A5051985478- Genetic factors in colorectal cancer
- BRCA gene mutations in cancer
- Eosinophilic Disorders and Syndromes
- Behavioral Health and Interventions
- Cancer Genomics and Diagnostics
- Smoking Behavior and Cessation
- Pneumocystis jirovecii pneumonia detection and treatment
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Nutrition, Genetics, and Disease
Mayo Clinic in Arizona
2023-2025
University of Nebraska Medical Center
2022
Abstract Background The prognosis in patients with advanced cardiac amyloidosis (CA) remains poor. Objectives We sought to describe survival post heart transplantation (HT) amyloid compared non‐amyloid recipients, highlight waitlist times within the new allocation system across three Organ Procurement and Transplantation Network (OPTN) regions, multiorgan (MOT) hereditary amyloidosis. Methods This is a retrospective review of end‐stage CA who underwent HT at Mayo Clinic from January 2007...
Abstract Introduction This study sought to examine reasons for youth e-cigarette use in association with vaping patterns and cessation behaviors. Aims Methods A national representative sample of current (past 30-day) users grades 6–12 was analyzed using the National Youth Tobacco Survey (NYTS), conducted from January March 2020. An exploratory oblique factor analysis a rotated pattern matrix select salient variable-factor relationships yielded four subscales related use. Multivariate...
The autosomal dominant cancer predisposition disorders hereditary breast and ovarian (HBOC) Lynch syndrome (LS) are genetic conditions for which early identification intervention have a positive effect on the individual public health. goals of this study were to determine whether germline screening using exome sequencing could be used efficiently identify carriers HBOC LS.
Abstract Two inherited autosomal dominant cancer predisposition conditions - BRCA related hereditary breast and ovarian (HBOC) Lynch syndrome (LS) are termed Centers for Disease Control Prevention Tier 1 (CDCT1) genetic conditions, which early identification intervention have a positive impact on public health. Selection of individuals testing these is based personal family history. The goal this study was to evaluate whether screening in tertiary medical center using exome sequencing could...