Combining rare genetic variant burden scores with common variant polygenic risk scores will benefit diagnosis and prognosis in psychiatry

Neuroscience Applied 2026 Open access

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Authors: E.F. Osimo, F. Mazzarotto, G. Murray
DOI: 10.1016/j.nsa.2025.106396
Cited by: 0

Fields of Study & Subjects

Genetic Associations and Epidemiology Genomics and Rare Diseases BRCA gene mutations in cancer

Publication details

Journal / source
Neuroscience Applied
Volume
5
Pages
106396–106396
Publication date
1 January 2026
Language
EN