Consensus recommendations for next-generation sequencing based genetic testing in Rare Neurological diseases

EJHG 2026: www.nature.com/ejhg

Consensus recommendations for NGS testing in rare neurological diseases
Developed by experts from ERN-RND and EMQN, this publication presents 27 consensus recommendations to improve the quality, consistency and harmonisation of next-generation sequencing (NGS) testing, interpretation and reporting for rare neurological diseases across Europe.
Consensus recommendations for next-generation sequencingbased genetic testing in Rare Neurological diseases