Progress towards therapies for disease modification in Parkinson's disease von Vijiaratnam, Nirosen, Simuni, Tanya, Bandmann, Oliver, Morris, Huw R, Foltynie, Thomas

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LRRK2 activation controls the repair of damaged endomembranes in macrophages von Herbst, Susanne, Campbell, Philip, Harvey, John, Bernard, Elliott M, Papayannopoulos, Venizelos, Wood, Nicholas W, Morris, Huw R, Gutierrez, Maximiliano G

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Astrogliopathy predominates the earliest stage of corticobasal degeneration pathology von Ling, Helen, Kovacs, Gabor G, Vonsattel, Jean Paul G, Davey, Karen, Mok, Kin Y, Hardy, John, Morris, Huw R, Warner, Thomas T, Holton, Janice L, Revesz, Tamas

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Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk von Lubbe, Steven J, Bustos, Bernabe I, Hu, Jing, Krainc, Dimitri, Joseph, Theresita, Hehir, Jason, Tan, Manuela, Zhang, Weijia, Escott-Price, Valentina, Williams, Nigel M, Blauwendraat, Cornelis, Singleton, Andrew B, Morris, Huw R

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The PINK1-Parkin mitophagy signalling pathway is not functional in peripheral blood mononuclear cells von Bradshaw, Aaron, Campbell, Philip, Schapira, Anthony H., Morris, Huw R., Taanman, Jan-Willem

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ATP10B and the risk for Parkinson’s disease von Real, Raquel, Moore, Anni, Blauwendraat, Cornelis, Morris, Huw R., Bandres-Ciga, Sara

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Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease von Hudson, Gavin, Nalls, Mike, Evans, Jonathan R, Breen, David P, Winder-Rhodes, Sophie, Morrison, Karen E, Morris, Huw R, Williams-Gray, Caroline H, Barker, Roger A, Singleton, Andrew B, Hardy, John, Wood, Nicholas E, Burn, David J, Chinnery, Patrick F

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Neurodegenerative Disease Risk in Carriers of Autosomal Recessive Disease von Vieira, Sophia R. L., Morris, Huw R.

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Progressive Supranuclear Palsy and Corticobasal Degeneration: Pathophysiology and Treatment Options von Lamb, Ruth, Rohrer, Jonathan D., Lees, Andrew J., Morris, Huw R.

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Variation in tau isoform expression in different brain regions and disease states von Majounie, Elisa, Cross, William, Newsway, Victoria, Dillman, Allissa, Vandrovcova, Jana, Morris, Christopher M, Nalls, Michael A, Ferrucci, Luigi, Owen, Michael J, O'Donovan, Michael C, Cookson, Mark R, Singleton, Andrew B, de Silva, Rohan, Morris, Huw R

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Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease von Ryan, Natalie S, Biessels, Geert-Jan, Kim, Lois, Nicholas, Jennifer M, Barber, Philip A, Walsh, Phoebe, Gami, Priya, Morris, Huw R, Bastos-Leite, António J, Schott, Jonathan M, Beck, Jon, Mead, Simon, Chavez-Gutierrez, Lucia, de Strooper, Bart, Rossor, Martin N, Revesz, Tamas, Lashley, Tammaryn, Fox, Nick C

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SGCE mutations cause psychiatric disorders: clinical and genetic characterization von PEALL, Kathryn J, SMITH, Daniel J, WHITE, Cathy, LUX, Andrew, JARDINE, Philip, BAJAJ, Narinder, LYNCH, Bryan, KIROV, George, O'RIORDAN, Sean, SAMUEL, Michael, LYNCH, Timothy, KING, Mary D, KURIAN, Manju A, CHINNERY, Patrick F, WARNER, Thomas T, BLAKE, Derek J, OWEN, Michael J, MORRIS, Huw R, WARDLE, Mark, WAITE, Adrian J, HEDDERLY, Tammy, LIN, Jean-Pierre, SMITH, Martin, WHONE, Alan, PALL, Hardev

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A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism von Leahy, Christopher B, Robinson, Andrew C, Jabbari, Edwin, Morris, Huw R, Lally, Imogen, Djoukhadar, Ibrahim, Roncaroli, Federico, Kobylecki, Christopher

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The pathogenesis of Parkinson's disease von Morris, Huw R, Spillantini, Maria Grazia, Sue, Carolyn M, Williams-Gray, Caroline H

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Making neurogenetics a global endeavour von Morris, Huw R.

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The motor phenotype of Parkinson's disease in relation to age at onset von Wickremaratchi, Mirdhu M., Knipe, M. Duleeka W., Sastry, B.S. Dwarakanath, Morgan, Elizabeth, Jones, Anne, Salmon, Rachel, Weiser, Richard, Moran, Maralyn, Davies, Debbie, Ebenezer, Louise, Raha, Sandip, Robertson, Neil P., Butler, Christopher C., Ben-Shlomo, Yoav, Morris, Huw R.

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Functional Magnetic Resonance Imaging Neurofeedback-guided Motor Imagery Training and Motor Training for Parkinson's Disease: Randomized Trial von Subramanian, Leena, Morris, Monica Busse, Brosnan, Meadhbh, Turner, Duncan L, Morris, Huw R, Linden, David E J

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Potential of Non-Coding RNA as Biomarkers for Progressive Supranuclear Palsy von Simoes, Fabio A, Joilin, Greig, Peters, Oliver, Schneider, Luisa-Sophie, Priller, Josef, Spruth, Eike Jakob, Vogt, Ina, Kimmich, Okka, Spottke, Annika, Hoffmann, Daniel C, Falkenburger, Björn, Brandt, Moritz, Prudlo, Johannes, Brockmann, Kathrin, Fries, Franca Laura, Rowe, James B, Church, Alistair, Respondek, Gesine, Newbury, Sarah F, Leigh, P Nigel, Morris, Huw R, Höglinger, Günter U, Hafezparast, Majid

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Utility of the new Movement Disorder Society clinical diagnostic criteria for Parkinson's disease applied retrospectively in a large cohort study of recent onset cases von Malek, Naveed, MD, Lawton, Michael A., MPhil, Grosset, Katherine A., MD, Bajaj, Nin, PhD, Barker, Roger A., PhD, Ben-Shlomo, Yoav, MD, PhD, Burn, David J., MD, Foltynie, Tom, PhD, Hardy, John, PhD, Morris, Huw R., PhD, Williams, Nigel M., PhD, Wood, Nicholas, PhD, Grosset, Donald G., MD

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Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: A systematic review von Wardle, Mark, Morris, Huw R., Robertson, Neil P.

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