3321 - 3330 of 8571 Results
Title
Year
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OPENTitle: SparkINFERNO: a scalable high-throughput pipeline for inferring molecular mechanisms of non-coding genetic variantsJournal Name: BioinformaticsPublisher: Oxford University Press (OUP)Vol: 36Issue #: 12Start Page: 3879End Page: 3881Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1093/bioinformatics/btaa246Best OA location URL: https://academic.oup.com/bioinformatics/article-pdf/36/12/3879/33437175/btaa246.pdfCitation Count: 12
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OPENTitle: Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutationsJournal Name: Brain CommunicationsPublisher: Oxford University Press (OUP)Vol: 6Issue #: 6Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-by, cc-byDOI - Digital Object Identifier: 10.1093/braincomms/fcae377Best OA location URL: https://academic.oup.com/braincomms/advance-article-pdf/doi/10.1093/braincomms/fcae377/60136284/fcae377.pdfCitation Count: 0
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OPENTitle: Bidirectional relationship between olfaction and Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1038/s41531-024-00838-4Best OA location URL: https://www.nature.com/articles/s41531-024-00838-4.pdfCitation Count: 0
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OPENTitle: Digital health technology for Parkinson's disease with comprehensive monitoring and artificial intelligence-enabled haptic biofeedback for bulbar dysfunctionJournal Name: Journal of Parkinson’s DiseasePublisher: SAGE PublicationsVol: 15Issue #: 3Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1177/1877718x251329354Best OA location URL: https://journals.sagepub.com/doi/pdf/10.1177/1877718X251329354Citation Count: 0
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OPENTitle: Missing Drivers with Dementia: Antecedents and RecoveryJournal Name: Journal of the American Geriatrics SocietyPublisher: WileyVol: 60Issue #: 11Start Page: 2063End Page: 2069Publication Date:Open Access(OA) Status: OPENLicense: public-domainDOI - Digital Object Identifier: 10.1111/j.1532-5415.2012.04159.xBest OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1532-5415.2012.04159.xCitation Count: 20
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RESTRICTEDTitle: Heartbeat signature for predicting motor and non-motor involvement among nonparkinsonian LRRK2 G2019S mutation carriersJournal Name: Clinical Autonomic ResearchPublisher: Springer Science and Business Media LLCVol: 35Issue #: 3Start Page:End Page:Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1007/s10286-024-01104-6Citation Count: 0
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OPENTitle: Peripheral immune cell abundance differences link blood mitochondrial DNA copy number and Parkinson’s diseaseJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 10Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-024-00831-xBest OA location URL: https://www.nature.com/articles/s41531-024-00831-x.pdfCitation Count: 3
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OPENTitle: Discovery of a Pyrrolopyrimidine (JH-II-127), a Highly Potent, Selective, and Brain Penetrant LRRK2 InhibitorJournal Name: ACS Medicinal Chemistry LettersPublisher: American Chemical Society (ACS)Vol: 6Issue #: 5Start Page: 584End Page: 589Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1021/acsmedchemlett.5b00064Best OA location URL: http://doi.org/10.1021/acsmedchemlett.5b00064Citation Count: 50
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RESTRICTEDTitle: Patients with Parkinson's disease and a history of falls have decreased cerebellar grey matter volumes in the cognitive cerebellumJournal Name: Revue NeurologiquePublisher: Elsevier BVVol: 178Issue #: 9Start Page: 924End Page: 931Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.neurol.2022.05.002Citation Count: 5
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OPENTitle: LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorderJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 52Issue #:Start Page: 98End Page: 101Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2018.03.019Best OA location URL: http://hdl.handle.net/11380/1206056Citation Count: 32