G. Watts

发表

A progressive translational mouse model of human valosin‐containing protein disease: The VCPR155H/+ mouse

V. Kimonis, J. Mukherjee, J. Vesa, 2013, Muscle & nerve.

Title A progressive translational mouse model of human valosin-containing protein disease : The VCP

V. Kimonis, J. Mukherjee, J. Vesa, 2013 .

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

D. Wallace, V. Kimonis, H. Su, 2010, PloS one.

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

Charles D. Smith, V. Kimonis, J. Mukherjee, 2011, Journal of Molecular Neuroscience.

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

V. Kimonis, S. Donkervoort, G. Watts, 2011 .

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

Charles D. Smith, D. Wallace, V. Kimonis, 2011 .

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

Charles D. Smith, D. Wallace, V. Kimonis, 2009, Neuromuscular Disorders.

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder.

V. Kimonis, J. Vesa, E. Fulchiero, 2008, Biochimica et biophysica acta.

Pathological consequences of VCP mutations on human striated muscle.

E. Wanker, A. Noegel, V. Kimonis, 2007, Brain : a journal of neurology.

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

K. Fliessbach, S. Mehta, V. Hans, 2005, Annals of neurology.

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

Charles D. Smith, S. Mehta, M. Forman, 2008, American journal of medical genetics. Part A.

The Homozygote VCPR155H/R155H Mouse Model Exhibits Accelerated Human VCP-Associated Disease Pathology

R. Edwards, V. Kimonis, N. Khanlou, 2012, PloS one.

mechanism with frontotemporal dementia muscle suggests a common pathogenic TDP-43 accumulation in inclusion body myopathy

Sara E. Miller, P. Hanson, M. Forman, 2009 .

Valosin-Containing Protein (VCP) Disease and Familial Alzheimer’s Disease: Contrasts and Overlaps

Charles D. Smith, V. Kimonis, J. Vesa, 2011 .

The Homozygote VCPR155H/R155H Mouse Model Exhibits Accelerated Human VCP-Associated Disease Pathology

R. Edwards, V. Kimonis, N. Khanlou, 2012, PloS one.

A Progressive Translational Mouse Model of Human VCP Disease: The VCP R155H/+ Mouse

V. Kimonis, J. Vesa, V. Caiozzo, 2013 .

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

A. Pestronk, V. Kimonis, G. Watts, 2003, Neuromuscular Disorders.

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

E. Ringelstein, J. Meuleman, T. Bird, 2005, Nature Genetics.

Primate genome gain and loss: a bone dysplasia, muscular dystrophy, and bone cancer syndrome resulting from mutated retroviral-derived MTAP transcripts.

V. Schramm, S. Mehta, J. Martignetti, 2012, American journal of human genetics.

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

A. Pestronk, S. Mehta, V. Kimonis, 2004, Nature Genetics.

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

S. Greenberg, V. Kimonis, A. Amato, 2007, Muscle & nerve.

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

S. Mehta, V. Kimonis, S. Mumm, 2006, American journal of medical genetics. Part A.

TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia

A. Pestronk, P. Hanson, M. Forman, 2008, Journal of Neurology, Neurosurgery, and Psychiatry.

Novel Ubiquitin Neuropathology in Frontotemporal Dementia With Valosin-Containing Protein Gene Mutations

Charles D. Smith, J. Karlawish, A. Pestronk, 2006, Journal of neuropathology and experimental neurology.

Breech presentation is a risk factor for dysplasia of the femoral trochlea

S. Donell, G. Watts, 2016, Acta orthopaedica.

Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy

T. Bird, P. Chance, G. Watts, 2001, Neurology.

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

S. Mehta, Chengfeng Zhao, V. Kimonis, 2005, Human Genetics.

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

Charles D. Smith, S. Mehta, M. Hutton, 2007, Genetics in Medicine.

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

V. Kimonis, Virginia E Kimonis, Giles D J Watts, 2005, Alzheimer disease and associated disorders.

A case of late-onset proximal and distal muscle weakness

R. Barohn, A. Amato, G. Watts, 2009, Neurology.

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

S. Mehta, L. Hocking, S. Ralston, 2006, Bone.

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

P. Chance, G. Watts, K. O'Briant, 2002, Human Genetics.

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

J. Meuleman, P. Chance, V. Timmerman, 2004, Muscle & nerve.

Molecular basis of hereditary neuropathies.

P. Chance, G. Watts, 2001, Advances in neurology.

Construction of a transcription map around the gene for ataxia telangiectasia: identification of at least four novel genes.

J. Riley, T. Stankovic, P. Byrd, 1997, Genomics.

Genotype–phenotype studies of VCP‐associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

J. Platt, M. Pasquali, K. Osann, 2013, Clinical genetics.

Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

D. Drachman, A. Kaminska, C. Weihl, 2007, Clinical genetics.