Gene fingerprint model for literature based detection of the associations among complex diseases: a case study of COPD.
Chen, Guocai; Jia, Yuxi; Zhu, Lisha; Li, Ping; Zhang, Lin; Tao, Cui; Jim Zheng, W.
BMC Med Inform Decis Mak
; 19(Suppl 1): 20, 2019 01 31.
Artigo em Inglês | MEDLINE | ID: mdl-30700303
Examining the role of unmeasured confounding in mediation analysis with genetic and genomic applications.
Deducting MicroRNA-Mediated Changes Common in Bronchial Epithelial Cells of Asthma and Chronic Obstructive Pulmonary Disease-A Next-Generation Sequencing-Guided Bioinformatic Approach.
The chronic bronchitis phenotype in chronic obstructive pulmonary disease: features and implications.
Microarray analysis of long non-coding RNAs in COPD lung tissue.
Human Lung DNA Methylation Quantitative Trait Loci Colocalize with Chronic Obstructive Pulmonary Disease Genome-Wide Association Loci.
Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study.
A candidate gene identification strategy utilizing mouse to human big-data mining: "3R-tenet" in COPD genetic research.
From comorbidities of chronic obstructive pulmonary disease to identification of shared molecular mechanisms by data integration.
Network modules uncover mechanisms of skeletal muscle dysfunction in COPD patients.
Association of thrombocytosis with COPD morbidity: the SPIROMICS and COPDGene cohorts.