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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
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Cites
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
Polymeropoulos, M. H., Lavedan, C., Leroy, E., Ide, S. E., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R., et al. (1997) · Science · doi:10.1126/science.276.5321.2045 · Cited by 8,240
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
Hutton, M., Lendon, C. L., Rizzu, P., Baker, M., Froelich, S., Houlden, H., Pickering-Brown, S., Chakraverty, S., Isaacs, A., Grover, A., et al. (1998) · Nature · doi:10.1038/31508 · Cited by 3,498
Self-citationHereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
Valente, E. M., Abou-Sleiman, P. M., Caputo, V., Muqit, M. M. K., Harvey, K., Gispert, S., Ali, Z., Del Turco, D., Bentivoglio, A. R., Healy, D. G., et al. (2004) · Science · doi:10.1126/science.1096284 · Cited by 3,481
α-synuclein locus duplication as a cause of familial Parkinson's disease
Chartier-Harlin, M.-C., Kachergus, J., Roumier, C., Mouroux, V., Douay, X., Lincoln, S., Levecque, C., Larvor, L., Andrieux, J., Hulihan, M., et al. (2004) · The Lancet · doi:10.1016/s0140-6736(04)17103-1 · Cited by 2,029
Self-citationInitiation and Synergistic Fibrillization of Tau and Alpha-Synuclein
Giasson, B. I., Forman, M. S., Higuchi, M., Golbe, L. I., Graves, C. L., Kotzbauer, P. T., Trojanowski, J. Q., & Lee, V. M.-Y. (2003) · Science · doi:10.1126/science.1082324 · Cited by 879
Research works printed but not linked: 25
- Arvanitakis, 2001, Recent advances in the understanding of tau protein and movement disorders, Curr. Opin. Neurol, 14, 491, 10.1097/00019052-200108000-00010 · DOI
- Bonifati, 2003, Mutations in the DJ-1 gene associated with autosomal recessive early-onset Parkinsonism, Science, 299, 256, 10.1126/science.1077209 · DOI · Paper page
- Bosgraaf, 2003, Roc, a Ras/GTPase domain in complex proteins, Biochim. Biophys. Acta, 1643, 5, 10.1016/j.bbamcr.2003.08.008 · DOI · Paper page
- Dickson, 1999, Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration, J. Neurol, 246, 6, 10.1007/BF03161076 · DOI · Paper page
- Duda, 2002, Concurrence of alpha-synuclein and tau brain pathology in the Contursi kindred, Acta Neuropathol. (Berl.), 104, 7, 10.1007/s00401-002-0563-3 · DOI · Paper page
- Farrer, 1999, The genetics of disorders with synuclein pathology and Parkinsonism, Hum. Mol. Genet, 8, 81, 10.1093/hmg/8.1.81 · DOI
- Funayama, 2002, A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1, Ann. Neurol, 51, 296, 10.1002/ana.10113 · DOI · Paper page
- Gasser, 1998, A susceptibility locus for Parkinson's disease maps to chromosome 2p13, Nat. Genet, 18, 262, 10.1038/ng0398-262 · DOI · Paper page
- Gotz, 2001, Formation of neurofibrillary tangles in P301l tau transgenic mice induced by Abeta 42 fibrils, Science, 293, 1491, 10.1126/science.1062097 · DOI · Paper page
- Hicks, 2002, A susceptibility gene for late-onset idiopathic Parkinson's disease, Ann. Neurol, 52, 549, 10.1002/ana.10324 · DOI · Paper page
- Hubbard, 2000, Protein tyrosine kinase structure and function, Annu. Rev. Biochem, 69, 373, 10.1146/annurev.biochem.69.1.373 · DOI · Paper page
- Kitada, 1998, Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism, Nature, 392, 605, 10.1038/33416 · DOI · Paper page
- Ishizawa, 2003, Colocalization of tau and alpha-synuclein epitopes in Lewy bodies, J. Neuropathol. Exp. Neurol, 62, 389, 10.1093/jnen/62.4.389 · DOI · Paper page
- Kobe, 2001, The leucine-rich repeat as a protein recognition motif, Curr. Opin. Struct. Biol, 11, 725, 10.1016/S0959-440X(01)00266-4 · DOI · Paper page
- Lewis, 2001, Enhanced neurofibrillary degeneration in transgenic mice expressing mutant tau and APP, Science, 293, 1487, 10.1126/science.1058189 · DOI · Paper page
- Paisán-Ruı́z, C., Jain, S., Evans, E.W., Gilks, W.P., Simón, J., van der Brug, M., López de Munain, A., Aparicio, S., Gil, A.M., Khan, N., et al. (2004). Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 44, this issue, 595–600. Published online October 22, 2004. · DOI · Paper page
- Pankratz, 2003, Significant linkage of Parkinson disease to chromosome 2q36–37, Am. J. Hum. Genet, 72, 1053, 10.1086/374383 · DOI
- Ridley, 2001, Rho family proteins, Trends Cell Biol, 11, 471, 10.1016/S0962-8924(01)02153-5 · DOI · Paper page
- Scott, 2000, Fine mapping of the chromosome 12 late-onset Alzheimer disease locus, Am. J. Hum. Genet, 66, 922, 10.1086/302828 · DOI
- Singleton, 2003, α-synuclein locus triplication causes Parkinson's disease, Science, 302, 841, 10.1126/science.1090278 · DOI · Paper page
- Smith, 1999, The WD repeat, Trends Biochem. Sci, 24, 181, 10.1016/S0968-0004(99)01384-5 · DOI · Paper page
- Tang, 1999, Chip-based genotyping by mass spectrometry, Proc. Natl. Acad. Sci. USA, 96, 10016, 10.1073/pnas.96.18.10016 · DOI · Paper page
- Wszolek, 1997, German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia—longitudinal observations, Parkinsonism Relat. Disord, 3, 125, 10.1016/S1353-8020(97)00013-8 · DOI
- Wszolek, 2004, Autosomal dominant parkinsonism associated with variable synuclein and tau pathology, Neurology, 62, 1619, 10.1212/01.WNL.0000125015.06989.DB · DOI · Paper page
- Zimprich, 2004, The PARK8 locus in autosomal dominant Parkinsonism, Am. J. Hum. Genet, 74, 11, 10.1086/380647 · DOI
Cited by
Pathological roles of MAPK signaling pathways in human diseases
Kim, E. K., & Choi, E.-J. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2009.12.009 · Cited by 2,472
The Role of Oxidative Stress in Parkinson's Disease
Dias, V., Junn, E., & Mouradian, M. M. (2013) · Journal of Parkinson’s Disease · doi:10.3233/jpd-130230 · Cited by 1,845
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Simón-Sánchez, J., Schulte, C., Bras, J. M., Sharma, M., Gibbs, J. R., Berg, D., Paisan-Ruiz, C., Lichtner, P., Scholz, S. W., Hernandez, D. G., et al. (2009) · Nature Genetics · doi:10.1038/ng.487 · Cited by 1,751
Self-citationInflammation and immune dysfunction in Parkinson disease
Tansey, M. G., Wallings, R. L., Houser, M. C., Herrick, M. K., Keating, C. E., & Joers, V. (2022) · Nature Reviews Immunology · doi:10.1038/s41577-022-00684-6 · Cited by 1,382
Healy, D. G., Falchi, M., O'Sullivan, S. S., Bonifati, V., Durr, A., Bressman, S., Brice, A., Aasly, J., Zabetian, C. P., Goldwurm, S., et al. (2008) · The Lancet Neurology · doi:10.1016/s1474-4422(08)70117-0 · Cited by 1,425
Self-citation
Metadata
- Authors
- Zimprich, A., Biskup, S., Leitner, P., Lichtner, P., Farrer, M., Lincoln, S., Kachergus, J., Hulihan, M., Uitti, R. J., Calne, D. B., Stoessl, A. J., Pfeiffer, R. F., Patenge, N., Carbajal, I. C., Vieregge, P., Asmus, F., Müller-Myhsok, B., Dickson, D. W., Meitinger, T., Strom, T. M., Wszolek, Z. K., & Gasser, T.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2004-11
- Volume
- 44
- Issue
- 4
- Pages
- 601-607
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2063127941
- Cited by
- 3,005
- References
- 5
- FWCI
- 89.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 3180 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
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- CoChat. (2026). Citation check: Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology. https://app.cochat.ai/papers/10.1016/j.neuron.2004.11.005
- The paper
- Zimprich, A., Biskup, S., Leitner, P., Lichtner, P., Farrer, M., Lincoln, S., Kachergus, J., Hulihan, M., Uitti, R. J., Calne, D. B., Stoessl, A. J., Pfeiffer, R. F., Patenge, N., Carbajal, I. C., Vieregge, P., Asmus, F., Müller-Myhsok, B., Dickson, D. W., Meitinger, T., . . . Gasser, T. (2004). Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology. Neuron. https://doi.org/10.1016/j.neuron.2004.11.005
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
