Tau gene and Parkinson’s disease: a case–control study and meta-analysis by Healy, D G, Abou-Sleiman, P M, Lees, A J, Casas, J P, Quinn, N, Bhatia, K, Hingorani, A D, Wood, N W

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The α-synuclein gene in multiple system atrophy by Ozawa, T, Healy, D G, Abou-Sleiman, P M, Ahmadi, K R, Quinn, N, Lees, A J, Shaw, K, Wullner, U, Berciano, J, Moller, J C, Kamm, C, Burk, K, Josephs, K A, Barone, P, Tolosa, E, Goldstein, D B, Wenning, G, Geser, F, Holton, J L, Gasser, T, Revesz, T, Wood, N W

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Genetic association studies of complex neurological diseases by Abou-Sleiman, P M, Hanna, M G, Wood, N W

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PINK1 protein in normal human brain and Parkinson's disease by Gandhi, S., Muqit, M. M. K., Stanyer, L., Healy, D. G., Abou-Sleiman, P. M., Hargreaves, I., Heales, S., Ganguly, M., Parsons, L., Lees, A. J., Latchman, D. S., Holton, J. L., Wood, N. W., Revesz, T.

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DJ-1 mutations in Parkinson’s disease by Healy, D G, Abou-Sleiman, P M, Valente, E M, Gilks, W P, Bhatia, K, Quinn, N, Lees, A J, Wood, N W

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The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease by Bandopadhyay, Rina, Kingsbury, Ann E., Cookson, Mark R., Reid, Andrew R., Evans, Ian M., Hope, Andrew D., Pittman, Alan M., Lashley, Tammaryn, Canet‐Aviles, Rosa, Miller, David W., McLendon, Chris, Strand, Catherine, Leonard, Andrew J., Abou‐Sleiman, Patrick M., Healy, Daniel G., Ariga, Hiroyashi, Wood, Nicholas W., de Silva, Rohan, Revesz, Tamas, Hardy, John A., Lees, Andrew J.

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Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration by Pittman, A M, Myers, A J, Abou-Sleiman, P, Fung, H C, Kaleem, M, Marlowe, L, Duckworth, J, Leung, D, Williams, D, Kilford, L, Thomas, N, Morris, C M, Dickson, D, Wood, N W, Hardy, J, Lees, A J, de Silva, R

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Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers by Apessos, A., Abou-Sleiman, P. M., Harper, J. C., Delhanty, J. D. A.

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Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome by Abou-Sleiman, P.M., Apessos, A., Harper, J.C., Serhal, P., Delhanty, J.D.A.

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First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2) by Abou-Sleiman, P. M., Apessos, A., Harper, J. C., Serhal, P., Winston, R. M. L., Delhanty, J. D. A.

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Population genetic approaches to neurological disease: Parkinson's disease as an example by Gandhi, S, Abou-Sleiman, P.M, Healy, D.G, Weale, M, Gilks, W, Ahmadi, K, Goldstein, D.B, Wood, N.W

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Genetic approaches to solving common diseases by ABOU-SLEIMAN, P. M, HEALY, D. G, WOOD, N. W

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Causes of Parkinson's disease: genetics of DJ-1 by Abou-Sleiman, Patrick M, Healy, Daniel G, Wood, Nicholas W

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A common LRRK2 mutation in idiopathic Parkinson's disease by Gilks, William P, Abou-Sleiman, Patrick M, Gandhi, Sonia, Jain, Shushant, Singleton, Andrew, Lees, Andrew J, Shaw, Karen, Bhatia, Kailash P, Bonifati, Vincenzo, Quinn, Niall P, Lynch, John, Healy, Daniel G, Holton, Janice L, Revesz, Tamas, Wood, Nicholas W

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Genetic causes of Parkinson's disease: UCHL-1 by Healy, Daniel G, Abou-Sleiman, Patrick M, Wood, Nicholas W

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The role of pathogenic DJ-1 mutations in Parkinson's disease by Abou-Sleiman, Patrick M., Healy, Daniel G., Quinn, Niall, Lees, Andrew J., Wood, Nicholas W.

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Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1 by Valente, Enza Maria, Abou-Sleiman, Patrick M., Caputo, Viviana, Miratul M. K. Muqit, Harvey, Kirsten, Gispert, Suzana, Ali, Zeeshan, Del Turco, Domenico, Bentivoglio, Anna Rita, Healy, Daniel G., Albanese, Alberto, Nussbaum, Robert, González-Maldonado, Rafael, Deller, Thomas, Salvi, Sergio, Cortelli, Pietro, Gilks, William P., Latchman, David S., Harvey, Robert J., Dallapiccola, Bruno, Auburger, Georg, Wood, Nicholas W.

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Hereditary motor and autonomic neuronopathy 1 maps to chromosome 20q13.2-13.3 by Marques, Jr, W, Davis, M B, Abou-Sleiman, P M, Marques, V D, Silva, Jr, W A, Zago, M A, Sobreira, C S, Barreira, A A

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Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data by Khan, Naheed L., Jain, Shushant, Lynch, John M., Pavese, Nicola, Abou-Sleiman, Patrick, Holton, Janice L., Healy, Daniel G., Gilks, William P., Sweeney, Mary G., Ganguly, Milan, Gibbons, Vaneesha, Gandhi, Sonia, Vaughan, Jenny, Eunson, Louise H., Katzenschlager, Regina, Gayton, Juliet, Lennox, Graham, Revesz, Tamas, Nicholl, David, Bhatia, Kailash P., Quinn, Niall, Brooks, David, Lees, Andrew J., Davis, Mary B., Piccini, Paola, Singleton, Andrew B., Wood, Nicholas W.

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Phenotype, genotype, and worldwide genetic penetrance of LRRK2 -associated Parkinson's disease: a case-control study by Healy, Daniel G, MD, Falchi, Mario, PhD, O'Sullivan, Sean S, MD, Bonifati, Vincenzo, MD, Durr, Alexandra, MD, Bressman, Susan, MD, Brice, Alexis, MD, Aasly, Jan, MD, Zabetian, Cyrus P, MD, Goldwurm, Stefano, PhD, Ferreira, Joaquim J, MD, Tolosa, Eduardo, MD, Kay, Denise M, PhD, Klein, Christine, MD, Williams, David R, MD, Marras, Connie, MD, Lang, Anthony E, MD, Wszolek, Zbigniew K, MD, Berciano, Jose, MD, Schapira, Anthony HV, MD, Lynch, Timothy, MD, Bhatia, Kailash P, MD, Gasser, Thomas, MD, Lees, Andrew J, MD, Wood, Nicholas W, MD

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