Items where Author is "Hardy, J"

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Number of items: 6.

Article

Allerton, F and Fishwick, J C and Paterson, S and Weller, R and Battersby, I and Doyle, R and Gould, D and Caddy, S and Dunning, M and Featherstone, H J and Hardy, J and Kent, A and Pedro, B and Smith, K and Swinbourne, F and Harrison, J and Heinrich, C and Lau-Gillard, P and Loeffler, A and Maddinson, R and Mason, C and Ramsey, I and Ridyard, A and Robin, L and Scudder, C and Seth, M and Tappin, S and Singleton, D and Smith, H and Southerden, P and Warland, J and Whitehead, M and Williams, J (2019) Call for coordinated antimicrobial approach at veterinary diagnostic laboratories. VETERINARY RECORD, 184 (26).

Noyce, A J and Kia, D A and Hemani, G and Nicolas, A and Price, T R and De Pablo-Fernandez, E and Haycock, P C and Lewis, P A and Foltynie, T and Smith, G D and Schrag, A and Lees, A J and Hardy, J and Singleton, A and Nalls, M A and Pearce, N and Lawlor, D A and Wood, N W (2017) Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study. PLOS Medicine, 14 (6).

Kara, E and Tucci, A and Manzoni, C and Lynch, DS and Elpidorou, M and Bettencourt, C and Chelban, V and Manole, A and Hamed, S and Federoff, M and Preza, E and Hughes, D and Pittman, A and Jaunmuktane, Z and Brandner, S and Xiromerisiou, G and Wiethoff, S and Schottlaender, L and Proukakis, C and Morris, HW and Warner, T and Bhatia, KP and Korlipara, P and Singleton, AB and Hardy, J and Wood, NW and Lewis, PA And Houlden, H (2016) Genetic and phenotypic characterisation of complex hereditary spastic paraplegia. BRAIN, 139 (7). pp. 1904-1918.

Kiely, A P and Ling, H and Asi, Y T and Kara, E and Proukakis, C and Schapira, A H and Morris, H R and Lubbe, S and Limousin, P and Lewis, P A and Lees, A J and Quinn, N and Hardy, J and Love, S and Revesz, T and Houlden, H and Holton, J L (2015) Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation. Molecular Neurodegeneration, 10. p. 41.

Mencacci, N E and Rubio-Agusti, I and Zdebik, A and Asmus, F and Ludtmann, M H R and Ryten, M and Plagnol, V and Hauser, A K and Bandres-Ciga, S and Bettencourt, C and Forabosco, P and Hughes, D and Soutar, M M and Peall, K and Morris, H R and Trabzuni, D and Tekman, M and Stanescu, H C and Kleta, R and Carecchio, M and Zorzi, G and Nardocci, N and Garavaglia, B and Lohmann, E and Weissbach, A and Klein, C and Hardy, J and Pittman, A M and Foltynie, T and Abramov, A Y and Gasser, T and Bhatia, K P and Wood, N W (2015) A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia. American Journal of Human Genetics, 96 (6). pp. 938-47.

Other

Soutar, MPM and Melandri, D and Annuario, E and Monaghan, AE and Welsh, NJ and D’Sa, K and Guelfi, S and Zhang, D and Pittman, A and Trabzuni, D and Pan, KS and Kia, DA and Bictash, M and Gandhi, S and Houlden, H and Cookson, MR and Wood, NW and Singleton, AB and Hardy, J and Whiting, PJ and Blauwendraat, C and Whitworth, AJ and Manzoni, C and Ryten, M and Lewis, PA and Plun-Favreau, H (2020) Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson’s disease at Chr16q11.2 and on the MAPT H1 allele. Cold Spring Harbor Laboratory. (Submitted)

This list was generated on Thu Dec 2 07:27:47 2021 GMT.