RNA modification-related variants in genomic loci associated with body mass index.
PMID:35879730
Genetic Variation in ATXN3 (Ataxin-3) 3'UTR: Insights into the Downstream Regulatory Elements of the Causative Gene of Machado-Joseph Disease/Spinocerebellar Ataxia Type 3.
PMID:35034258
CircleBase: an integrated resource and analysis platform for human eccDNAs.
PMID:34792166
In silico Analysis of Polymorphisms in microRNAs Deregulated in Alzheimer Disease.
PMID:33841080
Exploring Common Therapeutic Targets for Neurodegenerative Disorders Using Transcriptome Study.
PMID:33815473
AI-Driver: an ensemble method for identifying driver mutations in personal cancer genomes.
PMID:33575629
Identification and analysis of RNA structural disruptions induced by single nucleotide variants using Riprap and RiboSNitchDB.
PMID:33575608
Transcriptomic signatures and repurposing drugs for COVID-19 patients: findings of bioinformatics analyses.
PMID:33312453
Role of m6A RNA methylation in cardiovascular disease (Review).
PMID:33125109
RMVar: an updated database of functional variants involved in RNA modifications.
PMID:33021671
RMDisease: a database of genetic variants that affect RNA modifications, with implications for epitranscriptome pathogenesis.
PMID:33010174
Genetic variants in N6-methyladenosine are associated with bladder cancer risk in the Chinese population.
PMID:32964246
Somatic mutations in colorectal cancer are associated with the epigenetic modifications.
PMID:32865336
Integration Analysis of m6A-SNPs and eQTLs Associated With Sepsis Reveals Platelet Degranulation and Staphylococcus aureus Infection are Mediated by m6A mRNA Methylation.
PMID:32174955
Prevalence and architecture of posttranscriptionally impaired synonymous mutations in 8,320 genomes across 22 cancer types.
PMID:31950163
Gain-of-Function Mutations: An Emerging Advantage for Cancer Biology.
PMID:31047772
Discovery of Allele-Specific Protein-RNA Interactions in Human Transcriptomes.
PMID:30827501
OncoBase: a platform for decoding regulatory somatic mutations in human cancers.
PMID:30445567
Genome-wide identification of m6A-associated SNPs as potential functional variants for bone mineral density.
PMID:29980810
VarCards: an integrated genetic and clinical database for coding variants in the human genome.
PMID:29112736
Cellular network perturbations by disease-associated variants.
PMID:29057377
EpiDenovo: a platform for linking regulatory de novo mutations to developmental epigenetics and diseases.
PMID:29040751
m6AVar: a database of functional variants involved in m6A modification.
PMID:29036329
POSTAR: a platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins.
PMID:28053162