Phenomenological features and clinical impact of affective disorders in OCD: A focus on the bipolar disorder and OCD connection

Por Timpano, Kiara R., Rubenstein, Liza M., Murphy, Dennis L.
Publicado em 2011

The Relationship between Family Functioning and Adolescent Depressive Symptoms: The Role of Emotional Clarity

Por Freed, Rachel D., Rubenstein, Liza M., Daryanani, Issar, Olino, Thomas M., Alloy, Lauren B.
Publicado no J Youth Adolesc (2016)

Cognitive Attributions in Depression: Bridging the Gap between Research and Clinical Practice

Por Rubenstein, Liza M., Freed, Rachel D., Shapero, Benjamin G., Fauber, Robert L., Alloy, Lauren B.
Publicado no J Psychother Integr (2016)

The cyclical nature of depressed mood and future risk: Depression, rumination, and deficits in emotional clarity in adolescent girls

Por Rubenstein, Liza M., Hamilton, Jessica L., Stange, Jonathan P., Flynn, Megan, Abramson, Lyn Y., Alloy, Lauren B.
Publicado no J Adolesc (2015)

Anxiety and affective disorder comorbidity related to serotonin and other neurotransmitter systems: obsessive–compulsive disorder as an example of overlapping clinical and genetic...

Por Murphy, Dennis L., Moya, Pablo R., Fox, Meredith A., Rubenstein, Liza M., Wendland, Jens R., Timpano, Kiara R.
Publicado em 2013

Deficits in Emotional Clarity and Vulnerability to Peer Victimization and Internalizing Symptoms among Early Adolescents

Por Hamilton, Jessica L., Kleiman, Evan M., Rubenstein, Liza M., Stange, Jonathan P., Flynn, Megan, Abramson, Lyn Y., Alloy, Lauren B.
Publicado no J Youth Adolesc (2015)

Trait Affect, Emotion Regulation, and the Generation of Negative and Positive Interpersonal Events

Por Hamilton, Jessica L., Burke, Taylor A., Stange, Jonathan P., Kleiman, Evan M., Rubenstein, Liza M., Scopelliti, Kate A., Abramson, Lyn Y., Alloy, Lauren B.
Publicado no Behav Ther (2017)

Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette disorder

Por Moya, Pablo R, Wendland, Jens R, Rubenstein, Liza M, Timpano, Kiara R, Heiman, Gary A, Tischfield, Jay A, King, Robert A, Andrews, Anne M, Ramamoorthy, Samanda, McMahon, Francis J, Murphy, Dennis L
Publicado em 2013

Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes

Por Moya, Pablo R, Dodman, Nicholas H, Timpano, Kiara R, Rubenstein, Liza M, Rana, Zaker, Fried, Ruby L, Reichardt, Louis F, Heiman, Gary A, Tischfield, Jay A, King, Robert A, Galdzicka, Marzena, Ginns, Edward I, Wendland, Jens R
Publicado em 2013