Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk.
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| Title: | Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk. |
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| Authors: | Lake J; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Reed X; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Langston RG; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Nalls MA; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Center for Alzheimer's and Related Dementias, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA., Gan-Or Z; Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada.; Department of Human Genetics, McGill University, Montréal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada., Cookson MR; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Singleton AB; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Center for Alzheimer's and Related Dementias, National Institutes of Health, Bethesda, Maryland, USA., Blauwendraat C; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA., Leonard HL; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Center for Alzheimer's and Related Dementias, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany. |
| Corporate Authors: | International Parkinson's Disease Genomics Consortium (IPDGC) |
| Source: | Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2022 Jan; Vol. 37 (1), pp. 95-105. Date of Electronic Publication: 2021 Sep 20. |
| Publication Type: | Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8257 (Electronic) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 34542912 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Lake+J%22">Lake J</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Reed+X%22">Reed X</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Langston+RG%22">Langston RG</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Nalls+MA%22">Nalls MA</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Center for Alzheimer's and Related Dementias, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Gan-Or+Z%22">Gan-Or Z</searchLink>; Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada.; Department of Human Genetics, McGill University, Montréal, Quebec, Canada.; Department of Neurology and Neurosurgery, McGill University, Montréal, Quebec, Canada.<br /><searchLink fieldCode="AU" term="%22Cookson+MR%22">Cookson MR</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Singleton+AB%22">Singleton AB</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Center for Alzheimer's and Related Dementias, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Blauwendraat+C%22">Blauwendraat C</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Leonard+HL%22">Leonard HL</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.; Center for Alzheimer's and Related Dementias, National Institutes of Health, Bethesda, Maryland, USA.; Data Tecnica International, Glen Echo, Maryland, USA.; German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22International+Parkinson's+Disease+Genomics+Consortium+%28IPDGC%29%22">International Parkinson's Disease Genomics Consortium (IPDGC)</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228610688%22">Movement disorders : official journal of the Movement Disorder Society</searchLink> [Mov Disord] 2022 Jan; Vol. 37 (1), pp. 95-105. <i>Date of Electronic Publication: </i>2021 Sep 20. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Meta-Analysis; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S. – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Liss%22">Wiley-Liss </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8610688 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1531-8257 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2208853185%22">08853185 </searchLink><i>NLM ISO Abbreviation: </i>Mov Disord <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=34542912 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/mds.28787 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 95 Titles: – TitleFull: Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lake J – PersonEntity: Name: NameFull: Reed X – PersonEntity: Name: NameFull: Langston RG – PersonEntity: Name: NameFull: Nalls MA – PersonEntity: Name: NameFull: Gan-Or Z – PersonEntity: Name: NameFull: Cookson MR – PersonEntity: Name: NameFull: Singleton AB – PersonEntity: Name: NameFull: Blauwendraat C – PersonEntity: Name: NameFull: Leonard HL IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: 2022 Jan Type: published Y: 2022 Identifiers: – Type: issn-electronic Value: 1531-8257 Numbering: – Type: volume Value: 37 – Type: issue Value: 1 Titles: – TitleFull: Movement disorders : official journal of the Movement Disorder Society Type: main |
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