| Genetic studies of body mass index yield new insights for obesity biology AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ... Nature 518 (7538), 197-206, 2015 | 4611 | 2015 |
| A reference panel of 64,976 haplotypes for genotype imputation Nature genetics 48 (10), 1279-1283, 2016 | 2824 | 2016 |
| Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC ... Nature genetics 44 (9), 981-990, 2012 | 2143 | 2012 |
| Defining the role of common variation in the genomic and biological architecture of adult human height AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ... Nature genetics 46 (11), 1173-1186, 2014 | 2068 | 2014 |
| New genetic loci link adipose and insulin biology to body fat distribution D Shungin, TW Winkler, DC Croteau-Chonka, T Ferreira, AE Locke, ... Nature 518 (7538), 187-196, 2015 | 1597 | 2015 |
| Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium Nature genetics 46 (3), 234-244, 2014 | 897 | 2014 |
| 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 | 633 | 2017 |
| Biobank-driven genomic discovery yields new insight into atrial fibrillation biology JB Nielsen, RB Thorolfsdottir, LG Fritsche, W Zhou, MW Skov, SE Graham, ... Nature genetics 50 (9), 1234-1239, 2018 | 589 | 2018 |
| 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 | 531 | 2017 |
| Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology MA Ferreira, JM Vonk, H Baurecht, I Marenholz, C Tian, JD Hoffman, ... Nature genetics 49 (12), 1752-1757, 2017 | 497 | 2017 |
| 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 | 429 | 2016 |
| The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study TW Winkler, AE Justice, M Graff, L Barata, MF Feitosa, S Chu, ... PLoS genetics 11 (10), e1005378, 2015 | 425 | 2015 |
| Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci KJ Gaulton, T Ferreira, Y Lee, A Raimondo, R Mägi, ME Reschen, ... Nature genetics 47 (12), 1415-1425, 2015 | 408 | 2015 |
| 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 | 397 | 2016 |
| 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 | 324 | 2018 |
| 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 | 315 | 2016 |
| Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk OL Holmen, HE Zhang, Y Fan, DH Hovelson, EM Schmidt, W Zhou, Y Guo, ... Nature genetics 46 (4), 345-351, 2014 | 313 | 2014 |
| 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 | 245 | 2017 |
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014 | 236 | 2014 |
| Meta-analysis of gene-level tests for rare variant association DJ Liu, GM Peloso, X Zhan, OL Holmen, M Zawistowski, S Feng, ... Nature genetics 46 (2), 200-204, 2014 | 229 | 2014 |
