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27건, 그중 20건 표시.
Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes
McKay JD,
Hung RJ,
Han Y,
Zong X,
Carreras-Torres R,
Christiani DC,
Caporaso NE,
Johansson M,
Xiao X,
Li Y,
Byun J,
Dunning A
외 128명 — 모두 보기
Pooley KA,
Qian DC,
Ji X,
Liu G,
Timofeeva MN,
Bojesen SE,
Wu X,
Le Marchand L,
Albanes D,
Bickeböller H,
Aldrich MC,
Bush WS,
Tardon A,
Rennert G,
Teare MD,
Field JK,
Kiemeney LA,
Lazarus P,
Haugen A,
Lam S,
Schabath MB,
Andrew AS,
Shen H,
Hong YC,
Yuan JM,
Bertazzi PA,
Pesatori AC,
Ye Y,
Diao N,
Su L,
Zhang R,
Brhane Y,
Leighl N,
Johansen JS,
Mellemgaard A,
Saliba W,
Haiman CA,
Wilkens LR,
Fernandez-Somoano A,
Fernandez-Tardon G,
van der Heijden HFM,
Kim JH,
Dai J,
Hu Z,
Davies MPA,
Marcus MW,
Brunnström H,
Manjer J,
Melander O,
Muller DC,
Overvad K,
Trichopoulou A,
Tumino R,
Doherty JA,
Barnett MP,
Chen C,
Goodman GE,
Cox A,
Taylor F,
Woll P,
Brüske I,
Wichmann HE,
Manz J,
Muley TR,
Risch A,
Rosenberger A,
Grankvist K,
Johansson M,
Shepherd FA,
Tsao MS,
Arnold SM,
Haura EB,
Bolca C,
Holcatova I,
Janout V,
Kontic M,
Lissowska J,
Mukeria A,
Ognjanovic S,
Orlowski TM,
Scelo G,
Swiatkowska B,
Zaridze D,
Bakke P,
Skaug V,
Zienolddiny S,
Duell EJ,
Butler LM,
Koh WP,
Gao YT,
Houlston RS,
McLaughlin J,
Stevens VL,
Joubert P,
Lamontagne M,
Nickle DC,
Obeidat M,
Timens W,
Zhu B,
Song L,
Kachuri L,
Artigas MS,
Tobin MD,
Wain LV,
Rafnar T,
Thorgeirsson TE,
Reginsson GW,
Stefansson K,
Hancock DB,
Bierut LJ,
Spitz MR,
Gaddis NC,
Lutz SM,
Gu F,
Johnson EO,
Kamal A,
Pikielny C,
Zhu D,
Lindströem S,
Jiang X,
Tyndale RF,
Chenevix-Trench G,
Beesley J,
Bossé Y,
Chanock S,
Brennan P,
Landi MT,
Amos CI
SpiroMeta Consortium
Nature genetics · 2017 · PMID 28604730 · 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 association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Mullins N,
Forstner AJ,
O'Connell KS,
Coombes B,
Coleman JRI,
Qiao Z,
Als TD,
Bigdeli TB,
Børte S,
Bryois J,
Charney AW,
Drange OK
외 305명 — 모두 보기
Gandal MJ,
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Schilder BM,
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Steinberg S,
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Won HH,
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Anjorin A,
Antilla V,
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Beins EC,
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Bøcker Pedersen C,
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Brumpton BM,
Brunkhorst-Kanaan N,
Budde M,
Bybjerg-Grauholm J,
Byerley W,
Cairns M,
Casas M,
Cervantes P,
Clarke TK,
Cruceanu C,
Cuellar-Barboza A,
Cunningham J,
Curtis D,
Czerski PM,
Dale AM,
Dalkner N,
David FS,
Degenhardt F,
Djurovic S,
Dobbyn AL,
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Elvsåshagen T,
Escott-Price V,
Ferrier IN,
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Garnham J,
Gelernter J,
Giørtz Pedersen M,
Gizer IR,
Gordon SD,
Gordon-Smith K,
Greenwood TA,
Grove J,
Guzman-Parra J,
Ha K,
Haraldsson M,
Hautzinger M,
Heilbronner U,
Hellgren D,
Herms S,
Hoffmann P,
Holmans PA,
Huckins L,
Jamain S,
Johnson JS,
Kalman JL,
Kamatani Y,
Kennedy JL,
Kittel-Schneider S,
Knowles JA,
Kogevinas M,
Koromina M,
Kranz TM,
Kranzler HR,
Kubo M,
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Kushner SA,
Lavebratt C,
Lawrence J,
Leber M,
Lee HJ,
Lee PH,
Levy SE,
Lewis C,
Liao C,
Lucae S,
Lundberg M,
MacIntyre DJ,
Magnusson SH,
Maier W,
Maihofer A,
Malaspina D,
Maratou E,
Martinsson L,
Mattheisen M,
McCarroll SA,
McGregor NW,
McGuffin P,
McKay JD,
Medeiros H,
Medland SE,
Millischer V,
Montgomery GW,
Moran JL,
Morris DW,
Mühleisen TW,
O'Brien N,
O'Donovan C,
Olde Loohuis LM,
Oruc L,
Papiol S,
Pardiñas AF,
Perry A,
Pfennig A,
Porichi E,
Potash JB,
Quested D,
Raj T,
Rapaport MH,
DePaulo JR,
Regeer EJ,
Rice JP,
Rivas F,
Rivera M,
Roth J,
Roussos P,
Ruderfer DM,
Sánchez-Mora C,
Schulte EC,
Senner F,
Sharp S,
Shilling PD,
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Sirignano L,
Slaney C,
Smeland OB,
Smith DJ,
Sobell JL,
Søholm Hansen C,
Soler Artigas M,
Spijker AT,
Stein DJ,
Strauss JS,
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Terao C,
Thorgeirsson TE,
Toma C,
Tooney P,
Tsermpini EE,
Vawter MP,
Vedder H,
Walters JTR,
Witt SH,
Xi S,
Xu W,
Yang JMK,
Young AH,
Young H,
Zandi PP,
Zhou H,
Zillich L,
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Agartz I,
Alda M,
Alfredsson L,
Babadjanova G,
Backlund L,
Baune BT,
Bellivier F,
Bengesser S,
Berrettini WH,
Blackwood DHR,
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Breen G,
Carr VJ,
Catts S,
Corvin A,
Craddock N,
Dannlowski U,
Dikeos D,
Esko T,
Etain B,
Ferentinos P,
Frye M,
Fullerton JM,
Gawlik M,
Gershon ES,
Goes FS,
Green MJ,
Grigoroiu-Serbanescu M,
Hauser J,
Henskens F,
Hillert J,
Hong KS,
Hougaard DM,
Hultman CM,
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Iwata N,
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Jones I,
Jones LA,
Kahn RS,
Kelsoe JR,
Kirov G,
Landén M,
Leboyer M,
Lewis CM,
Li QS,
Lissowska J,
Lochner C,
Loughland C,
Martin NG,
Mathews CA,
Mayoral F,
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McMahon FJ,
Melle I,
Michie P,
Milani L,
Mitchell PB,
Morken G,
Mors O,
Mortensen PB,
Mowry B,
Müller-Myhsok B,
Myers RM,
Neale BM,
Nievergelt CM,
Nordentoft M,
Nöthen MM,
O'Donovan MC,
Oedegaard KJ,
Olsson T,
Owen MJ,
Paciga SA,
Pantelis C,
Pato C,
Pato MT,
Patrinos GP,
Perlis RH,
Posthuma D,
Ramos-Quiroga JA,
Reif A,
Reininghaus EZ,
Ribasés M,
Rietschel M,
Ripke S,
Rouleau GA,
Saito T,
Schall U,
Schalling M,
Schofield PR,
Schulze TG,
Scott LJ,
Scott RJ,
Serretti A,
Shannon Weickert C,
Smoller JW,
Stefansson H,
Stefansson K,
Stordal E,
Streit F,
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Turecki G,
Vaaler AE,
Vieta E,
Vincent JB,
Waldman ID,
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Zwart JA,
Biernacka JM,
Nurnberger JI,
Cichon S,
Edenberg HJ,
Stahl EA,
McQuillin A,
Di Florio A,
Ophoff RA,
Andreassen OA
HUNT All-In Psychiatry
Nature genetics · 2021 · PMID 34002096 · open access
페이지 12개+
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Hautakangas H,
Winsvold BS,
Ruotsalainen SE,
Bjornsdottir G,
Harder AVE,
Kogelman LJA,
Thomas LF,
Noordam R,
Benner C,
Gormley P,
Artto V,
Banasik K
외 59명 — 모두 보기
Bjornsdottir A,
Boomsma DI,
Brumpton BM,
Burgdorf KS,
Buring JE,
Chalmer MA,
de Boer I,
Dichgans M,
Erikstrup C,
Färkkilä M,
Garbrielsen ME,
Ghanbari M,
Hagen K,
Häppölä P,
Hottenga JJ,
Hrafnsdottir MG,
Hveem K,
Johnsen MB,
Kähönen M,
Kristoffersen ES,
Kurth T,
Lehtimäki T,
Lighart L,
Magnusson SH,
Malik R,
Pedersen OB,
Pelzer N,
Penninx BWJH,
Ran C,
Ridker PM,
Rosendaal FR,
Sigurdardottir GR,
Skogholt AH,
Sveinsson OA,
Thorgeirsson TE,
Ullum H,
Vijfhuizen LS,
Widén E,
van Dijk KW,
Aromaa A,
Belin AC,
Freilinger T,
Ikram MA,
Järvelin MR,
Raitakari OT,
Terwindt GM,
Kallela M,
Wessman M,
Olesen J,
Chasman DI,
Nyholt DR,
Stefánsson H,
Stefansson K,
van den Maagdenberg AMJM,
Hansen TF,
Ripatti S,
Zwart JA,
Palotie A,
Pirinen M
International Headache Genetics Consortium · HUNT All-in Headache 외 컨소시엄 1곳
Nature genetics · 2022 · PMID 35115687 · open access
페이지 12개+
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
Skuladottir AT,
Bjornsdottir G,
Ferkingstad E,
Einarsson G,
Stefansdottir L,
Nawaz MS,
Oddsson A,
Olafsdottir TA,
Saevarsdottir S,
Walters GB,
Magnusson SH,
Bjornsdottir A
외 18명 — 모두 보기
Sveinsson OA,
Vikingsson A,
Hansen TF,
Jacobsen RL,
Erikstrup C,
Schwinn M,
Brunak S,
Banasik K,
Ostrowski SR,
Troelsen A,
Henkel C,
Pedersen OB,
Jonsdottir I,
Gudbjartsson DF,
Sulem P,
Thorgeirsson TE,
Stefansson H,
Stefansson K
DBDS Genetic Consortium
Nature communications · 2022 · PMID 35332129 · open access
페이지 12개+
Genetic diversity fuels gene discovery for tobacco and alcohol use
Saunders GRB,
Wang X,
Chen F,
Jang SK,
Liu M,
Wang C,
Gao S,
Jiang Y,
Khunsriraksakul C,
Otto JM,
Addison C,
Akiyama M
외 205명 — 모두 보기
Albert CM,
Aliev F,
Alonso A,
Arnett DK,
Ashley-Koch AE,
Ashrani AA,
Barnes KC,
Barr RG,
Bartz TM,
Becker DM,
Bielak LF,
Benjamin EJ,
Bis JC,
Bjornsdottir G,
Blangero J,
Bleecker ER,
Boardman JD,
Boerwinkle E,
Boomsma DI,
Boorgula MP,
Bowden DW,
Brody JA,
Cade BE,
Chasman DI,
Chavan S,
Chen YI,
Chen Z,
Cheng I,
Cho MH,
Choquet H,
Cole JW,
Cornelis MC,
Cucca F,
Curran JE,
de Andrade M,
Dick DM,
Docherty AR,
Duggirala R,
Eaton CB,
Ehringer MA,
Esko T,
Faul JD,
Fernandes Silva L,
Fiorillo E,
Fornage M,
Freedman BI,
Gabrielsen ME,
Garrett ME,
Gharib SA,
Gieger C,
Gillespie N,
Glahn DC,
Gordon SD,
Gu CC,
Gu D,
Gudbjartsson DF,
Guo X,
Haessler J,
Hall ME,
Haller T,
Harris KM,
He J,
Herd P,
Hewitt JK,
Hickie I,
Hidalgo B,
Hokanson JE,
Hopfer C,
Hottenga J,
Hou L,
Huang H,
Hung YJ,
Hunter DJ,
Hveem K,
Hwang SJ,
Hwu CM,
Iacono W,
Irvin MR,
Jee YH,
Johnson EO,
Joo YY,
Jorgenson E,
Justice AE,
Kamatani Y,
Kaplan RC,
Kaprio J,
Kardia SLR,
Keller MC,
Kelly TN,
Kooperberg C,
Korhonen T,
Kraft P,
Krauter K,
Kuusisto J,
Laakso M,
Lasky-Su J,
Lee WJ,
Lee JJ,
Levy D,
Li L,
Li K,
Li Y,
Lin K,
Lind PA,
Liu C,
Lloyd-Jones DM,
Lutz SM,
Ma J,
Mägi R,
Manichaikul A,
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Mathur R,
Matoba N,
McArdle PF,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Meyers DA,
Millwood IY,
Mitchell BD,
Mohlke KL,
Moll M,
Montasser ME,
Morrison AC,
Mulas A,
Nielsen JB,
North KE,
Oelsner EC,
Okada Y,
Orrù V,
Palmer ND,
Palviainen T,
Pandit A,
Park SL,
Peters U,
Peters A,
Peyser PA,
Polderman TJC,
Rafaels N,
Redline S,
Reed RM,
Reiner AP,
Rice JP,
Rich SS,
Richmond NE,
Roan C,
Rotter JI,
Rueschman MN,
Runarsdottir V,
Saccone NL,
Schwartz DA,
Shadyab AH,
Shi J,
Shringarpure SS,
Sicinski K,
Skogholt AH,
Smith JA,
Smith NL,
Sotoodehnia N,
Stallings MC,
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Stefansson K,
Stitzel JA,
Sun X,
Syed M,
Tal-Singer R,
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Thai KK,
Tiwari H,
Turman C,
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Wall TL,
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Weir DR,
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White WB,
Whitfield JB,
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Willer CJ,
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Xu H,
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Yin J,
Young KL,
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Yu B,
Zhao W,
Zhou W,
Zöllner S,
Zuccolo L,
Batini C,
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Bierut LJ,
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Gagliano Taliun SA,
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Thorgeirsson TE,
Liu DJ,
Vrieze S
23andMe Research Team · Biobank Japan Project
Nature · 2022 · PMID 36477530 · open access
페이지 12개+
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Als TD,
Kurki MI,
Grove J,
Voloudakis G,
Therrien K,
Tasanko E,
Nielsen TT,
Naamanka J,
Veerapen K,
Levey DF,
Bendl J,
Bybjerg-Grauholm J
외 31명 — 모두 보기
Zeng B,
Demontis D,
Rosengren A,
Athanasiadis G,
Bækved-Hansen M,
Qvist P,
Bragi Walters G,
Thorgeirsson T,
Stefánsson H,
Musliner KL,
Rajagopal VM,
Farajzadeh L,
Thirstrup J,
Vilhjálmsson BJ,
McGrath JJ,
Mattheisen M,
Meier S,
Agerbo E,
Stefánsson K,
Nordentoft M,
Werge T,
Hougaard DM,
Mortensen PB,
Stein MB,
Gelernter J,
Hovatta I,
Roussos P,
Daly MJ,
Mors O,
Palotie A,
Børglum AD
Nature medicine · 2023 · PMID 37464041
페이지 12개+
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
Olafsson S,
Alexandersson KF,
Gizurarson JGK,
Hauksdottir K,
Gunnarsson O,
Olafsson K,
Gudmundsson J,
Stacey SN,
Sveinbjornsson G,
Saemundsdottir J,
Bjornsson ES,
Olafsson S
외 22명 — 모두 보기
Bjornsson S,
Orvar KB,
Vikingsson A,
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Arinbjarnarson S,
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Thorgeirsson TE,
Sigurdsson S,
Halldorsson GH,
Magnusson OT,
Masson G,
Holm H,
Jonsdottir I,
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Eyjolfsson GI,
Olafsson I,
Sulem P,
Thorsteinsdottir U,
Jonsson T,
Rafnar T,
Gudbjartsson DF,
Stefansson K
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2020 · PMID 31666285
페이지 11개
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
외 205명 — 모두 보기
Beekman AFT,
Bigdeli TB,
Binder EB,
Blackwood DRH,
Bryois J,
Buttenschøn HN,
Bybjerg-Grauholm J,
Cai N,
Castelao E,
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Clarke TK,
Coleman JIR,
Colodro-Conde L,
Couvy-Duchesne B,
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Crawford GE,
Crowley CA,
Dashti HS,
Davies G,
Deary IJ,
Degenhardt F,
Derks EM,
Direk N,
Dolan CV,
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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,
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Nature genetics · 2018 · PMID 29700475 · open access
페이지 10개
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외 20명 — 모두 보기
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Nature genetics · 2019 · PMID 31043756 · open access
페이지 6개
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외 19명 — 모두 보기
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페이지 4개
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외 16명 — 모두 보기
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페이지 3개
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Genetic Risk and Outcome in Psychosis (GROUP)
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페이지 2개
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption
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외 104명 — 모두 보기
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외 14명 — 모두 보기
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외 45명 — 모두 보기
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외 82명 — 모두 보기
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ENGAGE Consortium
Nature genetics · 2010 · PMID 20418888
페이지 1개
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가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.