The effects of gender and Catechol O-Methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in Velo-Cardio-Facial Syndrome (22q11.2 Deletion Syndrome): a fMRI st...

Por Coman, Ioana L., Gnirke, Matthew H., Middleton, Frank A., Antshel, Kevin M., Fremont, Wanda, Higgins, Anne Marie, Shprintzen, Robert J., Kates, Wendy R.
Publicado em 2010

White Matter Microstructural Abnormalities of the Cingulum Bundle in Youth with 22q11.2 Deletion Syndrome: Associations with Medication, Neuropsychological Function, and Prodromal...

Por Kates, Wendy R., Olszewski, Amy K., Gnirke, Matthew H., Kikinis, Zora, Nelson, Joshua, Antshel, Kevin M., Fremont, Wanda, Radoeva, Petya D., Middleton, Frank A., Shenton, Martha E., Coman, Ioana L.
Publicado no Schizophr Res (2014)

White Matter Abnormalities in 22q11.2 Deletion Syndrome: Preliminary Associations with the Nogo-66 Receptor Gene and Symptoms of Psychosis

Por Perlstein, Matthew D., Chohan, Moeed R., Coman, Ioana L., Antshel, Kevin M., Fremont, Wanda P., Gnirke, Matthew H., Kikinis, Zora, Middleton, Frank A., Radoeva, Petya D., Shenton, Martha E., Kates, Wendy R.
Publicado em 2013