Associations Between Perinatal Exposures and Neonatal DNA Methylation

A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals

Genetic variation in Down syndrome associated congenital heart defects

Stem cell derived monkey neural progenitor cells as a platform for translational research in Huntington's disease

MeCP2 Mediated Regulation of Small Noncoding RNA

Genetic variation caused by active retrotransposons in the humangenome

Identification of Aberrantly Expressed Synaptic Proteins in the Mouse Model of Fragile X Syndrome

Assessment of the clinical impact of sequence variants in the FMR1 gene

Pathogenesis of novel FMR1 mutations in fragile X syndrome