Childhood-onset schizophrenia case with 2.2 Mb deletion at chromosome 3p12.2–p12.1 and two large chromosomal abnormalities at 16q22.3–q24.3 and Xq23–q28

por Rudd, Danielle, Axelsen, Michael, Epping, Eric A, Andreasen, Nancy, Wassink, Thomas
Publicado 2015

Correlation of CAG repeat length between the maternal and paternal allele of the Huntingtin gene: evidence for assortative mating

por Nopoulos, Peg, Epping, Eric A, Wassink, Tom, Schlaggar, Bradley L, Perlmutter, Joel
Publicado 2011

Subcortical T1-Rho MRI Abnormalities in Juvenile-Onset Huntington’s Disease

por Tereshchenko, Alexander V., Schultz, Jordan L., Kunnath, Ansley J., Bruss, Joel E., Epping, Eric A., Magnotta, Vincent A., Nopoulos, Peg C.
Publicado 2020

Behavioral features in child and adolescent huntingtin gene‐mutation carriers

por Reasoner, Erin E., van der Plas, Ellen, Al‐Kaylani, Hend M., Langbehn, Douglas R., Conrad, Amy L., Schultz, Jordan L., Epping, Eric A., Magnotta, Vincent A., Nopoulos, Peggy C.
Publicado 2022

Depressive symptoms related to low fractional anisotropy of white matter underlying the right ventral anterior cingulate in older adults with atherosclerotic vascular disease

por Bijanki, Kelly R., Matsui, Joy T., Mayberg, Helen S., Magnotta, Vincent A., Arndt, Stephan, Johnson, Hans J., Nopoulos, Peg, Paradiso, Sergio, McCormick, Laurie M., Fiedorowicz, Jess G., Epping, Eric A., Moser, David J.
Publicado 2015