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Michael H. Cho
Michael H. Cho
Brigham and Women's Hospital, Harvard Medical School
在 channing.harvard.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
15762021
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
6292016
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
5232017
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
5152020
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
4922009
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
4752010
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
4262019
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
4212016
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
3842017
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
3842014
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
3532014
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
3172019
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
3062017
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
2752020
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
2712014
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
2682012
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
2462013
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
2442019
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
2432014
Genome-Wide Association Studies Identify CHRNA5/3 and HTR4 in the Development of Airflow Obstruction
JB Wilk, NRG Shrine, LR Loehr, JH Zhao, A Manichaikul, LM Lopez, ...
American journal of respiratory and critical care medicine 186 (7), 622-632, 2012
2332012
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