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Items where Author is "Manzoni, Dr Claudia"

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Costa, B., Manzoni, C. ORCID:, Bernal-Quiros, M., Kia, D. A., Aguilar, M., Alvarez, I., Alvarez, V., Andreassen, O. ORCID:, Anfossi, M., Bagnoli, S., Benussi, L., Bernardi, L., Binetti, G., Blackburn, D., Boada, M., Borroni, B., Bowns, L., Bråthen, G. ORCID:, Bruni, A. C., Chiang, H.-H., Clarimon, J., Colville, S., Conidi, M. E., Cope, T. E., Cruchaga, C., Cupidi, C., Di Battista, M. E., Diehl-Schmid, J., Diez-Fairen, M., Dols-Icardo, O., Durante, E., Flisar, D., Frangipane, F., Galimberti, D. ORCID:, Gallo, M., Gallucci, M., Ghidoni, R. ORCID:, Graff, C., Grafman, J. H., Grossman, M., Hardy, J., Hernández, I., Holloway, G. J. T., Huey, E. D., Illán-Gala, I. ORCID:, Karydas, A., Khoshnood, B., Kramberger, M. G., Kristiansen, M., Lewis, P. A., Lleó, A., Madhan, G. K., Maletta, R., Maver, A., Menendez-Gonzalez, M., Milan, G., Miller, B., Mol, M. O. ORCID:, Momeni, P., Moreno-Grau, S., Morris, C. M. ORCID:, Nacmias, B. ORCID:, Nilsson, C., Novelli, V., Öijerstedt, L., Padovani, A., Pal, S., Panchbhaya, Y., Pastor, P. ORCID:, Peterlin, B., Piaceri, I., Pickering-Brown, S., Pijnenburg, Y. A. L. ORCID:, Puca, A. A., Rainero, I., Rendina, A. ORCID:, Richardson, A. M. T., Rogaeva, E., Rogelj, B. ORCID:, Rollinson, S. ORCID:, Rossi, G., Rossmeier, C., Rowe, J. B., Rubino, E. ORCID:, Ruiz, A., Sanchez-Valle, R., Sando, S. B., Santillo, A. F., Saxon, J., Scarpini, E. ORCID:, Serpente, M., Smirne, N., Sorbi, S., Suh, E., Tagliavini, F., Thompson, J. C., Trojanowski, J. Q., Van Deerlin, V. M., Van der Zee, J. ORCID:, Van Broeckhoven, C. ORCID:, van Rooij, J., Van Swieten, J. C., Veronesi, A., Vitale, E. ORCID:, Waldö, M. L., Woodward, C., Yokoyama, J., Escott-Price, V., Polke, J. M. and Ferrari, R. (2020) C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts. Neurology, 95 (24). e3288-e3302. ISSN 0028-3878 doi:

Cogo, S., Manzoni, C., Lewis, P. A. and Greggio, E. (2020) Leucine‐rich repeat kinase 2 and lysosomal dyshomeostasis in Parkinson disease. Journal of Neurochemistry, 152 (3). pp. 273-283. ISSN 1471-4159 doi:

Manzoni, C., Lewis, P. A. and Ferrari, R. (2020) Network analysis for complex neurodegenerative diseases. Current Genetic Medicine Reports, 8 (1). pp. 17-25. ISSN 2167-4876 doi:

Tomkins, J. E., Ferrari, R., Vavouraki, N., Hardy, J., Lovering, R. C., Lewis, P. A., McGuffin, L. J. and Manzoni, C. (2020) PINOT: an intuitive resource for integrating protein-protein interactions. Cell Communication and Signaling, 18 (92). ISSN 1478-811X doi:

Bonham, L. W., Steele, N. Z. R., Karch, C. M., Broce, I., Geier, E. G., Wen, N. L., Momeni, P., Hardy, J., Miller, Z. A., Gorno-Tempini, M. L., Hess, C. P., Lewis, P., Miller, B. L., Seeley, W. W., Manzoni, C., Desikan, R. S., Baranzini, S. E., Ferrari, R. and Yokoyama, J. S. (2019) Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia. Scientific Reports, 9 (1). 10854. ISSN 2045-2322 doi:

Mamais, A., Manzoni, C., Nazish, I., Arber, C., Sonustun, B., Wray, S., Warner, T. T., Cookson, M. R., Lewis, P. A. and Bandopadhyay, R. (2018) Analysis of macroautophagy related proteins in G2019S LRRK2 Parkinson's disease brains with Lewy body pathology. Brain Research, 1701. pp. 75-84. ISSN 0006-8993 doi:

Price, A., Manzoni, C., Cookson, M. R. and Lewis, P. A. (2018) The LRRK2 signalling system. Cell and Tissue Research, 373 (1). pp. 39-50. ISSN 0302-766X doi:

Leksmono, C., Manzoni, C., Tomkins, J., Lucchesi, W., Cottrell, G. and Lewis, P. A. (2018) Measuring lactase enzymatic activity in the teaching lab. Journal of Visualized Experiments (138). e54377. ISSN 1940-087X doi:

Ferrari, R., Kia, D. A., Tomkins, J. E., Hardy, J., Wood, N. W., Lovering, R. C., Lewis, P. A. and Manzoni, C. (2018) Stratification of candidate genes for Parkinson’s disease using weighted protein interaction network analysis. BMC Genomics, 19. 452. ISSN 1471-2164 doi:

Tomkins, J. E., Dihanich, S., Beilina, A., Ferrari, R., Ilacqua, N., Cookson, M. R., Lewis, P. A. and Manzoni, C. (2018) Comparative protein interaction network analysis identifies shared and distinct functions for the human ROCO proteins. Proteomics, 18 (10). 1700444. ISSN 1615-9853 doi:

Manzoni, C., Mamais, A., Dihanich, S., Soutar, M. P. M., Plun-Favreau, H., Bandopadhyay, R., Abeti, R., Giunti, P., Hardy, J., Cookson, M. R., Tooze, S. A. and Lewis, P. A. (2018) mTOR independent alteration in ULK1 Ser758 phosphorylation following chronic LRRK2 kinase inhibition. Bioscience Reports, 38 (2). BSR20171669. ISSN 0144-8463 doi:

Manzoni, C., Kia, D. A., Vandrovcova, J., Hardy, J., Wood, N. W., Lewis, P. A. and Ferrari, R. (2018) Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences. Briefings In Bioinformatics, 19 (2). pp. 286-302. ISSN 1467-5463 doi:

Giacomina, R., Redaelli, V., Contiero, P., Fabiano, S., Tagliabue, G., Perego, P., Benussi, L., Bruni, A., Filippini, G., Farinotti, M., Giaccone, G., Buitatiotis, S., Manzoni, C., Ferrari, R. and Tagliavini, F. (2018) Tau mutations serve as a novel risk factor for cancer. Cancer Research, 78 (13). pp. 3731-3739. ISSN 0008-5472 doi:

Manzoni, C. and Lewis, P. A. (2017) LRRK2 and autophagy. In: Rideout, H. J. (ed.) Leucine-Rich Repeat Kinase 2 (LRRK2). Advances in Neurobiology (ISSN:2190-5215), 14. Springer International Publishing, Cham, Switzerland, pp. 89-105. ISBN 9783319499673 doi:

Ferrari, R., Lovering, R. C., Hardy, J., Lewis, P. A. and Manzoni, C. (2017) Weighted protein interaction network analysis of frontotemporal dementia. Journal of Proteome Research, 16 (2). pp. 999-1013. ISSN 1535-3907 doi:

Manzoni, C. (2017) The LRRK2-macroautophagy axis and its relevance to Parkinson's Disease. Biochemical Society Transactions, 45 (1). pp. 155-162. ISSN 1470-8752 doi:

Manzoni, C., Mamais, A., Roosen, D. A., Dihanich, S., Soutar, M. P. M., Plun-Favreau, H., Bandopadhyay, R., Hardy, J., Tooze, S. A., Cookson, M. R. and Lewis, P. A. (2016) mTOR independent regulation of macroautophagy by Leucine Rich Repeat Kinase 2 via Beclin-1. Scientific Reports, 6. 35106. ISSN 2045-2322 doi:

Kara, E., Tucci, A., Manzoni, C., Lynch, D. S., Elpidorou, M., Bettencourt, C., Chelban, V., Manole, A., Hamed, S., Haridy, N., Federoff, M., Preza, E., Hughes, D., Pittman, A., Jaunmuktane, Z., Brandner, S., Xiromerisiou, G., Wiethoff, S., Schottlaender, L., Proukakis, C., Morris, H., Warner, T., Bhatia, K., Korlipara, P., Singleton, A., Hardy, J., Wood, N., Lewis, P. and Houlden, H. (2016) Genetic and phenotypic characterization of complex hereditary spastic paraplegia. Brain : A Journal of Neurology, 139 (7). pp. 1904-1918. ISSN 1460-2156 doi:

Manzoni, C., Denny, P., Lovering, R. C. and Lewis, P. A. (2015) Computational analysis of the LRRK2 interactome. PeerJ, 3. 778. ISSN 2167-8359 doi:

Dihanich, S., Civiero, L., Manzoni, C., Mamais, A., Bandopadhyay, R., Greggio, E. and Lewis, P. A. (2014) GTP binding controls complex formation by the human ROCO protein MASL1. FEBS Journal, 281 (1). pp. 261-274. ISSN 1742-464X doi:

Schulte, E. C., Ellwanger, D. C., Dihanich, S., Manzoni, C., Stangl, K., Schormair, B., Graf, E., Eck, S., Mollenhauer, B., Haubenberger, D., Pirker, W., Zimprich, A., Brücke, T., Lichtner, P., Peters, A., Gieger, C., Trenkwalder, C., Mewes, H.-W., Meitinger, T., Lewis, P. A., Klünemann, H. H. and Winkelmann, J. (2014) Rare variants in LRRK1 and Parkinson's disease. Neurogenetics, 15 (1). pp. 49-57. ISSN 1364-6745 doi:

Manzoni, C., Mamais, A., Dihanich, S., McGoldrick, P., Devine, M. J., Zerle, J., Kara, E., Taanman, J.-W., Healy, D. G., Marti-Masso, J.-F., Schapira, A. H., Plun-Favreau, H., Tooze, S., Hardy, J., Bandopadhyay, R. and Lewis, P. A. (2013) Pathogenic Parkinson’s disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation. Biochemical and Biophysical Research Communications, 441 (4). pp. 862-866. ISSN 0006-291X doi:

Jebelli, J. D., Dihanich, S., Civiero, L., Manzoni, C., Greggio, E. and Lewis, P. A. (2012) GTP binding and intramolecular regulation by the ROC domain of Death Associated Protein Kinase 1. Scientific Reports, 2. 695. ISSN 2045-2322 doi:

This list was generated on Fri Jun 11 23:01:19 2021 UTC.

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