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17 matches for
Jones G.
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Demenais F,
Margaritte-Jeannin P,
Barnes KC,
Cookson WOC,
Altmüller J,
Ang W,
Barr RG,
Beaty TH,
Becker AB,
Beilby J,
Bisgaard H,
Bjornsdottir US
and 163 more — show all
Bleecker E,
Bønnelykke K,
Boomsma DI,
Bouzigon E,
Brightling CE,
Brossard M,
Brusselle GG,
Burchard E,
Burkart KM,
Bush A,
Chan-Yeung M,
Chung KF,
Couto Alves A,
Curtin JA,
Custovic A,
Daley D,
de Jongste JC,
Del-Rio-Navarro BE,
Donohue KM,
Duijts L,
Eng C,
Eriksson JG,
Farrall M,
Fedorova Y,
Feenstra B,
Ferreira MA,
Freidin MB,
Gajdos Z,
Gauderman J,
Gehring U,
Geller F,
Genuneit J,
Gharib SA,
Gilliland F,
Granell R,
Graves PE,
Gudbjartsson DF,
Haahtela T,
Heckbert SR,
Heederik D,
Heinrich J,
Heliövaara M,
Henderson J,
Himes BE,
Hirose H,
Hirschhorn JN,
Hofman A,
Holt P,
Hottenga J,
Hudson TJ,
Hui J,
Imboden M,
Ivanov V,
Jaddoe VWV,
James A,
Janson C,
Jarvelin MR,
Jarvis D,
Jones G,
Jonsdottir I,
Jousilahti P,
Kabesch M,
Kähönen M,
Kantor DB,
Karunas AS,
Khusnutdinova E,
Koppelman GH,
Kozyrskyj AL,
Kreiner E,
Kubo M,
Kumar R,
Kumar A,
Kuokkanen M,
Lahousse L,
Laitinen T,
Laprise C,
Lathrop M,
Lau S,
Lee YA,
Lehtimäki T,
Letort S,
Levin AM,
Li G,
Liang L,
Loehr LR,
London SJ,
Loth DW,
Manichaikul A,
Marenholz I,
Martinez FJ,
Matheson MC,
Mathias RA,
Matsumoto K,
Mbarek H,
McArdle WL,
Melbye M,
Melén E,
Meyers D,
Michel S,
Mohamdi H,
Musk AW,
Myers RA,
Nieuwenhuis MAE,
Noguchi E,
O'Connor GT,
Ogorodova LM,
Palmer CD,
Palotie A,
Park JE,
Pennell CE,
Pershagen G,
Polonikov A,
Postma DS,
Probst-Hensch N,
Puzyrev VP,
Raby BA,
Raitakari OT,
Ramasamy A,
Rich SS,
Robertson CF,
Romieu I,
Salam MT,
Salomaa V,
Schlünssen V,
Scott R,
Selivanova PA,
Sigsgaard T,
Simpson A,
Siroux V,
Smith LJ,
Solodilova M,
Standl M,
Stefansson K,
Strachan DP,
Stricker BH,
Takahashi A,
Thompson PJ,
Thorleifsson G,
Thorsteinsdottir U,
Tiesler CMT,
Torgerson DG,
Tsunoda T,
Uitterlinden AG,
van der Valk RJP,
Vaysse A,
Vedantam S,
von Berg A,
von Mutius E,
Vonk JM,
Waage J,
Wareham NJ,
Weiss ST,
White WB,
Wickman M,
Widén E,
Willemsen G,
Williams LK,
Wouters IM,
Yang JJ,
Zhao JH,
Moffatt MF,
Ober C,
Nicolae DL
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
12 pages+
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Schunkert H,
König IR,
Kathiresan S,
Reilly MP,
Assimes TL,
Holm H,
Preuss M,
Stewart AF,
Barbalic M,
Gieger C,
Absher D,
Aherrahrou Z
and 155 more — show all
Allayee H,
Altshuler D,
Anand SS,
Andersen K,
Anderson JL,
Ardissino D,
Ball SG,
Balmforth AJ,
Barnes TA,
Becker DM,
Becker LC,
Berger K,
Bis JC,
Boekholdt SM,
Boerwinkle E,
Braund PS,
Brown MJ,
Burnett MS,
Buysschaert I,
Carlquist JF,
Chen L,
Cichon S,
Codd V,
Davies RW,
Dedoussis G,
Dehghan A,
Demissie S,
Devaney JM,
Diemert P,
Do R,
Doering A,
Eifert S,
Mokhtari NE,
Ellis SG,
Elosua R,
Engert JC,
Epstein SE,
de Faire U,
Fischer M,
Folsom AR,
Freyer J,
Gigante B,
Girelli D,
Gretarsdottir S,
Gudnason V,
Gulcher JR,
Halperin E,
Hammond N,
Hazen SL,
Hofman A,
Horne BD,
Illig T,
Iribarren C,
Jones GT,
Jukema JW,
Kaiser MA,
Kaplan LM,
Kastelein JJ,
Khaw KT,
Knowles JW,
Kolovou G,
Kong A,
Laaksonen R,
Lambrechts D,
Leander K,
Lettre G,
Li M,
Lieb W,
Loley C,
Lotery AJ,
Mannucci PM,
Maouche S,
Martinelli N,
McKeown PP,
Meisinger C,
Meitinger T,
Melander O,
Merlini PA,
Mooser V,
Morgan T,
Mühleisen TW,
Muhlestein JB,
Münzel T,
Musunuru K,
Nahrstaedt J,
Nelson CP,
Nöthen MM,
Olivieri O,
Patel RS,
Patterson CC,
Peters A,
Peyvandi F,
Qu L,
Quyyumi AA,
Rader DJ,
Rallidis LS,
Rice C,
Rosendaal FR,
Rubin D,
Salomaa V,
Sampietro ML,
Sandhu MS,
Schadt E,
Schäfer A,
Schillert A,
Schreiber S,
Schrezenmeir J,
Schwartz SM,
Siscovick DS,
Sivananthan M,
Sivapalaratnam S,
Smith A,
Smith TB,
Snoep JD,
Soranzo N,
Spertus JA,
Stark K,
Stirrups K,
Stoll M,
Tang WH,
Tennstedt S,
Thorgeirsson G,
Thorleifsson G,
Tomaszewski M,
Uitterlinden AG,
van Rij AM,
Voight BF,
Wareham NJ,
Wells GA,
Wichmann HE,
Wild PS,
Willenborg C,
Witteman JC,
Wright BJ,
Ye S,
Zeller T,
Ziegler A,
Cambien F,
Goodall AH,
Cupples LA,
Quertermous T,
März W,
Hengstenberg C,
Blankenberg S,
Ouwehand WH,
Hall AS,
Deloukas P,
Thompson JR,
Stefansson K,
Roberts R,
Thorsteinsdottir U,
O'Donnell CJ,
McPherson R,
Erdmann J,
Samani NJ
Cardiogenics · CARDIoGRAM Consortium
Nature genetics · 2011 · PMID 21378990
7 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
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
Bønnelykke K,
Matheson MC,
Pers TH,
Granell R,
Strachan DP,
Alves AC,
Linneberg A,
Curtin JA,
Warrington NM,
Standl M,
Kerkhof M,
Jonsdottir I
and 58 more — show all
Bukvic BK,
Kaakinen M,
Sleimann P,
Thorleifsson G,
Thorsteinsdottir U,
Schramm K,
Baltic S,
Kreiner-Møller E,
Simpson A,
St Pourcain B,
Coin L,
Hui J,
Walters EH,
Tiesler CMT,
Duffy DL,
Jones G,
Ring SM,
McArdle WL,
Price L,
Robertson CF,
Pekkanen J,
Pekkanen J,
Tang CS,
Thiering E,
Montgomery GW,
Hartikainen AL,
Dharmage SC,
Husemoen LL,
Herder C,
Kemp JP,
Elliot P,
James A,
Waldenberger M,
Abramson MJ,
Fairfax BP,
Knight JC,
Knight JC,
Gupta R,
Thompson PJ,
Holt P,
Sly P,
Hirschhorn JN,
Blekic M,
Weidinger S,
Hakonarsson H,
Stefansson K,
Heinrich J,
Postma DS,
Custovic A,
Pennell CE,
Pennell CE,
Jarvelin MR,
Koppelman GH,
Timpson N,
Ferreira MA,
Ferreira MA,
Bisgaard H,
Henderson AJ
AAGC
Nature genetics · 2013 · PMID 23817571
7 pages
Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program
Klarin D,
Verma SS,
Judy R,
Dikilitas O,
Wolford BN,
Paranjpe I,
Levin MG,
Pan C,
Tcheandjieu C,
Spin JM,
Lynch J,
Assimes TL
and 41 more — show all
Åldstedt Nyrønning L,
Mattsson E,
Edwards TL,
Denny J,
Larson E,
Lee MTM,
Carrell D,
Zhang Y,
Jarvik GP,
Gharavi AG,
Harley J,
Mentch F,
Pacheco JA,
Hakonarson H,
Skogholt AH,
Thomas L,
Gabrielsen ME,
Hveem K,
Nielsen JB,
Zhou W,
Fritsche L,
Huang J,
Natarajan P,
Sun YV,
DuVall SL,
Rader DJ,
Cho K,
Chang KM,
Wilson PWF,
O'Donnell CJ,
Kathiresan S,
Scali ST,
Berceli SA,
Willer C,
Jones GT,
Bown MJ,
Nadkarni G,
Kullo IJ,
Ritchie M,
Damrauer SM,
Tsao PS
Veterans Affairs Million Veteran Program†
Circulation · 2020 · PMID 32981348 · open access
6 pages
Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors
Bakker MK,
van der Spek RAA,
van Rheenen W,
Morel S,
Bourcier R,
Hostettler IC,
Alg VS,
van Eijk KR,
Koido M,
Akiyama M,
Terao C,
Matsuda K
and 62 more — show all
Walters RG,
Lin K,
Li L,
Millwood IY,
Chen Z,
Rouleau GA,
Zhou S,
Rannikmäe K,
Sudlow CLM,
Houlden H,
van den Berg LH,
Dina C,
Naggara O,
Gentric JC,
Shotar E,
Eugène F,
Desal H,
Winsvold BS,
Børte S,
Johnsen MB,
Brumpton BM,
Sandvei MS,
Willer CJ,
Hveem K,
Zwart JA,
Verschuren WMM,
Friedrich CM,
Hirsch S,
Schilling S,
Dauvillier J,
Martin O,
Jones GT,
Bown MJ,
Ko NU,
Kim H,
Coleman JRI,
Breen G,
Zaroff JG,
Klijn CJM,
Malik R,
Dichgans M,
Sargurupremraj M,
Tatlisumak T,
Amouyel P,
Debette S,
Rinkel GJE,
Worrall BB,
Pera J,
Slowik A,
Gaál-Paavola EI,
Niemelä M,
Jääskeläinen JE,
von Und Zu Fraunberg M,
Lindgren A,
Broderick JP,
Werring DJ,
Woo D,
Redon R,
Bijlenga P,
Kamatani Y,
Veldink JH,
Ruigrok YM
HUNT All-In Stroke · China Kadoorie Biobank Collaborative Group and 5 more consortia
Nature genetics · 2020 · PMID 33199917
6 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
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci
Jones GT,
Tromp G,
Kuivaniemi H,
Gretarsdottir S,
Baas AF,
Giusti B,
Strauss E,
Van't Hof FN,
Webb TR,
Erdman R,
Ritchie MD,
Elmore JR
and 105 more — show all
Verma A,
Pendergrass S,
Kullo IJ,
Ye Z,
Peissig PL,
Gottesman O,
Verma SS,
Malinowski J,
Rasmussen-Torvik LJ,
Borthwick KM,
Smelser DT,
Crosslin DR,
de Andrade M,
Ryer EJ,
McCarty CA,
Böttinger EP,
Pacheco JA,
Crawford DC,
Carrell DS,
Gerhard GS,
Franklin DP,
Carey DJ,
Phillips VL,
Williams MJ,
Wei W,
Blair R,
Hill AA,
Vasudevan TM,
Lewis DR,
Thomson IA,
Krysa J,
Hill GB,
Roake J,
Merriman TR,
Oszkinis G,
Galora S,
Saracini C,
Abbate R,
Pulli R,
Pratesi C,
Saratzis A,
Verissimo AR,
Bumpstead S,
Badger SA,
Clough RE,
Cockerill G,
Hafez H,
Scott DJ,
Futers TS,
Romaine SP,
Bridge K,
Griffin KJ,
Bailey MA,
Smith A,
Thompson MM,
van Bockxmeer FM,
Matthiasson SE,
Thorleifsson G,
Thorsteinsdottir U,
Blankensteijn JD,
Teijink JA,
Wijmenga C,
de Graaf J,
Kiemeney LA,
Lindholt JS,
Hughes A,
Bradley DT,
Stirrups K,
Golledge J,
Norman PE,
Powell JT,
Humphries SE,
Hamby SE,
Goodall AH,
Nelson CP,
Sakalihasan N,
Courtois A,
Ferrell RE,
Eriksson P,
Folkersen L,
Franco-Cereceda A,
Eicher JD,
Johnson AD,
Betsholtz C,
Ruusalepp A,
Franzén O,
Schadt EE,
Björkegren JL,
Lipovich L,
Drolet AM,
Verhoeven EL,
Zeebregts CJ,
Geelkerken RH,
van Sambeek MR,
van Sterkenburg SM,
de Vries JP,
Stefansson K,
Thompson JR,
de Bakker PI,
Deloukas P,
Sayers RD,
Harrison SC,
van Rij AM,
Samani NJ,
Bown MJ
Circulation research · 2017 · PMID 27899403 · open access
3 pages
Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women
Jones G,
Trajanoska K,
Santanasto AJ,
Stringa N,
Kuo CL,
Atkins JL,
Lewis JR,
Duong T,
Hong S,
Biggs ML,
Luan J,
Sarnowski C
and 54 more — show all
Lunetta KL,
Tanaka T,
Wojczynski MK,
Cvejkus R,
Nethander M,
Ghasemi S,
Yang J,
Zillikens MC,
Walter S,
Sicinski K,
Kague E,
Ackert-Bicknell CL,
Arking DE,
Windham BG,
Boerwinkle E,
Grove ML,
Graff M,
Spira D,
Demuth I,
van der Velde N,
de Groot LCPGM,
Psaty BM,
Odden MC,
Fohner AE,
Langenberg C,
Wareham NJ,
Bandinelli S,
van Schoor NM,
Huisman M,
Tan Q,
Zmuda J,
Mellström D,
Karlsson M,
Bennett DA,
Buchman AS,
De Jager PL,
Uitterlinden AG,
Völker U,
Kocher T,
Teumer A,
Rodriguéz-Mañas L,
García FJ,
Carnicero JA,
Herd P,
Bertram L,
Ohlsson C,
Murabito JM,
Melzer D,
Kuchel GA,
Ferrucci L,
Karasik D,
Rivadeneira F,
Kiel DP,
Pilling LC
Nature communications · 2021 · PMID 33510174 · open access
3 pages
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction
Gudbjartsson DF,
Bjornsdottir US,
Halapi E,
Helgadottir A,
Sulem P,
Jonsdottir GM,
Thorleifsson G,
Helgadottir H,
Steinthorsdottir V,
Stefansson H,
Williams C,
Hui J
and 61 more — show all
Beilby J,
Warrington NM,
James A,
Palmer LJ,
Koppelman GH,
Heinzmann A,
Krueger M,
Boezen HM,
Wheatley A,
Altmuller J,
Shin HD,
Uh ST,
Cheong HS,
Jonsdottir B,
Gislason D,
Park CS,
Rasmussen LM,
Porsbjerg C,
Hansen JW,
Backer V,
Werge T,
Janson C,
Jönsson UB,
Ng MC,
Chan J,
So WY,
Ma R,
Shah SH,
Granger CB,
Quyyumi AA,
Levey AI,
Vaccarino V,
Reilly MP,
Rader DJ,
Williams MJ,
van Rij AM,
Jones GT,
Trabetti E,
Malerba G,
Pignatti PF,
Boner A,
Pescollderungg L,
Girelli D,
Olivieri O,
Martinelli N,
Ludviksson BR,
Ludviksdottir D,
Eyjolfsson GI,
Arnar D,
Thorgeirsson G,
Deichmann K,
Thompson PJ,
Wjst M,
Hall IP,
Postma DS,
Gislason T,
Gulcher J,
Kong A,
Jonsdottir I,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2009 · PMID 19198610
2 pages
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm
Gretarsdottir S,
Baas AF,
Thorleifsson G,
Holm H,
den Heijer M,
de Vries JP,
Kranendonk SE,
Zeebregts CJ,
van Sterkenburg SM,
Geelkerken RH,
van Rij AM,
Williams MJ
and 90 more — show all
Boll AP,
Kostic JP,
Jonasdottir A,
Jonasdottir A,
Walters GB,
Masson G,
Sulem P,
Saemundsdottir J,
Mouy M,
Magnusson KP,
Tromp G,
Elmore JR,
Sakalihasan N,
Limet R,
Defraigne JO,
Ferrell RE,
Ronkainen A,
Ruigrok YM,
Wijmenga C,
Grobbee DE,
Shah SH,
Granger CB,
Quyyumi AA,
Vaccarino V,
Patel RS,
Zafari AM,
Levey AI,
Austin H,
Girelli D,
Pignatti PF,
Olivieri O,
Martinelli N,
Malerba G,
Trabetti E,
Becker LC,
Becker DM,
Reilly MP,
Rader DJ,
Mueller T,
Dieplinger B,
Haltmayer M,
Urbonavicius S,
Lindblad B,
Gottsäter A,
Gaetani E,
Pola R,
Wells P,
Rodger M,
Forgie M,
Langlois N,
Corral J,
Vicente V,
Fontcuberta J,
España F,
Grarup N,
Jørgensen T,
Witte DR,
Hansen T,
Pedersen O,
Aben KK,
de Graaf J,
Holewijn S,
Folkersen L,
Franco-Cereceda A,
Eriksson P,
Collier DA,
Stefansson H,
Steinthorsdottir V,
Rafnar T,
Valdimarsson EM,
Magnadottir HB,
Sveinbjornsdottir S,
Olafsson I,
Magnusson MK,
Palmason R,
Haraldsdottir V,
Andersen K,
Onundarson PT,
Thorgeirsson G,
Kiemeney LA,
Powell JT,
Carey DJ,
Kuivaniemi H,
Lindholt JS,
Jones GT,
Kong A,
Blankensteijn JD,
Matthiasson SE,
Thorsteinsdottir U,
Stefansson K
Nature genetics · 2010 · PMID 20622881
2 pages
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
Thorgeirsson TE,
Geller F,
Sulem P,
Rafnar T,
Wiste A,
Magnusson KP,
Manolescu A,
Thorleifsson G,
Stefansson H,
Ingason A,
Stacey SN,
Bergthorsson JT
and 45 more — show all
Thorlacius S,
Gudmundsson J,
Jonsson T,
Jakobsdottir M,
Saemundsdottir J,
Olafsdottir O,
Gudmundsson LJ,
Bjornsdottir G,
Kristjansson K,
Skuladottir H,
Isaksson HJ,
Gudbjartsson T,
Jones GT,
Mueller T,
Gottsäter A,
Flex A,
Aben KKH,
de Vegt F,
Mulders PFA,
Isla D,
Vidal MJ,
Asin L,
Saez B,
Murillo L,
Blondal T,
Kolbeinsson H,
Stefansson JG,
Hansdottir I,
Runarsdottir V,
Pola R,
Lindblad B,
van Rij AM,
Dieplinger B,
Haltmayer M,
Mayordomo JI,
Kiemeney LA,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Gudbjartsson DF,
Gulcher JR,
Jonsson S,
Thorsteinsdottir U,
Kong A,
Stefansson K
Nature · 2008 · PMID 18385739
1 page
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior
Thorgeirsson TE,
Gudbjartsson DF,
Surakka I,
Vink JM,
Amin N,
Geller F,
Sulem P,
Rafnar T,
Esko T,
Walter S,
Gieger C,
Rawal R
and 82 more — show all
Mangino M,
Prokopenko I,
Mägi R,
Keskitalo K,
Gudjonsdottir IH,
Gretarsdottir S,
Stefansson H,
Thompson JR,
Aulchenko YS,
Nelis M,
Aben KK,
den Heijer M,
Dirksen A,
Ashraf H,
Soranzo N,
Valdes AM,
Steves C,
Uitterlinden AG,
Hofman A,
Tönjes A,
Kovacs P,
Hottenga JJ,
Willemsen G,
Vogelzangs N,
Döring A,
Dahmen N,
Nitz B,
Pergadia ML,
Saez B,
De Diego V,
Lezcano V,
Garcia-Prats MD,
Ripatti S,
Perola M,
Kettunen J,
Hartikainen AL,
Pouta A,
Laitinen J,
Isohanni M,
Huei-Yi S,
Allen M,
Krestyaninova M,
Hall AS,
Jones GT,
van Rij AM,
Mueller T,
Dieplinger B,
Haltmayer M,
Jonsson S,
Matthiasson SE,
Oskarsson H,
Tyrfingsson T,
Kiemeney LA,
Mayordomo JI,
Lindholt JS,
Pedersen JH,
Franklin WA,
Wolf H,
Montgomery GW,
Heath AC,
Martin NG,
Madden PA,
Giegling I,
Rujescu D,
Järvelin MR,
Salomaa V,
Stumvoll M,
Spector TD,
Wichmann HE,
Metspalu A,
Samani NJ,
Penninx BW,
Oostra BA,
Boomsma DI,
Tiemeier H,
van Duijn CM,
Kaprio J,
Gulcher JR,
McCarthy MI,
Peltonen L,
Thorsteinsdottir U,
Stefansson K
ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
1 page
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma
Ferreira MA,
Matheson MC,
Duffy DL,
Marks GB,
Hui J,
Le Souëf P,
Danoy P,
Baltic S,
Nyholt DR,
Jenkins M,
Hayden C,
Willemsen G
and 28 more — show all
Ang W,
Kuokkanen M,
Beilby J,
Cheah F,
de Geus EJ,
Ramasamy A,
Vedantam S,
Salomaa V,
Madden PA,
Heath AC,
Hopper JL,
Visscher PM,
Musk B,
Leeder SR,
Jarvelin MR,
Pennell C,
Boomsma DI,
Hirschhorn JN,
Walters H,
Martin NG,
James A,
Jones G,
Abramson MJ,
Robertson CF,
Dharmage SC,
Brown MA,
Montgomery GW,
Thompson PJ
Australian Asthma Genetics Consortium
Lancet (London, England) · 2011 · PMID 21907864
1 page
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants
Heap GA,
Weedon MN,
Bewshea CM,
Singh A,
Chen M,
Satchwell JB,
Vivian JP,
So K,
Dubois PC,
Andrews JM,
Annese V,
Bampton P
and 44 more — show all
Barnardo M,
Bell S,
Cole A,
Connor SJ,
Creed T,
Cummings FR,
D'Amato M,
Daneshmend TK,
Fedorak RN,
Florin TH,
Gaya DR,
Greig E,
Halfvarson J,
Hart A,
Irving PM,
Jones G,
Karban A,
Lawrance IC,
Lee JC,
Lees C,
Lev-Tzion R,
Lindsay JO,
Mansfield J,
Mawdsley J,
Mazhar Z,
Parkes M,
Parnell K,
Orchard TR,
Radford-Smith G,
Russell RK,
Reffitt D,
Satsangi J,
Silverberg MS,
Sturniolo GC,
Tremelling M,
Tsianos EV,
van Heel DA,
Walsh A,
Watermeyer G,
Weersma RK,
Zeissig S,
Rossjohn J,
Holden AL,
Ahmad T
International Serious Adverse Events Consortium · IBD Pharmacogenetics Study Group
Nature genetics · 2014 · PMID 25217962
1 page
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms
van 't Hof FN,
Ruigrok YM,
Lee CH,
Ripke S,
Anderson G,
de Andrade M,
Baas AF,
Blankensteijn JD,
Böttinger EP,
Bown MJ,
Broderick J,
Bijlenga P
and 59 more — show all
Carrell DS,
Crawford DC,
Crosslin DR,
Ebeling C,
Eriksson JG,
Eriksson JG,
Fornage M,
Foroud T,
von Und Zu Fraunberg M,
Friedrich CM,
Gaál EI,
Gottesman O,
Guo DC,
Harrison SC,
Hernesniemi J,
Hofman A,
Inoue I,
Jääskeläinen JE,
Jones GT,
Kiemeney LA,
Kivisaari R,
Ko N,
Koskinen S,
Kubo M,
Kullo IJ,
Kuivaniemi H,
Kurki MI,
Laakso A,
Lai D,
Leal SM,
Lehto H,
LeMaire SA,
Low SK,
Malinowski J,
McCarty CA,
Milewicz DM,
Mosley TH,
Nakamura Y,
Nakaoka H,
Niemelä M,
Pacheco J,
Peissig PL,
Pera J,
Rasmussen-Torvik L,
Ritchie MD,
Rivadeneira F,
van Rij AM,
Santos-Cortez RL,
Saratzis A,
Slowik A,
Takahashi A,
Tromp G,
Uitterlinden AG,
Verma SS,
Vermeulen SH,
Wang GT,
Han B,
Rinkel GJ,
de Bakker PI
Aneurysm Consortium; Vascular Research Consortium of New Zealand
Journal of the American Heart Association · 2016 · PMID 27418160 · open access
1 page
Genome-wide association study identifies susceptibility loci for acute myeloid leukemia
Lin WY,
Fordham SE,
Hungate E,
Sunter NJ,
Elstob C,
Xu Y,
Park C,
Quante A,
Strauch K,
Gieger C,
Skol A,
Rahman T
and 71 more — show all
Sucheston-Campbell L,
Wang J,
Hahn T,
Clay-Gilmour AI,
Jones GL,
Marr HJ,
Jackson GH,
Menne T,
Collin M,
Ivey A,
Hills RK,
Burnett AK,
Russell NH,
Fitzgibbon J,
Larson RA,
Le Beau MM,
Stock W,
Heidenreich O,
Alharbi A,
Allsup DJ,
Houlston RS,
Norden J,
Dickinson AM,
Douglas E,
Lendrem C,
Daly AK,
Palm L,
Piechocki K,
Jeffries S,
Bornhäuser M,
Röllig C,
Altmann H,
Ruhnke L,
Kunadt D,
Wagenführ L,
Cordell HJ,
Darlay R,
Andersen MK,
Fontana MC,
Martinelli G,
Marconi G,
Sanz MA,
Cervera J,
Gómez-Seguí I,
Cluzeau T,
Moreilhon C,
Raynaud S,
Sill H,
Voso MT,
Lo-Coco F,
Dombret H,
Cheok M,
Preudhomme C,
Gale RE,
Linch D,
Gaal-Wesinger J,
Masszi A,
Nowak D,
Hofmann WK,
Gilkes A,
Porkka K,
Milosevic Feenstra JD,
Kralovics R,
Grimwade D,
Meggendorfer M,
Haferlach T,
Krizsán S,
Bödör C,
Stölzel F,
Onel K,
Allan JM
Nature communications · 2021 · PMID 34716350 · open access
1 page
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