Publications by authors named "D Fasel"

Gyrotrons are essential for electron cyclotron resonance heating in fusion reactors, making efficient operation crucial for advancing fusion energy. Past experiments revealed instability issues due to trapped electrons in the magnetron injection gun (MIG) region, causing undesired currents and operational failures. To address this, tight manufacturing tolerances are required for the MIG geometry [Pagonakis et al.

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Leveraging linkage disequilibrium (LD) patterns as representative of population substructure enables the discovery of additive association signals in genome-wide association studies (GWASs). Standard GWASs are well-powered to interrogate additive models; however, new approaches are required for invesigating other modes of inheritance such as dominance and epistasis. Epistasis, or non-additive interaction between genes, exists across the genome but often goes undetected because of a lack of statistical power.

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The public health impact of genomic screening can be enhanced by cascade testing. However, cascade testing depends on communication of results to family members. While the barriers and facilitators of family communication have been researched following clinical genetic testing, the factors impacting the dissemination of genomic screening results are unknown.

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Article Synopsis
  • Researchers developed multiple polygenic risk scores (PRSs) for breast cancer but their applicability to diverse populations is still uncertain.
  • This study analyzed the effectiveness of these PRSs in a clinical setting, focusing on women of European, African, and Latinx ancestry using data from 39,591 women linked to electronic medical records.
  • Results showed that PRSs were significantly associated with breast cancer risk across all ancestry groups, with the strongest correlation found in women of European ancestry, indicating the potential usefulness of PRSs for risk assessment in diverse populations.
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Article Synopsis
  • Structured representation of clinical genetic results is crucial for enhancing precision medicine and integrating genetic data into electronic health records (EHR).
  • The eMERGE Network's Phase III program transitioned from a commercial XML format to a new standardized format based on HL7® FHIR® for better representation of genetic results.
  • These new standards aim to improve international healthcare interoperability and facilitate broader adoption of standardized practices in health information technology regarding genetic data management.
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