about
Studying Dynamic Features in Myocardial Infarction Progression by Integrating miRNA-Transcription Factor Co-Regulatory Networks and Time-Series RNA Expression Data from Peripheral Blood Mononuclear CellsSemFunSim: a new method for measuring disease similarity by integrating semantic and gene functional associationIntegration of Multiple Genomic and Phenotype Data to Infer Novel miRNA-Disease Associations.Estrogen deficiency is associated with hippocampal morphological remodeling of early postmenopausal miceSIDD: a semantically integrated database towards a global view of human disease.MicroRNA and transcription factor mediated regulatory network analysis reveals critical regulators and regulatory modules in myocardial infarctionIdentification and validation of potential prognostic lncRNA biomarkers for predicting survival in patients with multiple myeloma.BLAT2DOLite: An Online System for Identifying Significant Relationships between Genetic Sequences and Diseases.A potential prognostic long non-coding RNA signature to predict metastasis-free survival of breast cancer patientsPredicting disease-related genes using integrated biomedical networks.Prognostic and clinicopathological role of long non-coding RNA UCA1 in various carcinomas.A potential panel of six-long non-coding RNA signature to improve survival prediction of diffuse large-B-cell lymphoma.Characterization of long non-coding RNA-associated ceRNA network to reveal potential prognostic lncRNA biomarkers in human ovarian cancer.DisSim: an online system for exploring significant similar diseases and exhibiting potential therapeutic drugs.Relapse-related long non-coding RNA signature to improve prognosis prediction of lung adenocarcinomaOAHG: an integrated resource for annotating human genes with multi-level ontologies.IntNetLncSim: an integrative network analysis method to infer human lncRNA functional similarity.Discovery and validation of immune-associated long non-coding RNA biomarkers associated with clinically molecular subtype and prognosis in diffuse large B cell lymphomaConstruction and analysis of dysregulated lncRNA-associated ceRNA network identified novel lncRNA biomarkers for early diagnosis of human pancreatic cancer.Using Semantic Association to Extend and Infer Literature-Oriented Relativity Between Terms.Annotating the Function of the Human Genome with Gene Ontology and Disease Ontology.GAB2 rs2373115 variant contributes to Alzheimer's disease risk specifically in European population.MetSigDis: a manually curated resource for the metabolic signatures of diseases.Measuring disease similarity and predicting disease-related ncRNAs by a novel method.A novel method to identify pre-microRNA in various species knowledge base on various species.A framework for exploring associations between biomedical terms in PubMed.DincRNA: a comprehensive web-based bioinformatics toolkit for exploring disease associations and ncRNA function.Autoimmune disease variants regulate GSDMB gene expression in human immune cells and whole blood.Rs4878104 contributes to Alzheimer's disease risk and regulates DAPK1 gene expression.InfAcrOnt: calculating cross-ontology term similarities using information flow by a random walk.Identifying diseases-related metabolites using random walk.An Immune-Related Six-lncRNA Signature to Improve Prognosis Prediction of Glioblastoma Multiforme.Human Disease System BiologyExposing the Causal Effect of C-Reactive Protein on the Risk of Type 2 Diabetes Mellitus: A Mendelian Randomization StudyIdentification of Alzheimer's Disease-Related Genes Based on Data Integration MethodA Positive Causal Influence of IL-18 Levels on the Risk of T2DM: A Mendelian Randomization StudyDysbiosis of the Gut Microbiome in Lung CancerExposing the Causal Effect of Body Mass Index on the Risk of Type 2 Diabetes Mellitus: A Mendelian Randomization StudyA Review of Recent Advances and Research on Drug Target Identification MethodsIdentification of Cancer Dysfunctional Subpathways by Integrating DNA Methylation, Copy Number Variation, and Gene-Expression Data
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description
researcher (ORCID 0000-0002-6665-6710)
@en
name
Liang Cheng
@en
type
label
Liang Cheng
@en
prefLabel
Liang Cheng
@en
P2456
P31
P496
0000-0002-6665-6710