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성함이나 학술지명, PMID로 찾아보십시오.
Thorsteinsdottir U에 대해
145건, 그중 20건 표시.
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
Justice AE,
Karaderi T,
Highland HM,
Young KL,
Graff M,
Lu Y,
Turcot V,
Auer PL,
Fine RS,
Guo X,
Schurmann C,
Lempradl A
외 268명 — 모두 보기
Marouli E,
Mahajan A,
Winkler TW,
Winkler TW,
Locke AE,
Medina-Gomez C,
Esko T,
Vedantam S,
Giri A,
Lo KS,
Alfred T,
Mudgal P,
Ng MCY,
Heard-Costa NL,
Feitosa MF,
Manning AK,
Willems SM,
Sivapalaratnam S,
Abecasis G,
Alam DS,
Allison M,
Amouyel P,
Arzumanyan Z,
Balkau B,
Bastarache L,
Bergmann S,
Bielak LF,
Blüher M,
Boehnke M,
Boeing H,
Boerwinkle E,
Böger CA,
Bork-Jensen J,
Bottinger EP,
Bowden DW,
Brandslund I,
Broer L,
Burt AA,
Butterworth AS,
Caulfield MJ,
Cesana G,
Chambers JC,
Chasman DI,
Chen YI,
Chowdhury R,
Christensen C,
Chu AY,
Collins FS,
Cook JP,
Cox AJ,
Crosslin DS,
Danesh J,
de Bakker PIW,
Denus S,
Mutsert R,
Dedoussis G,
Demerath EW,
Dennis JG,
Denny JC,
Di Angelantonio E,
Dörr M,
Drenos F,
Dubé MP,
Dunning AM,
Easton DF,
Elliott P,
Evangelou E,
Farmaki AE,
Feng S,
Ferrannini E,
Ferrieres J,
Florez JC,
Fornage M,
Fox CS,
Franks PW,
Friedrich N,
Gan W,
Gandin I,
Gasparini P,
Giedraitis V,
Girotto G,
Gorski M,
Grallert H,
Grarup N,
Grove ML,
Gustafsson S,
Haessler J,
Hansen T,
Hattersley AT,
Hayward C,
Heid IM,
Holmen OL,
Hovingh GK,
Howson JMM,
Hu Y,
Hung YJ,
Hveem K,
Ikram MA,
Ingelsson E,
Jackson AU,
Jarvik GP,
Jia Y,
Jørgensen T,
Jousilahti P,
Justesen JM,
Kahali B,
Karaleftheri M,
Kardia SLR,
Karpe F,
Kee F,
Kitajima H,
Komulainen P,
Kooner JS,
Kovacs P,
Krämer BK,
Kuulasmaa K,
Kuusisto J,
Laakso M,
Lakka TA,
Lamparter D,
Lange LA,
Langenberg C,
Larson EB,
Lee NR,
Lee WJ,
Lehtimäki T,
Lewis CE,
Li H,
Li J,
Li-Gao R,
Lin LA,
Lin X,
Lind L,
Lindström J,
Linneberg A,
Liu CT,
Liu DJ,
Luan J,
Lyytikäinen LP,
MacGregor S,
Mägi R,
Männistö S,
Marenne G,
Marten J,
Masca NGD,
McCarthy MI,
Meidtner K,
Mihailov E,
Moilanen L,
Moitry M,
Mook-Kanamori DO,
Morgan A,
Morris AP,
Müller-Nurasyid M,
Munroe PB,
Narisu N,
Nelson CP,
Neville M,
Ntalla I,
O'Connell JR,
Owen KR,
Pedersen O,
Peloso GM,
Pennell CE,
Perola M,
Perry JA,
Perry JRB,
Pers TH,
Ewing A,
Polasek O,
Raitakari OT,
Rasheed A,
Raulerson CK,
Rauramaa R,
Reilly DF,
Reiner AP,
Ridker PM,
Rivas MA,
Robertson NR,
Robino A,
Rudan I,
Ruth KS,
Saleheen D,
Salomaa V,
Samani NJ,
Schreiner PJ,
Schulze MB,
Scott RA,
Segura-Lepe M,
Sim X,
Slater AJ,
Small KS,
Smith BH,
Smith JA,
Southam L,
Spector TD,
Speliotes EK,
Stefansson K,
Steinthorsdottir V,
Stirrups KE,
Strauch K,
Stringham HM,
Stumvoll M,
Sun L,
Surendran P,
Swart KMA,
Tardif JC,
Taylor KD,
Teumer A,
Thompson DJ,
Thorleifsson G,
Thorsteinsdottir U,
Thuesen BH,
Tönjes A,
Torres M,
Tsafantakis E,
Tuomilehto J,
Uitterlinden AG,
Uusitupa M,
van Duijn CM,
Vanhala M,
Varma R,
Vermeulen SH,
Vestergaard H,
Vitart V,
Vogt TF,
Vuckovic D,
Wagenknecht LE,
Walker M,
Wallentin L,
Wang F,
Wang CA,
Wang S,
Wareham NJ,
Warren HR,
Waterworth DM,
Wessel J,
White HD,
Willer CJ,
Wilson JG,
Wood AR,
Wu Y,
Yaghootkar H,
Yao J,
Yerges-Armstrong LM,
Young R,
Zeggini E,
Zhan X,
Zhang W,
Zhao JH,
Zhao W,
Zheng H,
Zhou W,
Zillikens MC,
Rivadeneira F,
Borecki IB,
Pospisilik JA,
Deloukas P,
Frayling TM,
Lettre G,
Mohlke KL,
Rotter JI,
Kutalik Z,
Hirschhorn JN,
Cupples LA,
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Lindgren CM
CHD Exome+ Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium 외 컨소시엄 8곳
Nature genetics · 2019 · PMID 30778226 · open access
페이지 12개+
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
외 174명 — 모두 보기
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,
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Lee JJ,
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Lind L,
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Liu J,
Loeffler M,
Lyytikäinen LP,
Mahajan A,
Maranville JC,
Mascalzoni D,
McMullen B,
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Miliku K,
Mook-Kanamori DO,
Müller-Nurasyid M,
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Ponte B,
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Rabelink TJ,
Raffield LM,
Reilly DF,
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Runz H,
Ryan KA,
Sabanayagam C,
Saum KU,
Schöttker B,
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Shi Y,
Smith AV,
Strauch K,
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Sun BB,
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Tai ES,
Tan NYQ,
Taylor KD,
Teren A,
Tham YC,
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Thio CHL,
Thomsen H,
Thorsteinsdottir U,
Tönjes A,
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Köttgen A
Nature communications · 2019 · PMID 31511532 · 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,
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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,
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Shaffer CM,
Smith AV,
Smith BH,
Spracklen CN,
Strauch K,
Stumvoll M,
Sulem P,
Tajuddin SM,
Teren A,
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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,
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Wilson JG,
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Ho K,
Parsa A,
Pramstaller PP,
Psaty BM,
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Snieder H,
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German Chronic Kidney Disease Study · Lifelines Cohort Study 외 컨소시엄 1곳
Nature genetics · 2019 · PMID 31578528 · open access
페이지 12개+
Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
Oskarsson GR,
Oddsson A,
Magnusson MK,
Kristjansson RP,
Halldorsson GH,
Ferkingstad E,
Zink F,
Helgadottir A,
Ivarsdottir EV,
Arnadottir GA,
Jensson BO,
Katrinardottir H
외 26명 — 모두 보기
Sveinbjornsson G,
Kristinsdottir AM,
Lee AL,
Saemundsdottir J,
Stefansdottir L,
Sigurdsson JK,
Davidsson OB,
Benonisdottir S,
Jonasdottir A,
Jonasdottir A,
Jonsson S,
Gudmundsson RL,
Asselbergs FW,
Tragante V,
Gunnarsson B,
Masson G,
Thorleifsson G,
Rafnar T,
Holm H,
Olafsson I,
Onundarson PT,
Gudbjartsson DF,
Norddahl GL,
Thorsteinsdottir U,
Sulem P,
Stefansson K
Communications biology · 2020 · PMID 32327693 · open access
페이지 12개+
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Ntalla I,
Weng LC,
Cartwright JH,
Hall AW,
Sveinbjornsson G,
Tucker NR,
Choi SH,
Chaffin MD,
Roselli C,
Barnes MR,
Mifsud B,
Warren HR
외 175명 — 모두 보기
Hayward C,
Marten J,
Cranley JJ,
Concas MP,
Gasparini P,
Boutin T,
Kolcic I,
Polasek O,
Rudan I,
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Lima-Costa MF,
Ribeiro ALP,
Souza RP,
Tarazona-Santos E,
Giedraitis V,
Ingelsson E,
Mahajan A,
Morris AP,
Del Greco M F,
Foco L,
Gögele M,
Hicks AA,
Cook JP,
Lind L,
Lindgren CM,
Sundström J,
Nelson CP,
Riaz MB,
Samani NJ,
Sinagra G,
Ulivi S,
Kähönen M,
Mishra PP,
Mononen N,
Nikus K,
Caulfield MJ,
Dominiczak A,
Padmanabhan S,
Montasser ME,
O'Connell JR,
Ryan K,
Shuldiner AR,
Aeschbacher S,
Conen D,
Risch L,
Thériault S,
Hutri-Kähönen N,
Lehtimäki T,
Lyytikäinen LP,
Raitakari OT,
Barnes CLK,
Campbell H,
Joshi PK,
Wilson JF,
Isaacs A,
Kors JA,
van Duijn CM,
Huang PL,
Gudnason V,
Harris TB,
Launer LJ,
Smith AV,
Bottinger EP,
Loos RJF,
Nadkarni GN,
Preuss MH,
Correa A,
Mei H,
Wilson J,
Meitinger T,
Müller-Nurasyid M,
Peters A,
Waldenberger M,
Mangino M,
Spector TD,
Rienstra M,
van de Vegte YJ,
van der Harst P,
Verweij N,
Kääb S,
Schramm K,
Sinner MF,
Strauch K,
Cutler MJ,
Fatkin D,
London B,
Olesen M,
Roden DM,
Benjamin Shoemaker M,
Gustav Smith J,
Biggs ML,
Bis JC,
Brody JA,
Psaty BM,
Rice K,
Sotoodehnia N,
De Grandi A,
Fuchsberger C,
Pattaro C,
Pramstaller PP,
Ford I,
Wouter Jukema J,
Macfarlane PW,
Trompet S,
Dörr M,
Felix SB,
Völker U,
Weiss S,
Havulinna AS,
Jula A,
Sääksjärvi K,
Salomaa V,
Guo X,
Heckbert SR,
Lin HJ,
Rotter JI,
Taylor KD,
Yao J,
de Mutsert R,
Maan AC,
Mook-Kanamori DO,
Noordam R,
Cucca F,
Ding J,
Lakatta EG,
Qian Y,
Tarasov KV,
Levy D,
Lin H,
Newton-Cheh CH,
Lunetta KL,
Murray AD,
Porteous DJ,
Smith BH,
Stricker BH,
Uitterlinden A,
van den Berg ME,
Haessler J,
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Nature communications · 2020 · PMID 32439900 · open access
페이지 12개+
FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease
Saevarsdottir S,
Olafsdottir TA,
Ivarsdottir EV,
Halldorsson GH,
Gunnarsdottir K,
Sigurdsson A,
Johannesson A,
Sigurdsson JK,
Juliusdottir T,
Lund SH,
Arnthorsson AO,
Styrmisdottir EL
외 34명 — 모두 보기
Gudmundsson J,
Grondal GM,
Steinsson K,
Alfredsson L,
Askling J,
Benediktsson R,
Bjarnason R,
Geirsson AJ,
Gudbjornsson B,
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Hreidarsson AB,
Klareskog L,
Kockum I,
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Love TJ,
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Olsson T,
Onundarson PT,
Orvar KB,
Padyukov L,
Sigurgeirsson B,
Tragante V,
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Masson G,
Sulem P,
Gudbjartsson DF,
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Thorleifsson G,
Norddahl GL,
Thorsteinsdottir U,
Jonsdottir I,
Stefansson K
Nature · 2020 · PMID 32581359
페이지 12개+
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
Surendran P,
Feofanova EV,
Lahrouchi N,
Ntalla I,
Karthikeyan S,
Cook J,
Chen L,
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Yao C,
Kraja AT,
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외 269명 — 모두 보기
Giri A,
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Akbarov A,
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Braithwaite VS,
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Gao H,
Giannakopoulou O,
Giulianini F,
Gudbjartsson DF,
Guo X,
Harris SE,
Havulinna AS,
Helgadottir A,
Huffman JE,
Hwang SJ,
Kanoni S,
Kontto J,
Larson MG,
Li-Gao R,
Lindström J,
Lotta LA,
Lu Y,
Luan J,
Mahajan A,
Malerba G,
Masca NGD,
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Mosen-Ansorena D,
Müller-Nurasyid M,
Paré G,
Paul DS,
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Poveda A,
Rauramaa R,
Richard M,
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Sepúlveda N,
Sim X,
Smith AV,
Smith JA,
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Stanáková A,
Sulem P,
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Thorsteinsdottir U,
Trompet S,
Varga TV,
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Weiss S,
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Young R,
Yu B,
Zhang W,
Zhao JH,
Zhao W,
Zhao W,
Evangelou E,
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Cho K,
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페이지 12개+
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VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
페이지 12개+
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
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외 169명 — 모두 보기
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Genes & Health Research Team · Estonian Biobank Research Team 외 컨소시엄 2곳
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페이지 12개+
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외 145명 — 모두 보기
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BioBank Japan Project · Regeneron Genetics Center 외 컨소시엄 1곳
Nature genetics · 2025 · PMID 40050429
페이지 12개+
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
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외 366명 — 모두 보기
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MAGIC · Procardis Consortium
Nature genetics · 2010 · PMID 20935630 · open access
페이지 11개
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
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외 162명 — 모두 보기
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Nature genetics · 2010 · PMID 21102462
페이지 11개
Ischemic stroke is associated with the ABO locus: the EuroCLOT study
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외 46명 — 모두 보기
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EuroCLOT Investigators · Wellcome Trust Case Control Consortium 2 외 컨소시엄 3곳
Annals of neurology · 2013 · PMID 23381943 · open access
페이지 11개
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어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
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.