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Eirini Marouli
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Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry
SL Pulit, C Stoneman, AP Morris, AR Wood, CA Glastonbury, J Tyrrell, ...
Human molecular genetics 28 (1), 166-174, 2019
9072019
Mapping the human genetic architecture of COVID-19
E Marouli
Nature, 2021
751*2021
Rare and low-frequency coding variants alter human adult height
E Marouli, et al
Nature, 2017
6542017
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
6232017
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
5452017
The power of genetic diversity in genome-wide association studies of lipids
SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ...
Nature 600 (7890), 675-679, 2021
4502021
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
4382016
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
4232018
Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
New England Journal of Medicine 374 (12), 1134-1144, 2016
4002016
A saturated map of common genetic variants associated with human height
L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ...
Nature 610 (7933), 704-712, 2022
3582022
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
3392018
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
3242016
Systematic evaluation of pleiotropy identifies 6 further loci associated with coronary artery disease
TR Webb, J Erdmann, KE Stirrups, NO Stitziel, NGD Masca, H Jansen, ...
Journal of the American College of Cardiology 69 (7), 823-836, 2017
2502017
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
2312015
Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci
AM Erzurumluoglu, M Liu, VE Jackson, DR Barnes, G Datta, ...
Molecular psychiatry 25 (10), 2392-2409, 2020
1342020
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
1002019
Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia
S Hackinger, B Prins, V Mamakou, E Zengini, E Marouli, L Brčić, ...
Translational psychiatry 8 (1), 252, 2018
852018
CARDIoGRAMplusC4D; UK Biobank CardioMetabolic Consortium CHD working group. 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, ...
Nat Genet 49 (9), 1385-1391, 2017
782017
Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function
JS Hawe, R Wilson, KT Schmid, L Zhou, LN Lakshmanan, BC Lehne, ...
Nature genetics 54 (1), 18-29, 2022
742022
Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use
DM Brazel, Y Jiang, JM Hughey, V Turcot, X Zhan, J Gong, C Batini, ...
Biological psychiatry 85 (11), 946-955, 2019
742019
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