Genetic variation in Down syndrome associated congenital heart defects

Telomere length: implications on the risk for chromosome 21 nondisjunction in oocytes

Assessment of cis and trans-acting factors for involvement in the altered recombination patterns associated with Trisomy 21

Genomics of Down Syndrome Associated Congenital Heart Defects

Development of Novel Analytic Methods for Improved Gene Mapping of Complex Human Traits

Identifying Variants in Neuroligin Pathway Genes Using Next Generation Sequencing Technologies

Genetic Variation in Recombination as a Risk Factor for Nondisjunction