M. Hutton

Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Marc Cruts, Cornelia M. van Duijn, H. Backhovens et al. · Human Molecular Genetics · 1998 · 434 citations · Full text

Genetics, Genetic Epidemiology, Genetic Contribution +17

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

Henry Houlden, Mary V. Baker, Huw R. Morris et al. · Neurology · 2001 · 412 citations

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene

I. R. A. Mackenzie, Matthew Baker, Stuart Pickering‐Brown et al. · Brain · 2006 · 297 citations

Corticobasal Degeneration, Genetics, Disease Gene Identification +18

Genetic association between intronic polymorphism in presenilin-1 gene and late-onset Alzheimer's disease

Michelle Wragg, Chris J. Talbot, M. Hutton et al. · The Lancet · 1996 · 245 citations

Neurodegenerative Diseases, Alzheimer's Disease, Genetics +10

Amyloid β protein (Aβ) deposition in chromosome 14–linked Alzheimer's disease: Predominance of Aβ₄₂₍₄₃₎

D.M.A. Mann, Takeshi Iwatsubo, N. J. Cairns et al. · Annals of Neurology · 1996 · 182 citations