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13 matches for
Jaddoe VWV.
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
Tachmazidou I,
Süveges D,
Min JL,
Ritchie GRS,
Steinberg J,
Walter K,
Iotchkova V,
Schwartzentruber J,
Huang J,
Memari Y,
McCarthy S,
Crawford AA
and 91 more — show all
Bombieri C,
Cocca M,
Farmaki AE,
Gaunt TR,
Jousilahti P,
Kooijman MN,
Lehne B,
Malerba G,
Männistö S,
Matchan A,
Medina-Gomez C,
Metrustry SJ,
Nag A,
Ntalla I,
Paternoster L,
Rayner NW,
Sala C,
Scott WR,
Shihab HA,
Southam L,
St Pourcain B,
Traglia M,
Trajanoska K,
Zaza G,
Zhang W,
Artigas MS,
Bansal N,
Benn M,
Chen Z,
Danecek P,
Lin WY,
Locke A,
Luan J,
Manning AK,
Mulas A,
Sidore C,
Tybjaerg-Hansen A,
Varbo A,
Zoledziewska M,
Finan C,
Hatzikotoulas K,
Hendricks AE,
Kemp JP,
Moayyeri A,
Panoutsopoulou K,
Szpak M,
Wilson SG,
Boehnke M,
Cucca F,
Di Angelantonio E,
Langenberg C,
Lindgren C,
McCarthy MI,
Morris AP,
Nordestgaard BG,
Scott RA,
Tobin MD,
Wareham NJ,
Burton P,
Chambers JC,
Smith GD,
Dedoussis G,
Felix JF,
Franco OH,
Gambaro G,
Gasparini P,
Hammond CJ,
Hofman A,
Jaddoe VWV,
Kleber M,
Kooner JS,
Perola M,
Relton C,
Ring SM,
Rivadeneira F,
Salomaa V,
Spector TD,
Stegle O,
Toniolo D,
Uitterlinden AG,
Barroso I,
Greenwood CMT,
Perry JRB,
Walker BR,
Butterworth AS,
Xue Y,
Durbin R,
Small KS,
Soranzo N,
Timpson NJ,
Zeggini E
SpiroMeta Consortium · GoT2D Consortium and 3 more consortia
American journal of human genetics · 2017 · PMID 28552196 · open access
12 pages+
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+
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
Waage J,
Standl M,
Curtin JA,
Jessen LE,
Thorsen J,
Tian C,
Schoettler N,
Flores C,
Abdellaoui A,
Ahluwalia TS,
Alves AC,
Amaral AFS
and 76 more — show all
Antó JM,
Arnold A,
Barreto-Luis A,
Baurecht H,
van Beijsterveldt CEM,
Bleecker ER,
Bonàs-Guarch S,
Boomsma DI,
Brix S,
Bunyavanich S,
Burchard EG,
Chen Z,
Curjuric I,
Custovic A,
den Dekker HT,
Dharmage SC,
Dmitrieva J,
Duijts L,
Ege MJ,
Gauderman WJ,
Georges M,
Gieger C,
Gilliland F,
Granell R,
Gui H,
Hansen T,
Heinrich J,
Henderson J,
Hernandez-Pacheco N,
Holt P,
Imboden M,
Jaddoe VWV,
Jarvelin MR,
Jarvis DL,
Jensen KK,
Jónsdóttir I,
Kabesch M,
Kaprio J,
Kumar A,
Lee YA,
Levin AM,
Li X,
Lorenzo-Diaz F,
Melén E,
Mercader JM,
Meyers DA,
Myers R,
Nicolae DL,
Nohr EA,
Palviainen T,
Paternoster L,
Pennell CE,
Pershagen G,
Pino-Yanes M,
Probst-Hensch NM,
Rüschendorf F,
Simpson A,
Stefansson K,
Sunyer J,
Sveinbjornsson G,
Thiering E,
Thompson PJ,
Torrent M,
Torrents D,
Tung JY,
Wang CA,
Weidinger S,
Weiss S,
Willemsen G,
Williams LK,
Ober C,
Hinds DA,
Ferreira MA,
Bisgaard H,
Strachan DP,
Bønnelykke K
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
Warrington NM,
Beaumont RN,
Horikoshi M,
Day FR,
Helgeland Ø,
Laurin C,
Bacelis J,
Peng S,
Hao K,
Feenstra B,
Wood AR,
Mahajan A
and 196 more — show all
Tyrrell J,
Robertson NR,
Rayner NW,
Qiao Z,
Moen GH,
Vaudel M,
Marsit CJ,
Chen J,
Nodzenski M,
Schnurr TM,
Zafarmand MH,
Bradfield JP,
Grarup N,
Kooijman MN,
Li-Gao R,
Geller F,
Ahluwalia TS,
Paternoster L,
Rueedi R,
Huikari V,
Hottenga JJ,
Lyytikäinen LP,
Cavadino A,
Metrustry S,
Cousminer DL,
Wu Y,
Thiering E,
Wang CA,
Have CT,
Vilor-Tejedor N,
Joshi PK,
Painter JN,
Ntalla I,
Myhre R,
Pitkänen N,
van Leeuwen EM,
Joro R,
Lagou V,
Richmond RC,
Espinosa A,
Barton SJ,
Inskip HM,
Holloway JW,
Santa-Marina L,
Estivill X,
Ang W,
Marsh JA,
Reichetzeder C,
Marullo L,
Hocher B,
Lunetta KL,
Murabito JM,
Relton CL,
Kogevinas M,
Chatzi L,
Allard C,
Bouchard L,
Hivert MF,
Zhang G,
Muglia LJ,
Heikkinen J,
Morgen CS,
van Kampen AHC,
van Schaik BDC,
Mentch FD,
Langenberg C,
Luan J,
Scott RA,
Zhao JH,
Hemani G,
Ring SM,
Bennett AJ,
Gaulton KJ,
Fernandez-Tajes J,
van Zuydam NR,
Medina-Gomez C,
de Haan HG,
Rosendaal FR,
Kutalik Z,
Marques-Vidal P,
Das S,
Willemsen G,
Mbarek H,
Müller-Nurasyid M,
Standl M,
Appel EVR,
Fonvig CE,
Trier C,
van Beijsterveldt CEM,
Murcia M,
Bustamante M,
Bonas-Guarch S,
Hougaard DM,
Mercader JM,
Linneberg A,
Schraut KE,
Lind PA,
Medland SE,
Shields BM,
Knight BA,
Chai JF,
Panoutsopoulou K,
Bartels M,
Sánchez F,
Stokholm J,
Torrents D,
Vinding RK,
Willems SM,
Atalay M,
Chawes BL,
Kovacs P,
Prokopenko I,
Tuke MA,
Yaghootkar H,
Ruth KS,
Jones SE,
Loh PR,
Murray A,
Weedon MN,
Tönjes A,
Stumvoll M,
Michaelsen KF,
Eloranta AM,
Lakka TA,
van Duijn CM,
Kiess W,
Körner A,
Niinikoski H,
Pahkala K,
Raitakari OT,
Jacobsson B,
Zeggini E,
Dedoussis GV,
Teo YY,
Saw SM,
Montgomery GW,
Campbell H,
Wilson JF,
Vrijkotte TGM,
Vrijheid M,
de Geus EJCN,
Hayes MG,
Kadarmideen HN,
Holm JC,
Beilin LJ,
Pennell CE,
Heinrich J,
Adair LS,
Borja JB,
Mohlke KL,
Eriksson JG,
Widén EE,
Hattersley AT,
Spector TD,
Kähönen M,
Viikari JS,
Lehtimäki T,
Boomsma DI,
Sebert S,
Vollenweider P,
Sørensen TIA,
Bisgaard H,
Bønnelykke K,
Murray JC,
Melbye M,
Nohr EA,
Mook-Kanamori DO,
Rivadeneira F,
Hofman A,
Felix JF,
Jaddoe VWV,
Hansen T,
Pisinger C,
Vaag AA,
Pedersen O,
Uitterlinden AG,
Järvelin MR,
Power C,
Hyppönen E,
Scholtens DM,
Lowe WL Jr,
Davey Smith G,
Timpson NJ,
Morris AP,
Wareham NJ,
Hakonarson H,
Grant SFA,
Frayling TM,
Lawlor DA,
Njølstad PR,
Johansson S,
Ong KK,
McCarthy MI,
Perry JRB,
Evans DM,
Freathy RM
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Wuttke M,
Li Y,
Li M,
Sieber KB,
Feitosa MF,
Gorski M,
Tin A,
Wang L,
Chu AY,
Hoppmann A,
Kirsten H,
Giri A
and 315 more — show all
Chai JF,
Sveinbjornsson G,
Tayo BO,
Nutile T,
Fuchsberger C,
Marten J,
Cocca M,
Ghasemi S,
Xu Y,
Horn K,
Noce D,
van der Most PJ,
Sedaghat S,
Yu Z,
Akiyama M,
Afaq S,
Ahluwalia TS,
Almgren P,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boehnke M,
Boerwinkle E,
Boissel M,
Bottinger EP,
Boutin TS,
Brenner H,
Brumat M,
Burkhardt R,
Butterworth AS,
Campana E,
Campbell A,
Campbell H,
Canouil M,
Carroll RJ,
Catamo E,
Chambers JC,
Chee ML,
Chee ML,
Chen X,
Cheng CY,
Cheng Y,
Christensen K,
Cifkova R,
Ciullo M,
Concas MP,
Cook JP,
Coresh J,
Corre T,
Sala CF,
Cusi D,
Danesh J,
Daw EW,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Delgado G,
Demirkan A,
Di Angelantonio E,
Dittrich K,
Divers J,
Dorajoo R,
Eckardt KU,
Ehret G,
Elliott P,
Endlich K,
Evans MK,
Felix JF,
Foo VHX,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Friedlander Y,
Froguel P,
Gansevoort RT,
Gao H,
Gasparini P,
Gaziano JM,
Giedraitis V,
Gieger C,
Girotto G,
Giulianini F,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hartman CA,
Hayward C,
Hellwege JN,
Heng CK,
Hicks AA,
Hofer E,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Indridason OS,
Ingelsson E,
Ising M,
Jaddoe VWV,
Jakobsdottir J,
Jonas JB,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kammerer CM,
Kanai M,
Kastarinen M,
Kerr SM,
Khor CC,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Kraja AT,
Krajcoviechova A,
Kramer H,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
Kuokkanen M,
Kuusisto J,
La Bianca M,
Laakso M,
Lange LA,
Langefeld CD,
Lee JJ,
Lehne B,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Liu J,
Loeffler M,
Loos RJF,
Lucae S,
Lukas MA,
Lyytikäinen LP,
Mägi R,
Magnusson PKE,
Mahajan A,
Martin NG,
Martins J,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Melander O,
Metspalu A,
Mikaelsdottir EK,
Milaneschi Y,
Miliku K,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Mychaleckyj JC,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell J,
O'Donoghue ML,
Olafsson I,
Oldehinkel AJ,
Orho-Melander M,
Ouwehand WH,
Padmanabhan S,
Palmer ND,
Palsson R,
Penninx BWJH,
Perls T,
Perola M,
Pirastu M,
Pirastu N,
Pistis G,
Podgornaia AI,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Pramstaller PP,
Preuss MH,
Prins BP,
Province MA,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Ridker PM,
Rivadeneira F,
Rizzi F,
Roberts DJ,
Robino A,
Rossing P,
Rudan I,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Sabanayagam C,
Salomaa V,
Salvi E,
Saum KU,
Schmidt H,
Schmidt R,
Schöttker B,
Schulz CA,
Schupf N,
Shaffer CM,
Shi Y,
Smith AV,
Smith BH,
Soranzo N,
Spracklen CN,
Strauch K,
Stringham HM,
Stumvoll M,
Svensson PO,
Szymczak S,
Tai ES,
Tajuddin SM,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorleifsson G,
Toniolo D,
Tönjes A,
Tremblay J,
Tzoulaki I,
Uitterlinden AG,
Vaccargiu S,
van Dam RM,
van der Harst P,
van Duijn CM,
Velez Edward DR,
Verweij N,
Vogelezang S,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Wallentin L,
Wang YX,
Wang C,
Waterworth DM,
Bin Wei W,
White H,
Whitfield JB,
Wild SH,
Wilson JF,
Wojczynski MK,
Wong C,
Wong TY,
Xu L,
Yang Q,
Yasuda M,
Yerges-Armstrong LM,
Zhang W,
Zonderman AB,
Rotter JI,
Bochud M,
Psaty BM,
Vitart V,
Wilson JG,
Dehghan A,
Parsa A,
Chasman DI,
Ho K,
Morris AP,
Devuyst O,
Akilesh S,
Pendergrass SA,
Sim X,
Böger CA,
Okada Y,
Edwards TL,
Snieder H,
Stefansson K,
Hung AM,
Heid IM,
Scholz M,
Teumer A,
Köttgen A,
Pattaro C
Lifelines Cohort Study · V. A. Million Veteran Program
Nature genetics · 2019 · PMID 31152163
12 pages+
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria
Teumer A,
Li Y,
Ghasemi S,
Prins BP,
Wuttke M,
Hermle T,
Giri A,
Sieber KB,
Qiu C,
Kirsten H,
Tin A,
Chu AY
and 174 more — show all
Bansal N,
Feitosa MF,
Wang L,
Chai JF,
Cocca M,
Fuchsberger C,
Gorski M,
Hoppmann A,
Horn K,
Li M,
Marten J,
Noce D,
Nutile T,
Sedaghat S,
Sveinbjornsson G,
Tayo BO,
van der Most PJ,
Xu Y,
Yu Z,
Gerstner L,
Ärnlöv J,
Bakker SJL,
Baptista D,
Biggs ML,
Boerwinkle E,
Brenner H,
Burkhardt R,
Carroll RJ,
Chee ML,
Chee ML,
Chen M,
Cheng CY,
Cook JP,
Coresh J,
Corre T,
Danesh J,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Degenhardt F,
Dittrich K,
Divers J,
Eckardt KU,
Ehret G,
Endlich K,
Felix JF,
Franco OH,
Franke A,
Freedman BI,
Freitag-Wolf S,
Gansevoort RT,
Giedraitis V,
Gögele M,
Grundner-Culemann F,
Gudbjartsson DF,
Gudnason V,
Hamet P,
Harris TB,
Hicks AA,
Holm H,
Foo VHX,
Hwang SJ,
Ikram MA,
Ingelsson E,
Jaddoe VWV,
Jakobsdottir J,
Josyula NS,
Jung B,
Kähönen M,
Khor CC,
Kiess W,
Koenig W,
Körner A,
Kovacs P,
Kramer H,
Krämer BK,
Kronenberg F,
Lange LA,
Langefeld CD,
Lee JJ,
Lehtimäki T,
Lieb W,
Lim SC,
Lind L,
Lindgren CM,
Liu J,
Loeffler M,
Lyytikäinen LP,
Mahajan A,
Maranville JC,
Mascalzoni D,
McMullen B,
Meisinger C,
Meitinger T,
Miliku K,
Mook-Kanamori DO,
Müller-Nurasyid M,
Mychaleckyj JC,
Nauck M,
Nikus K,
Ning B,
Noordam R,
Connell JO,
Olafsson I,
Palmer ND,
Peters A,
Podgornaia AI,
Ponte B,
Poulain T,
Pramstaller PP,
Rabelink TJ,
Raffield LM,
Reilly DF,
Rettig R,
Rheinberger M,
Rice KM,
Rivadeneira F,
Runz H,
Ryan KA,
Sabanayagam C,
Saum KU,
Schöttker B,
Shaffer CM,
Shi Y,
Smith AV,
Strauch K,
Stumvoll M,
Sun BB,
Szymczak S,
Tai ES,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
Thiery J,
Thio CHL,
Thomsen H,
Thorsteinsdottir U,
Tönjes A,
Tremblay J,
Uitterlinden AG,
van der Harst P,
Verweij N,
Vogelezang S,
Völker U,
Waldenberger M,
Wang C,
Wilson OD,
Wong C,
Wong TY,
Yang Q,
Yasuda M,
Akilesh S,
Bochud M,
Böger CA,
Devuyst O,
Edwards TL,
Ho K,
Morris AP,
Parsa A,
Pendergrass SA,
Psaty BM,
Rotter JI,
Stefansson K,
Wilson JG,
Susztak K,
Snieder H,
Heid IM,
Scholz M,
Butterworth AS,
Hung AM,
Pattaro C,
Köttgen A
Nature communications · 2019 · PMID 31511532 · open access
12 pages+
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error
Fan Q,
Pozarickij A,
Tan NYQ,
Guo X,
Verhoeven VJM,
Vitart V,
Guggenheim JA,
Miyake M,
Tideman JWL,
Khawaja AP,
Zhang L,
MacGregor S
and 46 more — show all
Höhn R,
Chen P,
Biino G,
Wedenoja J,
Saffari SE,
Tedja MS,
Xie J,
Lanca C,
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Sahebjada S,
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1 page
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