Sequence analysis of chromosome translocations in neurodevelopmental disorders

The Role of Insulators and Transcription Factors in Genome Organization and Function in Drosophila

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

Serum Dopamine Beta Hydroxylase (DβH) enzyme activity changes within individual women according to stage of pregnancy: Evidence that regulation of expression of DβH differs during pregnancy in women carrying different genotypes at rs1611115.

Population Genetics of Raccoons in the Eastern United States With Implications for Rabies Transmission and Spread

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

The Origin and Spread of Drug Resistant Malaria in South America

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

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

Mutations in APH(3')-IIIa Increase Activity Against Amikacin

Genomics of Down Syndrome Associated Congenital Heart Defects

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

Evolution of Purine Metabolism

Novel Germline and Somatic Retrotransposon Insertions in Humans

Identifying Variants in Neuroligin Pathway Genes Using Next Generation Sequencing Technologies

Genetic and environmental contributions to gastrointestinal health

Genetic Variation in Recombination as a Risk Factor for Nondisjunction

Identification and Evaluation of Novel Epilepsy-Associated Variants