Publications by authors named "Carolyn Chow"

Article Synopsis
  • Some people with dementia and their families prefer to stay at home as they feel it's the best care, but this isn't the same for everyone.
  • A study with interviews found that many families avoid moving to care facilities until it's absolutely necessary, often because of fear or guilt.
  • It's important for care programs to consider all the reasons families make decisions about where to live and to help them understand their options better.
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Background: Many patients hospitalized for COVID-19 experience prolonged symptoms months after discharge. Little is known abou t patients' personal experiences recovering from COVID-19 in the United States (US), where medically underserved populations are at particular risk of adverse outcomes.

Objective: To explore patients' perspectives on the impact of COVID-19 hospitalization and barriers to and facilitators of recovery 1 year after hospital discharge in a predominantly Black American study population with high neighborhood-level socioeconomic disadvantage.

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Article Synopsis
  • Genomic sequencing is increasing, making it hard to offer genetic counseling to everyone, so a hybrid approach of in-person communication for actionable results and mail for other results is being explored.
  • In a study, participants who received neutral genomic screening results by mail reported high satisfaction and generally understood their results, though a few had misunderstandings about their disease risk.
  • The study found that receiving neutral results by mail did not lead to distress or negative health behavior changes, but some individuals may still benefit from extra genetic counseling for context regarding their results.
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Background: 22q11.2 Microdeletion syndrome (22q11DS) is associated with elevated rates of autism spectrum disorders (ASDs), although the diagnosis is controversial. In order to determine whether there is a biological substrate of ASD in 22q11DS, we examined neurocognitive and structural neuroanatomic differences between those with 22q11DS and an ASD diagnosis (22q11DS-ASD+) and those with 22q11DS without ASD (22q11DS-ASD-); we then determined whether these differences were better characterized within a categorical or dimensional framework.

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22q11.2 deletion syndrome (22q11DS) is a neurogenetic disorder associated with elevated rates of developmental neuropsychiatric disorders and impaired executive function (EF). Disrupted brain structure-function relationships may underlie EF deficits in 22q11DS.

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Background: 22q11.2 Deletion Syndrome (22q11DS) represents one of the greatest known genetic risk factors for the development of psychotic illness, and is also associated with high rates of autistic spectrum disorders (ASD) in childhood. We performed integrated genomic analyses of 22q11DS to identify genes and pathways related to specific phenotypes.

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22q11.2 Microdeletion Syndrome (22q11DS) is a highly penetrant genetic mutation associated with a significantly increased risk for psychosis. Aberrant neurodevelopment may lead to inappropriate neural circuit formation and cerebral dysconnectivity in 22q11DS, which may contribute to symptom development.

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Introduction: 22q11.2 deletion syndrome (22q11DS) represents one of the largest known genetic risk factors for psychosis, yet the neurobiological mechanisms underlying symptom development are not well understood. Here we conducted a cross-sectional study of 22q11DS to decompose cortical volume into its constituent parts, cortical thickness (CT) and surface area (SA), which are believed to have distinct neurodevelopmental origins.

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22q11.2 deletion syndrome (22q11DS) is a genetic mutation associated with disorders of cortical connectivity and social dysfunction. However, little is known about the functional connectivity (FC) of the resting brain in 22q11DS and its relationship with social behavior.

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Article Synopsis
  • * A study analyzed 389 DNA samples from families with 22q11DS and found a significant bias for the deletion to originate from the mother (56% maternal vs. 44% paternal).
  • * The research also indicated that maternal age at conception was around 29.5 years, similar to general population trends, and suggested that higher female recombination rates in this chromosome region may contribute to the maternal bias in origins.
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22q11.2 deletion syndrome (22qDS) represents one of the largest known genetic risk factors for schizophrenia. Approximately 30% of individuals with 22qDS develop psychotic illness in adolescence or young adulthood.

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  • Velo-cardio-facial syndrome (VCFS) is linked to a genetic mutation that raises the risk of Autism Spectrum Disorder (ASD), and this study focused on analyzing Theory of Mind (ToM) skills in individuals with VCFS compared to typically developing individuals.
  • A video-based task was used to evaluate participants' ability to understand complex mental states (ToM condition) and simple movements (Random condition) across two universities.
  • Results showed that individuals with VCFS, regardless of an ASD diagnosis, performed worse in understanding mental states, suggesting that these social perception difficulties contribute to challenges in real-life social interactions and highlighting the need for tailored interventions.
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Do graduate record examination (GRE) scores serve as strong predictors of student success in graduate school in nursing, and if so, is the extent to which they may indicate success outweighed by their perceived role as a barrier to application to graduate school in nursing? Academic ability, defined as cumulative grade point average (GPA), was used as the outcome indicator for success in graduate school and was compared with admission GRE scores for 217 students admitted to graduate programs at the University of Washington School of Nursing over a 1-year period. The GRE presented a large barrier to application that far outweighed the limited benefit of predicting 5% to 8% of explained variance in GPA.

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