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Aberrant methylation and downregulation of sall3 in human hepatocellular carcinoma
Association Study of Candidate Gene Polymorphisms with Amnestic Mild Cognitive Impairment in a Chinese Population
Effector CD4+ T Cell Expression Signatures and Immune-Mediated Disease Associated Genes
New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis
Selenium, Selenoenzymes, Oxidative Stress and Risk of Neoplastic Progression from Barrett’s Esophagus: Results from Biomarkers and Genetic Variants
Markers of Endogenous Desaturase Activity and Risk of Coronary Heart Disease in the CAREMA Cohort Study
The Aromatase Gene CYP19A1: Several Genetic and Functional Lines of Evidence Supporting a Role in Reading, Speech and Language
Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen Study
High-Throughput Mutation Profiling Identifies Frequent Somatic Mutations in Advanced Gastric Adenocarcinoma
Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
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