Back to search

Article

Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care Centre

2024-05-13

Abstract excerpt

<h4>Background: </h4> The findings of variants of uncertain significance (VUS) on a clinical genetic testing report pose a challenge for attending healthcare professionals (HCPs) in patient care. Here, we describe the outcomes of multidisciplinary VUS Rounds, implemented at a neurological disease tertiary care centre, which aid in interpreting and communicating VUS identified in our neurogenetics patient populatio...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
6dc5784b-3c66-5858-9282-d14eaa1a4d96
DOI
10.1101/2024.05.13.24307186
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care CentreDOI 10.1101/2024.05.13.24307186
Select a neighboring publication to make it the new centre.