Open Access. Powered by Scholars. Published by Universities.®
- Keyword
-
- Amplitude (1)
- Amygdala (1)
- Attention Deficit Hyperactivity Disorder (1)
- Autosomal recessive (1)
- Behavioral neuroscience (1)
-
- Brain Volume (1)
- Conduct Disorder (1)
- EEG (1)
- Family Income (1)
- Genetic disorder (1)
- Integration (1)
- JOVI (1)
- Knockout mice (1)
- Latency (1)
- MRI (1)
- Oppositional Defiant Disorder (1)
- Orbitofrontal Cortex (1)
- P200 (1)
- SNAP (1)
- Schizophrenia (1)
- Sensorineural hearing loss (1)
- Ultrasonic vocalizations (1)
- Ush2a (1)
- Usher syndrome (1)
- Usher syndrome type 2 (1)
Articles 1 - 3 of 3
Full-Text Articles in Cognitive Psychology
The Relationship Between Amygdala And Orbitofrontal Cortex Volume In The Context Of Oppositional Defiant Disorder, Rahul Alla
Honors Scholar Theses
Disobedient and rebellious attitude in children is on the rise and this type of behavior is categorized as Oppositional Defiant Disorder (ODD). ODD in children can be identified as a persistent pattern of angry or irritable mood, argumentative or defiant behavior or vindictiveness toward others according to the Diagnostic and Statistical Manual (DSM-5, Fifth Edition) of Mental Disorders.1 Children with ODD typically have difficulty regulating and processing their emotions. Issues with regulating emotions is defined as the process by which individuals “influence which emotions they have, when they have them, and how they experience and express them”.2 Dysregulation of emotions …
The Ush2a Gene: An Analysis Of Ultrasonic Vocalizations In A Mouse Model Of Usher Syndrome Type 2, Kiana R. Akhundzadeh
The Ush2a Gene: An Analysis Of Ultrasonic Vocalizations In A Mouse Model Of Usher Syndrome Type 2, Kiana R. Akhundzadeh
Honors Scholar Theses
Usher syndrome type 2 is a complex autosomal recessive genetic disorder that is characterized by moderate to severe congenital sensorineural hearing loss, the onset of retinitis pigmentosa in the second decade of life, and in some cases, vestibular dysfunction. Mutations in the USH2A gene account for 85% of cases of type 2. The USH2A gene is responsible for encoding the protein usherin, which has an important role in the development and function of inner ear hair cells and retinal photoreceptors. Until recently, it has been believed that carriers of the USH2A mutation were phenotype free. However, recent data has suggested …
Electrophysiological Changes In P200 Latency And Amplitude Of Jittered Orientation Visual Integration Task In Healthy Participants: A Multi-Block Design Eeg Study, Monika M. Rozynski, Chi-Ming Chen
Electrophysiological Changes In P200 Latency And Amplitude Of Jittered Orientation Visual Integration Task In Healthy Participants: A Multi-Block Design Eeg Study, Monika M. Rozynski, Chi-Ming Chen
Honors Scholar Theses
Visual integration, the ability to fuse environmental information such as light, color, shades, and motion to form a representation of a whole cohesive higher-order visual image, is impaired in persons with schizophrenia. Little is known how the P200 component, an event-related potential (ERP) in the parieto-occipital region, is affected in persons with schizophrenia while they perform visual integration tasks, when compared to healthy persons. This study administered Gabor contours that varied in high and low degrees of orientational jitter through the Jitter Orientation Visual Integration (JOVI) task to investigate visual integration by analyzing latency and amplitude of the P200 component. …