Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication von FUCHS, J, NILSSON, C, GASSER, T, FARRER, M. J, KACHERGUS, J, MUNZ, M, LARSSON, E.-M, SCHÜLE, B, LANGSTON, J. W, MIDDLETON, F. A, ROSS, O. A, HULIHAN, M

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Progression of dopaminergic dysfunction in a LRRK2 kindred : A multitracer PET study von NANDHAGOPAL, R, MAK, E, STOESSL, A. J, SCHULZER, M, MCKENZIE, J, MCCORMICK, S, SOSSI, V, RUTH, T. J, STRONGOSKY, A, FARRER, M. J, WSZOLEK, Z. K

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Retromer-dependent neurotransmitter receptor trafficking to synapses is altered by the Parkinson's disease VPS35 mutation p.D620N von Munsie, L N, Milnerwood, A J, Seibler, P, Beccano-Kelly, D A, Tatarnikov, I, Khinda, J, Volta, M, Kadgien, C, Cao, L P, Tapia, L, Klein, C, Farrer, M J

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Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease von HAUGARVOLL, K, RADEMAKERS, R, GUIDI, M, RIBOLDAZZI, G, BROWN, L, WALTER, U, BENECKE, R, BERG, D, GASSER, T, THEUNS, J, PALS, P, CRAS, P, KACHERGUS, J. M, DE DEYN, P. Paul, ENGELBORGHS, S, PICKUT, B, UITTI, R. J, FOROUD, T, NICHOLS, W. C, HAGENAH, J, KLEIN, C, SAMII, A, ZABETIAN, C. P, NUYTEMANS, K, BONIFATI, V, VAN BROECKHOVEN, C, FARRER, M. J, WSZOLEK, Z. K, ROSS, O. A, GIBSON, J. M, TAN, E.-K, GAIG, C, TOLOSA, E, GOLDWURM, S

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Autosomal dominant parkinsonism associated with variable synuclein and tau pathology von WSZOLEK, Z. K, PFEIFFER, R. F, GASSER, T, CALNE, D. B, DICKSON, D. W, TSUBOI, Y, UITTI, R. J, MCCOMB, R. D, STOESSL, A. J, STRONGOSKY, A. J, ZIMPRICH, A, MÜLLER-MYHSOK, B, FARRER, M. J

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MAPT H1 HAPLOTYPE IS A RISK FACTOR FOR ESSENTIAL TREMOR AND MULTIPLE SYSTEM ATROPHY von VILARINO-GÜELL, C, SOTO-ORTOLAZA, A. I, FARRER, M. J, ROSS, O. A, RAJPUT, A, MASH, D. C, PAPAPETROPOULOS, S, PAHWA, R, LYONS, K. E, UITTI, R. J, WSZOLEK, Z. K, DICKSON, D. W

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Progressive dopaminergic alterations and mitochondrial abnormalities in LRRK2 G2019S knock-in mice von Yue, M, Hinkle, K.M, Davies, P, Trushina, E, Fiesel, F.C, Christenson, T.A, Schroeder, A.S, Zhang, L, Bowles, E, Behrouz, B, Lincoln, S.J, Beevers, J.E, Milnerwood, A.J, Kurti, A, McLean, P.J, Fryer, J.D, Springer, W, Dickson, D.W, Farrer, M.J, Melrose, H.L

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Parkinsonism, Lrrk2 G2019S, and tau neuropathology von Rajput, A, Dickson, D W, Robinson, C A, Ross, O A, Dächsel, J C, Lincoln, S J, Cobb, S A, Rajput, M L, Farrer, M J

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PINK1 mutations and parkinsonism von ISHIHARA-PAUL, L, HULIHAN, M. M, ZOUARI, M, SASSI, S. B, YAHMED, S. B, EL EUCH-FAYECHE, G, MATTHEWS, P. M, MIDDLETON, L. T, GIBSON, R. A, HENTATI, F, FARRER, M. J, KACHERGUS, J, UPMANYU, R, WARREN, L, AMOURI, R, ELANGO, R, PRINJHA, R. K, SOTO, A, KEFI, M

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A family with parkinsonism, essential tremor, restless legs syndrome, and depression von PUSCHMANN, A, PFEIFFER, R. F, DICKSON, D. W, WSZOLEK, Z. K, STOESSL, A. J, KURIAKOSE, R, LASH, J. L, SEARCY, J. A, STRONGOSKY, A. J, VILARINO-GÜELL, C, FARRER, M. J, ROSS, O. A

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Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population von TOFT, M, PIELSTICKER, L, ROSS, O. A, AASLY, J. O, FARRER, M. J

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Characterization of DCTN1 genetic variability in neurodegeneration von VILARINO-GÜELL, C, WIDER, C, UITTI, R. J, GRAFF-RADFORD, N. R, BOEVE, B. F, JOSEPHS, K. A, MILLER, B, BOYLAN, K. B, GWINN, K, ADLER, C. H, AASLY, J. O, HENTATI, F, SOTO-ORTOLAZA, A. I, DESTEE, A, KRYGOWSKA-WAJS, A, CHARTIER-HARLIN, M.-C, ROSS, O. A, RADEMAKERS, R, FARRER, M. J, COBB, S. A, KACHERGUS, J. M, KEELING, B. H, DACHSEL, J. C, HULIHAN, M. M, DICKSON, D. W, WSZOLEK, Z. K

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A comparative analysis of leucine-rich repeat kinase 2 (Lrrk2) expression in mouse brain and Lewy body disease von Melrose, H.L, Kent, C.B, Taylor, J.P, Dachsel, J.C, Hinkle, K.M, Lincoln, S.J, Mok, S.S, Culvenor, J.G, Masters, C.L, Tyndall, G.M, Bass, D.I, Ahmed, Z, Andorfer, C.A, Ross, O.A, Wszolek, Z.K, Delldonne, A, Dickson, D.W, Farrer, M.J

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Α-Synuclein, pesticides, and Parkinson disease : A case-control study von BRIGHINA, L, FRIGERIO, R, MARAGANORE, D. M, SCHNEIDER, N. K, LESNICK, T. G, DE ANDRADE, M, CUNNINGHAM, J. M, FARRER, M. J, LINCOLN, S. J, CHECKOWAY, H, ROCCA, W. A

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Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1 : Redefining DYT14 as DYT5 von WIDER, C, MELQUIST, S, STEPHAN, D. A, SCHORDERET, D. F, GHIKA, J, BURKHARD, P. R, KAPATOS, G, HUTTON, M, FARRER, M. J, WSZOLEK, Z. K, VINGERHOETS, F. J. G, HAUF, M, SOLIDA, A, COBB, S. A, KACHERGUS, J. M, GASS, J, COON, K. D, BAKER, M, CANNON, A

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Lrrk2 localization in the primate basal ganglia and thalamus: A light and electron microscopic analysis in monkeys von Lee, H., Melrose, H.L., Yue, M., Pare, Jean-Francois, Farrer, M.J., Smith, Y.

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Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease von MARAGANORE, D. M, FARRER, M. J, HARDY, J. A, LINCOLN, S. J, MCDONNELL, S. K, ROCCA, W. A

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Adult neurogenesis and neurite outgrowth are impaired in LRRK2 G2019S mice von Winner, B, Melrose, H.L, Zhao, C, Hinkle, K.M, Yue, M, Kent, C, Braithwaite, A.T, Ogholikhan, S, Aigner, R, Winkler, J, Farrer, M.J, Gage, F.H

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Identification of FUS p.R377W in essential tremor von Rajput, A., Rajput, A. H., Rajput, M. L., Encarnacion, M., Bernales, C. Q., Ross, J. P., Farrer, M. J., Vilariño-Güell, C.

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Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic mice von Melrose, H.L, Dächsel, J.C, Behrouz, B, Lincoln, S.J, Yue, M, Hinkle, K.M, Kent, C.B, Korvatska, E, Taylor, J.P, Witten, L, Liang, Y.-Q, Beevers, J.E, Boules, M, Dugger, B.N, Serna, V.A, Gaukhman, A, Yu, X, Castanedes-Casey, M, Braithwaite, A.T, Ogholikhan, S, Yu, N, Bass, D, Tyndall, G, Schellenberg, G.D, Dickson, D.W, Janus, C, Farrer, M.J

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