受强制性开放获取政策约束的文章 - Joanna Howson了解详情
可在其他位置公开访问的文章：93 篇
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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
JA Todd, NM Walker, JD Cooper, DJ Smyth, K Downes, V Plagnol, ...
Nature genetics 39 (7), 857-864, 2007
强制性开放获取政策： British Heart Foundation
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Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ...
Nature genetics 50 (4), 524-537, 2018
强制性开放获取政策： US National Institutes of Health, British Heart Foundation, UK Medical …
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
E Evangelou, HR Warren, D Mosen-Ansorena, B Mifsud, R Pazoki, H Gao, ...
Nature genetics 50 (10), 1412-1425, 2018
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health, US …
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The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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Shared and distinct genetic variants in type 1 diabetes and celiac disease
DJ Smyth, V Plagnol, NM Walker, JD Cooper, K Downes, JHM Yang, ...
New England Journal of Medicine 359 (26), 2767-2777, 2008
强制性开放获取政策： US National Institutes of Health, British Heart Foundation
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Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
强制性开放获取政策： US National Institutes of Health, UK Biotechnology and Biological Sciences …
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Association analyses based on false discovery rate implicate new loci for coronary artery disease
CP Nelson, A Goel, AS Butterworth, S Kanoni, TR Webb, E Marouli, ...
Nature genetics 49 (9), 1385-1391, 2017
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
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Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk
HR Warren, E Evangelou, CP Cabrera, H Gao, M Ren, B Mifsud, I Ntalla, ...
Nature genetics 49 (3), 403-415, 2017
强制性开放获取政策： US National Institutes of Health, UK Biotechnology and Biological Sciences …
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Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease
P Zanoni, SA Khetarpal, DB Larach, WF Hancock-Cerutti, JS Millar, ...
Science 351 (6278), 1166-1171, 2016
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Exome-wide association study of plasma lipids in> 300,000 individuals
DJ Liu, GM Peloso, H Yu, AS Butterworth, X Wang, A Mahajan, ...
Nature genetics 49 (12), 1758-1766, 2017
强制性开放获取政策： US National Institutes of Health, British Heart Foundation, UK Medical …
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The polygenic and monogenic basis of blood traits and diseases
D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ...
Cell 182 (5), 1214-1231. e11, 2020
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs, UK …
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Bayesian refinement of association signals for 14 loci in 3 common diseases
JB Maller, G McVean, J Byrnes, D Vukcevic, K Palin, Z Su, JMM Howson, ...
Nature genetics 44 (12), 1294-1301, 2012
强制性开放获取政策： Versus Arthritis, UK, British Heart Foundation
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Association of LPA variants with risk of coronary disease and the implications for lipoprotein (a)-lowering therapies: a Mendelian randomization analysis
S Burgess, BA Ference, JR Staley, DF Freitag, AM Mason, SF Nielsen, ...
JAMA cardiology 3 (7), 619-627, 2018
强制性开放获取政策： British Heart Foundation, UK Medical Research Council, National Institute …
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Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations
MH Chen, LM Raffield, A Mousas, S Sakaue, JE Huffman, A Moscati, ...
Cell 182 (5), 1198-1213. e14, 2020
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs …
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A robust and efficient method for Mendelian randomization with hundreds of genetic variants
S Burgess, CN Foley, E Allara, JR Staley, JMM Howson
Nature communications 11 (1), 376, 2020
强制性开放获取政策： British Heart Foundation, UK Medical Research Council, National Institute …
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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
A Mahajan, J Wessel, SM Willems, W Zhao, NR Robertson, AY Chu, ...
Nature genetics 50 (4), 559-571, 2018
强制性开放获取政策： US National Institutes of Health, British Heart Foundation, UK Medical …
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Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease.
NO Stitziel, KE Stirrups, NG Masca, J Erdmann, PG Ferrario, IR König, ...
The New England journal of medicine 374 (12), 1134-1144, 2016
强制性开放获取政策： US National Institutes of Health, American Heart Association, German …
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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
A Giri, JN Hellwege, JM Keaton, J Park, C Qiu, HR Warren, ES Torstenson, ...
Nature genetics 51 (1), 51-62, 2019
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs, British …
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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health …
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
P Surendran, F Drenos, R Young, H Warren, JP Cook, AK Manning, ...
Nature genetics 48 (10), 1151-1161, 2016
强制性开放获取政策： US National Institutes of Health, UK Biotechnology and Biological Sciences …
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