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| Patterns of growth and decline in lung function in persistent childhood asthma MJ McGeachie, KP Yates, X Zhou, F Guo, AL Sternberg, ML Van Natta, ... New England Journal of Medicine 374 (19), 1842-1852, 2016 | 651 | 2016 |
| 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 | 557 | 2020 |
| Association between telomere length and risk of cancer and non-neoplastic diseases: a Mendelian randomization study PC Haycock, S Burgess, A Nounu, J Zheng, GN Okoli, J Bowden, ... JAMA oncology 3 (5), 636-651, 2017 | 552 | 2017 |
| MMP12, lung function, and COPD in high-risk populations GM Hunninghake, MH Cho, Y Tesfaigzi, ME Soto-Quiros, L Avila, ... New England Journal of Medicine 361 (27), 2599-2608, 2009 | 498 | 2009 |
| Variants in FAM13A are associated with chronic obstructive pulmonary disease MH Cho, N Boutaoui, BJ Klanderman, JS Sylvia, JP Ziniti, CP Hersh, ... Nature genetics 42 (3), 200-202, 2010 | 480 | 2010 |
| New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries N Shrine, AL Guyatt, AM Erzurumluoglu, VE Jackson, BD Hobbs, ... Nature genetics 51 (3), 481-493, 2019 | 438 | 2019 |
| Association between interstitial lung abnormalities and all-cause mortality RK Putman, H Hatabu, T Araki, G Gudmundsson, W Gao, M Nishino, ... Jama 315 (7), 672-681, 2016 | 435 | 2016 |
| Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis BD Hobbs, K De Jong, M Lamontagne, Y Bossé, N Shrine, MS Artigas, ... Nature genetics 49 (3), 426-432, 2017 | 390 | 2017 |
| Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis MH Cho, MLN McDonald, X Zhou, M Mattheisen, PJ Castaldi, CP Hersh, ... The lancet Respiratory medicine 2 (3), 214-225, 2014 | 389 | 2014 |
| The clinical and genetic features of COPD-asthma overlap syndrome M Hardin, M Cho, ML McDonald, T Beaty, J Ramsdell, S Bhatt, ... European Respiratory Journal 44 (2), 341-350, 2014 | 361 | 2014 |
| Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations P Sakornsakolpat, D Prokopenko, M Lamontagne, NF Reeve, AL Guyatt, ... Nature genetics 51 (3), 494-505, 2019 | 332 | 2019 |
| Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets LV Wain, N Shrine, MS Artigas, AM Erzurumluoglu, B Noyvert, ... Nature genetics 49 (3), 416-425, 2017 | 310 | 2017 |
| Epidemiology, genetics, and subtyping of preserved ratio impaired spirometry (PRISm) in COPDGene ES Wan, PJ Castaldi, MH Cho, JE Hokanson, EA Regan, BJ Make, ... Respiratory research 15, 1-13, 2014 | 289 | 2014 |
| Genome-wide association study of susceptibility to idiopathic pulmonary fibrosis RJ Allen, B Guillen-Guio, JM Oldham, SF Ma, A Dressen, ML Paynton, ... American journal of respiratory and critical care medicine 201 (5), 564-574, 2020 | 287 | 2020 |
| A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13 MH Cho, PJ Castaldi, ES Wan, M Siedlinski, CP Hersh, DL Demeo, ... Human molecular genetics 21 (4), 947-957, 2012 | 270 | 2012 |
| Genetic diversity fuels gene discovery for tobacco and alcohol use GRB Saunders, X Wang, F Chen, SK Jang, M Liu, C Wang, S Gao, ... Nature 612 (7941), 720-724, 2022 | 264 | 2022 |
| Use of> 100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in … MH Kowalski, H Qian, Z Hou, JD Rosen, AL Tapia, Y Shan, D Jain, ... PLoS genetics 15 (12), e1008500, 2019 | 257 | 2019 |
| Computed tomographic measures of pulmonary vascular morphology in smokers and their clinical implications RSJ Estépar, GL Kinney, JL Black-Shinn, RP Bowler, GL Kindlmann, ... American journal of respiratory and critical care medicine 188 (2), 231-239, 2013 | 251 | 2013 |
| 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 | 246 | 2014 |
Ed SilvermanVerified email at channing.harvard.edu
