David G. Ashbrook

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions

Mechanisms of autophagy–lysosome dysfunction in neurodegenerative diseases

A natural mutator allele shapes mutation spectrum variation in mice

Identification of cyclin D1 as a major modulator of 3-nitropropionic acid-induced striatal neurodegeneration