Perl Programming for Biologists: By D. Curtis Jamison. Hoboken, NJ: John Wiley & Sons, Inc., 2003; 191 pages; $42.95

Por Thornton-Wells, Tricia A., Johnson, Kevin B.
Publicado em 2004

Association Rule Discovery Has the Ability to Model Complex Genetic Effects

Por Bush, William S., Thornton-Wells, Tricia A., Ritchie, Marylyn D.
Publicado em 2007

Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic data

Por Thornton-Wells, Tricia A, Moore, Jason H, Haines, Jonathan L
Publicado em 2006

Using novel control groups to dissect the amygdala's role in Williams syndrome

Por Thornton-Wells, Tricia A., Avery, Suzanne N., Blackford, Jennifer Urbano
Publicado em 2011

Regional Brain Differences in Cortical Thickness, Surface Area and Subcortical Volume in Individuals with Williams Syndrome

Por Meda, Shashwath A., Pryweller, Jennifer R., Thornton-Wells, Tricia A.
Publicado em 2012

Correction: Regional Brain Differences in Cortical Thickness, Surface Area and Subcortical Volume in Individuals with Williams Syndrome

Por Meda, Shashwath A., Pryweller, Jennifer R., Thornton-Wells, Tricia A.
Publicado em 2012

Genetic Interactions Found Between Calcium Channel Genes Modulate Amyloid Load Measured by Positron Emission Tomography

Por Koran, Mary Ellen I., Hohman, Timothy J., Thornton-Wells, Tricia A.
Publicado em 2013

Genetic variation modifies risk for neurodegeneration based on biomarker status

Por Hohman, Timothy J., Koran, Mary Ellen I., Thornton-Wells, Tricia A.
Publicado em 2014

Genetic Modification of the Relationship between Phosphorylated Tau and Neurodegeneration

Por Hohman, Timothy J., Koran, Mary Ellen I., Thornton-Wells, Tricia A.
Publicado em 2014

Alterations in diffusion properties of white matter in Williams syndrome

Por Arlinghaus, Lori R., Thornton-Wells, Tricia A., Dykens, Elisabeth M., Anderson, Adam W.
Publicado em 2011

White matter integrity deficits in prefrontal-amygdala pathways in Williams syndrome

Por Avery, Suzanne N., Thornton-Wells, Tricia A., Anderson, Adam W, Blackford, Jennifer Urbano
Publicado em 2011

Genetic interactions within inositol-related pathways are associated with longitudinal changes in ventricle size

Por Koran, Mary Ellen I., Hohman, Timothy J., Meda, Shashwath A., Thornton-Wells, Tricia A.
Publicado em 2014

Neural Correlates of Amusia in Williams Syndrome

Por Lense, Miriam D., Dankner, Nathan, Pryweller, Jennifer R., Thornton-Wells, Tricia A., Dykens, Elisabeth M.
Publicado no Brain Sci (2014)

Effect of Non-rigid Registration Algorithms on Deformation Based Morphometry: A Comparative Study with Control and Williams Syndrome Subjects

Por Han, Zhaoying, Thornton-Wells, Tricia A., Dykens, Elisabeth M., Gore, John C., Dawant, Benoit M.
Publicado no Magn Reson Imaging (2012)

The effect of intellectual ability on functional activation in a neurodevelopmental disorder: preliminary evidence from multiple fMRI studies in Williams syndrome

Por Pryweller, Jennifer R, Avery, Suzanne N, Blackford, Jennifer U, Dykens, Elisabeth M, Thornton-Wells, Tricia A
Publicado em 2012

Resting-State Functional Connectivity in Individuals with Down Syndrome and Williams Syndrome Compared with Typically Developing Controls

Por Vega, Jennifer N., Hohman, Timothy J., Pryweller, Jennifer R., Dykens, Elisabeth M., Thornton-Wells, Tricia A.
Publicado no Brain Connect (2015)

Confronting Complexity in Late-Onset Alzheimer Disease: Application of Two-Stage Analysis Approach Addressing Heterogeneity and Epistasis

Por Thornton-Wells, Tricia A., Moore, Jason H., Martin, Eden R., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado em 2008

Genetic interactions associated with 12-mo atrophy in hippocampus and entorhinal cortex in ADNI

Por A.Meda, Shashwath, Koran, Mary Ellen I., Pryweller, Jennifer R., Vega, Jennifer N., Thornton-Wells, Tricia A.
Publicado em 2012

Auditory Attraction: Activation of visual cortex by music and sound in Williams syndrome

Por Thornton-Wells, Tricia A., Cannistraci, Chris J., Anderson, Adam, Kim, Chai-Youn, Eapen, Mariam, Gore, John C., Blake, Randolph, Dykens, Elisabeth M.
Publicado em 2010

Associations Between KCNJ6 (GIRK2) Gene Polymorphisms and Pain-Related Phenotypes

Por Bruehl, Stephen, Denton, Jerod S., Lonergan, Daniel, Koran, Mary Ellen, Chont, Melissa, Sobey, Christopher, Fernando, Shanik, Bush, William S., Mishra, Puneet, Thornton-Wells, Tricia A.
Publicado em 2013