Publications by authors named "Katherine Crawford"

Social service professionals routinely use screening tools to assess for cognitive decline or identify suspected dementia in nursing home residents. Published literature lacks details about the specific tools used and how professionals use and perceive them in practice. The aim of this study is to better understand cognitive screening roles performed by nursing home social service professionals and how they view their use and efficacy.

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Purpose: Children with behavioral issues in residential care settings have high rates of trauma, with a range of trauma experiences such as abuse and neglect, issues with attachment, and multiple disruptions in placements. Staff in these settings should have an understanding of trauma, its impact, and how to engage in trauma-informed practice.

Unlabelled: The purpose of this study was to examine whether a trauma-informed training, developed specifically based on the identified needs of a residential group care facility, had an impact on future staff attitudes and behaviors.

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Non-alcoholic fatty liver disease (NAFLD) is the most pervasive liver pathology worldwide. Here, we demonstrate that the ubiquitin E3 ligase Huwe1 is vital in NAFLD pathogenesis. Using mass spectrometry and RNA sequencing, we reveal that liver-specific deletion of Huwe1 () in 1-year-old mice (approximately middle age in humans) elicits extensive lipid metabolic reprogramming that involves downregulation of lipogenesis and fatty acid uptake, upregulation of fatty acid β-oxidation, and increased oxidative phosphorylation.

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The COVID-19 outbreak in March 2020 resulted in a shift to telemedicine for cancer genetic counseling (GC). The objective of this study was to determine the effect of telehealth (TH) services on patient acceptance of recommended genetic testing, time to test completion, and follow-up test-disclosure GC appointment, as well as compliance with National Comprehensive Cancer Network (NCCN) recommendations for medical screenings when testing positive for a genetic variant. Data for this retrospective cohort study were collected at a tertiary-care academic health center using the electronic medical record and laboratory portal.

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  • During the Zika Virus Response by the CDC, birth defects surveillance was adapted to track issues potentially linked to Zika virus infections in pregnant women from January 2016 to June 2017 across 22 U.S. states and territories.
  • Researchers categorized areas by their level of Zika transmission and calculated the prevalence of brain and eye defects per 10,000 live births, finding significant increases in areas with widespread transmission.
  • Nine specific birth defects showed notably higher prevalence in regions with extensive Zika spread, particularly intracranial calcifications and chorioretinal abnormalities, suggesting that ongoing monitoring of certain defects could be beneficial.
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To evaluate the hypothesis that patients with a history of intravenous drug misuse (IVDM) initiated on weight-based heparin infusions require higher than expected infusion rates to achieve therapeutic activated partial thromboplastin time (aPTT). This study is a multicenter, retrospective chart review of patients with a history of IVDM who were admitted to an acute care site between 10/1/2015 and 9/30/2020 and treated with continuous heparin infusions. Patients were identified using ICD9 and ICD10 codes and included if they had a documented history of IVDM within the past six months.

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Animal and human studies have documented the existence of developmental windows (or sensitive periods) when experience can have lasting effects on brain structure or function, behavior, and disease. Although sensitive periods for depression likely arise through a complex interplay of genes and experience, this possibility has not yet been explored in humans. We examined the effect of genetic pathways regulating sensitive periods, alone and in interaction with common childhood adversities, on depression risk.

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We propose a dedicated research effort on the determinants of settlement persistence in the ancient world, with the potential to significantly advance the scientific understanding of urban sustainability today. Settlements (cities, towns, villages) are locations with two key attributes: They frame human interactions and activities in space, and they are where people dwell or live. Sustainability, in this case, focuses on the capacity of structures and functions of a settlement system (geography, demography, institutions) to provide for continuity of safe habitation.

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  • The study investigates the genetic basis of lacunar stroke, which is often not well understood, by analyzing data from newly recruited patients and existing genome-wide association studies (GWAS) to identify new genetic associations.
  • A pooled analysis included over 7,000 cases of lacunar stroke and nearly 255,000 controls, incorporating various ancestry groups, and revealed five loci significantly associated with the condition, along with additional loci linked to related brain traits.
  • The findings contribute to understanding the genetic underpinnings of lacunar stroke and highlight potential pathways and risk factors involved in the disease's development.
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Purpose: Pathogenic variants in SCN2A cause a wide range of neurodevelopmental phenotypes. Reports of genotype-phenotype correlations are often anecdotal, and the available phenotypic data have not been systematically analyzed.

Methods: We extracted phenotypic information from primary descriptions of SCN2A-related disorders in the literature between 2001 and 2019, which we coded in Human Phenotype Ontology (HPO) terms.

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Cancer is a major public health problem and the second leading cause of death worldwide. The burden of cancer continues to grow and is projected to double by 2040. This situation calls for coordinated action and emphasizes the need to join efforts on worldwide initiatives, including World Cancer Research Day (WCRD), which aims to create and consolidate a yearly momentum to raise awareness and commitment for research on cancer.

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Social cognitive deficits can have many negative consequences, spanning social withdrawal to psychopathology. Prior work has shown that child maltreatment may associate with poorer social cognitive skills in later life. However, no studies have examined this association from early childhood into adolescence.

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HUWE1 is a HECT-domain ubiquitin E3 ligase expressed in various tissues. Although HUWE1 is known to promote degradation of the tumor suppressor p53, given a growing list of its substrates, functions of HUWE1 remain elusive. Here, we investigated the role of HUWE1 in the female reproductive system.

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Pet ownership is common. Growing evidence suggests children form deep emotional attachments to their pets. Yet, little is known about children's emotional reactions to a pet's death.

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Article Synopsis
  • * From January 2016 to June 2017, the CDC studied over 2 million live births and identified 3,359 cases of birth defects that may be linked to Zika virus, with a prevalence rate of 1.7 per 1,000 live births.
  • * In regions with widespread Zika transmission, birth defects increased significantly, peaking at 5.6 per 1,000 live births in early 2017, indicating a fourfold rise compared to the same period the previous year.
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  • Genetic studies on intracerebral hemorrhage (ICH) have primarily involved white participants, raising concerns about how genetic risk varies in nonwhite populations due to different coexposures.
  • The objective of the study was to analyze how the APOE ε4 allele, a significant genetic risk factor for ICH, relates to ICH risk across different racial and ethnic groups.
  • The study included over 13,000 participants and found that while the APOE ε2 and ε4 alleles were linked to increased lobar ICH risk in white participants, no such associations were observed in Hispanic and black participants, even after controlling for hypertension.
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We sought to determine whether a small pool of ancestry-informative DNA markers (AIMs) improves modeling of intracerebral hemorrhage (ICH) risk in heterogeneous populations, compared with self-identified race/ethnicity (SIRE) alone. We genotyped 15 preselected AIMs to perform principal component (PC) analysis in the ERICH study (a multi-center case-control study of ICH in whites, blacks, and Hispanics). We used multivariate logistic regression and tests for independent samples to compare associations for genetic ancestry and SIRE with ICH-associated vascular risk factors (VRFs).

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Background: Emotion recognition skills are essential for social communication. Deficits in these skills have been implicated in mental disorders. Prior studies of clinical and high-risk samples have consistently shown that children exposed to adversity are more likely than their unexposed peers to have emotion recognition skills deficits.

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Background: Although childhood adversity is a potent determinant of psychopathology, relatively little is known about how the characteristics of adversity exposure, including its developmental timing or duration, influence subsequent mental health outcomes. This study compared three models from life course theory (recency, accumulation, sensitive period) to determine which one(s) best explained this relationship.

Methods: Prospective data came from the Avon Longitudinal Study of Parents and Children (n = 7476).

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Background And Objective: Due to conflicting results in multiple studies, uncertainty remains regarding sex differences in severity and mortality after intracerebral hemorrhage (ICH). We investigated the impact of sex on ICH severity, expansion, and mortality.

Methods: We analyzed prospectively collected ICH patients and assessed clinical variables and mortality rate.

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Low levels of serum albumin may increase the risk of infections and mortality in critically ill patients. We tested the hypothesis that admission hypoalbuminemia predicted infectious complications and poor outcome in subjects with acute intracerebral hemorrhage (ICH). We analyzed a single center cohort of ICH patients collected between 1994 and 2015.

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