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Hansen T에 대해
90건, 그중 20건 표시.
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
Mahajan A,
Spracklen CN,
Zhang W,
Ng MCY,
Petty LE,
Kitajima H,
Yu GZ,
Rüeger S,
Speidel L,
Kim YJ,
Horikoshi M,
Mercader JM
외 337명 — 모두 보기
Taliun D,
Moon S,
Kwak SH,
Robertson NR,
Rayner NW,
Loh M,
Kim BJ,
Chiou J,
Miguel-Escalada I,
Della Briotta Parolo P,
Lin K,
Bragg F,
Preuss MH,
Takeuchi F,
Nano J,
Guo X,
Lamri A,
Nakatochi M,
Scott RA,
Lee JJ,
Huerta-Chagoya A,
Graff M,
Chai JF,
Parra EJ,
Yao J,
Bielak LF,
Tabara Y,
Hai Y,
Steinthorsdottir V,
Cook JP,
Kals M,
Grarup N,
Schmidt EM,
Pan I,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Long J,
Sun M,
Tong L,
Chen WM,
Ahmad M,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Lecoeur C,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Jensen RA,
Tajuddin S,
Kabagambe EK,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Flanagan J,
Abaitua F,
Adair LS,
Adeyemo A,
Aguilar-Salinas CA,
Akiyama M,
Anand SS,
Bertoni A,
Bian Z,
Bork-Jensen J,
Brandslund I,
Brody JA,
Brummett CM,
Buchanan TA,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Das SK,
de Silva HJ,
Dedoussis G,
Dimitrov L,
Doumatey AP,
Du S,
Duan Q,
Eckardt KU,
Emery LS,
Evans DS,
Evans MK,
Fischer K,
Floyd JS,
Ford I,
Fornage M,
Franco OH,
Frayling TM,
Freedman BI,
Fuchsberger C,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Goodarzi MO,
Gordon-Larsen P,
Gorkin D,
Gross M,
Guo Y,
Hackinger S,
Han S,
Hattersley AT,
Herder C,
Howard AG,
Hsueh W,
Huang M,
Huang W,
Hung YJ,
Hwang MY,
Hwu CM,
Ichihara S,
Ikram MA,
Ingelsson M,
Islam MT,
Isono M,
Jang HM,
Jasmine F,
Jiang G,
Jonas JB,
Jørgensen ME,
Jørgensen T,
Kamatani Y,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
Kho AN,
Khor CC,
Kibriya MG,
Kim DH,
Kohara K,
Kriebel J,
Kronenberg F,
Kuusisto J,
Läll K,
Lange LA,
Lee MS,
Lee NR,
Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
Luan J,
Luk AO,
Luo X,
Lv J,
Lyssenko V,
Mamakou V,
Mani KR,
Meitinger T,
Metspalu A,
Morris AD,
Nadkarni GN,
Nadler JL,
Nalls MA,
Nayak U,
Nongmaithem SS,
Ntalla I,
Okada Y,
Orozco L,
Patel SR,
Pereira MA,
Peters A,
Pirie FJ,
Porneala B,
Prasad G,
Preissl S,
Rasmussen-Torvik LJ,
Reiner AP,
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Roll K,
Sabanayagam C,
Sander M,
Sandow K,
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Schönherr S,
Schurmann C,
Shahriar M,
Shi J,
Shin DM,
Shriner D,
Smith JA,
So WY,
Stančáková A,
Stilp AM,
Strauch K,
Suzuki K,
Takahashi A,
Taylor KD,
Thorand B,
Thorleifsson G,
Thorsteinsdottir U,
Tomlinson B,
Torres JM,
Tsai FJ,
Tuomilehto J,
Tusie-Luna T,
Udler MS,
Valladares-Salgado A,
van Dam RM,
van Klinken JB,
Varma R,
Vujkovic M,
Wacher-Rodarte N,
Wheeler E,
Whitsel EA,
Wickremasinghe AR,
van Dijk KW,
Witte DR,
Yajnik CS,
Yamamoto K,
Yamauchi T,
Yengo L,
Yoon K,
Yu C,
Yuan JM,
Yusuf S,
Zhang L,
Zheng W,
Raffel LJ,
Igase M,
Ipp E,
Redline S,
Cho YS,
Lind L,
Province MA,
Hanis CL,
Peyser PA,
Ingelsson E,
Zonderman AB,
Psaty BM,
Wang YX,
Rotimi CN,
Becker DM,
Matsuda F,
Liu Y,
Zeggini E,
Yokota M,
Rich SS,
Kooperberg C,
Pankow JS,
Engert JC,
Chen YI,
Froguel P,
Wilson JG,
Sheu WHH,
Kardia SLR,
Wu JY,
Hayes MG,
Ma RCW,
Wong TY,
Groop L,
Mook-Kanamori DO,
Chandak GR,
Collins FS,
Bharadwaj D,
Paré G,
Sale MM,
Ahsan H,
Motala AA,
Shu XO,
Park KS,
Jukema JW,
Cruz M,
McKean-Cowdin R,
Grallert H,
Cheng CY,
Bottinger EP,
Dehghan A,
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Kato N,
Laakso M,
Köttgen A,
Koh WP,
Palmer CNA,
Liu S,
Abecasis G,
Kooner JS,
Loos RJF,
North KE,
Haiman CA,
Florez JC,
Saleheen D,
Hansen T,
Pedersen O,
Mägi R,
Langenberg C,
Wareham NJ,
Maeda S,
Kadowaki T,
Lee J,
Millwood IY,
Walters RG,
Stefansson K,
Myers SR,
Ferrer J,
Gaulton KJ,
Meigs JB,
Mohlke KL,
Gloyn AL,
Bowden DW,
Below JE,
Chambers JC,
Sim X,
Boehnke M,
Rotter JI,
McCarthy MI,
Morris AP
FinnGen · eMERGE Consortium
Nature genetics · 2022 · PMID 35551307 · open access
페이지 12개+
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
Young WJ,
Lahrouchi N,
Isaacs A,
Duong T,
Foco L,
Ahmed F,
Brody JA,
Salman R,
Noordam R,
Benjamins JW,
Haessler J,
Lyytikäinen LP
외 154명 — 모두 보기
Repetto L,
Concas MP,
van den Berg ME,
Weiss S,
Baldassari AR,
Bartz TM,
Cook JP,
Evans DS,
Freudling R,
Hines O,
Isaksen JL,
Lin H,
Mei H,
Moscati A,
Müller-Nurasyid M,
Nursyifa C,
Qian Y,
Richmond A,
Roselli C,
Ryan KA,
Tarazona-Santos E,
Thériault S,
van Duijvenboden S,
Warren HR,
Yao J,
Raza D,
Aeschbacher S,
Ahlberg G,
Alonso A,
Andreasen L,
Bis JC,
Boerwinkle E,
Campbell A,
Catamo E,
Cocca M,
Cutler MJ,
Darbar D,
De Grandi A,
De Luca A,
Ding J,
Ellervik C,
Ellinor PT,
Felix SB,
Froguel P,
Fuchsberger C,
Gögele M,
Graff C,
Graff M,
Guo X,
Hansen T,
Heckbert SR,
Huang PL,
Huikuri HV,
Hutri-Kähönen N,
Ikram MA,
Jackson RD,
Junttila J,
Kavousi M,
Kors JA,
Leal TP,
Lemaitre RN,
Lin HJ,
Lind L,
Linneberg A,
Liu S,
MacFarlane PW,
Mangino M,
Meitinger T,
Mezzavilla M,
Mishra PP,
Mitchell RN,
Mononen N,
Montasser ME,
Morrison AC,
Nauck M,
Nauffal V,
Navarro P,
Nikus K,
Pare G,
Patton KK,
Pelliccione G,
Pittman A,
Porteous DJ,
Pramstaller PP,
Preuss MH,
Raitakari OT,
Reiner AP,
Ribeiro ALP,
Rice KM,
Risch L,
Schlessinger D,
Schotten U,
Schurmann C,
Shen X,
Shoemaker MB,
Sinagra G,
Sinner MF,
Soliman EZ,
Stoll M,
Strauch K,
Tarasov K,
Taylor KD,
Tinker A,
Trompet S,
Uitterlinden A,
Völker U,
Völzke H,
Waldenberger M,
Weng LC,
Whitsel EA,
Wilson JG,
Avery CL,
Conen D,
Correa A,
Cucca F,
Dörr M,
Gharib SA,
Girotto G,
Grarup N,
Hayward C,
Jamshidi Y,
Järvelin MR,
Jukema JW,
Kääb S,
Kähönen M,
Kanters JK,
Kooperberg C,
Lehtimäki T,
Lima-Costa MF,
Liu Y,
Loos RJF,
Lubitz SA,
Mook-Kanamori DO,
Morris AP,
O'Connell JR,
Olesen MS,
Orini M,
Padmanabhan S,
Pattaro C,
Peters A,
Psaty BM,
Rotter JI,
Stricker B,
van der Harst P,
van Duijn CM,
Verweij N,
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Lambiase PD,
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Newton-Cheh C,
Munroe PB
Nature communications · 2022 · PMID 36050321 · open access
페이지 12개+
Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention
Wang Z,
Emmerich A,
Pillon NJ,
Moore T,
Hemerich D,
Cornelis MC,
Mazzaferro E,
Broos S,
Ahluwalia TS,
Bartz TM,
Bentley AR,
Bielak LF
외 206명 — 모두 보기
Chong M,
Chu AY,
Berry D,
Dorajoo R,
Dueker ND,
Kasbohm E,
Feenstra B,
Feitosa MF,
Gieger C,
Graff M,
Hall LM,
Haller T,
Hartwig FP,
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Huikari V,
Heard-Costa N,
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Jackson AU,
Johansson Å,
Jørgensen AM,
Kaakinen MA,
Karlsson R,
Kerr KF,
Kim B,
Koolhaas CM,
Kutalik Z,
Lagou V,
Lind PA,
Lorentzon M,
Lyytikäinen LP,
Mangino M,
Metzendorf C,
Monroe KR,
Pacolet A,
Pérusse L,
Pool R,
Richmond RC,
Rivera NV,
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Schraut KE,
Schulz CA,
Stringham HM,
Tanaka T,
Teumer A,
Turman C,
van der Most PJ,
Vanmunster M,
van Rooij FJA,
van Vliet-Ostaptchouk JV,
Zhang X,
Zhao JH,
Zhao W,
Balkhiyarova Z,
Balslev-Harder MN,
Baumeister SE,
Beilby J,
Blangero J,
Boomsma DI,
Brage S,
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Brody JA,
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Cole JW,
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Kardia SLR,
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Lifelines Cohort Study
Nature genetics · 2022 · PMID 36071172 · open access
페이지 12개+
A saturated map of common genetic variants associated with human height
Yengo L,
Vedantam S,
Marouli E,
Sidorenko J,
Bartell E,
Sakaue S,
Graff M,
Eliasen AU,
Jiang Y,
Raghavan S,
Miao J,
Arias JD
외 610명 — 모두 보기
Graham SE,
Mukamel RE,
Spracklen CN,
Yin X,
Chen SH,
Ferreira T,
Highland HH,
Ji Y,
Karaderi T,
Lin K,
Lüll K,
Malden DE,
Medina-Gomez C,
Machado M,
Moore A,
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Sim X,
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23andMe Research Team · VA Million Veteran Program 외 컨소시엄 5곳
Nature · 2022 · PMID 36224396 · open access
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VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
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페이지 10개
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페이지 10개
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페이지 8개
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페이지 7개
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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.