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Author Details

Michael H Cho
Brigham and Women's Hospital Channing Division of Network Medicine
2006
277
51
Trey Ideker (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37611073Early Evidence of Chronic Obstructive Pulmonary Disease Obscured by Race-Specific Prediction Equations.Am J Respir Crit Care Med2024
37611073Early Evidence of Chronic Obstructive Pulmonary Disease Obscured by Race-Specific Prediction Equations.Am J Respir Crit Care Med2024
36216496Integrative analyses for the identification of idiopathic pulmonary fibrosis-associated genes and shared loci with other diseases.Thorax2023
36229050Bronchial gene expression alterations associated with radiological bronchiectasis.Eur Respir J2023
35953101Zinc finger protein 33B demonstrates sex interaction with atopy-related markers in childhood asthma.Eur Respir J2023
36216496Integrative analyses for the identification of idiopathic pulmonary fibrosis-associated genes and shared loci with other diseases.Thorax2023
35930450Suspected Interstitial Lung Disease in COPDGene Study.Am J Respir Crit Care Med2023
36255742FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies.Hum Mol Genet2023
35780812Quantitative Interstitial Abnormality Progression and Outcomes in the Genetic Epidemiology of COPD and Pittsburgh Lung Screening Study Cohorts.Chest2023
37749248Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.Nat Genet2023
37595761Polygenic risk scores identify heterogeneity in asthma and chronic obstructive pulmonary disease.J Allergy Clin Immunol2023
37734371The COPD GWAS gene ADGRG6 instructs function and injury response in human iPSC-derived type II alveolar epithelial cells.Am J Hum Genet2023
37905118Determinants of mosaic chromosomal alteration fitness.medRxiv2023
37904051Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.Nat Genet2023
37788444Clonal Somatic Mutations in Chronic Lung Diseases Are Associated with Reduced Lung Function.Am J Respir Crit Care Med2023
37782931Suspected Bronchiectasis and Mortality in Adults With a History of Smoking Who Have Normal and Impaired Lung Function : A Cohort Study.Ann Intern Med2023
37961722Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability.bioRxiv2023
37869564Multivariate adaptive shrinkage improves cross-population transcriptome prediction and association studies in underrepresented populations.HGG Adv2023
37286633Large scale proteomic studies create novel privacy considerations.Sci Rep2023
37160347Heterogeneity and Progression of Chronic Obstructive Pulmonary Disease: Emphysema-Predominant and Non-Emphysema-Predominant Disease.Am J Epidemiol2023
37474940Bilirubin-associated single nucleotide polymorphism (SNP) and respiratory health outcomes: a mendelian randomization study.Respir Res2023
36778386Structural variation across 138,134 samples in the TOPMed consortium.Res Sq2023
37210745Airway-Occluding Mucus Plugs and Mortality in Patients With Chronic Obstructive Pulmonary Disease.JAMA2023
36898128Traction Bronchiectasis/Bronchiolectasis in Interstitial Lung Abnormality: Follow-up in the COPDGene Study.Am J Respir Crit Care Med2023
36961916Who Modifies the Modifiers: A High-Resolution View of the Genetic Modifiers of Cystic Fibrosis.Am J Respir Crit Care Med2023
37268414Pulmonary emphysema subtypes defined by unsupervised machine learning on CT scans.Thorax2023
36952240Variability in <i>MUC5B</i> Expression Is Dependent on Genotype and Endotype in Idiopathic Pulmonary Fibrosis.Am J Respir Crit Care Med2023
37398003Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.medRxiv2023
37072532Use of the Spirometric "Fixed-Ratio" Underdiagnoses COPD in African-Americans in a Longitudinal Cohort Study.J Gen Intern Med2023
37069358Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models.Nat Genet2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
37066248Prediction and stratification of longitudinal risk for chronic obstructive pulmonary disease across smoking behaviors.medRxiv2023
36747810Structural variation across 138,134 samples in the TOPMed consortium.bioRxiv2023
36865145Identifying COPD subtypes using multi-trait genetics.medRxiv2023
36798214Multivariate adaptive shrinkage improves cross-population transcriptome prediction for transcriptome-wide association studies in underrepresented populations.bioRxiv2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
37041558Identifying chronic obstructive pulmonary disease from integrative omics and clustering in lung tissue.BMC Pulm Med2023
36602845Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.Am J Respir Crit Care Med2023
37228113Hierarchical association of COPD to principal genetic components of biological systems.PLoS One2023
36918970Cluster analysis of COVID-19 recovery center patients at a clinic in Boston, MA 2021-2022: impact on strategies for access and personalized care.Arch Public Health2023
36726148X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study.Respir Res2023
37523715A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities.Am J Respir Crit Care Med2023
37523391A statistical framework to identify cell types whose genetically regulated proportions are associated with complex diseases.PLoS Genet2023
36780661Integrating Genetics, Transcriptomics, and Proteomics in Lung Tissue to Investigate Chronic Obstructive Pulmonary Disease.Am J Respir Cell Mol Biol2023
37595761Polygenic risk scores identify heterogeneity in asthma and chronic obstructive pulmonary disease.J Allergy Clin Immunol2023
37961722Trait selection strategy in multi-trait GWAS: Boosting SNPs discoverability.bioRxiv2023
37523715A Polygenic Risk Score for Idiopathic Pulmonary Fibrosis and Interstitial Lung Abnormalities.Am J Respir Crit Care Med2023
37905118Determinants of mosaic chromosomal alteration fitness.medRxiv2023
37523391A statistical framework to identify cell types whose genetically regulated proportions are associated with complex diseases.PLoS Genet2023
37904051Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing.Nat Genet2023
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Collaborators

Brigham and Women's Hospital
Co-authored papers 200
Co-authored papers 78
Harvard Medical School
Co-authored papers 67
Co-authored papers 55
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Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 28
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Co-authored papers 25
Co-authored papers 23
Boston University School of Medicine
Co-authored papers 21
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Co-authored papers 18
Brigham and Women's Hospital and Harvard Medical School
Co-authored papers 18
Co-authored papers 17
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Co-authored papers 16
Co-authored papers 15
Co-authored papers 15
University of Michigan School of Public Health ann arbor
Co-authored papers 14
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Co-authored papers 14
Brigham and Women's Hospital
Co-authored papers 14