Richard Crook

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Matt Baker, Ian R. Mackenzie, Stuart Pickering‐Brown et al. · Nature · 2006 · 2.1K citations

Neurodegenerative Diseases, Alzheimer's Disease, Mendelian Disorder +11

Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy

David F. Tang‐Wai, N. R. Graff-Radford, Bradley F. Boeve et al. · Neurology · 2004 · 625 citations

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Jennifer Gass, Ashley Cannon, Ian R. Mackenzie et al. · Human Molecular Genetics · 2006 · 569 citations

The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families

Robert Clark, M. Hutton, M. Fuldner et al. · Nature Genetics · 1995 · 470 citations

Allelic Variant, Genetic Disorder, Genetics +7

Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis

Nicola J. Rutherford, Yong‐Jie Zhang, Matt Baker et al. · PLoS Genetics · 2008 · 458 citations · Full text

Neurodegenerative Diseases, Ubiquitin Inclusions, Amyotrophic Lateral Sclerosis +13