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Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutations.
Whole-Exome Sequencing for the Identification of Susceptibility Genes of Kashinâ€“Beck Disease
Biology of breast cancer during pregnancy using genomic profiling
Whole-Genome Sequencing of Individuals from a Founder Population Identifies Candidate Genes for Asthma
Association of serine racemase gene variants with type 2 diabetes in the Chinese Han population
YIA4 Genetic Risk Markers for Atrial Fibrillation Influence Allelic Expression of Nearby Candidate Genes
Polymorphisms in ERCC1 gene could predict clinical outcome of platinum-based chemotherapy for non-small cell lung cancer patients
ZNF300P1 Encodes a lincRNA that regulates cell polarity and is epigenetically silenced in type II epithelial ovarian cancer
Interleukin-10 gene promoter polymorphism and susceptibility to liver cirrhosis
Common TLR1 Genetic Variation Is Not Associated with Death from Melioidosis, a Common Cause of Sepsis in Rural Thailand