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16 matches for
Rawal R.
Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
Wain LV,
Shrine N,
Artigas MS,
Erzurumluoglu AM,
Noyvert B,
Bossini-Castillo L,
Obeidat M,
Henry AP,
Portelli MA,
Hall RJ,
Billington CK,
Rimington TL
and 94 more — show all
Fenech AG,
John C,
Blake T,
Jackson VE,
Allen RJ,
Prins BP,
Campbell A,
Porteous DJ,
Jarvelin MR,
Wielscher M,
James AL,
Hui J,
Wareham NJ,
Zhao JH,
Wilson JF,
Joshi PK,
Stubbe B,
Rawal R,
Schulz H,
Imboden M,
Probst-Hensch NM,
Karrasch S,
Gieger C,
Deary IJ,
Harris SE,
Marten J,
Rudan I,
Enroth S,
Gyllensten U,
Kerr SM,
Polasek O,
Kähönen M,
Surakka I,
Vitart V,
Hayward C,
Lehtimäki T,
Raitakari OT,
Evans DM,
Henderson AJ,
Pennell CE,
Wang CA,
Sly PD,
Wan ES,
Busch R,
Hobbs BD,
Litonjua AA,
Sparrow DW,
Gulsvik A,
Bakke PS,
Crapo JD,
Beaty TH,
Hansel NN,
Mathias RA,
Ruczinski I,
Barnes KC,
Bossé Y,
Joubert P,
van den Berge M,
Brandsma CA,
Paré PD,
Sin DD,
Nickle DC,
Hao K,
Gottesman O,
Dewey FE,
Bruse SE,
Carey DJ,
Kirchner HL,
Jonsson S,
Thorleifsson G,
Jonsdottir I,
Gislason T,
Stefansson K,
Schurmann C,
Nadkarni G,
Bottinger EP,
Loos RJ,
Walters RG,
Chen Z,
Millwood IY,
Vaucher J,
Kurmi OP,
Li L,
Hansell AL,
Brightling C,
Zeggini E,
Cho MH,
Silverman EK,
Sayers I,
Trynka G,
Morris AP,
Strachan DP,
Hall IP,
Tobin MD
Understanding Society Scientific Group · Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics · 2017 · PMID 28166213 · open access
12 pages+
Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits
Justice AE,
Winkler TW,
Feitosa MF,
Graff M,
Fisher VA,
Young K,
Barata L,
Deng X,
Czajkowski J,
Hadley D,
Ngwa JS,
Ahluwalia TS
and 305 more — show all
Chu AY,
Heard-Costa NL,
Lim E,
Perez J,
Eicher JD,
Kutalik Z,
Xue L,
Mahajan A,
Renström F,
Wu J,
Qi Q,
Ahmad S,
Alfred T,
Amin N,
Bielak LF,
Bonnefond A,
Bragg J,
Cadby G,
Chittani M,
Coggeshall S,
Corre T,
Direk N,
Eriksson J,
Fischer K,
Gorski M,
Neergaard Harder M,
Horikoshi M,
Huang T,
Huffman JE,
Jackson AU,
Justesen JM,
Kanoni S,
Kinnunen L,
Kleber ME,
Komulainen P,
Kumari M,
Lim U,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Marten J,
Middelberg RPS,
Müller-Nurasyid M,
Navarro P,
Pérusse L,
Pervjakova N,
Sarti C,
Smith AV,
Smith JA,
Stančáková A,
Strawbridge RJ,
Stringham HM,
Sung YJ,
Tanaka T,
Teumer A,
Trompet S,
van der Laan SW,
van der Most PJ,
Van Vliet-Ostaptchouk JV,
Vedantam SL,
Verweij N,
Vink JM,
Vitart V,
Wu Y,
Yengo L,
Zhang W,
Hua Zhao J,
Zimmermann ME,
Zubair N,
Abecasis GR,
Adair LS,
Afaq S,
Afzal U,
Bakker SJL,
Bartz TM,
Beilby J,
Bergman RN,
Bergmann S,
Biffar R,
Blangero J,
Boerwinkle E,
Bonnycastle LL,
Bottinger E,
Braga D,
Buckley BM,
Buyske S,
Campbell H,
Chambers JC,
Collins FS,
Curran JE,
de Borst GJ,
de Craen AJM,
de Geus EJC,
Dedoussis G,
Delgado GE,
den Ruijter HM,
Eiriksdottir G,
Eriksson AL,
Esko T,
Faul JD,
Ford I,
Forrester T,
Gertow K,
Gigante B,
Glorioso N,
Gong J,
Grallert H,
Grammer TB,
Grarup N,
Haitjema S,
Hallmans G,
Hamsten A,
Hansen T,
Harris TB,
Hartman CA,
Hassinen M,
Hastie ND,
Heath AC,
Hernandez D,
Hindorff L,
Hocking LJ,
Hollensted M,
Holmen OL,
Homuth G,
Jan Hottenga J,
Huang J,
Hung J,
Hutri-Kähönen N,
Ingelsson E,
James AL,
Jansson JO,
Jarvelin MR,
Jhun MA,
Jørgensen ME,
Juonala M,
Kähönen M,
Karlsson M,
Koistinen HA,
Kolcic I,
Kolovou G,
Kooperberg C,
Krämer BK,
Kuusisto J,
Kvaløy K,
Lakka TA,
Langenberg C,
Launer LJ,
Leander K,
Lee NR,
Lind L,
Lindgren CM,
Linneberg A,
Lobbens S,
Loh M,
Lorentzon M,
Luben R,
Lubke G,
Ludolph-Donislawski A,
Lupoli S,
Madden PAF,
Männikkö R,
Marques-Vidal P,
Martin NG,
McKenzie CA,
McKnight B,
Mellström D,
Menni C,
Montgomery GW,
Musk AB,
Narisu N,
Nauck M,
Nolte IM,
Oldehinkel AJ,
Olden M,
Ong KK,
Padmanabhan S,
Peyser PA,
Pisinger C,
Porteous DJ,
Raitakari OT,
Rankinen T,
Rao DC,
Rasmussen-Torvik LJ,
Rawal R,
Rice T,
Ridker PM,
Rose LM,
Bien SA,
Rudan I,
Sanna S,
Sarzynski MA,
Sattar N,
Savonen K,
Schlessinger D,
Scholtens S,
Schurmann C,
Scott RA,
Sennblad B,
Siemelink MA,
Silbernagel G,
Slagboom PE,
Snieder H,
Staessen JA,
Stott DJ,
Swertz MA,
Swift AJ,
Taylor KD,
Tayo BO,
Thorand B,
Thuillier D,
Tuomilehto J,
Uitterlinden AG,
Vandenput L,
Vohl MC,
Völzke H,
Vonk JM,
Waeber G,
Waldenberger M,
Westendorp RGJ,
Wild S,
Willemsen G,
Wolffenbuttel BHR,
Wong A,
Wright AF,
Zhao W,
Zillikens MC,
Baldassarre D,
Balkau B,
Bandinelli S,
Böger CA,
Boomsma DI,
Bouchard C,
Bruinenberg M,
Chasman DI,
Chen YD,
Chines PS,
Cooper RS,
Cucca F,
Cusi D,
Faire U,
Ferrucci L,
Franks PW,
Froguel P,
Gordon-Larsen P,
Grabe HJ,
Gudnason V,
Haiman CA,
Hayward C,
Hveem K,
Johnson AD,
Wouter Jukema J,
Kardia SLR,
Kivimaki M,
Kooner JS,
Kuh D,
Laakso M,
Lehtimäki T,
Marchand LL,
März W,
McCarthy MI,
Metspalu A,
Morris AP,
Ohlsson C,
Palmer LJ,
Pasterkamp G,
Pedersen O,
Peters A,
Peters U,
Polasek O,
Psaty BM,
Qi L,
Rauramaa R,
Smith BH,
Sørensen TIA,
Strauch K,
Tiemeier H,
Tremoli E,
van der Harst P,
Vestergaard H,
Vollenweider P,
Wareham NJ,
Weir DR,
Whitfield JB,
Wilson JF,
Tyrrell J,
Frayling TM,
Barroso I,
Boehnke M,
Deloukas P,
Fox CS,
Hirschhorn JN,
Hunter DJ,
Spector TD,
Strachan DP,
van Duijn CM,
Heid IM,
Mohlke KL,
Marchini J,
Loos RJF,
Kilpeläinen TO,
Liu CT,
Borecki IB,
North KE,
Cupples LA
Nature communications · 2017 · PMID 28443625 · open access
12 pages+
Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults
Graff M,
Scott RA,
Justice AE,
Young KL,
Feitosa MF,
Barata L,
Winkler TW,
Chu AY,
Mahajan A,
Hadley D,
Xue L,
Workalemahu T
and 269 more — show all
Heard-Costa NL,
den Hoed M,
Ahluwalia TS,
Qi Q,
Ngwa JS,
Renström F,
Quaye L,
Eicher JD,
Hayes JE,
Cornelis M,
Kutalik Z,
Lim E,
Luan J,
Huffman JE,
Zhang W,
Zhao W,
Griffin PJ,
Haller T,
Ahmad S,
Marques-Vidal PM,
Bien S,
Yengo L,
Teumer A,
Smith AV,
Kumari M,
Harder MN,
Justesen JM,
Kleber ME,
Hollensted M,
Lohman K,
Rivera NV,
Whitfield JB,
Zhao JH,
Stringham HM,
Lyytikäinen LP,
Huppertz C,
Willemsen G,
Peyrot WJ,
Wu Y,
Kristiansson K,
Demirkan A,
Fornage M,
Hassinen M,
Bielak LF,
Cadby G,
Tanaka T,
Mägi R,
van der Most PJ,
Jackson AU,
Bragg-Gresham JL,
Vitart V,
Marten J,
Navarro P,
Bellis C,
Pasko D,
Johansson Å,
Snitker S,
Cheng YC,
Eriksson J,
Lim U,
Aadahl M,
Adair LS,
Amin N,
Balkau B,
Auvinen J,
Beilby J,
Bergman RN,
Bergmann S,
Bertoni AG,
Blangero J,
Bonnefond A,
Bonnycastle LL,
Borja JB,
Brage S,
Busonero F,
Buyske S,
Campbell H,
Chines PS,
Collins FS,
Corre T,
Smith GD,
Delgado GE,
Dueker N,
Dörr M,
Ebeling T,
Eiriksdottir G,
Esko T,
Faul JD,
Fu M,
Færch K,
Gieger C,
Gläser S,
Gong J,
Gordon-Larsen P,
Grallert H,
Grammer TB,
Grarup N,
van Grootheest G,
Harald K,
Hastie ND,
Havulinna AS,
Hernandez D,
Hindorff L,
Hocking LJ,
Holmens OL,
Holzapfel C,
Hottenga JJ,
Huang J,
Huang T,
Hui J,
Huth C,
Hutri-Kähönen N,
James AL,
Jansson JO,
Jhun MA,
Juonala M,
Kinnunen L,
Koistinen HA,
Kolcic I,
Komulainen P,
Kuusisto J,
Kvaløy K,
Kähönen M,
Lakka TA,
Launer LJ,
Lehne B,
Lindgren CM,
Lorentzon M,
Luben R,
Marre M,
Milaneschi Y,
Monda KL,
Montgomery GW,
De Moor MHM,
Mulas A,
Müller-Nurasyid M,
Musk AW,
Männikkö R,
Männistö S,
Narisu N,
Nauck M,
Nettleton JA,
Nolte IM,
Oldehinkel AJ,
Olden M,
Ong KK,
Padmanabhan S,
Paternoster L,
Perez J,
Perola M,
Peters A,
Peters U,
Peyser PA,
Prokopenko I,
Puolijoki H,
Raitakari OT,
Rankinen T,
Rasmussen-Torvik LJ,
Rawal R,
Ridker PM,
Rose LM,
Rudan I,
Sarti C,
Sarzynski MA,
Savonen K,
Scott WR,
Sanna S,
Shuldiner AR,
Sidney S,
Silbernagel G,
Smith BH,
Smith JA,
Snieder H,
Stančáková A,
Sternfeld B,
Swift AJ,
Tammelin T,
Tan ST,
Thorand B,
Thuillier D,
Vandenput L,
Vestergaard H,
van Vliet-Ostaptchouk JV,
Vohl MC,
Völker U,
Waeber G,
Walker M,
Wild S,
Wong A,
Wright AF,
Zillikens MC,
Zubair N,
Haiman CA,
Lemarchand L,
Gyllensten U,
Ohlsson C,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Pérusse L,
Wilson JF,
Hayward C,
Polasek O,
Cucca F,
Hveem K,
Hartman CA,
Tönjes A,
Bandinelli S,
Palmer LJ,
Kardia SLR,
Rauramaa R,
Sørensen TIA,
Tuomilehto J,
Salomaa V,
Penninx BWJH,
de Geus EJC,
Boomsma DI,
Lehtimäki T,
Mangino M,
Laakso M,
Bouchard C,
Martin NG,
Kuh D,
Liu Y,
Linneberg A,
März W,
Strauch K,
Kivimäki M,
Harris TB,
Gudnason V,
Völzke H,
Qi L,
Järvelin MR,
Chambers JC,
Kooner JS,
Froguel P,
Kooperberg C,
Vollenweider P,
Hallmans G,
Hansen T,
Pedersen O,
Metspalu A,
Wareham NJ,
Langenberg C,
Weir DR,
Porteous DJ,
Boerwinkle E,
Chasman DI,
Abecasis GR,
Barroso I,
McCarthy MI,
Frayling TM,
O'Connell JR,
van Duijn CM,
Boehnke M,
Heid IM,
Mohlke KL,
Strachan DP,
Fox CS,
Liu CT,
Hirschhorn JN,
Klein RJ,
Johnson AD,
Borecki IB,
Franks PW,
North KE,
Cupples LA,
Loos RJF,
Kilpeläinen TO
CHARGE Consortium · EPIC-InterAct Consortium and 1 more consortia
PLoS genetics · 2017 · PMID 28448500 · open access
12 pages+
Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation
Teumer A,
Chaker L,
Groeneweg S,
Li Y,
Di Munno C,
Barbieri C,
Schultheiss UT,
Traglia M,
Ahluwalia TS,
Akiyama M,
Appel EVR,
Arking DE
and 116 more — show all
Arnold A,
Astrup A,
Beekman M,
Beilby JP,
Bekaert S,
Boerwinkle E,
Brown SJ,
De Buyzere M,
Campbell PJ,
Ceresini G,
Cerqueira C,
Cucca F,
Deary IJ,
Deelen J,
Eckardt KU,
Ekici AB,
Eriksson JG,
Ferrrucci L,
Fiers T,
Fiorillo E,
Ford I,
Fox CS,
Fuchsberger C,
Galesloot TE,
Gieger C,
Gögele M,
De Grandi A,
Grarup N,
Greiser KH,
Haljas K,
Hansen T,
Harris SE,
van Heemst D,
den Heijer M,
Hicks AA,
den Hollander W,
Homuth G,
Hui J,
Ikram MA,
Ittermann T,
Jensen RA,
Jing J,
Jukema JW,
Kajantie E,
Kamatani Y,
Kasbohm E,
Kaufman JM,
Kiemeney LA,
Kloppenburg M,
Kronenberg F,
Kubo M,
Lahti J,
Lapauw B,
Li S,
Liewald DCM,
Lim EM,
Linneberg A,
Marina M,
Mascalzoni D,
Matsuda K,
Medenwald D,
Meisinger C,
Meulenbelt I,
De Meyer T,
Meyer Zu Schwabedissen HE,
Mikolajczyk R,
Moed M,
Netea-Maier RT,
Nolte IM,
Okada Y,
Pala M,
Pattaro C,
Pedersen O,
Petersmann A,
Porcu E,
Postmus I,
Pramstaller PP,
Psaty BM,
Ramos YFM,
Rawal R,
Redmond P,
Richards JB,
Rietzschel ER,
Rivadeneira F,
Roef G,
Rotter JI,
Sala CF,
Schlessinger D,
Selvin E,
Slagboom PE,
Soranzo N,
Sørensen TIA,
Spector TD,
Starr JM,
Stott DJ,
Taes Y,
Taliun D,
Tanaka T,
Thuesen B,
Tiller D,
Toniolo D,
Uitterlinden AG,
Visser WE,
Walsh JP,
Wilson SG,
Wolffenbuttel BHR,
Yang Q,
Zheng HF,
Cappola A,
Peeters RP,
Naitza S,
Völzke H,
Sanna S,
Köttgen A,
Visser TJ,
Medici M
Lifelines Cohort Study
Nature communications · 2018 · PMID 30367059 · open access
12 pages+
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Howard DM,
Adams MJ,
Clarke TK,
Hafferty JD,
Gibson J,
Shirali M,
Coleman JRI,
Hagenaars SP,
Ward J,
Wigmore EM,
Alloza C,
Shen X
and 26 more — show all
Barbu MC,
Xu EY,
Whalley HC,
Marioni RE,
Porteous DJ,
Davies G,
Deary IJ,
Hemani G,
Berger K,
Teismann H,
Rawal R,
Arolt V,
Baune BT,
Dannlowski U,
Domschke K,
Tian C,
Hinds DA,
Trzaskowski M,
Byrne EM,
Ripke S,
Smith DJ,
Sullivan PF,
Wray NR,
Breen G,
Lewis CM,
McIntosh AM
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
12 pages+
New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries
Shrine N,
Guyatt AL,
Erzurumluoglu AM,
Jackson VE,
Hobbs BD,
Melbourne CA,
Batini C,
Fawcett KA,
Song K,
Sakornsakolpat P,
Li X,
Boxall R
and 99 more — show all
Reeve NF,
Obeidat M,
Zhao JH,
Wielscher M,
Weiss S,
Kentistou KA,
Kentistou KA,
Cook JP,
Sun BB,
Zhou J,
Hui J,
Karrasch S,
Imboden M,
Harris SE,
Marten J,
Enroth S,
Kerr SM,
Surakka I,
Vitart V,
Lehtimäki T,
Allen RJ,
Bakke PS,
Beaty TH,
Bleecker ER,
Bossé Y,
Brandsma CA,
Chen Z,
Crapo JD,
Danesh J,
DeMeo DL,
Dudbridge F,
Ewert R,
Gieger C,
Gulsvik A,
Hansell AL,
Hao K,
Hoffman JD,
Hokanson JE,
Homuth G,
Joshi PK,
Joubert P,
Langenberg C,
Li X,
Li L,
Lin K,
Lind L,
Locantore N,
Luan J,
Mahajan A,
Maranville JC,
Murray A,
Nickle DC,
Packer R,
Parker MM,
Paynton ML,
Porteous DJ,
Porteous DJ,
Prokopenko D,
Qiao D,
Rawal R,
Runz H,
Sayers I,
Sin DD,
Smith BH,
Soler Artigas M,
Sparrow D,
Tal-Singer R,
Timmers PRHJ,
Van den Berge M,
Whittaker JC,
Woodruff PG,
Yerges-Armstrong LM,
Troyanskaya OG,
Raitakari OT,
Kähönen M,
Polašek O,
Gyllensten U,
Rudan I,
Deary IJ,
Probst-Hensch NM,
Schulz H,
James AL,
Wilson JF,
Stubbe B,
Zeggini E,
Jarvelin MR,
Wareham N,
Silverman EK,
Hayward C,
Morris AP,
Butterworth AS,
Scott RA,
Walters RG,
Meyers DA,
Cho MH,
Strachan DP,
Hall IP,
Tobin MD,
Wain LV
Understanding Society Scientific Group
Nature genetics · 2019 · PMID 30804560 · open access
12 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
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation
Soler Artigas M,
Wain LV,
Miller S,
Kheirallah AK,
Huffman JE,
Ntalla I,
Shrine N,
Obeidat M,
Trochet H,
McArdle WL,
Alves AC,
Hui J
and 78 more — show all
Zhao JH,
Joshi PK,
Teumer A,
Albrecht E,
Imboden M,
Rawal R,
Lopez LM,
Marten J,
Enroth S,
Surakka I,
Polasek O,
Lyytikäinen LP,
Granell R,
Hysi PG,
Flexeder C,
Mahajan A,
Beilby J,
Bossé Y,
Brandsma CA,
Campbell H,
Gieger C,
Gläser S,
González JR,
Grallert H,
Hammond CJ,
Harris SE,
Hartikainen AL,
Heliövaara M,
Henderson J,
Hocking L,
Horikoshi M,
Hutri-Kähönen N,
Ingelsson E,
Johansson Å,
Kemp JP,
Kolcic I,
Kumar A,
Lind L,
Melén E,
Musk AW,
Navarro P,
Nickle DC,
Padmanabhan S,
Raitakari OT,
Ried JS,
Ripatti S,
Schulz H,
Scott RA,
Sin DD,
Starr JM,
Viñuela A,
Völzke H,
Wild SH,
Wright AF,
Zemunik T,
Jarvis DL,
Spector TD,
Evans DM,
Lehtimäki T,
Vitart V,
Kähönen M,
Gyllensten U,
Rudan I,
Deary IJ,
Karrasch S,
Probst-Hensch NM,
Heinrich J,
Stubbe B,
Wilson JF,
Wareham NJ,
James AL,
Morris AP,
Jarvelin MR,
Hayward C,
Sayers I,
Strachan DP,
Hall IP,
Tobin MD
UK BiLEVE
Nature communications · 2015 · PMID 26635082 · open access
8 pages
Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk
Teumer A,
Rawal R,
Homuth G,
Ernst F,
Heier M,
Evert M,
Dombrowski F,
Völker U,
Nauck M,
Radke D,
Ittermann T,
Biffar R
and 7 more — show all
American journal of human genetics · 2011 · PMID 21565293
6 pages
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease
Medici M,
Porcu E,
Pistis G,
Teumer A,
Brown SJ,
Jensen RA,
Rawal R,
Roef GL,
Plantinga TS,
Vermeulen SH,
Lahti J,
Simmonds MJ
and 106 more — show all
Husemoen LL,
Freathy RM,
Shields BM,
Pietzner D,
Nagy R,
Broer L,
Chaker L,
Korevaar TI,
Plia MG,
Sala C,
Völker U,
Richards JB,
Sweep FC,
Gieger C,
Corre T,
Kajantie E,
Thuesen B,
Taes YE,
Visser WE,
Hattersley AT,
Kratzsch J,
Hamilton A,
Li W,
Homuth G,
Lobina M,
Mariotti S,
Soranzo N,
Cocca M,
Nauck M,
Spielhagen C,
Ross A,
Arnold A,
van de Bunt M,
Liyanarachchi S,
Heier M,
Grabe HJ,
Masciullo C,
Galesloot TE,
Lim EM,
Reischl E,
Leedman PJ,
Lai S,
Delitala A,
Bremner AP,
Philips DI,
Beilby JP,
Mulas A,
Vocale M,
Abecasis G,
Forsen T,
James A,
Widen E,
Hui J,
Prokisch H,
Rietzschel EE,
Palotie A,
Feddema P,
Fletcher SJ,
Schramm K,
Rotter JI,
Kluttig A,
Radke D,
Traglia M,
Surdulescu GL,
He H,
Franklyn JA,
Tiller D,
Vaidya B,
de Meyer T,
Jørgensen T,
Eriksson JG,
O'Leary PC,
Wichmann E,
Hermus AR,
Psaty BM,
Ittermann T,
Hofman A,
Bosi E,
Schlessinger D,
Wallaschofski H,
Pirastu N,
Aulchenko YS,
de la Chapelle A,
Netea-Maier RT,
Gough SC,
Meyer Zu Schwabedissen H,
Frayling TM,
Kaufman JM,
Linneberg A,
Räikkönen K,
Smit JW,
Kiemeney LA,
Rivadeneira F,
Uitterlinden AG,
Walsh JP,
Meisinger C,
den Heijer M,
Visser TJ,
Spector TD,
Wilson SG,
Völzke H,
Cappola A,
Toniolo D,
Sanna S,
Naitza S,
Peeters RP
PLoS genetics · 2014 · PMID 24586183 · open access
3 pages
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
Kettunen J,
Demirkan A,
Würtz P,
Draisma HH,
Haller T,
Rawal R,
Vaarhorst A,
Kangas AJ,
Lyytikäinen LP,
Pirinen M,
Pool R,
Sarin AP
and 38 more — show all
Soininen P,
Tukiainen T,
Wang Q,
Tiainen M,
Tynkkynen T,
Amin N,
Zeller T,
Beekman M,
Deelen J,
van Dijk KW,
Esko T,
Hottenga JJ,
van Leeuwen EM,
Lehtimäki T,
Mihailov E,
Rose RJ,
de Craen AJ,
Gieger C,
Kähönen M,
Perola M,
Blankenberg S,
Savolainen MJ,
Verhoeven A,
Viikari J,
Willemsen G,
Boomsma DI,
van Duijn CM,
Eriksson J,
Jula A,
Järvelin MR,
Kaprio J,
Metspalu A,
Raitakari O,
Salomaa V,
Slagboom PE,
Waldenberger M,
Ripatti S,
Ala-Korpela M
Nature communications · 2016 · PMID 27005778 · open access
3 pages
KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference
Schumann G,
Liu C,
O'Reilly P,
Gao H,
Song P,
Xu B,
Ruggeri B,
Amin N,
Jia T,
Preis S,
Segura Lepe M,
Akira S
and 115 more — show all
Barbieri C,
Baumeister S,
Cauchi S,
Clarke TK,
Enroth S,
Fischer K,
Hällfors J,
Harris SE,
Hieber S,
Hofer E,
Hottenga JJ,
Johansson Å,
Joshi PK,
Kaartinen N,
Laitinen J,
Lemaitre R,
Loukola A,
Luan J,
Lyytikäinen LP,
Mangino M,
Manichaikul A,
Mbarek H,
Milaneschi Y,
Moayyeri A,
Mukamal K,
Nelson C,
Nettleton J,
Partinen E,
Rawal R,
Robino A,
Rose L,
Sala C,
Satoh T,
Schmidt R,
Schraut K,
Scott R,
Smith AV,
Starr JM,
Teumer A,
Trompet S,
Uitterlinden AG,
Venturini C,
Vergnaud AC,
Verweij N,
Vitart V,
Vuckovic D,
Wedenoja J,
Yengo L,
Yu B,
Zhang W,
Zhao JH,
Boomsma DI,
Chambers J,
Chasman DI,
Daniela T,
de Geus E,
Deary I,
Eriksson JG,
Esko T,
Eulenburg V,
Franco OH,
Froguel P,
Gieger C,
Grabe HJ,
Gudnason V,
Gyllensten U,
Harris TB,
Hartikainen AL,
Heath AC,
Hocking L,
Hofman A,
Huth C,
Jarvelin MR,
Jukema JW,
Kaprio J,
Kooner JS,
Kutalik Z,
Lahti J,
Langenberg C,
Lehtimäki T,
Liu Y,
Madden PA,
Martin N,
Morrison A,
Penninx B,
Pirastu N,
Psaty B,
Raitakari O,
Ridker P,
Rose R,
Rotter JI,
Samani NJ,
Schmidt H,
Spector TD,
Stott D,
Strachan D,
Tzoulaki I,
van der Harst P,
van Duijn CM,
Marques-Vidal P,
Vollenweider P,
Wareham NJ,
Whitfield JB,
Wilson J,
Wolffenbuttel B,
Bakalkin G,
Evangelou E,
Liu Y,
Rice KM,
Desrivières S,
Kliewer SA,
Mangelsdorf DJ,
Müller CP,
Levy D,
Elliott P
Proceedings of the National Academy of Sciences of the United States of America · 2016 · PMID 27911795
3 pages
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption
Cornelis MC,
Byrne EM,
Esko T,
Nalls MA,
Ganna A,
Paynter N,
Monda KL,
Amin N,
Fischer K,
Renstrom F,
Ngwa JS,
Huikari V
and 142 more — show all
Cavadino A,
Nolte IM,
Teumer A,
Yu K,
Marques-Vidal P,
Rawal R,
Manichaikul A,
Wojczynski MK,
Vink JM,
Zhao JH,
Burlutsky G,
Lahti J,
Mikkilä V,
Lemaitre RN,
Eriksson J,
Musani SK,
Tanaka T,
Geller F,
Luan J,
Hui J,
Mägi R,
Dimitriou M,
Garcia ME,
Ho WK,
Wright MJ,
Rose LM,
Magnusson PK,
Pedersen NL,
Couper D,
Oostra BA,
Hofman A,
Ikram MA,
Tiemeier HW,
Uitterlinden AG,
van Rooij FJ,
Barroso I,
Johansson I,
Xue L,
Kaakinen M,
Milani L,
Power C,
Snieder H,
Stolk RP,
Baumeister SE,
Biffar R,
Gu F,
Bastardot F,
Kutalik Z,
Jacobs DR Jr,
Forouhi NG,
Mihailov E,
Lind L,
Lindgren C,
Michaëlsson K,
Morris A,
Jensen M,
Khaw KT,
Luben RN,
Wang JJ,
Männistö S,
Perälä MM,
Kähönen M,
Lehtimäki T,
Viikari J,
Mozaffarian D,
Mukamal K,
Psaty BM,
Döring A,
Heath AC,
Montgomery GW,
Dahmen N,
Carithers T,
Tucker KL,
Ferrucci L,
Boyd HA,
Melbye M,
Treur JL,
Mellström D,
Hottenga JJ,
Prokopenko I,
Tönjes A,
Deloukas P,
Kanoni S,
Lorentzon M,
Houston DK,
Liu Y,
Danesh J,
Rasheed A,
Mason MA,
Zonderman AB,
Franke L,
Kristal BS,
Karjalainen J,
Reed DR,
Westra HJ,
Evans MK,
Saleheen D,
Harris TB,
Dedoussis G,
Curhan G,
Stumvoll M,
Beilby J,
Pasquale LR,
Feenstra B,
Bandinelli S,
Ordovas JM,
Chan AT,
Peters U,
Ohlsson C,
Gieger C,
Martin NG,
Waldenberger M,
Siscovick DS,
Raitakari O,
Eriksson JG,
Mitchell P,
Hunter DJ,
Kraft P,
Rimm EB,
Boomsma DI,
Borecki IB,
Loos RJ,
Wareham NJ,
Vollenweider P,
Caporaso N,
Grabe HJ,
Neuhouser ML,
Wolffenbuttel BH,
Hu FB,
Hyppönen E,
Järvelin MR,
Cupples LA,
Franks PW,
Ridker PM,
van Duijn CM,
Heiss G,
Metspalu A,
North KE,
Ingelsson E,
Nettleton JA,
van Dam RM,
Chasman DI
Coffee and Caffeine Genetics Consortium · International Parkinson’s Disease Genomics Consortium (IPDGC) and 2 more consortia
Molecular psychiatry · 2015 · PMID 25288136
2 pages
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
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function
Rawal R,
Teumer A,
Völzke H,
Wallaschofski H,
Ittermann T,
Åsvold BO,
Bjøro T,
Greiser KH,
Tiller D,
Werdan K,
Meyer zu Schwabedissen HE,
Doering A
and 4 more — show all
Human molecular genetics · 2012 · PMID 22494929
1 page
Meta-analysis of exome array data identifies six novel genetic loci for lung function
Jackson VE,
Latourelle JC,
Wain LV,
Smith AV,
Grove ML,
Bartz TM,
Obeidat M,
Province MA,
Gao W,
Qaiser B,
Porteous DJ,
Cassano PA
and 95 more — show all
Ahluwalia TS,
Grarup N,
Li J,
Altmaier E,
Marten J,
Harris SE,
Manichaikul A,
Pottinger TD,
Li-Gao R,
Lind-Thomsen A,
Mahajan A,
Lahousse L,
Imboden M,
Teumer A,
Prins B,
Lyytikäinen LP,
Eiriksdottir G,
Franceschini N,
Sitlani CM,
Brody JA,
Bossé Y,
Timens W,
Kraja A,
Loukola A,
Tang W,
Liu Y,
Bork-Jensen J,
Justesen JM,
Linneberg A,
Lange LA,
Rawal R,
Karrasch S,
Huffman JE,
Smith BH,
Davies G,
Burkart KM,
Mychaleckyj JC,
Bonten TN,
Enroth S,
Lind L,
Brusselle GG,
Kumar A,
Stubbe B,
Kähönen M,
Wyss AB,
Psaty BM,
Heckbert SR,
Hao K,
Rantanen T,
Kritchevsky SB,
Lohman K,
Skaaby T,
Pisinger C,
Hansen T,
Schulz H,
Polasek O,
Campbell A,
Starr JM,
Rich SS,
Mook-Kanamori DO,
Johansson Å,
Ingelsson E,
Uitterlinden AG,
Weiss S,
Raitakari OT,
Gudnason V,
North KE,
Gharib SA,
Sin DD,
Taylor KD,
O'Connor GT,
Kaprio J,
Harris TB,
Pederson O,
Vestergaard H,
Wilson JG,
Strauch K,
Hayward C,
Kerr S,
Deary IJ,
Barr RG,
de Mutsert R,
Gyllensten U,
Morris AP,
Ikram MA,
Probst-Hensch N,
Gläser S,
Zeggini E,
Lehtimäki T,
Strachan DP,
Dupuis J,
Morrison AC,
Hall IP,
Tobin MD,
London SJ
Understanding Society Scientific Group
Wellcome open research · 2018 · PMID 30175238 · open access
1 page
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