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High Resolution X Chromosome Copy Number Variation in Autism
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Genomics studies of population structure and evolution in Neisseria gonorrhoeae
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A Biochemical Model of Hybridization on DNA Microarrays and its Application to Single Nucleotide Polymorphism and Copy Number Variation Genotyping in Trisomy 21 Individuals
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Genetic variation in Down syndrome associated congenital heart
defects
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Assessment of cis and trans-acting factors for involvement in the
altered recombination patterns associated with Trisomy 21
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Assessment of the clinical impact of sequence variants in the
FMR1 gene
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Effects of Life History and Genome Architecture on ssRNA Virus
Evolution and Extinction
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An Investigation of the Properties of Gene-Based Tests of GWAS Data: Simulations and Analyses of ADHD GWAS Data
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Genomics of Down Syndrome Associated Congenital Heart Defects
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Identifying Variants in Neuroligin Pathway Genes Using Next
Generation Sequencing Technologies
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