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Academic

Dr Giles Watts

Job Title Contact Location
Lecturer in Cell Biology/Biochemistry  Giles dot Watts at uea dot ac dot uk
Tel: +44 (0)1603 59 1159  
Bio-Medical Research Centre (BMRC) 02.01B 
  • Publications
Jump to: Article
Number of items: 17.

Article

Nalbandian, A, Donkervoort, S, Dec, E, Badadani, M, Katheria, V, Rana, P, Nguyen, C, Mukherjee, J, Caiozzo, V, Martin, B, Watts, GD, Vesa, J, Smith, C and Kimonis, VE (2011) The Multiple Faces of Valosin-Containing Protein-Associated Diseases: Inclusion Body Myopathy with Paget's Disease of Bone, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis. Journal of Molecular Neuroscience, Epub ahead of print.

Vij, Neeraj, Badadani, Mallikarjun, Nalbandian, Angèle, Watts, Giles D, Vesa, Jouni, Kitazawa, Masashi, Su, Hailing, Tanaja, Jasmin, Dec, Eric, Wallace, Douglas C., Mukherjee, Jogeshwar, Caiozzo, Vincent, Warman, Matthew and Kimonis, Virginia E. (2010) VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease. PLoS ONE, 5 (10). e13183. ISSN 1932-6203

Barohn, RJ, Watts, GD and Amato, AA (2009) A case of late-onset proximal and distal muscle weakness. Neurology, 73 (19). pp. 1592-1597.

Vesa, J, Su, H, Watts, GD, Krause, S, Walter, MC, Martin, B, Smith, C, Wallace, DC and Kimonis, VE (2009) Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts. Neuromuscul Disord, 19 (11). pp. 766-772.

Kimonis, VE, Fulchiero, EC, Vesa, J and Watts, GD (2008) VCP Disease associated with myopathy, Paget Disease of Bone and Frontotemporal Dementia: Review of a new disorder. Biochimica et Biophysica Acta, 1782 (12). pp. 744-748.

Kimonis, VE, Mehta, SG, Fulchiero, EC, Thomasova, D, Pasquali, M, Boycott, K, Neilan, EG, Kartashov, A, Forman, MS, Tucker, S, Kimonis, K, Mumm, S, Whyte, MP, Smith, CD and Watts, GD (2008) Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia. Am J Med Genet, 46A. pp. 745-757.

Wiehl, CC, Temiz, P, Miller, SE, Watts, GD, Smith, C, Forman, M, Hanson, PI, Kimonis, VE and Pestronk, A (2008) TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia. J Neurol Neurosurg Psychiatry, 79 (10). pp. 1186-1189.

Greenberg, SA, Watts, GD, Kimonis, VE, Amato, AA and Pinkus, JL (2007) Nuclear localization of valosin-containing protein in normal muscle and muscle affected by inclusion-body myositis. Muscle Nerve, 36 (4). pp. 447-454.

Mehta, SG, Watts, GD, Adamson, AL, Hutton, M, Umberger, G, Xiong, S, Ramdeen, S, Lovell, MA, Kimonis, VE and Smith, CD (2007) APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD). Genet Med, 9 (1). pp. 9-13.

Watts, GD, Thomasova, D, Ramdeen, SK, Fulchiero, EC, Mehta, SG, Drachman, DA, Weihl, CC, Jamrozik, Z, Kwiecinski, H, Kaminska, A and Kimonis, VE (2007) Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. Clin Genet, 72. pp. 420-426.

Forman, MS, Mackenzie, IR, Cairns, NJ, Swanson, E, Boyer, PJ, Drachman, DA, Jhaveri, BS, Karlawish, JH, McKeel, DW, Pestronk, A, Smith, TW, Watts, GD, Markesbery, WR, Smith, CD and Kimonis, VE (2006) Novel ubiquitin neuropathology in frontotemporal dementia with VCP gene mutations. J. Neuropathol. Exp. Neurol, 65 (6). pp. 571-581.

Hubbers, CU, Clemen, CS, Kesper, K, Boddrich, A, Hofmann, A, Kamarainen, O, Tolksdorf, K, Stumpf, M, Reichelt, J, Roth, U, Krause, S, Watts, GD, Kimonis, VE, Wattjes, MP, Reimann, J, Thal, DR, Biermann, K, Evert, O, Lochmuller, H, Wanker, EE, Schoser, BG, Noegel, AA and Schroder, R (2006) Pathological consequences of VCP mutations on human striated muscle. Brain, 130 (2). pp. 381-393.

Mehta, SG, Watts, GD, Mumm, S, Hamilton, SJ, Ramdeen, S, Seton, M, Briggs, C, Whyte, MP, McGillivray, B and Kimonis, VE (2006) Manifestations in a Family with Autosomal Dominant Bpne Fragility and Limb-girdle Myopathy. Am J Med Genet, 140. pp. 322-330.

Kimonis, VE and Watts, GD (2005) Autosomal Dominant Inclusion Body Myopathy, Paget Disease of Bone and Frontotemporal Dementia. Alzheimer Dis Assoc Disord, 1. pp. 44-47.

Kuhlenbaumer, G, Hannibal, MC, Nelis, E, Schirmacher, A, Verpoorten, N, Meuleman, J, Watts, GD, De Vriendt, E, Young, P, Stogbauer, F, Halfter, H, Betz, BG, Kurleman, G, Bird, TD, Airaksinen, E, Mononen, T, Pou Serradell, A, Prats, JM and Van Broeckhoven, C (2005) Mutations in the human septin 0 gene (SEPT9) cause hereditary neuralgic amyotrophy (HNA). Nat. Genet, 37 (10). pp. 1044-1046.

Schroder, R, Watts, GD, Mehta, SG, Evert, BO, Broich, P, Fliessbach, K, Pauls, K, Hans, VH, Kimonis, VE and Thal, DR (2005) Mutant valosin-containing protein causes a novel type of frontotemporal dementia. Ann Neurol, 57 (3). pp. 457-461.

Watts, GD, Mehta, SG, Zhao, C, Ramdeen, S, Hamilton, SJ, Mumm, S, Whyte, MP, McGillivray, B and Kimonis, VE (2005) Mapping of Autosomal Dominant Progressive Myopathy of a Limb-Girdle Distribution and Bone Fragility to Chromosome 9p21-22: Identification of a Novel Locus for a Musculoskeletal Syndrome. Hum. Genet, 118 (3-4). pp. 508-514.

This list was generated on Sun May 19 09:53:38 2013 BST.
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