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Davies G,
showing the first 20.
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
Porcu E,
Medici M,
Pistis G,
Volpato CB,
Wilson SG,
Cappola AR,
Bos SD,
Deelen J,
den Heijer M,
Freathy RM,
Lahti J,
Liu C
and 82 more — show all
Lopez LM,
Nolte IM,
O'Connell JR,
Tanaka T,
Trompet S,
Arnold A,
Bandinelli S,
Beekman M,
Böhringer S,
Brown SJ,
Buckley BM,
Camaschella C,
de Craen AJ,
Davies G,
de Visser MC,
Ford I,
Forsen T,
Frayling TM,
Fugazzola L,
Gögele M,
Hattersley AT,
Hermus AR,
Hofman A,
Houwing-Duistermaat JJ,
Jensen RA,
Kajantie E,
Kloppenburg M,
Lim EM,
Masciullo C,
Mariotti S,
Minelli C,
Mitchell BD,
Nagaraja R,
Netea-Maier RT,
Palotie A,
Persani L,
Piras MG,
Psaty BM,
Räikkönen K,
Richards JB,
Rivadeneira F,
Sala C,
Sabra MM,
Sattar N,
Shields BM,
Soranzo N,
Starr JM,
Stott DJ,
Sweep FC,
Usala G,
van der Klauw MM,
van Heemst D,
van Mullem A,
Vermeulen SH,
Visser WE,
Walsh JP,
Westendorp RG,
Widen E,
Zhai G,
Cucca F,
Deary IJ,
Eriksson JG,
Ferrucci L,
Fox CS,
Jukema JW,
Kiemeney LA,
Pramstaller PP,
Schlessinger D,
Shuldiner AR,
Slagboom EP,
Uitterlinden AG,
Vaidya B,
Visser TJ,
Wolffenbuttel BH,
Meulenbelt I,
Rotter JI,
Spector TD,
Hicks AA,
Toniolo D,
Sanna S,
Peeters RP,
Naitza S
PLoS genetics · 2013 · PMID 23408906 · open access
10 pages
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Okbay A,
Baselmans BM,
De Neve JE,
Turley P,
Nivard MG,
Fontana MA,
Meddens SF,
Linnér RK,
Rietveld CA,
Derringer J,
Gratten J,
Lee JJ
and 180 more — show all
Liu JZ,
de Vlaming R,
Ahluwalia TS,
Buchwald J,
Cavadino A,
Frazier-Wood AC,
Furlotte NA,
Garfield V,
Geisel MH,
Gonzalez JR,
Haitjema S,
Karlsson R,
van der Laan SW,
Ladwig KH,
Lahti J,
van der Lee SJ,
Lind PA,
Liu T,
Matteson L,
Mihailov E,
Miller MB,
Minica CC,
Nolte IM,
Mook-Kanamori D,
van der Most PJ,
Oldmeadow C,
Qian Y,
Raitakari O,
Rawal R,
Realo A,
Rueedi R,
Schmidt B,
Smith AV,
Stergiakouli E,
Tanaka T,
Taylor K,
Thorleifsson G,
Wedenoja J,
Wellmann J,
Westra HJ,
Willems SM,
Zhao W,
Amin N,
Bakshi A,
Bergmann S,
Bjornsdottir G,
Boyle PA,
Cherney S,
Cox SR,
Davies G,
Davis OS,
Ding J,
Direk N,
Eibich P,
Eibich P,
Emeny RT,
Fatemifar G,
Faul JD,
Ferrucci L,
Ferrucci L,
Forstner AJ,
Gieger C,
Gupta R,
Harris TB,
Harris JM,
Holliday EG,
Hottenga JJ,
De Jager PL,
Kaakinen MA,
Kajantie E,
Karhunen V,
Kolcic I,
Kumari M,
Launer LJ,
Franke L,
Franke L,
Li-Gao R,
Liewald DC,
Koini M,
Loukola A,
Marques-Vidal P,
Montgomery GW,
Mosing MA,
Paternoster L,
Pattie A,
Petrovic KE,
Pulkki-Råback L,
Quaye L,
Räikkönen K,
Rudan I,
Scott RJ,
Smith JA,
Sutin AR,
Trzaskowski M,
Vinkhuyzen AE,
Yu L,
Zabaneh D,
Attia JR,
Bennett DA,
Berger K,
Bertram L,
Boomsma DI,
Snieder H,
Chang SC,
Cucca F,
Deary IJ,
van Duijn CM,
Eriksson JG,
Bültmann U,
de Geus EJ,
Groenen PJ,
Gudnason V,
Hansen T,
Hartman CA,
Haworth CM,
Haworth CM,
Hayward C,
Heath AC,
Hinds DA,
Hyppönen E,
Iacono WG,
Järvelin MR,
Jöckel KH,
Kaprio J,
Kardia SL,
Keltikangas-Järvinen L,
Kraft P,
Kubzansky LD,
Lehtimäki T,
Magnusson PK,
Martin NG,
McGue M,
Metspalu A,
Mills M,
de Mutsert R,
Oldehinkel AJ,
Pasterkamp G,
Pedersen NL,
Plomin R,
Polasek O,
Power C,
Rich SS,
Rosendaal FR,
den Ruijter HM,
Schlessinger D,
Schmidt H,
Svento R,
Schmidt R,
Alizadeh BZ,
Sørensen TI,
Spector TD,
Starr JM,
Stefansson K,
Steptoe A,
Terracciano A,
Thorsteinsdottir U,
Thurik AR,
Timpson NJ,
Tiemeier H,
Uitterlinden AG,
Vollenweider P,
Vollenweider P,
Wagner GG,
Weir DR,
Yang J,
Conley DC,
Smith GD,
Hofman A,
Johannesson M,
Laibson DI,
Medland SE,
Meyer MN,
Pickrell JK,
Esko T,
Krueger RF,
Beauchamp JP,
Koellinger PD,
Benjamin DJ,
Bartels M,
Cesarini D
LifeLines Cohort Study
Nature genetics · 2016 · PMID 27089181 · open access
10 pages
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Wray NR,
Ripke S,
Mattheisen M,
Trzaskowski M,
Byrne EM,
Abdellaoui A,
Adams MJ,
Agerbo E,
Air TM,
Andlauer TMF,
Bacanu SA,
Bækvad-Hansen M
and 205 more — show all
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
Christensen JH,
Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
Craddock N,
Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
Dunn EC,
Eley TC,
Eriksson N,
Escott-Price V,
Kiadeh FHF,
Finucane HK,
Forstner AJ,
Frank J,
Gaspar HA,
Gill M,
Giusti-Rodríguez P,
Goes FS,
Gordon SD,
Grove J,
Hall LS,
Hannon E,
Hansen CS,
Hansen TF,
Herms S,
Hickie IB,
Hoffmann P,
Homuth G,
Horn C,
Hottenga JJ,
Hougaard DM,
Hu M,
Hyde CL,
Ising M,
Jansen R,
Jansen R,
Jin F,
Jorgenson E,
Knowles JA,
Kohane IS,
Kraft J,
Kretzschmar WW,
Krogh J,
Kutalik Z,
Lane JM,
Li Y,
Li Y,
Lind PA,
Liu X,
Lu L,
MacIntyre DJ,
MacKinnon DF,
Maier RM,
Maier W,
Marchini J,
Mbarek H,
McGrath P,
McGuffin P,
Medland SE,
Mehta D,
Middeldorp CM,
Mihailov E,
Milaneschi Y,
Milani L,
Mill J,
Mondimore FM,
Montgomery GW,
Mostafavi S,
Mullins N,
Nauck M,
Ng B,
Nivard MG,
Nyholt DR,
O'Reilly PF,
Oskarsson H,
Owen MJ,
Painter JN,
Pedersen CB,
Pedersen MG,
Peterson RE,
Pettersson E,
Peyrot WJ,
Pistis G,
Posthuma D,
Purcell SM,
Quiroz JA,
Qvist P,
Rice JP,
Riley BP,
Rivera M,
Saeed Mirza S,
Saxena R,
Schoevers R,
Schulte EC,
Shen L,
Shi J,
Shyn SI,
Sigurdsson E,
Sinnamon GBC,
Smit JH,
Smith DJ,
Stefansson H,
Steinberg S,
Stockmeier CA,
Streit F,
Strohmaier J,
Tansey KE,
Teismann H,
Teumer A,
Thompson W,
Thomson PA,
Thorgeirsson TE,
Tian C,
Traylor M,
Treutlein J,
Trubetskoy V,
Uitterlinden AG,
Umbricht D,
Van der Auwera S,
van Hemert AM,
Viktorin A,
Visscher PM,
Wang Y,
Webb BT,
Weinsheimer SM,
Wellmann J,
Willemsen G,
Witt SH,
Wu Y,
Xi HS,
Yang J,
Zhang F,
Arolt V,
Baune BT,
Berger K,
Boomsma DI,
Cichon S,
Dannlowski U,
de Geus ECJ,
DePaulo JR,
Domenici E,
Domschke K,
Esko T,
Grabe HJ,
Hamilton SP,
Hayward C,
Heath AC,
Hinds DA,
Kendler KS,
Kloiber S,
Lewis G,
Li QS,
Lucae S,
Madden PFA,
Magnusson PK,
Martin NG,
McIntosh AM,
Metspalu A,
Mors O,
Mortensen PB,
Müller-Myhsok B,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Paciga SA,
Pedersen NL,
Penninx BWJH,
Perlis RH,
Porteous DJ,
Potash JB,
Preisig M,
Rietschel M,
Schaefer C,
Schulze TG,
Smoller JW,
Stefansson K,
Tiemeier H,
Uher R,
Völzke H,
Weissman MM,
Werge T,
Winslow AR,
Lewis CM,
Levinson DF,
Breen G,
Børglum AD,
Sullivan PF
eQTLGen · 23andMe and 1 more consortia
Nature genetics · 2018 · PMID 29700475 · open access
10 pages
Genetic architecture of subcortical brain structures in 38,851 individuals
Satizabal CL,
Adams HHH,
Hibar DP,
White CC,
Knol MJ,
Stein JL,
Scholz M,
Sargurupremraj M,
Jahanshad N,
Roshchupkin GV,
Smith AV,
Bis JC
and 277 more — show all
Jian X,
Luciano M,
Hofer E,
Teumer A,
van der Lee SJ,
Yang J,
Yanek LR,
Lee TV,
Li S,
Hu Y,
Koh JY,
Eicher JD,
Desrivières S,
Arias-Vasquez A,
Chauhan G,
Athanasiu L,
Rentería ME,
Kim S,
Hoehn D,
Armstrong NJ,
Chen Q,
Holmes AJ,
den Braber A,
Kloszewska I,
Andersson M,
Espeseth T,
Grimm O,
Abramovic L,
Alhusaini S,
Milaneschi Y,
Papmeyer M,
Axelsson T,
Ehrlich S,
Roiz-Santiañez R,
Kraemer B,
Håberg AK,
Jones HJ,
Pike GB,
Stein DJ,
Stevens A,
Bralten J,
Vernooij MW,
Harris TB,
Filippi I,
Witte AV,
Guadalupe T,
Wittfeld K,
Mosley TH,
Becker JT,
Doan NT,
Hagenaars SP,
Saba Y,
Cuellar-Partida G,
Amin N,
Hilal S,
Nho K,
Mirza-Schreiber N,
Arfanakis K,
Becker DM,
Ames D,
Goldman AL,
Lee PH,
Boomsma DI,
Lovestone S,
Giddaluru S,
Le Hellard S,
Mattheisen M,
Bohlken MM,
Kasperaviciute D,
Schmaal L,
Lawrie SM,
Agartz I,
Walton E,
Tordesillas-Gutierrez D,
Davies GE,
Shin J,
Ipser JC,
Vinke LN,
Hoogman M,
Jia T,
Burkhardt R,
Klein M,
Crivello F,
Janowitz D,
Carmichael O,
Haukvik UK,
Aribisala BS,
Schmidt H,
Strike LT,
Cheng CY,
Risacher SL,
Pütz B,
Fleischman DA,
Assareh AA,
Mattay VS,
Buckner RL,
Mecocci P,
Dale AM,
Cichon S,
Boks MP,
Matarin M,
Penninx BWJH,
Calhoun VD,
Chakravarty MM,
Marquand AF,
Macare C,
Kharabian Masouleh S,
Oosterlaan J,
Amouyel P,
Hegenscheid K,
Rotter JI,
Schork AJ,
Liewald DCM,
de Zubicaray GI,
Wong TY,
Shen L,
Sämann PG,
Brodaty H,
Roffman JL,
de Geus EJC,
Tsolaki M,
Erk S,
van Eijk KR,
Cavalleri GL,
van der Wee NJA,
McIntosh AM,
Gollub RL,
Bulayeva KB,
Bernard M,
Richards JS,
Himali JJ,
Loeffler M,
Rommelse N,
Hoffmann W,
Westlye LT,
Valdés Hernández MC,
Hansell NK,
van Erp TGM,
Wolf C,
Kwok JBJ,
Vellas B,
Heinz A,
Olde Loohuis LM,
Delanty N,
Ho BC,
Ching CRK,
Shumskaya E,
Singh B,
Hofman A,
van der Meer D,
Homuth G,
Psaty BM,
Bastin ME,
Montgomery GW,
Foroud TM,
Reppermund S,
Hottenga JJ,
Simmons A,
Meyer-Lindenberg A,
Cahn W,
Whelan CD,
van Donkelaar MMJ,
Yang Q,
Hosten N,
Green RC,
Thalamuthu A,
Mohnke S,
Hulshoff Pol HE,
Lin H,
Jack CR Jr,
Schofield PR,
Mühleisen TW,
Maillard P,
Potkin SG,
Wen W,
Fletcher E,
Toga AW,
Gruber O,
Huentelman M,
Davey Smith G,
Launer LJ,
Nyberg L,
Jönsson EG,
Crespo-Facorro B,
Koen N,
Greve DN,
Uitterlinden AG,
Weinberger DR,
Steen VM,
Fedko IO,
Groenewold NA,
Niessen WJ,
Toro R,
Tzourio C,
Longstreth WT Jr,
Ikram MK,
Smoller JW,
van Tol MJ,
Sussmann JE,
Paus T,
Lemaître H,
Schroeter ML,
Mazoyer B,
Andreassen OA,
Holsboer F,
Depondt C,
Veltman DJ,
Turner JA,
Pausova Z,
Schumann G,
van Rooij D,
Djurovic S,
Deary IJ,
McMahon KL,
Müller-Myhsok B,
Brouwer RM,
Soininen H,
Pandolfo M,
Wassink TH,
Cheung JW,
Wolfers T,
Martinot JL,
Zwiers MP,
Nauck M,
Melle I,
Martin NG,
Kanai R,
Westman E,
Kahn RS,
Sisodiya SM,
White T,
Saremi A,
van Bokhoven H,
Brunner HG,
Völzke H,
Wright MJ,
van 't Ent D,
Nöthen MM,
Ophoff RA,
Buitelaar JK,
Fernández G,
Sachdev PS,
Rietschel M,
van Haren NEM,
Fisher SE,
Beiser AS,
Francks C,
Saykin AJ,
Mather KA,
Romanczuk-Seiferth N,
Hartman CA,
DeStefano AL,
Heslenfeld DJ,
Weiner MW,
Walter H,
Hoekstra PJ,
Nyquist PA,
Franke B,
Bennett DA,
Grabe HJ,
Johnson AD,
Chen C,
van Duijn CM,
Lopez OL,
Fornage M,
Wardlaw JM,
Schmidt R,
DeCarli C,
De Jager PL,
Villringer A,
Debette S,
Gudnason V,
Medland SE,
Shulman JM,
Thompson PM,
Seshadri S,
Ikram MA
Nature genetics · 2019 · PMID 31636452
10 pages
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease
Sabater-Lleal M,
Huang J,
Chasman D,
Naitza S,
Dehghan A,
Johnson AD,
Teumer A,
Reiner AP,
Folkersen L,
Basu S,
Rudnicka AR,
Trompet S
and 133 more — show all
Mälarstig A,
Baumert J,
Bis JC,
Guo X,
Hottenga JJ,
Shin SY,
Lopez LM,
Lahti J,
Tanaka T,
Yanek LR,
Oudot-Mellakh T,
Wilson JF,
Navarro P,
Huffman JE,
Zemunik T,
Redline S,
Mehra R,
Pulanic D,
Rudan I,
Wright AF,
Kolcic I,
Polasek O,
Wild SH,
Campbell H,
Curb JD,
Wallace R,
Liu S,
Eaton CB,
Becker DM,
Becker LC,
Bandinelli S,
Räikkönen K,
Widen E,
Palotie A,
Fornage M,
Green D,
Gross M,
Davies G,
Harris SE,
Liewald DC,
Starr JM,
Williams FM,
Grant PJ,
Spector TD,
Strawbridge RJ,
Silveira A,
Sennblad B,
Rivadeneira F,
Uitterlinden AG,
Franco OH,
Hofman A,
van Dongen J,
Willemsen G,
Boomsma DI,
Yao J,
Swords Jenny N,
Haritunians T,
McKnight B,
Lumley T,
Taylor KD,
Rotter JI,
Psaty BM,
Peters A,
Gieger C,
Illig T,
Grotevendt A,
Homuth G,
Völzke H,
Kocher T,
Goel A,
Franzosi MG,
Seedorf U,
Clarke R,
Steri M,
Tarasov KV,
Sanna S,
Schlessinger D,
Stott DJ,
Sattar N,
Buckley BM,
Rumley A,
Lowe GD,
McArdle WL,
Chen MH,
Tofler GH,
Song J,
Boerwinkle E,
Folsom AR,
Rose LM,
Franco-Cereceda A,
Teichert M,
Ikram MA,
Mosley TH,
Bevan S,
Dichgans M,
Rothwell PM,
Sudlow CL,
Hopewell JC,
Chambers JC,
Saleheen D,
Kooner JS,
Danesh J,
Nelson CP,
Erdmann J,
Reilly MP,
Kathiresan S,
Schunkert H,
Morange PE,
Ferrucci L,
Eriksson JG,
Jacobs D,
Deary IJ,
Soranzo N,
Witteman JC,
de Geus EJ,
Tracy RP,
Hayward C,
Koenig W,
Cucca F,
Jukema JW,
Eriksson P,
Seshadri S,
Markus HS,
Watkins H,
Samani NJ,
Wallaschofski H,
Smith NL,
Tregouet D,
Ridker PM,
Tang W,
Strachan DP,
Hamsten A,
O'Donnell CJ
VTE Consortium · STROKE Consortium and 3 more consortia
Circulation · 2013 · PMID 23969696
9 pages
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways
Stolk L,
Perry JR,
Chasman DI,
He C,
Mangino M,
Sulem P,
Barbalic M,
Broer L,
Byrne EM,
Ernst F,
Esko T,
Franceschini N
and 167 more — show all
Gudbjartsson DF,
Hottenga JJ,
Kraft P,
McArdle PF,
Porcu E,
Shin SY,
Smith AV,
van Wingerden S,
Zhai G,
Zhuang WV,
Albrecht E,
Alizadeh BZ,
Aspelund T,
Bandinelli S,
Lauc LB,
Beckmann JS,
Boban M,
Boerwinkle E,
Broekmans FJ,
Burri A,
Campbell H,
Chanock SJ,
Chen C,
Cornelis MC,
Corre T,
Coviello AD,
d'Adamo P,
Davies G,
de Faire U,
de Geus EJ,
Deary IJ,
Dedoussis GV,
Deloukas P,
Ebrahim S,
Eiriksdottir G,
Emilsson V,
Eriksson JG,
Fauser BC,
Ferreli L,
Ferrucci L,
Fischer K,
Folsom AR,
Garcia ME,
Gasparini P,
Gieger C,
Glazer N,
Grobbee DE,
Hall P,
Haller T,
Hankinson SE,
Hass M,
Hayward C,
Heath AC,
Hofman A,
Ingelsson E,
Janssens AC,
Johnson AD,
Karasik D,
Kardia SL,
Keyzer J,
Kiel DP,
Kolcic I,
Kutalik Z,
Lahti J,
Lai S,
Laisk T,
Laven JS,
Lawlor DA,
Liu J,
Lopez LM,
Louwers YV,
Magnusson PK,
Marongiu M,
Martin NG,
Klaric IM,
Masciullo C,
McKnight B,
Medland SE,
Melzer D,
Mooser V,
Navarro P,
Newman AB,
Nyholt DR,
Onland-Moret NC,
Palotie A,
Paré G,
Parker AN,
Pedersen NL,
Peeters PH,
Pistis G,
Plump AS,
Polasek O,
Pop VJ,
Psaty BM,
Räikkönen K,
Rehnberg E,
Rotter JI,
Rudan I,
Sala C,
Salumets A,
Scuteri A,
Singleton A,
Smith JA,
Snieder H,
Soranzo N,
Stacey SN,
Starr JM,
Stathopoulou MG,
Stirrups K,
Stolk RP,
Styrkarsdottir U,
Sun YV,
Tenesa A,
Thorand B,
Toniolo D,
Tryggvadottir L,
Tsui K,
Ulivi S,
van Dam RM,
van der Schouw YT,
van Gils CH,
van Nierop P,
Vink JM,
Visscher PM,
Voorhuis M,
Waeber G,
Wallaschofski H,
Wichmann HE,
Widen E,
Wijnands-van Gent CJ,
Willemsen G,
Wilson JF,
Wolffenbuttel BH,
Wright AF,
Yerges-Armstrong LM,
Zemunik T,
Zgaga L,
Zillikens MC,
Zygmunt M,
Arnold AM,
Boomsma DI,
Buring JE,
Crisponi L,
Demerath EW,
Gudnason V,
Harris TB,
Hu FB,
Hunter DJ,
Launer LJ,
Metspalu A,
Montgomery GW,
Oostra BA,
Ridker PM,
Sanna S,
Schlessinger D,
Spector TD,
Stefansson K,
Streeten EA,
Thorsteinsdottir U,
Uda M,
Uitterlinden AG,
van Duijn CM,
Völzke H,
Murray A,
Murabito JM,
Visser JA,
Lunetta KL
LifeLines Cohort Study
Nature genetics · 2012 · PMID 22267201 · open access
8 pages
Genome-wide association study identifies 48 common genetic variants associated with handedness
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LifeLines Cohort Study
American journal of human genetics · 2012 · PMID 23022100
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LifeLines Cohort Study · CARDIoGRAM Consortium and 3 more consortia
Nature genetics · 2013 · PMID 23263486
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GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
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LifeLines Cohort Study
Science (New York, N.Y.) · 2013 · PMID 23722424
3 pages
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