Lista de obras - Kathryn L. McCabe - Dominio Público Uruguay

A Web-Based Telehealth Training Platform Incorporating Automated Nonverbal Behavior Feedback for Teaching Communication Skills to Medical Students: A Randomized Crossover Study

artículo científico publicado en 2016

Application of Synchronous Text-Based Dialogue Systems in Mental Health Interventions: Systematic Review

artículo científico publicado en 2017

Australian Schizophrenia Research Bank: a database of comprehensive clinical, endophenotypic and genetic data for aetiological studies of schizophrenia

artículo científico publicado en 2010

Development and evaluation of an Internet-based program to improve the mental health and wellbeing of young men

Differential susceptibility to performance degradation across categories of facial emotion--a model confirmation

artículo científico publicado en 2003

Divergent patterns of social cognition performance in autism and 22q11.2 deletion syndrome (22q11DS).

artículo científico publicado en 2013

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

artículo científico publicado en 2020

Improving Moderator Responsiveness in Online Peer Support Through Automated Triage

scientific article published on 26 April 2019

Investigating the Lived Experience of Recovery in People Who Hear Voices

artículo científico publicado en 2015

Is theory of mind related to social dysfunction and emotional problems in 22q11.2 deletion syndrome (velo-cardio-facial syndrome)?

artículo científico publicado en 2011

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size

artículo científico publicado en 2018

Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS).

artículo científico publicado en 2014

Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome

artículo científico publicado en 2019

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome