Introduction: Williams Syndrome

Por Morris, Colleen A.
Publicado em 2010

Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and E...

Por Mervis Carolyn B, Morris Colleen A, Osborne Lucy R
Publicado em 2011-02-01

BAC-FISH refutes report of an 8p22–8p23.1 inversion or duplication in 8 patients with Kabuki syndrome

Por Kimberley, Kendra W, Morris, Colleen A, Hobart, Holly H
Publicado em 2006

Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and E...

Por Morris, Colleen A, Mervis, Carolyn B, Osborne, Lucy R
Publicado em 2011

The Effect of Football Shoulder Pads on Pulmonary Function

Por Coast, J. Richard, Baronas, Jessica L., Morris, Colleen, Willeford, K. Sean
Publicado em 2005

Longitudinal Assessment of Intellectual Abilities of Children with Williams Syndrome: Multilevel Modeling of Performance on the Kaufman Brief Intelligence Test-2

Por Mervis, Carolyn B., Kistler, Doris J., John, Angela E., Morris, Colleen A.
Publicado em 2012

Genetic Counseling of Adults with Williams Syndrome: A First Study

Por Farwig, Katrina, Harmon, Amanda G., Fontana, Kristina M., Mervis, Carolyn B., Morris, Colleen A.
Publicado em 2010

Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome

Por Morris, Colleen A., Pani, Ariel M., Mervis, Carolyn B., Rios, Cecilia M., Kistler, Doris J., Gregg, Ronald G.
Publicado em 2010

Abnormalities in neural processing of emotional stimuli in Williams syndrome vary according to social vs. non-social content

Por Muñoz, Karen E., Meyer-Lindenberg, Andreas, Hariri, Ahmad R., Mervis, Carolyn B., Mattay, Venkata S., Morris, Colleen A., Berman, Karen Faith
Publicado em 2009

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23

Por Strong, Emma, Butcher, Darci T., Singhania, Rajat, Mervis, Carolyn B., Morris, Colleen A., De Carvalho, Daniel, Weksberg, Rosanna, Osborne, Lucy R.
Publicado no Am J Hum Genet (2015)

The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and function

Por Jabbi, Mbemba, Kippenhan, J. Shane, Kohn, Philip, Marenco, Stefano, Mervis, Carolyn B., Morris, Colleen A., Meyer-Lindenberg, Andreas, Berman, Karen Faith
Publicado em 2012

The Common Inversion of the Williams–Beuren Syndrome Region at 7q11.23 Does Not Cause Clinical Symptoms

Por Tam, Elaine, Young, Edwin J., Morris, Colleen A., Marshall, Christian R., Loo, Wayne, Scherer, Stephen W., Mervis, Carolyn B., Osborne, Lucy R.
Publicado em 2008

A Genetic Model for Understanding Higher Order Visual Processing: Functional Interactions of the Ventral Visual Stream in Williams Syndrome

Por Sarpal, Deepak, Buchsbaum, Bradley R., Kohn, Philip D., Kippenhan, J. Shane, Mervis, Carolyn B., Morris, Colleen A., Meyer-Lindenberg, Andreas, Berman, Karen Faith
Publicado em 2008

Retinotopically defined primary visual cortex in Williams syndrome

Por Olsen, Rosanna K., Kippenhan, J. Shane, Japee, Shruti, Kohn, Philip, Mervis, Carolyn B., Saad, Ziad S., Morris, Colleen A., Meyer-Lindenberg, Andreas, Berman, Karen Faith
Publicado em 2009

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome

Por Hobart, Holly H., Morris, Colleen A., Mervis, Carolyn B., Pani, Ariel M., Kistler, Doris J., Rios, Cecilia M., Kimberley, Kendra W., Gregg, Ronald G., Bray-Ward, Patricia
Publicado em 2010

Children with 7q11.23 Duplication Syndrome: Psychological Characteristics

Por Mervis, Carolyn B., Klein-Tasman, Bonita P., Huffman, Myra J., Velleman, Shelley L., Pitts, C. Holley, Henderson, Danielle R., Woodruff-Borden, Janet, Morris, Colleen A., Osborne, Lucy R.
Publicado no Am J Med Genet A (2015)

Duplication of GTF2I Results in Separation Anxiety in Mice and Humans

Por Mervis, Carolyn B., Dida, Joana, Lam, Emily, Crawford-Zelli, Nicole A., Young, Edwin J., Henderson, Danielle R., Onay, Tuncer, Morris, Colleen A., Woodruff-Borden, Janet, Yeomans, John, Osborne, Lucy R.
Publicado em 2012

Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome

Por Meyer-Lindenberg, Andreas, Mervis, Carolyn B., Sarpal, Deepak, Koch, Paul, Steele, Sonya, Kohn, Philip, Marenco, Stefano, Morris, Colleen A., Das, Saumitra, Kippenhan, Shane, Mattay, Venkata S., Weinberger, Daniel R., Berman, Karen Faith
Publicado em 2005

Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome

Por Marenco, Stefano, Siuta, Michael A., Kippenhan, J. Shane, Grodofsky, Samuel, Chang, Wei-li, Kohn, Philip, Mervis, Carolyn B., Morris, Colleen A., Weinberger, Daniel R., Meyer-Lindenberg, Andreas, Pierpaoli, Carlo, Berman, Karen Faith
Publicado em 2007

Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome

Por Pani, Ariel M., Hobart, Holly H., Morris, Colleen A., Mervis, Carolyn B., Bray-Ward, Patricia, Kimberley, Kendra W., Rios, Cecilia M., Clark, Robin C., Gulbronson, Maricela D., Gowans, Gordon C., Gregg, Ronald G.
Publicado em 2010