1351 - 1375 of 9030 Results
Title
Year
- Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions2010OPENTitle: Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusionsJournal Name: Nature GeneticsPublisher: Springer Science and Business Media LLCVol: 42Issue #: 3Start Page: 234End Page: 239Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/ng.536Best OA location URL: http://doi.org/10.1038/ng.536Citation Count: 604
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OPENTitle: Clinical and demographic characteristics related to onset site and spread of cervical dystoniaJournal Name: Movement DisordersPublisher: WileyVol: 31Issue #: 12Start Page: 1874End Page: 1882Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.26817Best OA location URL: http://doi.org/10.1002/mds.26817Citation Count: 47
- Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter Hyperintensities2020RESTRICTEDTitle: Parkinson's Disease, NOTCH3 Genetic Variants, and White Matter HyperintensitiesJournal Name: Movement DisordersPublisher: WileyVol: 35Issue #: 11Start Page: 2090End Page: 2095Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1002/mds.28171Citation Count: 28
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OPENTitle: Suitability of Automated Writing Measures for Clinical Trial Outcome in Writer's CrampJournal Name: Movement DisordersPublisher: WileyVol: 38Issue #: 1Start Page: 123End Page: 132Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.29237Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9851940Citation Count: 8
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OPENTitle: Longitudinal Clinical and Biological Characteristics in Juvenile‐Onset Huntington's DiseaseJournal Name: Movement DisordersPublisher: WileyVol: 38Issue #: 1Start Page: 113End Page: 122Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.29251Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9851979Citation Count: 15
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OPENTitle: Pathogenic Parkinson’s disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvationJournal Name: Biochemical and Biophysical Research CommunicationsPublisher: Elsevier BVVol: 441Issue #: 4Start Page: 862End Page: 866Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.bbrc.2013.10.159Best OA location URL: https://doi.org/10.1016/j.bbrc.2013.10.159Citation Count: 86
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OPENTitle: Characterization of TAE684 as a potent LRRK2 kinase inhibitorJournal Name: Bioorganic & Medicinal Chemistry LettersPublisher: Elsevier BVVol: 22Issue #: 5Start Page: 1864End Page: 1869Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.bmcl.2012.01.084Best OA location URL: http://hdl.handle.net/10871/35667Citation Count: 88
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OPENTitle: Analysis of macroautophagy related proteins in G2019S LRRK2 Parkinson’s disease brains with Lewy body pathologyJournal Name: Brain ResearchPublisher: Elsevier BVVol: 1701Issue #:Start Page: 75End Page: 84Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.brainres.2018.07.023Best OA location URL: https://doi.org/10.1016/j.brainres.2018.07.023Citation Count: 41
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OPENTitle: Genetic variability in the regulation of gene expression in ten regions of the human brainJournal Name: Nature NeurosciencePublisher: Springer Science and Business Media LLCVol: 17Issue #: 10Start Page: 1418End Page: 1428Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/nn.3801Best OA location URL: http://doi.org/10.1038/nn.3801Citation Count: 705
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OPENTitle: Role of Elongation and Secondary Pathways in S6 Amyloid Fibril GrowthJournal Name: Biophysical JournalPublisher: Elsevier BVVol: 102Issue #: 9Start Page: 2167End Page: 2175Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.bpj.2012.03.047Best OA location URL: http://www.cell.com/article/S0006349512003888/pdfCitation Count: 35
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OPENTitle: Hippocampal Neuroinflammation, Functional Connectivity, and Depressive Symptoms in Multiple SclerosisJournal Name: Biological PsychiatryPublisher: Elsevier BVVol: 80Issue #: 1Start Page: 62End Page: 72Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1016/j.biopsych.2015.11.022Best OA location URL: https://kclpure.kcl.ac.uk/ws/files/46558917/1_s2.0_S0006322315010252_main.pdfCitation Count: 146
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OPENTitle: Rare variants in LRRK1 and Parkinson's diseaseJournal Name: neurogeneticsPublisher: Springer Science and Business Media LLCVol: 15Issue #: 1Start Page: 49End Page: 57Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1007/s10048-013-0383-8Best OA location URL: https://link.springer.com/content/pdf/10.1007/s10048-013-0383-8.pdfCitation Count: 32
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OPENTitle: Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar DegenerationJournal Name: Archives of NeurologyPublisher: American Medical Association (AMA)Vol: 68Issue #: 4Start Page: 488End Page: 488Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1001/archneurol.2011.53Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/3160280Citation Count: 121
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OPENTitle: Differential Associations of Apolipoprotein E ε4 Genotype With Attentional Abilities Across the Life Span of Individuals With Down SyndromeJournal Name: JAMA Network OpenPublisher: American Medical Association (AMA)Vol: 3Issue #: 9Start Page: e2018221End Page: e2018221Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1001/jamanetworkopen.2020.18221Best OA location URL: https://jamanetwork.com/journals/jamanetworkopen/articlepdf/2770878/dsouza_2020_oi_200657_1605807465.21177.pdfCitation Count: 10
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OPENTitle: Mitochondrial complex IV defects induce metabolic and signaling perturbations that expose potential vulnerabilities in HCT116 cellsJournal Name: FEBS Open BioPublisher: WileyVol: 12Issue #: 5Start Page: 959End Page: 982Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1002/2211-5463.13398Best OA location URL: https://doi.org/10.1002/2211-5463.13398Citation Count: 9
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OPENTitle: Genome-wide association study identifies four novel loci associated with Alzheimer’s endophenotypes and disease modifiersJournal Name: Acta NeuropathologicaPublisher: Springer Science and Business Media LLCVol: 133Issue #: 5Start Page: 839End Page: 856Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1007/s00401-017-1685-yBest OA location URL: http://doi.org/10.1007/s00401-017-1685-yCitation Count: 250
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OPENTitle: Investigation of Autosomal Genetic Sex Differences in Parkinson's DiseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 90Issue #: 1Start Page: 35End Page: 42Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc, cc-by-ncDOI - Digital Object Identifier: 10.1002/ana.26090Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.26090Citation Count: 61
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OPENTitle: Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architectureJournal Name: Nature GeneticsPublisher: Springer Science and Business Media LLCVol: 53Issue #: 3Start Page: 294End Page: 303Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41588-021-00785-3Best OA location URL: https://escholarship.org/uc/item/7qn6v913Citation Count: 474
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OPENTitle: Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s diseaseJournal Name: Nature GeneticsPublisher: Springer Science and Business Media LLCVol: 52Issue #: 5Start Page: 482End Page: 493Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41588-020-0610-9Best OA location URL: https://kclpure.kcl.ac.uk/ws/files/151614623/Genetic_Identification_of_Cell_Types_Underlying_Brain_Complex_BREEN_Published27April2020_GREEN_AAM.pdfCitation Count: 375
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OPENTitle: Identification of evolutionarily conserved gene networks mediating neurodegenerative dementiaJournal Name: Nature MedicinePublisher: Springer Science and Business Media LLCVol: 25Issue #: 1Start Page: 152End Page: 164Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41591-018-0223-3Best OA location URL: https://escholarship.org/uc/item/7f81n266Citation Count: 154
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OPENTitle: Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson diseaseJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 111Issue #: 7Start Page: 2626End Page: 2631Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1073/pnas.1318306111Best OA location URL: https://www.pnas.org/content/pnas/111/7/2626.full.pdfCitation Count: 365
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OPENTitle: Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegenerationJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 17Start Page: 4621End Page: 4638Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddu178Best OA location URL: https://academic.oup.com/hmg/article-pdf/23/17/4621/2215861/ddu178.pdfCitation Count: 174
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OPENTitle: A multi-ancestry genome-wide study incorporating gene–smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressureJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 28Issue #: 15Start Page: 2615End Page: 2633Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddz070Best OA location URL: https://academic.oup.com/hmg/article-pdf/28/15/2615/28936234/ddz070.pdfCitation Count: 47
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OPENTitle: Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson’s diseaseJournal Name: Nature GeneticsPublisher: Springer Science and Business Media LLCVol: 53Issue #: 6Start Page: 787End Page: 793Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41588-021-00847-6Best OA location URL: http://hdl.handle.net/1887/3249471Citation Count: 137
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OPENTitle: Structure of LRRK2 in Parkinson’s disease and model for microtubule interactionJournal Name: NaturePublisher: Springer Science and Business Media LLCVol: 588Issue #: 7837Start Page: 344End Page: 349Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1038/s41586-020-2673-2Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/7726071Citation Count: 243