meitinger T,
Metspalu A,
Metzger M,
Mihailov E,
Mitchell P,
Nauck M,
Oldehinkel AJ,
Olden M,
Wjh Penninx B,
Pistis G,
Pramstaller PP,
Probst-Hensch N,
Raitakari OT,
Rettig R,
Ridker PM,
Rivadeneira F,
Robino A,
Rosas SE,
Ruderfer D,
Ruggiero D,
Saba Y,
Sala C,
Schmidt H,
Schmidt R,
Scott RJ,
Sedaghat S,
Smith AV,
Sorice R,
Stengel B,
Stracke S,
Strauch K,
Toniolo D,
Uitterlinden AG,
Ulivi S,
Viikari JS,
Völker U,
Vollenweider P,
Völzke H,
Vuckovic D,
Waldenberger M,
Jin Wang J,
Yang Q,
Chasman DI,
Tromp G,
Snieder H,
Heid IM,
Fox CS,
Köttgen A,
Pattaro C,
Böger CA,
Fuchsberger C
Scientific reports · 2017 · PMID 28452372 · open access
4 pages
Genome-wide association study of blood pressure and hypertension
Levy D,
Ehret GB,
Rice K,
Verwoert GC,
Launer LJ,
Dehghan A,
Glazer NL,
Morrison AC,
Johnson AD,
Aspelund T,
Aulchenko Y,
Lumley T
and 32 more — show all
Köttgen A,
Vasan RS,
Rivadeneira F,
Eiriksdottir G,
Guo X,
Arking DE,
Mitchell GF,
Mattace-Raso FU,
Smith AV,
Taylor K,
Scharpf RB,
Hwang SJ,
Sijbrands EJ,
Bis J,
Harris TB,
Ganesh SK,
O'Donnell CJ,
Hofman A,
Rotter JI,
Coresh J,
Benjamin EJ,
Uitterlinden AG,
Heiss G,
Fox CS,
Witteman JC,
Boerwinkle E,
Wang TJ,
Gudnason V,
Larson MG,
Chakravarti A,
Psaty BM,
van Duijn CM
Nature genetics · 2009 · PMID 19430479
3 pages
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution
Lindgren CM,
Heid IM,
Randall JC,
Lamina C,
Steinthorsdottir V,
Qi L,
Speliotes EK,
Thorleifsson G,
Willer CJ,
Herrera BM,
Jackson AU,
Lim N
and 131 more — show all
Scheet P,
Soranzo N,
Amin N,
Aulchenko YS,
Chambers JC,
Drong A,
Luan J,
Lyon HN,
Rivadeneira F,
Sanna S,
Timpson NJ,
Zillikens MC,
Zhao JH,
Almgren P,
Bandinelli S,
Bennett AJ,
Bergman RN,
Bonnycastle LL,
Bumpstead SJ,
Chanock SJ,
Cherkas L,
Chines P,
Coin L,
Cooper C,
Crawford G,
Doering A,
Dominiczak A,
Doney AS,
Ebrahim S,
Elliott P,
Erdos MR,
Estrada K,
Ferrucci L,
Fischer G,
Forouhi NG,
Gieger C,
Grallert H,
Groves CJ,
Grundy S,
Guiducci C,
Hadley D,
Hamsten A,
Havulinna AS,
Hofman A,
Holle R,
Holloway JW,
Illig T,
Isomaa B,
Jacobs LC,
Jameson K,
Jousilahti P,
Karpe F,
Kuusisto J,
Laitinen J,
Lathrop GM,
Lawlor DA,
Mangino M,
McArdle WL,
Meitinger T,
Morken MA,
Morris AP,
Munroe P,
Narisu N,
Nordström A,
Nordström P,
Oostra BA,
Palmer CN,
Payne F,
Peden JF,
Prokopenko I,
Renström F,
Ruokonen A,
Salomaa V,
Sandhu MS,
Scott LJ,
Scuteri A,
Silander K,
Song K,
Yuan X,
Stringham HM,
Swift AJ,
Tuomi T,
Uda M,
Vollenweider P,
Waeber G,
Wallace C,
Walters GB,
Weedon MN,
Witteman JC,
Zhang C,
Zhang W,
Caulfield MJ,
Collins FS,
Davey Smith G,
Day IN,
Franks PW,
Hattersley AT,
Hu FB,
Jarvelin MR,
Kong A,
Kooner JS,
Laakso M,
Lakatta E,
Mooser V,
Morris AD,
Peltonen L,
Samani NJ,
Spector TD,
Strachan DP,
Tanaka T,
Tuomilehto J,
Uitterlinden AG,
van Duijn CM,
Wareham NJ,
Hugh Watkins,
Waterworth DM,
Boehnke M,
Deloukas P,
Groop L,
Hunter DJ,
Thorsteinsdottir U,
Schlessinger D,
Wichmann HE,
Frayling TM,
Abecasis GR,
Hirschhorn JN,
Loos RJ,
Stefansson K,
Mohlke KL,
Barroso I,
McCarthy MI
Wellcome Trust Case Control Consortium · Procardis Consortia and 1 more consortia
PLoS genetics · 2009 · PMID 19557161 · open access
3 pages
Common genetic determinants of vitamin D insufficiency: a genome-wide association study
Wang TJ,
Zhang F,
Richards JB,
Kestenbaum B,
van Meurs JB,
Berry D,
Kiel DP,
Streeten EA,
Ohlsson C,
Koller DL,
Peltonen L,
Cooper JD
and 64 more — show all
O'Reilly PF,
Houston DK,
Glazer NL,
Vandenput L,
Peacock M,
Shi J,
Rivadeneira F,
McCarthy MI,
Anneli P,
de Boer IH,
Mangino M,
Kato B,
Smyth DJ,
Booth SL,
Jacques PF,
Burke GL,
Goodarzi M,
Cheung CL,
Wolf M,
Rice K,
Goltzman D,
Hidiroglou N,
Ladouceur M,
Wareham NJ,
Hocking LJ,
Hart D,
Arden NK,
Cooper C,
Malik S,
Fraser WD,
Hartikainen AL,
Zhai G,
Macdonald HM,
Forouhi NG,
Loos RJ,
Reid DM,
Hakim A,
Dennison E,
Liu Y,
Power C,
Stevens HE,
Jaana L,
Vasan RS,
Soranzo N,
Bojunga J,
Psaty BM,
Lorentzon M,
Foroud T,
Harris TB,
Hofman A,
Jansson JO,
Cauley JA,
Uitterlinden AG,
Gibson Q,
Järvelin MR,
Karasik D,
Siscovick DS,
Econs MJ,
Kritchevsky SB,
Florez JC,
Todd JA,
Dupuis J,
Hyppönen E,
Spector TD
Lancet (London, England) · 2010 · PMID 20541252
3 pages
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
Heid IM,
Jackson AU,
Randall JC,
Winkler TW,
Qi L,
Steinthorsdottir V,
Thorleifsson G,
Zillikens MC,
Speliotes EK,
Mägi R,
Workalemahu T,
White CC
and 290 more — show all
Bouatia-Naji N,
Harris TB,
Berndt SI,
Ingelsson E,
Willer CJ,
Weedon MN,
Luan J,
Vedantam S,
Esko T,
Kilpeläinen TO,
Kutalik Z,
Li S,
Monda KL,
Dixon AL,
Holmes CC,
Kaplan LM,
Liang L,
Min JL,
Moffatt MF,
Molony C,
Nicholson G,
Schadt EE,
Zondervan KT,
Feitosa MF,
Ferreira T,
Lango Allen H,
Weyant RJ,
Wheeler E,
Wood AR,
Estrada K,
Goddard ME,
Lettre G,
Mangino M,
Nyholt DR,
Purcell S,
Smith AV,
Visscher PM,
Yang J,
McCarroll SA,
Nemesh J,
Voight BF,
Absher D,
Amin N,
Aspelund T,
Coin L,
Glazer NL,
Hayward C,
Heard-Costa NL,
Hottenga JJ,
Johansson A,
Johnson T,
Kaakinen M,
Kapur K,
Ketkar S,
Knowles JW,
Kraft P,
Kraja AT,
Lamina C,
Leitzmann MF,
McKnight B,
Morris AP,
Ong KK,
Perry JR,
Peters MJ,
Polasek O,
Prokopenko I,
Rayner NW,
Ripatti S,
Rivadeneira F,
Robertson NR,
Sanna S,
Sovio U,
Surakka I,
Teumer A,
van Wingerden S,
Vitart V,
Zhao JH,
Cavalcanti-Proença C,
Chines PS,
Fisher E,
Kulzer JR,
Lecoeur C,
Narisu N,
Sandholt C,
Scott LJ,
Silander K,
Stark K,
Tammesoo ML,
Teslovich TM,
Timpson NJ,
Watanabe RM,
Welch R,
Chasman DI,
Cooper MN,
Jansson JO,
Kettunen J,
Lawrence RW,
Pellikka N,
Perola M,
Vandenput L,
Alavere H,
Almgren P,
Atwood LD,
Bennett AJ,
Biffar R,
Bonnycastle LL,
Bornstein SR,
Buchanan TA,
Campbell H,
Day IN,
Dei M,
Dörr M,
Elliott P,
Erdos MR,
Eriksson JG,
Freimer NB,
Fu M,
Gaget S,
Geus EJ,
Gjesing AP,
Grallert H,
Grässler J,
Groves CJ,
Guiducci C,
Hartikainen AL,
Hassanali N,
Havulinna AS,
Herzig KH,
Hicks AA,
Hui J,
Igl W,
Jousilahti P,
Jula A,
Kajantie E,
Kinnunen L,
Kolcic I,
Koskinen S,
Kovacs P,
Kroemer HK,
Krzelj V,
Kuusisto J,
Kvaloy K,
Laitinen J,
Lantieri O,
Lathrop GM,
Lokki ML,
Luben RN,
Ludwig B,
McArdle WL,
McCarthy A,
Morken MA,
Nelis M,
Neville MJ,
Paré G,
Parker AN,
Peden JF,
Pichler I,
Pietiläinen KH,
Platou CG,
Pouta A,
Ridderstråle M,
Samani NJ,
Saramies J,
Sinisalo J,
Smit JH,
Strawbridge RJ,
Stringham HM,
Swift AJ,
Teder-Laving M,
Thomson B,
Usala G,
van Meurs JB,
van Ommen GJ,
Vatin V,
Volpato CB,
Wallaschofski H,
Walters GB,
Widen E,
Wild SH,
Willemsen G,
Witte DR,
Zgaga L,
Zitting P,
Beilby JP,
James AL,
James AL,
Kähönen M,
Lehtimäki T,
Nieminen MS,
Ohlsson C,
Palmer LJ,
Raitakari O,
Ridker PM,
Stumvoll M,
Tönjes A,
Viikari J,
Balkau B,
Ben-Shlomo Y,
Bergman RN,
Boeing H,
Smith GD,
Ebrahim S,
Froguel P,
Hansen T,
Hengstenberg C,
Hveem K,
Isomaa B,
Jørgensen T,
Karpe F,
Khaw KT,
Laakso M,
Lawlor DA,
Marre M,
Meitinger T,
Metspalu A,
Midthjell K,
Pedersen O,
Salomaa V,
Schwarz PE,
Schwarz PE,
Tuomi T,
Tuomilehto J,
Valle TT,
Wareham NJ,
Arnold AM,
Beckmann JS,
Bergmann S,
Boerwinkle E,
Boomsma DI,
Caulfield MJ,
Collins FS,
Eiriksdottir G,
Gudnason V,
Gyllensten U,
Hamsten A,
Hattersley AT,
Hofman A,
Hu FB,
Illig T,
Iribarren C,
Jarvelin MR,
Kao WH,
Kaprio J,
Launer LJ,
Munroe PB,
Oostra B,
Penninx BW,
Pramstaller PP,
Psaty BM,
Quertermous T,
Rissanen A,
Rudan I,
Shuldiner AR,
Soranzo N,
Spector TD,
Syvanen AC,
Uda M,
Uitterlinden A,
Völzke H,
Vollenweider P,
Wilson JF,
Witteman JC,
Wright AF,
Abecasis GR,
Boehnke M,
Borecki IB,
Deloukas P,
Frayling TM,
Groop LC,
Haritunians T,
Hunter DJ,
Kaplan RC,
North KE,
O'Connell JR,
Peltonen L,
Schlessinger D,
Strachan DP,
Hirschhorn JN,
Assimes TL,
Wichmann HE,
Thorsteinsdottir U,
van Duijn CM,
Stefansson K,
Cupples LA,
Loos RJ,
Barroso I,
McCarthy MI,
Fox CS,
Mohlke KL,
Lindgren CM
MAGIC
Nature genetics · 2010 · PMID 20935629
3 pages
Multiple loci are associated with white blood cell phenotypes
Nalls MA,
Couper DJ,
Tanaka T,
van Rooij FJ,
Chen MH,
Smith AV,
Toniolo D,
Zakai NA,
Yang Q,
Greinacher A,
Wood AR,
Garcia M
and 81 more — show all
Gasparini P,
Liu Y,
Lumley T,
Folsom AR,
Reiner AP,
Gieger C,
Lagou V,
Felix JF,
Völzke H,
Gouskova NA,
Biffi A,
Döring A,
Völker U,
Chong S,
Wiggins KL,
Rendon A,
Dehghan A,
Moore M,
Taylor K,
Wilson JG,
Lettre G,
Hofman A,
Bis JC,
Pirastu N,
Fox CS,
Meisinger C,
Sambrook J,
Arepalli S,
Nauck M,
Prokisch H,
Stephens J,
Glazer NL,
Cupples LA,
Okada Y,
Takahashi A,
Kamatani Y,
Matsuda K,
Tsunoda T,
Tanaka T,
Kubo M,
Nakamura Y,
Yamamoto K,
Kamatani N,
Stumvoll M,
Tönjes A,
Prokopenko I,
Illig T,
Patel KV,
Garner SF,
Kuhnel B,
Mangino M,
Oostra BA,
Thein SL,
Coresh J,
Wichmann HE,
Menzel S,
Lin J,
Pistis G,
Uitterlinden AG,
Spector TD,
Teumer A,
Eiriksdottir G,
Gudnason V,
Bandinelli S,
Frayling TM,
Chakravarti A,
van Duijn CM,
Melzer D,
Ouwehand WH,
Levy D,
Boerwinkle E,
Singleton AB,
Hernandez DG,
Longo DL,
Soranzo N,
Witteman JC,
Psaty BM,
Ferrucci L,
Harris TB,
O'Donnell CJ,
Ganesh SK
PLoS genetics · 2011 · PMID 21738480 · open access
3 pages
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
Ellinor PT,
Lunetta KL,
Albert CM,
Glazer NL,
Ritchie MD,
Smith AV,
Arking DE,
Müller-Nurasyid M,
Krijthe BP,
Lubitz SA,
Bis JC,
Chung MK
and 77 more — show all
Dörr M,
Ozaki K,
Roberts JD,
Smith JG,
Pfeufer A,
Sinner MF,
Lohman K,
Ding J,
Smith NL,
Smith JD,
Rienstra M,
Rice KM,
Van Wagoner DR,
Magnani JW,
Wakili R,
Clauss S,
Rotter JI,
Steinbeck G,
Launer LJ,
Davies RW,
Borkovich M,
Harris TB,
Lin H,
Völker U,
Völzke H,
Milan DJ,
Hofman A,
Boerwinkle E,
Chen LY,
Soliman EZ,
Voight BF,
Li G,
Chakravarti A,
Kubo M,
Tedrow UB,
Rose LM,
Ridker PM,
Conen D,
Tsunoda T,
Furukawa T,
Sotoodehnia N,
Xu S,
Kamatani N,
Levy D,
Nakamura Y,
Parvez B,
Mahida S,
Furie KL,
Rosand J,
Muhammad R,
Psaty BM,
Meitinger T,
Perz S,
Wichmann HE,
Witteman JC,
Kao WH,
Kathiresan S,
Roden DM,
Uitterlinden AG,
Rivadeneira F,
McKnight B,
Sjögren M,
Newman AB,
Liu Y,
Gollob MH,
Melander O,
Tanaka T,
Stricker BH,
Felix SB,
Alonso A,
Darbar D,
Barnard J,
Chasman DI,
Heckbert SR,
Benjamin EJ,
Gudnason V,
Kääb S
Nature genetics · 2012 · PMID 22544366
3 pages
Discovery and fine mapping of serum protein loci through transethnic meta-analysis
Franceschini N,
van Rooij FJ,
Prins BP,
Feitosa MF,
Karakas M,
Eckfeldt JH,
Folsom AR,
Kopp J,
Vaez A,
Andrews JS,
Baumert J,
Boraska V
and 89 more — show all
Broer L,
Hayward C,
Ngwa JS,
Okada Y,
Polasek O,
Westra HJ,
Wang YA,
Del Greco M F,
Glazer NL,
Kapur K,
Kema IP,
Lopez LM,
Schillert A,
Smith AV,
Winkler CA,
Zgaga L,
Bandinelli S,
Bergmann S,
Boban M,
Bochud M,
Chen YD,
Davies G,
Dehghan A,
Ding J,
Doering A,
Durda JP,
Ferrucci L,
Franco OH,
Franke L,
Gunjaca G,
Hofman A,
Hsu FC,
Kolcic I,
Kraja A,
Kubo M,
Lackner KJ,
Launer L,
Loehr LR,
Li G,
Meisinger C,
Nakamura Y,
Schwienbacher C,
Starr JM,
Takahashi A,
Torlak V,
Uitterlinden AG,
Vitart V,
Waldenberger M,
Wild PS,
Kirin M,
Zeller T,
Zemunik T,
Zhang Q,
Ziegler A,
Blankenberg S,
Boerwinkle E,
Borecki IB,
Campbell H,
Deary IJ,
Frayling TM,
Gieger C,
Harris TB,
Hicks AA,
Koenig W,
O' Donnell CJ,
Fox CS,
Pramstaller PP,
Psaty BM,
Reiner AP,
Rotter JI,
Rudan I,
Snieder H,
Tanaka T,
van Duijn CM,
Vollenweider P,
Waeber G,
Wilson JF,
Witteman JC,
Wolffenbuttel BH,
Wright AF,
Wu Q,
Liu Y,
Jenny NS,
North KE,
Felix JF,
Alizadeh BZ,
Cupples LA,
Perry JR,
Morris AP
LifeLines Cohort Study
American journal of human genetics · 2012 · PMID 23022100
3 pages
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations
Köttgen A,
Albrecht E,
Teumer A,
Vitart V,
Krumsiek J,
Hundertmark C,
Pistis G,
Ruggiero D,
O'Seaghdha CM,
Haller T,
Yang Q,
Tanaka T
and 214 more — show all
Johnson AD,
Kutalik Z,
Smith AV,
Shi J,
Struchalin M,
Middelberg RP,
Brown MJ,
Gaffo AL,
Pirastu N,
Li G,
Hayward C,
Zemunik T,
Huffman J,
Yengo L,
Zhao JH,
Demirkan A,
Feitosa MF,
Liu X,
Malerba G,
Lopez LM,
van der Harst P,
Li X,
Kleber ME,
Hicks AA,
Nolte IM,
Johansson A,
Murgia F,
Wild SH,
Bakker SJ,
Peden JF,
Dehghan A,
Steri M,
Tenesa A,
Lagou V,
Salo P,
Mangino M,
Rose LM,
Lehtimäki T,
Woodward OM,
Okada Y,
Tin A,
Müller C,
Oldmeadow C,
Putku M,
Czamara D,
Kraft P,
Frogheri L,
Thun GA,
Grotevendt A,
Gislason GK,
Harris TB,
Launer LJ,
McArdle P,
Shuldiner AR,
Boerwinkle E,
Coresh J,
Schmidt H,
Schallert M,
Martin NG,
Montgomery GW,
Kubo M,
Nakamura Y,
Tanaka T,
Munroe PB,
Samani NJ,
Jacobs DR Jr,
Liu K,
D'Adamo P,
Ulivi S,
Rotter JI,
Psaty BM,
Vollenweider P,
Waeber G,
Campbell S,
Devuyst O,
Navarro P,
Kolcic I,
Hastie N,
Balkau B,
Froguel P,
Esko T,
Salumets A,
Khaw KT,
Langenberg C,
Wareham NJ,
Isaacs A,
Kraja A,
Zhang Q,
Wild PS,
Scott RJ,
Holliday EG,
Org E,
Org E,
Viigimaa M,
Bandinelli S,
Metter JE,
Lupo A,
Trabetti E,
Sorice R,
Döring A,
Lattka E,
Strauch K,
Theis F,
Waldenberger M,
Wichmann HE,
Davies G,
Gow AJ,
Bruinenberg M,
Stolk RP,
Kooner JS,
Zhang W,
Winkelmann BR,
Boehm BO,
Lucae S,
Penninx BW,
Smit JH,
Curhan G,
Mudgal P,
Plenge RM,
Portas L,
Persico I,
Kirin M,
Wilson JF,
Mateo Leach I,
van Gilst WH,
Goel A,
Ongen H,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Imboden M,
von Eckardstein A,
Cucca F,
Nagaraja R,
Piras MG,
Nauck M,
Schurmann C,
Budde K,
Ernst F,
Farrington SM,
Theodoratou E,
Prokopenko I,
Stumvoll M,
Jula A,
Perola M,
Salomaa V,
Shin SY,
Spector TD,
Sala C,
Ridker PM,
Kähönen M,
Viikari J,
Hengstenberg C,
Nelson CP,
Meschia JF,
Nalls MA,
Sharma P,
Singleton AB,
Kamatani N,
Zeller T,
Burnier M,
Attia J,
Laan M,
Klopp N,
Hillege HL,
Kloiber S,
Choi H,
Pirastu M,
Tore S,
Probst-Hensch NM,
Völzke H,
Gudnason V,
Parsa A,
Schmidt R,
Whitfield JB,
Fornage M,
Gasparini P,
Siscovick DS,
Polašek O,
Campbell H,
Rudan I,
Bouatia-Naji N,
Metspalu A,
Loos RJ,
van Duijn CM,
Borecki IB,
Ferrucci L,
Gambaro G,
Deary IJ,
Wolffenbuttel BH,
Chambers JC,
März W,
Pramstaller PP,
Snieder H,
Gyllensten U,
Wright AF,
Navis G,
Watkins H,
Witteman JC,
Sanna S,
Schipf S,
Dunlop MG,
Tönjes A,
Ripatti S,
Soranzo N,
Toniolo D,
Chasman DI,
Raitakari O,
Kao WH,
Ciullo M,
Fox CS,
Caulfield M,
Bochud M,
Gieger C
LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
3 pages
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
Rietveld CA,
Medland SE,
Derringer J,
Yang J,
Esko T,
Martin NW,
Westra HJ,
Shakhbazov K,
Abdellaoui A,
Agrawal A,
Albrecht E,
Alizadeh BZ
and 191 more — show all
Amin N,
Barnard J,
Baumeister SE,
Benke KS,
Bielak LF,
Boatman JA,
Boyle PA,
Davies G,
de Leeuw C,
Eklund N,
Evans DS,
Ferhmann R,
Fischer K,
Gieger C,
Gjessing HK,
Hägg S,
Harris JR,
Hayward C,
Holzapfel C,
Ibrahim-Verbaas CA,
Ingelsson E,
Jacobsson B,
Joshi PK,
Jugessur A,
Kaakinen M,
Kanoni S,
Karjalainen J,
Kolcic I,
Kristiansson K,
Kutalik Z,
Lahti J,
Lee SH,
Lin P,
Lind PA,
Liu Y,
Lohman K,
Loitfelder M,
McMahon G,
Vidal PM,
Meirelles O,
Milani L,
Myhre R,
Nuotio ML,
Oldmeadow CJ,
Petrovic KE,
Peyrot WJ,
Polasek O,
Quaye L,
Reinmaa E,
Rice JP,
Rizzi TS,
Schmidt H,
Schmidt R,
Smith AV,
Smith JA,
Tanaka T,
Terracciano A,
van der Loos MJ,
Vitart V,
Völzke H,
Wellmann J,
Yu L,
Zhao W,
Allik J,
Attia JR,
Bandinelli S,
Bastardot F,
Beauchamp J,
Bennett DA,
Berger K,
Bierut LJ,
Boomsma DI,
Bültmann U,
Campbell H,
Chabris CF,
Cherkas L,
Chung MK,
Cucca F,
de Andrade M,
De Jager PL,
De Neve JE,
Deary IJ,
Dedoussis GV,
Deloukas P,
Dimitriou M,
Eiríksdóttir G,
Elderson MF,
Eriksson JG,
Evans DM,
Faul JD,
Ferrucci L,
Garcia ME,
Grönberg H,
Guðnason V,
Hall P,
Harris JM,
Harris TB,
Hastie ND,
Heath AC,
Hernandez DG,
Hoffmann W,
Hofman A,
Holle R,
Holliday EG,
Hottenga JJ,
Iacono WG,
Illig T,
Järvelin MR,
Kähönen M,
Kaprio J,
Kirkpatrick RM,
Kowgier M,
Latvala A,
Launer LJ,
Lawlor DA,
Lehtimäki T,
Li J,
Lichtenstein P,
Lichtner P,
Liewald DC,
Madden PA,
Magnusson PK,
Mäkinen TE,
Masala M,
McGue M,
Metspalu A,
Mielck A,
Miller MB,
Montgomery GW,
Mukherjee S,
Nyholt DR,
Oostra BA,
Palmer LJ,
Palotie A,
Penninx BW,
Perola M,
Peyser PA,
Preisig M,
Räikkönen K,
Raitakari OT,
Realo A,
Ring SM,
Ripatti S,
Rivadeneira F,
Rudan I,
Rustichini A,
Salomaa V,
Sarin AP,
Schlessinger D,
Scott RJ,
Snieder H,
St Pourcain B,
Starr JM,
Sul JH,
Surakka I,
Svento R,
Teumer A,
Tiemeier H,
van Rooij FJ,
Van Wagoner DR,
Vartiainen E,
Viikari J,
Vollenweider P,
Vonk JM,
Waeber G,
Weir DR,
Wichmann HE,
Widen E,
Willemsen G,
Wilson JF,
Wright AF,
Conley D,
Davey-Smith G,
Franke L,
Groenen PJ,
Hofman A,
Johannesson M,
Kardia SL,
Krueger RF,
Laibson D,
Martin NG,
Meyer MN,
Posthuma D,
Thurik AR,
Timpson NJ,
Uitterlinden AG,
van Duijn CM,
Visscher PM,
Benjamin DJ,
Cesarini D,
Koellinger PD
LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
Genome-wide meta-analysis identifies new susceptibility loci for migraine
Anttila V,
Winsvold BS,
Gormley P,
Kurth T,
Bettella F,
McMahon G,
Kallela M,
Malik R,
de Vries B,
Terwindt G,
Medland SE,
Todt U
and 85 more — show all
McArdle WL,
Quaye L,
Koiranen M,
Ikram MA,
Lehtimäki T,
Stam AH,
Ligthart L,
Wedenoja J,
Dunham I,
Neale BM,
Palta P,
Hamalainen E,
Schürks M,
Rose LM,
Buring JE,
Ridker PM,
Steinberg S,
Stefansson H,
Jakobsson F,
Lawlor DA,
Evans DM,
Ring SM,
Färkkilä M,
Artto V,
Kaunisto MA,
Freilinger T,
Schoenen J,
Frants RR,
Pelzer N,
Weller CM,
Zielman R,
Heath AC,
Madden PAF,
Montgomery GW,
Martin NG,
Borck G,
Göbel H,
Heinze A,
Heinze-Kuhn K,
Williams FMK,
Hartikainen AL,
Pouta A,
van den Ende J,
Uitterlinden AG,
Hofman A,
Amin N,
Hottenga JJ,
Vink JM,
Heikkilä K,
Alexander M,
Muller-Myhsok B,
Schreiber S,
Meitinger T,
Wichmann HE,
Aromaa A,
Eriksson JG,
Traynor B,
Trabzuni D,
Rossin E,
Lage K,
Jacobs SBR,
Jacobs SBR,
Gibbs JR,
Birney E,
Kaprio J,
Penninx BW,
Boomsma DI,
van Duijn C,
van Duijn C,
Raitakari O,
Jarvelin MR,
Zwart JA,
Cherkas L,
Strachan DP,
Kubisch C,
Ferrari MD,
van den Maagdenberg AMJM,
Dichgans M,
Wessman M,
Smith GD,
Stefansson K,
Daly MJ,
Nyholt DR,
Chasman D,
Palotie A
North American Brain Expression Consortium · UK Brain Expression Consortium
Nature genetics · 2013 · PMID 23793025 · open access
3 pages
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
Evangelou E,
Kerkhof HJ,
Styrkarsdottir U,
Ntzani EE,
Bos SD,
Esko T,
Evans DS,
Metrustry S,
Panoutsopoulou K,
Ramos YF,
Thorleifsson G,
Tsilidis KK
and 54 more — show all
Arden N,
Aslam N,
Bellamy N,
Birrell F,
Blanco FJ,
Carr A,
Chapman K,
Day-Williams AG,
Deloukas P,
Doherty M,
Engström G,
Helgadottir HT,
Hofman A,
Ingvarsson T,
Jonsson H,
Keis A,
Keurentjes JC,
Kloppenburg M,
Lind PA,
McCaskie A,
Martin NG,
Milani L,
Montgomery GW,
Nelissen RG,
Nevitt MC,
Nilsson PM,
Ollier WE,
Parimi N,
Rai A,
Ralston SH,
Reed MR,
Riancho JA,
Rivadeneira F,
Rodriguez-Fontenla C,
Southam L,
Thorsteinsdottir U,
Tsezou A,
Wallis GA,
Wilkinson JM,
Gonzalez A,
Lane NE,
Lohmander LS,
Loughlin J,
Metspalu A,
Uitterlinden AG,
Jonsdottir I,
Stefansson K,
Slagboom PE,
Zeggini E,
Meulenbelt I,
Ioannidis JP,
Spector TD,
van Meurs JB,
Valdes AM
arcOGEN Consortium
Annals of the rheumatic diseases · 2014 · PMID 23989986 · open access
3 pages
Questions about this list
Why is my paper here? I never gave you permission.
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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
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My name is misspelt, or the paper is wrong.
Tell us and it is fixed. Names come from the public record and initials are
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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
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