オープン アクセスを義務付けられた論文 - Wei Zhao詳細
一般公開: 32 件
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A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease
Nature genetics 47 (10), 1121-1130, 2015
委任: US National Institutes of Health, British Heart Foundation, UK Medical …
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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
委任: US National Institutes of Health, Canadian Institutes of Health Research …
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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
委任: US National Institutes of Health, UK Biotechnology and Biological Sciences …
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Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
D Saleheen, R Scott, S Javad, W Zhao, A Rodrigues, A Picataggi, ...
The Lancet Diabetes & Endocrinology 3 (7), 507-513, 2015
委任: US National Institutes of Health, Cancer Research UK, UK Medical Research …
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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
GB Ehret, T Ferreira, DI Chasman, AU Jackson, EM Schmidt, T Johnson, ...
Nature Genetics 48 (10), 1171-1184, 2016
委任: US National Institutes of Health, Versus Arthritis, UK, British Heart …
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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
委任: US National Institutes of Health, British Heart Foundation, UK Medical …
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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
委任: Swiss National Science Foundation, US National Institutes of Health …
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Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity
D Saleheen, P Natarajan, IM Armean, W Zhao, A Rasheed, SA Khetarpal, ...
Nature 544 (7649), 235-239, 2017
委任: US National Institutes of Health, British Heart Foundation, UK Medical …
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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
委任: US National Institutes of Health, UK Biotechnology and Biological Sciences …
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Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms
JMM Howson, W Zhao, DR Barnes, WK Ho, R Young, DS Paul, LL Waite, ...
Nature genetics 49 (7), 1113-1119, 2017
委任: US National Institutes of Health, British Heart Foundation, UK Medical …
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Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
W Zhao, A Rasheed, E Tikkanen, JJ Lee, AS Butterworth, JMM Howson, ...
Nature genetics 49 (10), 1450-1457, 2017
委任: US National Institutes of Health, American Heart Association, Natural …
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Apolipoprotein (a) isoform size, lipoprotein (a) concentration, and coronary artery disease: a mendelian randomisation analysis
D Saleheen, PC Haycock, W Zhao, A Rasheed, A Taleb, A Imran, ...
The Lancet Diabetes & Endocrinology 5 (7), 524-533, 2017
委任: US National Institutes of Health, British Heart Foundation, UK Medical …
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Causal assessment of serum urate levels in cardiometabolic diseases through a Mendelian randomization study
T Keenan, W Zhao, A Rasheed, WK Ho, R Malik, JF Felix, R Young, ...
Journal of the American College of Cardiology 67 (4), 407-416, 2016
委任: US National Institutes of Health, American Heart Association, British Heart …
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Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes
M Imamura, A Takahashi, T Yamauchi, K Hara, K Yasuda, N Grarup, ...
Nature communications 7 (1), 10531, 2016
委任: US National Institutes of Health, National Natural Science Foundation of …
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Low-frequency and common genetic variation in ischemic stroke: the METASTROKE collaboration
R Malik, M Traylor, SL Pulit, S Bevan, JC Hopewell, EG Holliday, W Zhao, ...
Neurology 86 (13), 1217-1226, 2016
委任: US National Institutes of Health, US Department of Veterans Affairs …
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Loss of function of GALNT2 lowers high-density lipoproteins in humans, nonhuman primates, and rodents
SA Khetarpal, KT Schjoldager, C Christoffersen, A Raghavan, ...
Cell metabolism 24 (2), 234-245, 2016
委任: US National Institutes of Health, German Research Foundation, Danish Council …
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A Novel MMP12 Locus Is Associated with Large Artery Atherosclerotic Stroke Using a Genome-Wide Age-at-Onset Informed Approach
M Traylor, KM Mäkelä, LL Kilarski, EG Holliday, WJ Devan, MA Nalls, ...
PLoS genetics 10 (7), e1004469, 2014
委任: US National Institutes of Health, National Health and Medical Research …
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Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2
YC Cheng, TM Stanne, AK Giese, WK Ho, M Traylor, P Amouyel, ...
Stroke 47 (2), 307-316, 2016
委任: US National Institutes of Health, US Department of Veterans Affairs …
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Systolic Blood Pressure and Risk of Type 2 Diabetes: A Mendelian Randomization Study
RC Aikens, W Zhao, D Saleheen, MP Reilly, SE Epstein, E Tikkanen, ...
Diabetes 66 (2), 543-550, 2017
委任: US National Institutes of Health, American Heart Association
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Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions
D Saleheen, W Zhao, R Young, CP Nelson, WK Ho, JF Ferguson, ...
Circulation 135 (24), 2336-2353, 2017
委任: US National Institutes of Health, British Heart Foundation, UK Medical …
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