1341 - 1350 of 6420 Results
Title
Year
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OPENTitle: Long genes are more frequently affected by somatic mutations and show reduced expression in Alzheimer's disease: Implications for disease etiologyJournal Name: Alzheimer's & DementiaPublisher: WileyVol: 17Issue #: 3Start Page: 489End Page: 499Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1002/alz.12211Best OA location URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/alz.12211Citation Count: 29
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OPENTitle: Loss of One Engrailed1 Allele Enhances Induced α-SynucleinopathyJournal Name: Journal of Parkinson's DiseasePublisher: SAGE PublicationsVol: 9Issue #: 2Start Page: 315End Page: 326Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.3233/jpd-191590Best OA location URL: https://content.iospress.com:443/download/journal-of-parkinsons-disease/jpd191590?id=journal-of-parkinsons-disease%2Fjpd191590Citation Count: 15
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OPENTitle: Common and rare GCH1 variants are associated with Parkinson's diseaseJournal Name: Neurobiology of AgingPublisher: Elsevier BVVol: 73Issue #:Start Page: 231.e1End Page: 231.e6Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1016/j.neurobiolaging.2018.09.008Citation Count: 29
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OPENTitle: Prevalence and Clinical Implications of a β-Amyloid–Negative, Tau-Positive Cerebrospinal Fluid Biomarker Profile in Alzheimer DiseaseJournal Name: JAMA NeurologyPublisher: American Medical Association (AMA)Vol: 80Issue #: 9Start Page: 969End Page: 969Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1001/jamaneurol.2023.2338Best OA location URL: https://jamanetwork.com/journals/jamaneurology/articlepdf/2807607/jamaneurology_erickson_2023_oi_230049_1689611082.26721.pdfCitation Count: 32
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OPENTitle: Consumption of Dairy Products and Risk of Parkinson's DiseaseJournal Name: American Journal of EpidemiologyPublisher: Oxford University Press (OUP)Vol: 165Issue #: 9Start Page: 998End Page: 1006Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/aje/kwk089Best OA location URL: https://academic.oup.com/aje/article-pdf/165/9/998/204475/kwk089.pdfCitation Count: 184
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OPENTitle: In situ structural analysis reveals membrane shape transitions during autophagosome formationJournal Name: Proceedings of the National Academy of SciencesPublisher: Proceedings of the National Academy of SciencesVol: 119Issue #: 39Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-nd, cc-by-nc-ndDOI - Digital Object Identifier: 10.1073/pnas.2209823119Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9522377Citation Count: 79
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OPENTitle: Altered SOD1 maturation and post-translational modification in amyotrophic lateral sclerosis spinal cordJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 145Issue #: 9Start Page: 3108End Page: 3130Publication Date:Open Access(OA) Status: OPENLicense: cc-by-ncDOI - Digital Object Identifier: 10.1093/brain/awac165Best OA location URL: https://academic.oup.com/brain/article-pdf/145/9/3108/45824171/awac165.pdfCitation Count: 54
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OPENTitle: A Markov random field model-based approach for differentially expressed gene detection from single-cell RNA-seq dataJournal Name: Briefings in BioinformaticsPublisher: Oxford University Press (OUP)Vol: 23Issue #: 5Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.1093/bib/bbac166Best OA location URL: https://academic.oup.com/bib/article-pdf/23/5/bbac166/45937268/bbac166.pdfCitation Count: 6
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OPENTitle: Association of Olfactory Performance With Motor Decline and Age at Onset in People With Parkinson Disease and the LRRK2 G2019S VariantJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 99Issue #: 8Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0000000000200737Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/9484727Citation Count: 8
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OPENTitle: Use of Whole-Genome Sequencing for Mitochondrial Disease DiagnosisJournal Name: NeurologyPublisher: Ovid Technologies (Wolters Kluwer Health)Vol: 99Issue #: 7Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1212/wnl.0000000000200745Best OA location URL: https://n.neurology.org/content/neurology/99/7/e730.full.pdfCitation Count: 52