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성함이나 학술지명, PMID로 찾아보십시오.
Gordon S에 대해
45건, 그중 20건 표시.
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
Davies G,
Lam M,
Harris SE,
Trampush JW,
Luciano M,
Hill WD,
Hagenaars SP,
Ritchie SJ,
Marioni RE,
Fawns-Ritchie C,
Liewald DCM,
Okely JA
외 212명 — 모두 보기
Ahola-Olli AV,
Barnes CLK,
Bertram L,
Bis JC,
Burdick KE,
Christoforou A,
DeRosse P,
Djurovic S,
Espeseth T,
Giakoumaki S,
Giddaluru S,
Gustavson DE,
Hayward C,
Hofer E,
Ikram MA,
Karlsson R,
Knowles E,
Lahti J,
Leber M,
Li S,
Mather KA,
Melle I,
Morris D,
Oldmeadow C,
Palviainen T,
Payton A,
Pazoki R,
Petrovic K,
Reynolds CA,
Sargurupremraj M,
Scholz M,
Smith JA,
Smith AV,
Terzikhan N,
Thalamuthu A,
Trompet S,
van der Lee SJ,
Ware EB,
Windham BG,
Wright MJ,
Yang J,
Yu J,
Ames D,
Amin N,
Amouyel P,
Andreassen OA,
Armstrong NJ,
Assareh AA,
Attia JR,
Attix D,
Avramopoulos D,
Bennett DA,
Böhmer AC,
Boyle PA,
Brodaty H,
Campbell H,
Cannon TD,
Cirulli ET,
Congdon E,
Conley ED,
Corley J,
Cox SR,
Dale AM,
Dehghan A,
Dick D,
Dickinson D,
Eriksson JG,
Evangelou E,
Faul JD,
Ford I,
Freimer NA,
Gao H,
Giegling I,
Gillespie NA,
Gordon SD,
Gottesman RF,
Griswold ME,
Gudnason V,
Harris TB,
Hartmann AM,
Hatzimanolis A,
Heiss G,
Holliday EG,
Joshi PK,
Kähönen M,
Kardia SLR,
Karlsson I,
Kleineidam L,
Knopman DS,
Kochan NA,
Konte B,
Kwok JB,
Le Hellard S,
Lee T,
Lehtimäki T,
Li SC,
Lill CM,
Liu T,
Koini M,
London E,
Longstreth WT Jr,
Lopez OL,
Loukola A,
Luck T,
Lundervold AJ,
Lundquist A,
Lyytikäinen LP,
Martin NG,
Montgomery GW,
Murray AD,
Need AC,
Noordam R,
Nyberg L,
Ollier W,
Papenberg G,
Pattie A,
Polasek O,
Poldrack RA,
Psaty BM,
Reppermund S,
Riedel-Heller SG,
Rose RJ,
Rotter JI,
Roussos P,
Rovio SP,
Saba Y,
Sabb FW,
Sachdev PS,
Satizabal CL,
Satizabal CL,
Schmid M,
Scott RJ,
Scult MA,
Simino J,
Slagboom PE,
Smyrnis N,
Soumaré A,
Stefanis NC,
Stott DJ,
Straub RE,
Sundet K,
Taylor AM,
Taylor KD,
Tzoulaki I,
Tzourio C,
Uitterlinden A,
Vitart V,
Voineskos AN,
Kaprio J,
Wagner M,
Wagner H,
Weinhold L,
Wen KH,
Widen E,
Yang Q,
Zhao W,
Adams HHH,
Arking DE,
Bilder RM,
Bitsios P,
Boerwinkle E,
Chiba-Falek O,
Corvin A,
De Jager PL,
Debette S,
Donohoe G,
Elliott P,
Fitzpatrick AL,
Gill M,
Glahn DC,
Hägg S,
Hansell NK,
Hariri AR,
Ikram MK,
Jukema JW,
Jukema JW,
Vuoksimaa E,
Keller MC,
Kremen WS,
Launer L,
Lindenberger U,
Palotie A,
Pedersen NL,
Pendleton N,
Porteous DJ,
Räikkönen K,
Raitakari OT,
Ramirez A,
Reinvang I,
Rudan I,
Dan Rujescu,
Schmidt R,
Schmidt H,
Schofield PW,
Schofield PR,
Starr JM,
Steen VM,
Trollor JN,
Turner ST,
Van Duijn CM,
Villringer A,
Weinberger DR,
Weir DR,
Wilson JF,
Malhotra A,
McIntosh AM,
Gale CR,
Seshadri S,
Mosley TH Jr,
Bressler J,
Lencz T,
Deary IJ
Nature communications · 2018 · PMID 29844566 · open access
페이지 12개+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
외 111명 — 모두 보기
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
페이지 12개+
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci
Dudding T,
Haworth S,
Lind PA,
Sathirapongsasuti JF,
Tung JY,
Mitchell R,
Colodro-Conde L,
Medland SE,
Gordon S,
Elsworth B,
Paternoster L,
Franks PW
외 3명 — 모두 보기
23andMe Research Team
Nature communications · 2019 · PMID 30837455 · open access
페이지 12개+
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
외 315명 — 모두 보기
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
페이지 12개+
Combined analysis of keratinocyte cancers identifies novel genome-wide loci
Liyanage UE,
Law MH,
Han X,
An J,
Ong JS,
Gharahkhani P,
Gordon S,
Neale RE,
Olsen CM,
MacGregor S,
Whiteman DC
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
페이지 12개+
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Tin A,
Marten J,
Halperin Kuhns VL,
Li Y,
Wuttke M,
Kirsten H,
Sieber KB,
Qiu C,
Gorski M,
Yu Z,
Giri A,
Sveinbjornsson G
외 213명 — 모두 보기
Li M,
Chu AY,
Hoppmann A,
O'Connor LJ,
Prins B,
Nutile T,
Noce D,
Akiyama M,
Cocca M,
Ghasemi S,
van der Most PJ,
Horn K,
Xu Y,
Fuchsberger C,
Sedaghat S,
Afaq S,
Amin N,
Ärnlöv J,
Bakker SJL,
Bansal N,
Baptista D,
Bergmann S,
Biggs ML,
Biino G,
Boerwinkle E,
Bottinger EP,
Boutin TS,
Brumat M,
Burkhardt R,
Campana E,
Campbell A,
Campbell H,
Carroll RJ,
Catamo E,
Chambers JC,
Ciullo M,
Concas MP,
Coresh J,
Corre T,
Cusi D,
Felicita SC,
de Borst MH,
De Grandi A,
de Mutsert R,
de Vries APJ,
Delgado G,
Demirkan A,
Devuyst O,
Dittrich K,
Eckardt KU,
Ehret G,
Endlich K,
Evans MK,
Gansevoort RT,
Gasparini P,
Giedraitis V,
Gieger C,
Girotto G,
Gögele M,
Gordon SD,
Gudbjartsson DF,
Gudnason V,
Haller T,
Hamet P,
Harris TB,
Hayward C,
Hicks AA,
Hofer E,
Holm H,
Huang W,
Hutri-Kähönen N,
Hwang SJ,
Ikram MA,
Lewis RM,
Ingelsson E,
Jakobsdottir J,
Jonsdottir I,
Jonsson H,
Joshi PK,
Josyula NS,
Jung B,
Kähönen M,
Kamatani Y,
Kanai M,
Kerr SM,
Kiess W,
Kleber ME,
Koenig W,
Kooner JS,
Körner A,
Kovacs P,
Krämer BK,
Kronenberg F,
Kubo M,
Kühnel B,
La Bianca M,
Lange LA,
Lehne B,
Lehtimäki T,
Liu J,
Loeffler M,
Loos RJF,
Lyytikäinen LP,
Magi R,
Mahajan A,
Martin NG,
März W,
Mascalzoni D,
Matsuda K,
Meisinger C,
Meitinger T,
Metspalu A,
Milaneschi Y,
O'Donnell CJ,
Wilson OD,
Gaziano JM,
Mishra PP,
Mohlke KL,
Mononen N,
Montgomery GW,
Mook-Kanamori DO,
Müller-Nurasyid M,
Nadkarni GN,
Nalls MA,
Nauck M,
Nikus K,
Ning B,
Nolte IM,
Noordam R,
O'Connell JR,
Olafsson I,
Padmanabhan S,
Penninx BWJH,
Perls T,
Peters A,
Pirastu M,
Pirastu N,
Pistis G,
Polasek O,
Ponte B,
Porteous DJ,
Poulain T,
Preuss MH,
Rabelink TJ,
Raffield LM,
Raitakari OT,
Rettig R,
Rheinberger M,
Rice KM,
Rizzi F,
Robino A,
Rudan I,
Krajcoviechova A,
Cifkova R,
Rueedi R,
Ruggiero D,
Ryan KA,
Saba Y,
Salvi E,
Schmidt H,
Schmidt R,
Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
Thiery J,
Thio CHL,
Thorsteinsdottir U,
Toniolo D,
Tönjes A,
Tremblay J,
Uitterlinden AG,
Vaccargiu S,
van der Harst P,
van Duijn CM,
Verweij N,
Völker U,
Vollenweider P,
Waeber G,
Waldenberger M,
Whitfield JB,
Wild SH,
Wilson JF,
Yang Q,
Zhang W,
Zonderman AB,
Bochud M,
Wilson JG,
Pendergrass SA,
Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
Böger CA,
Snieder H,
Butterworth AS,
Okada Y,
Edwards TL,
Stefansson K,
Susztak K,
Scholz M,
Heid IM,
Hung AM,
Teumer A,
Pattaro C,
Woodward OM,
Vitart V,
Köttgen A
German Chronic Kidney Disease Study · Lifelines Cohort Study 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31578528 · open access
페이지 12개+
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Gallagher CS,
Mäkinen N,
Harris HR,
Rahmioglu N,
Uimari O,
Cook JP,
Shigesi N,
Ferreira T,
Velez-Edwards DR,
Edwards TL,
Mortlock S,
Ruhioglu Z
외 24명 — 모두 보기
Day F,
Becker CM,
Karhunen V,
Martikainen H,
Järvelin MR,
Cantor RM,
Ridker PM,
Terry KL,
Buring JE,
Gordon SD,
Medland SE,
Montgomery GW,
Nyholt DR,
Hinds DA,
Tung JY,
Perry JRB,
Lind PA,
Painter JN,
Martin NG,
Morris AP,
Chasman DI,
Missmer SA,
Zondervan KT,
Morton CC
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
페이지 12개+
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
Landi MT,
Bishop DT,
MacGregor S,
Machiela MJ,
Stratigos AJ,
Ghiorzo P,
Brossard M,
Calista D,
Choi J,
Fargnoli MC,
Zhang T,
Rodolfo M
외 140명 — 모두 보기
Trower AJ,
Menin C,
Martinez J,
Hadjisavvas A,
Song L,
Stefanaki I,
Scolyer R,
Yang R,
Goldstein AM,
Potrony M,
Kypreou KP,
Pastorino L,
Queirolo P,
Pellegrini C,
Cattaneo L,
Zawistowski M,
Gimenez-Xavier P,
Rodriguez A,
Elefanti L,
Manoukian S,
Rivoltini L,
Smith BH,
Loizidou MA,
Del Regno L,
Massi D,
Mandala M,
Khosrotehrani K,
Akslen LA,
Amos CI,
Andresen PA,
Avril MF,
Azizi E,
Soyer HP,
Bataille V,
Dalmasso B,
Bowdler LM,
Burdon KP,
Chen WV,
Codd V,
Craig JE,
Dębniak T,
Falchi M,
Fang S,
Friedman E,
Simi S,
Galan P,
Garcia-Casado Z,
Gillanders EM,
Gordon S,
Green A,
Gruis NA,
Hansson J,
Harland M,
Harris J,
Helsing P,
Henders A,
Hočevar M,
Höiom V,
Hunter D,
Ingvar C,
Kumar R,
Lang J,
Lathrop GM,
Lee JE,
Li X,
Lubiński J,
Mackie RM,
Malt M,
Malvehy J,
McAloney K,
Mohamdi H,
Molven A,
Moses EK,
Neale RE,
Novaković S,
Nyholt DR,
Olsson H,
Orr N,
Fritsche LG,
Puig-Butille JA,
Qureshi AA,
Radford-Smith GL,
Randerson-Moor J,
Requena C,
Rowe C,
Samani NJ,
Sanna M,
Schadendorf D,
Schulze HJ,
Simms LA,
Smithers M,
Song F,
Swerdlow AJ,
van der Stoep N,
Kukutsch NA,
Visconti A,
Wallace L,
Ward SV,
Wheeler L,
Sturm RA,
Hutchinson A,
Jones K,
Malasky M,
Vogt A,
Zhou W,
Pooley KA,
Elder DE,
Han J,
Hicks B,
Hayward NK,
Kanetsky PA,
Brummett C,
Montgomery GW,
Olsen CM,
Hayward C,
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23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
페이지 12개+
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
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외 205명 — 모두 보기
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23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
페이지 12개+
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
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AURORA Study · Estonian Biobank Research Team 외 컨소시엄 2곳
Nature genetics · 2024 · PMID 38637617
페이지 12개+
Genetic architecture reconciles linkage and association studies of complex traits
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Estonian Biobank Research Team · Lifelines Cohort Study
Nature genetics · 2024 · PMID 39375568
페이지 12개+
Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
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International Visible Trait Genetics Consortium
Nature genetics · 2018 · PMID 29662168 · open access
페이지 10개
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
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eQTLGen · 23andMe 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29700475 · open access
페이지 10개
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
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International Headache Genetics Consortium
Nature genetics · 2016 · PMID 27322543
페이지 9개
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
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Nature genetics · 2025 · PMID 40962958
페이지 9개
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
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