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45건, 그중 20건 표시.
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Aragam KG,
Jiang T,
Goel A,
Kanoni S,
Wolford BN,
Atri DS,
Weeks EM,
Wang M,
Hindy G,
Zhou W,
Grace C,
Roselli C
외 83명 — 모두 보기
Marston NA,
Kamanu FK,
Surakka I,
Venegas LM,
Sherliker P,
Koyama S,
Ishigaki K,
Åsvold BO,
Brown MR,
Brumpton B,
de Vries PS,
Giannakopoulou O,
Giardoglou P,
Gudbjartsson DF,
Güldener U,
Haider SMI,
Helgadottir A,
Ibrahim M,
Kastrati A,
Kessler T,
Kyriakou T,
Konopka T,
Li L,
Ma L,
Meitinger T,
Mucha S,
Munz M,
Murgia F,
Nielsen JB,
Nöthen MM,
Pang S,
Reinberger T,
Schnitzler G,
Smedley D,
Thorleifsson G,
von Scheidt M,
Ulirsch JC,
Arnar DO,
Burtt NP,
Costanzo MC,
Flannick J,
Ito K,
Jang DK,
Kamatani Y,
Khera AV,
Komuro I,
Kullo IJ,
Lotta LA,
Nelson CP,
Roberts R,
Thorgeirsson G,
Thorsteinsdottir U,
Webb TR,
Baras A,
Björkegren JLM,
Boerwinkle E,
Dedoussis G,
Holm H,
Hveem K,
Melander O,
Morrison AC,
Orho-Melander M,
Rallidis LS,
Ruusalepp A,
Sabatine MS,
Stefansson K,
Zalloua P,
Ellinor PT,
Farrall M,
Danesh J,
Ruff CT,
Finucane HK,
Hopewell JC,
Clarke R,
Gupta RM,
Erdmann J,
Samani NJ,
Schunkert H,
Watkins H,
Willer CJ,
Deloukas P,
Kathiresan S,
Butterworth AS
Biobank Japan · EPIC-CVD 외 컨소시엄 1곳
Nature genetics · 2022 · PMID 36474045 · open access
페이지 12개+
Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets
Zhao JH,
Stacey D,
Eriksson N,
Macdonald-Dunlop E,
Hedman ÅK,
Kalnapenkis A,
Enroth S,
Cozzetto D,
Digby-Bell J,
Marten J,
Folkersen L,
Herder C
외 29명 — 모두 보기
Jonsson L,
Bergen SE,
Gieger C,
Needham EJ,
Surendran P,
Paul DS,
Polasek O,
Thorand B,
Grallert H,
Roden M,
Võsa U,
Esko T,
Hayward C,
Johansson Å,
Gyllensten U,
Powell N,
Hansson O,
Mattsson-Carlgren N,
Joshi PK,
Danesh J,
Padyukov L,
Klareskog L,
Landén M,
Wilson JF,
Siegbahn A,
Wallentin L,
Mälarstig A,
Butterworth AS,
Peters JE
Estonian Biobank Research Team
Nature immunology · 2023 · PMID 37563310 · open access
페이지 12개+
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology
Akbari P,
Vuckovic D,
Stefanucci L,
Jiang T,
Kundu K,
Kreuzhuber R,
Bao EL,
Collins JH,
Downes K,
Grassi L,
Guerrero JA,
Kaptoge S
외 20명 — 모두 보기
Knight JC,
Meacham S,
Sambrook J,
Seyres D,
Stegle O,
Verboon JM,
Walter K,
Watkins NA,
Danesh J,
Roberts DJ,
Di Angelantonio E,
Sankaran VG,
Frontini M,
Burgess S,
Kuijpers T,
Peters JE,
Butterworth AS,
Ouwehand WH,
Soranzo N,
Astle WJ
Nature communications · 2023 · PMID 37596262 · open access
페이지 12개+
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Suzuki K,
Hatzikotoulas K,
Southam L,
Taylor HJ,
Yin X,
Lorenz KM,
Mandla R,
Huerta-Chagoya A,
Melloni GEM,
Kanoni S,
Rayner NW,
Bocher O
외 351명 — 모두 보기
Arruda AL,
Sonehara K,
Namba S,
Lee SSK,
Preuss MH,
Petty LE,
Schroeder P,
Vanderwerff B,
Kals M,
Bragg F,
Lin K,
Guo X,
Zhang W,
Yao J,
Kim YJ,
Graff M,
Takeuchi F,
Nano J,
Lamri A,
Nakatochi M,
Moon S,
Scott RA,
Cook JP,
Lee JJ,
Pan I,
Taliun D,
Parra EJ,
Chai JF,
Bielak LF,
Tabara Y,
Hai Y,
Thorleifsson G,
Grarup N,
Sofer T,
Wuttke M,
Sarnowski C,
Gieger C,
Nousome D,
Trompet S,
Kwak SH,
Long J,
Sun M,
Tong L,
Chen WM,
Nongmaithem SS,
Noordam R,
Lim VJY,
Tam CHT,
Joo YY,
Chen CH,
Raffield LM,
Prins BP,
Nicolas A,
Yanek LR,
Chen G,
Brody JA,
Kabagambe E,
An P,
Xiang AH,
Choi HS,
Cade BE,
Tan J,
Broadaway KA,
Williamson A,
Kamali Z,
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Thangam M,
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Adeyemo A,
Aguilar-Salinas CA,
Ahluwalia TS,
Anand SS,
Bertoni A,
Bork-Jensen J,
Brandslund I,
Buchanan TA,
Burant CF,
Butterworth AS,
Canouil M,
Chan JCN,
Chang LC,
Chee ML,
Chen J,
Chen SH,
Chen YT,
Chen Z,
Chuang LM,
Cushman M,
Danesh J,
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,
Franco OH,
Frayling TM,
Freedman BI,
Genter P,
Gerstein HC,
Giedraitis V,
González-Villalpando C,
González-Villalpando ME,
Gordon-Larsen P,
Gross M,
Guare LA,
Hackinger S,
Hakaste L,
Han S,
Hattersley AT,
Herder C,
Horikoshi M,
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 T,
Kamanu FK,
Kandeel FR,
Kasturiratne A,
Katsuya T,
Kaur V,
Kawaguchi T,
Keaton JM,
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Khor CC,
Kibriya MG,
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Läll K,
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Lee KM,
Lee MS,
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Leong A,
Li L,
Li Y,
Li-Gao R,
Ligthart S,
Lindgren CM,
Linneberg A,
Liu CT,
Liu J,
Locke AE,
Louie T,
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Luk AO,
Luo X,
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Lyssenko V,
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Mamakou V,
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Metspalu A,
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Moura FA,
Nadler JL,
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Polikowsky HG,
Porneala B,
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Sabanayagam C,
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Schönherr S,
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Rotter JI,
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Voight BF,
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Zeggini E
VA Million Veteran Program
Nature · 2024 · PMID 38374256 · open access
페이지 12개+
Genome-wide characterization of circulating metabolic biomarkers
Karjalainen MK,
Karthikeyan S,
Oliver-Williams C,
Sliz E,
Allara E,
Fung WT,
Surendran P,
Zhang W,
Jousilahti P,
Kristiansson K,
Salomaa V,
Goodwin M
외 75명 — 모두 보기
Hughes DA,
Boehnke M,
Fernandes Silva L,
Yin X,
Mahajan A,
Neville MJ,
van Zuydam NR,
de Mutsert R,
Li-Gao R,
Mook-Kanamori DO,
Demirkan A,
Liu J,
Noordam R,
Trompet S,
Chen Z,
Kartsonaki C,
Li L,
Lin K,
Hagenbeek FA,
Hottenga JJ,
Pool R,
Ikram MA,
van Meurs J,
Haller T,
Milaneschi Y,
Kähönen M,
Mishra PP,
Joshi PK,
Macdonald-Dunlop E,
Mangino M,
Zierer J,
Acar IE,
Hoyng CB,
Lechanteur YTE,
Franke L,
Kurilshikov A,
Zhernakova A,
Beekman M,
van den Akker EB,
Kolcic I,
Polasek O,
Rudan I,
Gieger C,
Waldenberger M,
Asselbergs FW,
Hayward C,
Fu J,
den Hollander AI,
Menni C,
Spector TD,
Wilson JF,
Lehtimäki T,
Raitakari OT,
Penninx BWJH,
Esko T,
Walters RG,
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Sattar N,
Ghanbari M,
Willems van Dijk K,
Karpe F,
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Perola M,
Kooner JS,
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van Duijn C,
Slagboom PE,
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Danesh J,
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Butterworth AS,
Kettunen J
China Kadoorie Biobank Collaborative Group · Estonian Biobank Research Team 외 컨소시엄 1곳
Nature · 2024 · PMID 38448586 · open access
페이지 12개+
Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Keaton JM,
Kamali Z,
Xie T,
Vaez A,
Williams A,
Goleva SB,
Ani A,
Evangelou E,
Hellwege JN,
Yengo L,
Young WJ,
Traylor M
외 135명 — 모두 보기
Giri A,
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Morris AP,
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Conen D,
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Sun YV,
Wilson PWF,
Cho K,
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Denny JC,
Levy D,
Edwards TL,
Munroe PB,
Snieder H,
Warren HR
Million Veteran Program · Lifelines Cohort Study 외 컨소시엄 2곳
Nature genetics · 2024 · PMID 38689001 · open access
페이지 12개+
Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction
Schormair B,
Zhao C,
Bell S,
Didriksen M,
Nawaz MS,
Schandra N,
Stefani A,
Högl B,
Dauvilliers Y,
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Kemlink D,
Sonka K
외 55명 — 모두 보기
Paulus W,
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Oexle K,
Winkelmann J
23andMe Research Team · D.E.S.I.R. study group
Nature genetics · 2024 · PMID 38839884 · open access
페이지 12개+
Novel loci and biomedical consequences of iron homoeostasis variation
Allara E,
Bell S,
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Gill D,
Gaziano L,
Morselli Gysi D,
Wang F,
Tragante V,
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Lumbers RT
외 60명 — 모두 보기
Bonglack E,
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Di Angelantonio E
DBDS Genomic Consortium · FinnGen Consortium
Communications biology · 2024 · PMID 39643614 · open access
페이지 12개+
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Surendran P,
Drenos F,
Young R,
Warren H,
Cook JP,
Manning AK,
Grarup N,
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외 198명 — 모두 보기
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CHARGE-Heart Failure Consortium · EchoGen Consortium 외 컨소시엄 12곳
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페이지 11개
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외 78명 — 모두 보기
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CHD Exome+ Consortium · EPIC-CVD Consortium 외 컨소시엄 2곳
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페이지 11개
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Charge Diabetes Working Group · EPIC-InterAct Consortium 외 컨소시엄 3곳
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페이지 11개
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
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외 39명 — 모두 보기
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23andMe Research Team · DESIR study group
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페이지 10개
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외 164명 — 모두 보기
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페이지 7개
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외 11명 — 모두 보기
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Nature communications · 2019 · PMID 30837465 · open access
페이지 7개
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외 228명 — 모두 보기
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ExomeBP Consortium · MAGIC Consortium 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29632382 · open access
페이지 6개
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
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외 84명 — 모두 보기
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페이지 4개
Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels
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외 93명 — 모두 보기
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페이지 2개
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease
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외 12명 — 모두 보기
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Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations
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외 30명 — 모두 보기
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Diabetes care · 2021 · PMID 33203707 · open access
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Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative
Little A,
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외 55명 — 모두 보기
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Human molecular genetics · 2022 · PMID 34553764
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