Analysis of shared heritability in common disorders of the brain.
Times cited: 206
TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosis.
Times cited: 138
Evidence for a role of the rare p.A152T variant in mapt in increasing the risk for FTD-spectrum and Alzheimer's diseases.
Human Molecular Genetics.
Times cited: 126