Artificial Intelligence, Healthcare, Clinical Genomics, and Pharmacogenomics Approaches in Precision Medicine. 
 PMID:35873469
                                    
                                
                                    Distinct Roles of NANOS1 and NANOS3 in the Cell Cycle and NANOS3-PUM1-FOXM1 Axis to Control G2/M Phase in a Human Primordial Germ Cell Model. 
 PMID:35743036
                                    
                                
                                    Integrated Analysis of Tissue-Specific Gene Expression in Diabetes by Tensor Decomposition Can Identify Possible Associated Diseases. 
 PMID:35741859
                                    
                                
                                    Defining characteristics and conservation of poorly annotated genes in Caenorhabditis elegans using WormCat 2.0. 
 PMID:35587742
                                    
                                
                                    MOSES: A New Approach to Integrate Interactome Topology and Functional Features for Disease Gene Prediction. 
 PMID:34828319
                                    
                                
                                    A computational approach for identification of core modules from a co-expression network and GWAS data. 
 PMID:34467232
                                    
                                
                                    Advancing clinical genomics and precision medicine with GVViZ: FAIR bioinformatics platform for variable gene-disease annotation, visualization, and expression analysis. 
 PMID:34174938
                                    
                                
                                    Mapping OMIM Disease-Related Variations on Protein Domains Reveals an Association Among Variation Type, Pfam Models, and Disease Classes. 
 PMID:34026820
                                    
                                
                                    Network bioinformatics analysis provides insight into drug repurposing for COVID-19. 
 PMID:33817623
                                    
                                
                                    Approaches to Identify and Characterise the Post-Transcriptional Roles of lncRNAs in Cancer. 
 PMID:33803328
                                    
                                
                                    High-depth African genomes inform human migration and health. 
 PMID:33116287
                                    
                                
                                    Highlighting Human Enzymes Active in Different Metabolic Pathways and Diseases: The Case Study of EC 1.2.3.1 and EC 2.3.1.9. 
 PMID:32751059
                                    
                                
                                    Precise breakpoint detection in a patient with 9p- syndrome. 
 PMID:32532883
                                    
                                
                                    Human gene and disease associations for clinical-genomics and precision medicine research. 
 PMID:32508008
                                    
                                
                                    TS-GOEA: a web tool for tissue-specific gene set enrichment analysis based on gene ontology. 
 PMID:31760951
                                    
                                
                                    NPInter v4.0: an integrated database of ncRNA interactions. 
 PMID:31670377
                                    
                                
                                    VarSite: Disease variants and protein structure. 
 PMID:31606900
                                    
                                
                                    Debutant iOS app and gene-disease complexities in clinical genomics and precision medicine. 
 PMID:31586224
                                    
                                
                                    A pediatric perspective on genomics and prevention in the twenty-first century. 
 PMID:31578042
                                    
                                
                                    CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases. 
 PMID:31322791
                                    
                                
                                    PhenPath: a tool for characterizing biological functions underlying different phenotypes. 
 PMID:31307376
                                    
                                
                                    Active repurposing of drug candidates for melanoma based on GWAS, PheWAS and a wide range of omics data. 
 PMID:31221082
                                    
                                
                                    Protein-Protein Interaction Network Analysis Reveals Several Diseases Highly Associated with Polycystic Ovarian Syndrome. 
 PMID:31216618
                                    
                                
                                    PanglaoDB: a web server for exploration of mouse and human single-cell RNA sequencing data. 
 PMID:30951143
                                    
                                
                                    Functional and Structural Features of Disease-Related Protein Variants. 
 PMID:30934684
                                    
                                
                                    GM604 regulates developmental neurogenesis pathways and the expression of genes associated with amyotrophic lateral sclerosis. 
 PMID:30524706