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ONCOGENE MUTATION PROFILING OF PEDIATRIC SOLID TUMORS REVEALS SIGNIFICANT SUBSETS OF EMBRYONAL RHABDOMYOSARCOMA AND NEUROBLASTOMA WITH MUTATED GENES IN GROWTH SIGNALING PATHWAYS
Genome-Wide Gene-Environment Study Identifies Glutamate Receptor Gene GRIN2A as a Parkinsonâ€™s Disease Modifier Gene via Interaction with Coffee
Plasma adrenomedullin level is related to a single nucleotide polymorphism in the adrenomedullin gene
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease
Acetylation of H2A.Z is a key epigenetic modification associated with gene deregulation and epigenetic remodeling in cancer
Late-replicating heterochromatin is characterized by decreased cytosine methylation in the human genome
Identification of improved IL28B SNPs and haplotypes for prediction of drug response in treatment of hepatitis C using massively parallel sequencing in a cross-sectional European cohort
DNA methylation is associated with downregulation of the organic cation transporter OCT1 (SLC22A1) in human hepatocellular carcinoma
Septin 9 isoform expression, localization and epigenetic changes during human and mouse breast cancer progression
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers