| Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ... Nature 590 (7845), 290-299, 2021 | 1417 | 2021 |
| Association analysis identifies 65 new breast cancer risk loci K Michailidou, S Lindström, J Dennis, J Beesley, S Hui, S Kar, A Lemaçon, ... Nature 551 (7678), 92-94, 2017 | 1375 | 2017 |
| Polygenic risk scores for prediction of breast cancer and breast cancer subtypes N Mavaddat, K Michailidou, J Dennis, M Lush, L Fachal, A Lee, JP Tyrer, ... The American Journal of Human Genetics 104 (1), 21-34, 2019 | 950 | 2019 |
| Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease JC Crosby, GM Peloso, PL Auer, et al. New England Journal of Medicine 371, 22-31, 2014 | 841 | 2014 |
| Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, P Angelica Merlini, ... Nature 518 (7537), 102-106, 2015 | 763 | 2015 |
| 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 | 655 | 2017 |
| A population-based study of genes previously implicated in breast cancer C Hu, SN Hart, R Gnanaolivu, H Huang, KY Lee, J Na, C Gao, J Lilyquist, ... New England Journal of Medicine 384 (5), 440-451, 2021 | 621 | 2021 |
| Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ... Nature 526 (7571), 112-117, 2015 | 548 | 2015 |
| 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 | 547 | 2017 |
| Statistical design and analysis of RNA sequencing data PL Auer, RW Doerge Genetics 185 (2), 405-416, 2010 | 516 | 2010 |
| Inherited causes of clonal haematopoiesis in 97,691 whole genomes AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ... Nature 586 (7831), 763-768, 2020 | 467 | 2020 |
| Inactivating Mutations in NPC1L1 and Protection from Coronary Heart Disease NO Stitziel, HH Won, AC Morrison, GM Peloso, R Do, LA Lange, ... The New England Journal of Medicine 371, 2072-2082, 2014 | 467* | 2014 |
| The polygenic and monogenic basis of blood traits and diseases D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ... Cell 182 (5), 1214-1231. e11, 2020 | 464 | 2020 |
| Trans-ethnic and ancestry-specific blood-cell genetics in 746,667 individuals from 5 global populations MH Chen, LM Raffield, A Mousas, S Sakaue, JE Huffman, A Moscati, ... Cell 182 (5), 1198-1213. e14, 2020 | 427 | 2020 |
| 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 | 400 | 2016 |
| Breast cancer risk from modifiable and nonmodifiable risk factors among white women in the United States P Maas, M Barrdahl, AD Joshi, PL Auer, MM Gaudet, RL Milne, ... JAMA oncology 2 (10), 1295-1302, 2016 | 393 | 2016 |
| Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks GM Peloso, PL Auer, JC Bis, A Voorman, AC Morrison, NO Stitziel, ... The American Journal of Human Genetics 94 (2), 223-232, 2014 | 382 | 2014 |
| Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer RL Milne, KB Kuchenbaecker, K Michailidou, J Beesley, S Kar, ... Nature genetics 49 (12), 1767-1778, 2017 | 373 | 2017 |
| Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses H Zhang, TU Ahearn, J Lecarpentier, D Barnes, J Beesley, G Qi, X Jiang, ... Nature genetics 52 (6), 572-581, 2020 | 341 | 2020 |
| 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 | 339 | 2018 |
