Author

Giles D. J. Watts

Observed names: G.D.J. Watts, Giles D J Watts, Giles D. J Watts, Giles D. Watts, Giles D.J Watts, Giles D.J. Watts, Giles Dj Watts

Observed institutions: University of East Anglia, Brigham and Women's Hospital, Boston Children's Hospital, Seattle Children's Hospital, Mayo Clinic, Harvard University, University of Washington, University of Washington Medical Center, University of Kansas Medical Center, University of Birmingham

OpenAlex ID: A5111679916

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

2004 · Giles D J Watts, Jill Wymer, et al. · Nature Genetics · 1,378

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Mutations in SEPT9 cause hereditary neuralgic amyotrophy

2005 · Gregor Kuhlenbäumer, Mark C Hannibal, et al. · Nature Genetics · 260

Novel Ubiquitin Neuropathology in Frontotemporal Dementia WithValosin-Containing ProteinGene Mutations

2006 · Mark S. Forman, Ian R. Mackenzie, et al. · Journal of Neuropathology & Experimental Neurology · 226

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

2005 · Rolf Schröder, Giles D. J. Watts, et al. · Annals of Neurology · 176

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

2008 · Virginia. E. Kimonis, Sarju G. Mehta, et al. · American Journal of Medical Genetics Part A · 174

The Multiple Faces of Valosin-Containing Protein-Associated Diseases: Inclusion Body Myopathy with Paget’s Disease of Bone, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis

2011 · Angèle Nalbandian, Sandra Donkervoort, et al. · Journal of Molecular Neuroscience · 135

VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease

2010 · Mallikarjun Badadani, Angèle Nalbandian, et al. · PLoS ONE · 121

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Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts

2009 · Jouni Vesa, Hailing Su, et al. · Neuromuscular Disorders · 61

Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes

2003 · Giles D.J Watts, M Thorne, et al. · Neuromuscular Disorders · 58

Autosomal Dominant Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia

2005 · Virginia E Kimonis, Giles D. J Watts · Alzheimer Disease & Associated Disorders · 56

APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)

2007 · Sarju G. Mehta, Giles Dj Watts, et al. · Genetics in Medicine · 53

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Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone

2005 · Gavin J.A. Lucas, Sarju G. Mehta, et al. · Bone · 39

Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy

2001 · Pierre–Yves Jeannet, Giles D.J. Watts, et al. · Neurology · 39

Evidence for genetic heterogeneity in hereditary neuralgic amyotrophy

2001 · G.D.J. Watts, K.C. O’Briant, et al. · Neurology · 32

Nuclear localization of valosin‐containing protein in normal muscle and muscle affected by inclusion‐body myositis

2007 · Steven A. Greenberg, Giles D. Watts, et al. · Muscle & Nerve · 24

Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families

2001 · Giles D. Watts, Kathy C. O'Briant, et al. · Human Genetics · 23

Construction of a Transcription Map around the Gene for Ataxia Telangiectasia: Identification of at Least Four Novel Genes

1997 · Tatjana Stankovic, Philip J. Byrd, et al. · Genomics · 23

Manifestations in a family with autosomal dominant bone fragility and limb‐girdle myopathy

2006 · Sarju G. Mehta, Giles D.J. Watts, et al. · American Journal of Medical Genetics Part A · 11

A case of late-onset proximal and distal muscle weakness

2009 · Richard J. Barohn, Giles D.J. Watts, et al. · Neurology · 5

Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: a novel locus for a musculoskeletal syndrome

2005 · Giles D.J. Watts, Sarju G. Mehta, et al. · Human Genetics · 5

Molecular basis of hereditary neuropathies.

2002 · Giles D J Watts, Phillip F Chance · PubMed · 3

Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy

2004 · Gert Hünermund, Anja Schirmacher, et al. · Muscle & Nerve · 1

Clinical Spectrum of VCP Myopathy, Paget Disease, and fronTotemporal Dementia: Experimental Models and Potential Treatments

2011 · Virginia E. Kimonis, Eric Dec, et al. · Wiley eBooks

Works count: 24

Citation count: 2,903

H-index: 17

I10-index: 18