Lrrk2 pathogenic substitutions in Parkinson's disease
MATA, Ignacio F, KACHERGUS, Jennifer M, LAHOZ, Carlos, WSZOLEK, Zbigniew K, FARRER, Matthew J, TAYLOR, Julie P, LINCOLN, Sarah, AASLY, Jan, LYNCH, Timothy, HULIHAN, Mary M, COBB, Stephanie A, WU, Ruey-Meei, LU, Chin-Song
Published in Neurogenetics (01.12.2005)
Published in Neurogenetics (01.12.2005)
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Genetics of restless legs syndrome
Mata, Ignacio F., Bodkin, Cynthia L., Adler, Charles H., Lin, Siong-chi, Uitti, Ryan J., Farrer, Matthew J., Wszolek, Zbigniew K.
Published in Parkinsonism & related disorders (2006)
Published in Parkinsonism & related disorders (2006)
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Retromer-dependent neurotransmitter receptor trafficking to synapses is altered by the Parkinson's disease VPS35 mutation p.D620N
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
Published in Human molecular genetics (15.03.2015)
Published in Human molecular genetics (15.03.2015)
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LRRK2 in Parkinson's disease: protein domains and functional insights
Mata, Ignacio F., Wedemeyer, William J., Farrer, Matthew J., Taylor, Julie P., Gallo, Kathleen A.
Published in Trends in neurosciences (Regular ed.) (01.05.2006)
Published in Trends in neurosciences (Regular ed.) (01.05.2006)
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Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication
Fuchs, J, Nilsson, C, Kachergus, J, Munz, M, Larsson, E-M, Schüle, B, Langston, J W, Middleton, F A, Ross, O A, Hulihan, M, Gasser, T, Farrer, M J
Published in Neurology (20.03.2007)
Published in Neurology (20.03.2007)
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Clinical heterogeneity of α-synuclein gene duplication in Parkinson's disease
Nishioka, Kenya, Hayashi, Shin, Farrer, Matthew J., Singleton, Andrew B., Yoshino, Hiroyo, Imai, Hisamasa, Kitami, Toshiaki, Sato, Kenichi, Kuroda, Ryu, Tomiyama, Hiroyuki, Mizoguchi, Koichi, Murata, Miho, Toda, Tatsushi, Imoto, Issei, Inazawa, Johji, Mizuno, Yoshikuni, Hattori, Nobutaka
Published in Annals of neurology (01.02.2006)
Published in Annals of neurology (01.02.2006)
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Parkinsonism, Lrrk2 G2019S, and tau neuropathology
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
Published in Neurology (24.10.2006)
Published in Neurology (24.10.2006)
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High-Resolution Whole-Genome Association Study of Parkinson Disease
Maraganore, Demetrius M., de Andrade, Mariza, Lesnick, Timothy G., Strain, Kari J., Farrer, Matthew J., Rocca, Walter A., Pant, P.V. Krishna, Frazer, Kelly A., Cox, David R., Ballinger, Dennis G.
Published in American journal of human genetics (01.11.2005)
Published in American journal of human genetics (01.11.2005)
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P.109 Diagnostic Yield of Targeted Exome Sequencing in West Syndrome
Parfyonov, M, Guella, I, Evans, DM, Adam, S, DeGuzman, C, Van Allen, MI, Boelman, C, Nelson, TN, Farrer, MJ, Connolly, MB, Demos, M
Published in Canadian journal of neurological sciences (01.11.2021)
Published in Canadian journal of neurological sciences (01.11.2021)
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Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations
Kachergus, Jennifer, Mata, Ignacio F., Hulihan, Mary, Taylor, Julie P., Lincoln, Sarah, Aasly, Jan, Gibson, J. Mark, Ross, Owen A., Lynch, Timothy, Wiley, Joseph, Payami, Haydeh, Nutt, John, Maraganore, Demetrius M., Czyzewski, Krzysztof, Styczynska, Maria, Wszolek, Zbigniew K., Farrer, Matthew J., Toft, Mathias
Published in American journal of human genetics (01.04.2005)
Published in American journal of human genetics (01.04.2005)
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Progression of dopaminergic dysfunction in a LRRK2 kindred: a multitracer PET study
Nandhagopal, R, Mak, E, Schulzer, M, McKenzie, J, McCormick, S, Sossi, V, Ruth, T J, Strongosky, A, Farrer, M J, Wszolek, Z K, Stoessl, A J
Published in Neurology (25.11.2008)
Published in Neurology (25.11.2008)
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Biochemical and pathological characterization of Lrrk2
Giasson, Benoit I., Covy, Jason P., Bonini, Nancy M., Hurtig, Howard I., Farrer, Matthew J., Trojanowski, John Q., Van Deerlin, Vivianna M.
Published in Annals of neurology (01.02.2006)
Published in Annals of neurology (01.02.2006)
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Lrrk2 and Lewy body disease
Ross, Owen A., Toft, Mathias, Whittle, Andrew J., Johnson, Joseph L., Papapetropoulos, Spiridon, Mash, Deborah C., Litvan, Irene, Gordon, Mark F., Wszolek, Zbigniew K., Farrer, Matthew J., Dickson, Dennis W.
Published in Annals of neurology (01.02.2006)
Published in Annals of neurology (01.02.2006)
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P.016 A novel de novo GABRA1 mutation linked to epileptic encephalopathy: pathophysiology and potential therapeutic options
Chiu, M, Bai, Y, Chan, EH, Huh, L, Guella, I, Farrer, MJ, Connolly, M, Liu, L, Demos, M, Wang, Y
Published in Canadian journal of neurological sciences (01.06.2018)
Published in Canadian journal of neurological sciences (01.06.2018)
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Parkin genetics: one model for Parkinson's disease
Mata, Ignacio F., Lockhart, Paul J., Farrer, Matthew J.
Published in Human molecular genetics (01.04.2004)
Published in Human molecular genetics (01.04.2004)
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α-Synuclein promoter confers susceptibility to Parkinson's disease
Pals, Philippe, Lincoln, Sarah, Manning, Jonathan, Heckman, Michael, Skipper, Lisa, Hulihan, Mary, Van den Broeck, Marleen, De Pooter, Tim, Cras, Patrick, Crook, Julia, Van Broeckhoven, Christine, Farrer, Matt J.
Published in Annals of neurology (01.10.2004)
Published in Annals of neurology (01.10.2004)
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Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
Wszolek, Z K, Pfeiffer, R F, Tsuboi, Y, Uitti, R J, McComb, R D, Stoessl, A J, Strongosky, A J, Zimprich, A, Müller-Myhsok, B, Farrer, M J, Gasser, T, Calne, D B, Dickson, D W
Published in Neurology (11.05.2004)
Published in Neurology (11.05.2004)
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Journal Article
LRRK2: a common pathway for parkinsonism, pathogenesis and prevention?
Taylor, Julie P., Mata, Ignacio F., Farrer, Matt J.
Published in Trends in molecular medicine (01.02.2006)
Published in Trends in molecular medicine (01.02.2006)
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