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Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles
Aberrant methylation of Pax3 gene and neural tube defects in association with exposure to polycyclic aromatic hydrocarbons
Large-scale genome-wide association study of East Asians identifies loci associated with risk for colorectal cancer
Genetic analysis of the relation between IL2RA/IL2RB and rheumatoid arthritis risk
Body Mass Index in Multiple Sclerosis modulates ceramide-induced DNA methylation and disease course
Association of expression quantitative trait loci for long noncoding RNAs with lung cancer risk in Asians
CLAVATA signaling pathway genes modulating flowering time and flower number in chickpea
DNA-Based Sequencing Assays
The rs1126616 Single Nucleotide Polymorphism of the Osteopontin Gene Is Independently Associated with Cardiovascular Events in a Chronic Kidney Disease Cohort
Association between CNTNAP2 polymorphisms and autism: A family‐based study in the chinese han population and a meta‐analysis combined with GWAS data of psychiatric genomics consortium