3071 - 3080 of 9131 Results
Title
Year
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OPENTitle: Prediction of dyskinesia in Parkinson’s disease patients using machine learning algorithmsJournal Name: Scientific ReportsPublisher: Springer Science and Business Media LLCVol: 13Issue #: 1Start Page: 22426End Page: 22426Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41598-023-49617-wBest OA location URL: https://www.nature.com/articles/s41598-023-49617-w.pdfCitation Count: 9
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OPENTitle: Genetic risk scores and hallucinations in patients with Parkinson diseaseJournal Name: Neurology GeneticsPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 6Issue #: 5Start Page: e492End Page: e492Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/nxg.0000000000000492Best OA location URL: https://escholarship.org/uc/item/22d7k5j8Citation Count: 25
- A Parkinson's disease Circ RNA s Resource reveals a link between circ SLC 8A1 and oxidative stress2020OPENTitle: A Parkinson's disease Circ RNA s Resource reveals a link between circ SLC 8A1 and oxidative stressJournal Name: EMBO Molecular MedicinePublisher: Springer Science and Business Media LLCVol: 12Issue #: 9Start Page: e11942End Page: e11942Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.15252/emmm.201911942Best OA location URL: https://doi.org/10.15252/emmm.201911942Citation Count: 150
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OPENTitle: Lack of evidence for genetic association of saposins A, B, C and D with Parkinson’s diseaseJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 143Issue #: 9Start Page: e72End Page: e72Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/brain/awaa214Best OA location URL: https://academic.oup.com/brain/article-pdf/143/9/e72/34280049/awaa214.pdfCitation Count: 14
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OPENTitle: Different impulse control disorder evolution patterns and white matter microstructural damage in the progression of Parkinson’s diseaseJournal Name: Frontiers in Aging NeurosciencePublisher: Frontiers Media SAVol: 15Issue #:Start Page: 1260630End Page: 1260630Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnagi.2023.1260630Best OA location URL: https://www.frontiersin.org/articles/10.3389/fnagi.2023.1260630/pdf?isPublishedV2=FalseCitation Count: 0
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OPENTitle: Epigenome-wide association study of Alzheimer’s disease replicates 22 differentially methylated positions and 30 differentially methylated regionsJournal Name: Clinical EpigeneticsPublisher: Springer Science and Business Media LLCVol: 12Issue #: 1Start Page: 149End Page: 149Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1186/s13148-020-00944-zBest OA location URL: https://clinicalepigeneticsjournal.biomedcentral.com/track/pdf/10.1186/s13148-020-00944-zCitation Count: 80
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OPENTitle: PyRates—A code-generation tool for modeling dynamical systems in biology and beyondJournal Name: PLOS Computational BiologyPublisher: Public Library of Science (PLoS)Vol: 19Issue #: 12Start Page: e1011761End Page: e1011761Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1371/journal.pcbi.1011761Best OA location URL: https://doi.org/10.1371/journal.pcbi.1011761Citation Count: 7
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RESTRICTEDTitle: Altered dynamic functional network connectivity in drug-naïve Parkinson’s disease patients with excessive daytime sleepinessJournal Name: Frontiers in Aging NeurosciencePublisher: Frontiers Media SAVol: 15Issue #:Start Page: 1282962End Page: 1282962Publication Date:Open Access(OA) Status: RESTRICTEDLicense: cc-byDOI - Digital Object Identifier: 10.3389/fnagi.2023.1282962Best OA location URL: https://www.frontiersin.org/articles/10.3389/fnagi.2023.1282962/pdf?isPublishedV2=FalseCitation Count: 23
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OPENTitle: Decreasing the intrinsically disordered protein α-synuclein levels by targeting its structured mRNA with a ribonuclease-targeting chimeraJournal Name: Proceedings of the National Academy of SciencesPublisher: National Academy of SciencesVol: 121Issue #: 2Start Page: e2306682120End Page: e2306682120Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1073/pnas.2306682120Best OA location URL: https://www.pnas.org/doi/pdf/10.1073/pnas.2306682120Citation Count: 44
- Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly2023OPENTitle: Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephalyJournal Name: European Journal of Human GeneticsPublisher: Springer Science and Business Media LLCVol: 32Issue #: 1Start Page: 52End Page: 60Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41431-023-01461-2Best OA location URL: https://www.nature.com/articles/s41431-023-01461-2.pdfCitation Count: 11