Giles D. Watts - Concepedia

Author

Giles D. Watts

Also Known As

G. D. WATTS, G.D.J. Watts, Giles 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

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Boston Children's Hospital Harvard University Washington University in St. Louis University of Kentucky University of California, Irvine

About

Giles D. Watts is an author at Boston Children's Hospital specializing in medicine, genetics, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	2.4K
2	Social Sciences	2	2	479
3	Cell Biology	2	2	116
4	Cellular Physiology	1	1	60
5	Molecular Biology	1	1	56

Giles D. Watts

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
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, Nature Genetics Mutant Valosin-containing ProteinAlzheimer's DiseaseInclusion Body MyopathyPathologyDegenerative Disease	2004	1.4K
Mutations in SEPT9 cause hereditary neuralgic amyotrophy Gregor Kuhlenbäumer, Mark Hannibal, Eva Nelis, Nature Genetics Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMolecular NeuroscienceGenetic DisorderGenetics	2005	259
Novel Ubiquitin Neuropathology in Frontotemporal Dementia With<i>Valosin-Containing Protein</i>Gene Mutations Mark S. Forman, Ian R. Mackenzie, Nigel J. Cairns, Journal of Neuropathology & Experimental Neurology GeneticsPathologyDisease Gene IdentificationUbiquitin PathologySocial Sciences	2006	220
Mutant valosin‐containing protein causes a novel type of frontotemporal dementia Rolf Schröder, Giles D. Watts, Sarju Mehta, Annals of Neurology Mutant VcpGeneticsPathologyDisease Gene IdentificationMendelian Disorder	2005	176
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia Virginia Kimonis, Sarju Mehta, Erin Fulchiero, American Journal of Medical Genetics Part A	2008	173
VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease Mallikarjun Badadani, Angèle Nalbandian, Giles D. Watts, PLoS ONE	2010	122
Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts Jouni Vesa, Hailing Su, Giles D. Watts, Neuromuscular Disorders Inclusion BodyAutophagyHistopathologyPathologyCell Fusion	2009	60
Autosomal Dominant Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia Virginia Kimonis, Giles D. Watts Alzheimer Disease & Associated Disorders GeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationOrthopaedic Surgery	2005	56
Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes Giles D. Watts, Marielle Thorne, Margaret J. Kovach, Neuromuscular Disorders Chromosome 9PGenetic DisorderMedicineGeneticsPathology	2003	54
APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD) Sarju Mehta, Giles D. Watts, Jennifer Adamson, Genetics in Medicine Neurodegenerative DiseasesMedicineDementiaGeneticsFrontotemporal Dementia	2007	53

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