Now showing items 1-5 of 5

    • McCauley, Jacob Lee (2005-03-09)
      Department: Molecular Physiology and Biophysics
      Autism is a severe neurodevelopmental disorder characterized by deficits in language and social interaction, and patterns of repetitive and stereotyped behaviors, interests and activities. Evidence indicates that autism ...
    • Liang, Xueying (2007-04-16)
      Department: Human Genetics
      With the exception of ApoE gene, no universally accepted genetic association has been identified with the complex Late-onset Alzheimer Disease (LOAD). A broad region of chromosome 10 has engendered continued interest ...
    • Davis, Mary Feller (2013-04-15)
      Department: Interdisciplinary Studies: Applied Statistics
      Previous evidence has shown that Parkinson disease (PD) has a heritable component, but only a small proportion of the total genetic contribution to PD has been identified. Genetic heterogeneity complicates the verification ...
    • Cummings, Anna Christine (2012-12-07)
      Department: Interdisciplinary Studies: Applied Statistics
      Studying population isolates with large, complex pedigrees has many advantages for discovering genetic susceptibility loci; however, statistical analyses can be computationally challenging. Allelic association tests need ...
    • Delahanty, Ryan James (2010-01-29)
      Department: Human Genetics
      TOWARD AN UNDERSTANDING OF THE ROLE OF CHROMOSOME 15Q11-Q13 IN IDIOPATHIC AUTISM RYAN JAMES DELAHANTY Dissertation under the direction of Dr. James S. Sutcliffe The 15q11-q13 region is a genomic interval ...