受强制性开放获取政策约束的文章 - Jennifer Wessel了解详情
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Enrichment Analysis Informs Rare Variant Association Tests of Type 2 Diabetes and Glycemic Traits in CHARGE Whole‑Genome Sequence
S Lent, A Manning, J Wessel, J Dupuis, JB Meigs
Diabetes 66, A478-A478, 2017
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：40 篇
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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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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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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
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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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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
J Flannick, JM Mercader, C Fuchsberger, MS Udler, A Mahajan, J Wessel, ...
Nature 570 (7759), 71-76, 2019
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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
J Wessel, AY Chu, SM Willems, S Wang, H Yaghootkar, JA Brody, ...
Nature communications 6 (1), 5897, 2015
强制性开放获取政策： US Department of Energy, Swiss National Science Foundation, US National …
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A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease
RA Scott, DF Freitag, L Li, AY Chu, P Surendran, R Young, N Grarup, ...
Science translational medicine 8 (341), 341ra76-341ra76, 2016
强制性开放获取政策： US National Institutes of Health, Danish Council for Independent Research …
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Genome-wide meta-analyses of smoking behaviors in African Americans
SP David, A Hamidovic, GK Chen, AW Bergen, J Wessel, JL Kasberger, ...
Translational psychiatry 2 (5), e119-e119, 2012
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Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution
AE Justice, T Karaderi, HM Highland, KL Young, M Graff, Y Lu, V Turcot, ...
Nature genetics 51 (3), 452-469, 2019
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CACNA1C Gene Polymorphisms, Cardiovascular Disease Outcomes, and Treatment Response
AL Beitelshees, H Navare, D Wang, Y Gong, J Wessel, JI Moss, ...
Circulation: Cardiovascular Genetics 2 (4), 362-370, 2009
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Resequencing of nicotinic acetylcholine receptor genes and association of common and rare variants with the Fagerström test for nicotine dependence
J Wessel, SM McDonald, DA Hinds, RP Stokowski, HS Javitz, ...
Neuropsychopharmacology 35 (12), 2392-2402, 2010
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Maternal lipid profile differs by gestational diabetes physiologic subtype
J Layton, C Powe, C Allard, MC Battista, M Doyon, L Bouchard, P Perron, ...
Metabolism 91, 39-42, 2019
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A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk
A Manning, HM Highland, J Gasser, X Sim, T Tukiainen, P Fontanillas, ...
Diabetes 66 (7), 2019-2032, 2017
强制性开放获取政策： US National Institutes of Health, Helmholtz Association, Danish Council for …
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SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function
M Li, Y Li, O Weeks, V Mijatovic, A Teumer, JE Huffman, G Tromp, ...
Journal of the American Society of Nephrology 28 (3), 981-994, 2017
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, National …
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Impact of rare and common genetic variants on diabetes diagnosis by hemoglobin A1c in multi-ancestry cohorts: the trans-omics for precision medicine program
C Sarnowski, A Leong, LM Raffield, P Wu, PS de Vries, D DiCorpo, X Guo, ...
The American Journal of Human Genetics 105 (4), 706-718, 2019
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Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes
GE Swan, HS Javitz, LM Jack, J Wessel, M Michel, DA Hinds, ...
The pharmacogenomics journal 12 (4), 349-358, 2012
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Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits
AM Valle, Z Radić, BK Rana, V Mahboubi, J Wessel, PB Shih, F Rao, ...
The Journal of pharmacology and experimental therapeutics 338 (1), 125-133, 2011
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Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya
TM Temu, KA Lane, C Shen, L Ng'ang'a, CO Akwanalo, PS Chen, ...
PLoS One 12 (9), e0185204, 2017
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Human tyrosine hydroxylase natural allelic variation: influence on autonomic function and hypertension
F Rao, K Zhang, L Zhang, BK Rana, J Wessel, MM Fung, ...
Cellular and molecular neurobiology 30, 1391-1394, 2010
强制性开放获取政策： US National Institutes of Health
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