Giles D. Watts

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

Giles D. Watts, Jill Wymer, Margaret J. Kovach et al. · Nature Genetics · 2004 · 1.4K citations · Full text

Mutant Valosin-containing Protein, Alzheimer's Disease, Inclusion Body Myopathy +9

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis et al. · Nature Genetics · 2005 · 259 citations

Neurodegenerative Diseases, Amyotrophic Lateral Sclerosis, Molecular Neuroscience +8

Novel Ubiquitin Neuropathology in Frontotemporal Dementia With<i>Valosin-Containing Protein</i>Gene Mutations

Mark S. Forman, Ian R. Mackenzie, Nigel J. Cairns et al. · Journal of Neuropathology & Experimental Neurology · 2006 · 220 citations · Full text

Genetics, Pathology, Disease Gene Identification +19

Mutant valosin‐containing protein causes a novel type of frontotemporal dementia

Rolf Schröder, Giles D. Watts, Sarju Mehta et al. · Annals of Neurology · 2005 · 176 citations · Full text

Mutant Vcp, Genetics, Pathology +16

Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia

Virginia Kimonis, Sarju Mehta, Erin Fulchiero et al. · American Journal of Medical Genetics Part A · 2008 · 173 citations · Full text