Eirini Marouli
TitleCited byYear
Rare and low-frequency coding variants alter human adult height
E Marouli, et al
Nature, 2017
2882017
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
2012016
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
1972017
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
1692017
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
1462016
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
1332015
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
1122017
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
1062018
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
962018
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
642016
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
412019
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
362017
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
292017
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
232019
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
202017
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
182016
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
92019
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
82019
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), 1-10, 2018
82018
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Articles 1–20