Eirini Marouli
Title
Cited by
Cited by
Year
Rare and low-frequency coding variants alter human adult height
E Marouli, et al
Nature, 2017
3172017
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, 2017
2292017
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
2112016
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, 2017
1922017
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
1502016
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), 1-16, 2015
1392015
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
1242017
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
1162018
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, 2018
1162018
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
682016
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
562019
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
422017
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
302017
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
262017
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
242019
Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators
NO Stitziel, KE Stirrups, NG Masca, J Erdmann, PG Ferrario, IR König, ...
Coding variation in ANGPTL4, LPL, and SVEP1 and the risk of coronary disease …, 2016
192016
Both youth and long-term vitamin D status is associated with risk of type 2 diabetes mellitus in adulthood: a cohort study
F Wu, M Juonala, N Pitkänen, A Jula, T Lehtimäki, MA Sabin, K Pahkala, ...
Annals of medicine 50 (1), 74-82, 2018
142018
No association of coronary artery disease with X-chromosomal variants in comprehensive international meta-analysis
C Loley, M Alver, TL Assimes, A Bjonnes, A Goel, S Gustafsson, ...
Scientific reports 6, 35278, 2016
142016
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
132019
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, 1-18, 2019
132019
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Articles 1–20