2201 - 2210 of 6466 Results
Title
Year
- Global network and local vulnerabilities underlie brain atrophy across Parkinson’s disease stages2025OPENTitle: Global network and local vulnerabilities underlie brain atrophy across Parkinson’s disease stagesJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 149Issue #: 7Start Page: 2380End Page: 2394Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/brain/awaf432Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awaf432/65292384/awaf432.pdfCitation Count: 2
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OPENTitle: SETD7-mediated monomethylation is enriched on soluble Tau in Alzheimer’s diseaseJournal Name: Molecular NeurodegenerationPublisher: Springer Science and Business Media LLCVol: 16Issue #: 1Start Page: 46End Page: 46Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13024-021-00468-xBest OA location URL: https://molecularneurodegeneration.biomedcentral.com/counter/pdf/10.1186/s13024-021-00468-xCitation Count: 27
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OPENTitle: Genomewide Association Studies of LRRK2 Modifiers of Parkinson's DiseaseJournal Name: Annals of NeurologyPublisher: WileyVol: 90Issue #: 1Start Page: 76End Page: 88Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/ana.26094Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ana.26094Citation Count: 50
- Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome2024OPENTitle: Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndromeJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 5Start Page: 1822End Page: 1836Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awae010Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae010/55676562/awae010.pdfCitation Count: 13
- The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders2024OPENTitle: The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disordersJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 8Start Page: 2775End Page: 2790Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awae056Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae056/56907442/awae056.pdfCitation Count: 13
- RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity2024OPENTitle: RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticityJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 7Start Page: 2334End Page: 2343Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awae091Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae091/57089091/awae091.pdfCitation Count: 8
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OPENTitle: Somatic instability of the FGF14 -SCA27B GAA•TTC repeat reveals a marked expansion bias in the cerebellumJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 148Issue #: 4Start Page: 1258End Page: 1270Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/brain/awae312Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awae312/59644388/awae312.pdfCitation Count: 16
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OPENTitle: LRRK2 Modulates the Exocyst Complex Assembly by Interacting with Sec8Journal Name: CellsPublisher: MDPI AGVol: 10Issue #: 2Start Page: 203End Page: 203Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/cells10020203Best OA location URL: https://www.mdpi.com/2073-4409/10/2/203/pdf?version=1611625974Citation Count: 1
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OPENTitle: From trials to clinical practice: Temporal trends in the coverage of specialized allied health services for Parkinson's diseaseJournal Name: European Journal of NeurologyPublisher: WileyVol: 28Issue #: 3Start Page: 775End Page: 782Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1111/ene.14627Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/ene.14627Citation Count: 16
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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: 388