The Global Parkinson's Disease Genetics (GP2) Genome Browser.
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| Title: | The Global Parkinson's Disease Genetics (GP2) Genome Browser. |
|---|---|
| Authors: | Fang ZH; DataTecnica, Washington, District of Columbia, USA.; German Center for Neurodegenerative Disease (DZNE), Tübingen, Germany., Grant RH; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Vitale D; DataTecnica, Washington, District of Columbia, USA.; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA., Hernandez CF; Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Santiago, Chile., Hong S; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA., Leonard HL; DataTecnica, Washington, District of Columbia, USA.; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA., Makarious MB; DataTecnica, Washington, District of Columbia, USA., Lange LM; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA., Solomonson M; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Heutink P; Global Parkinson's Genetics Program, Bethesda, Maryland, USA., Dilliott AA; Parkinson's Foundation, New York, New York, USA., Galvelis KG; Parkinson's Foundation, New York, New York, USA., Nalls MA; DataTecnica, Washington, District of Columbia, USA.; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA., Singleton AB; Global Parkinson's Genetics Program, Bethesda, Maryland, USA., Blauwendraat C; Global Parkinson's Genetics Program, Bethesda, Maryland, USA.; Coalition for Aligning Science, Chevy Chase, Maryland, USA. |
| Corporate Authors: | Global Parkinson's Genetics Program (GP2) |
| Source: | Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2026 Apr 19. Date of Electronic Publication: 2026 Apr 19. |
| Publication Type: | Journal Article |
| 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 |
| FullText | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 42003207 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: The Global Parkinson's Disease Genetics (GP2) Genome Browser. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Fang+ZH%22">Fang ZH</searchLink>; DataTecnica, Washington, District of Columbia, USA.; German Center for Neurodegenerative Disease (DZNE), Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Grant+RH%22">Grant RH</searchLink>; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.<br /><searchLink fieldCode="AU" term="%22Vitale+D%22">Vitale D</searchLink>; DataTecnica, Washington, District of Columbia, USA.; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Hernandez+CF%22">Hernandez CF</searchLink>; Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Santiago, Chile.<br /><searchLink fieldCode="AU" term="%22Hong+S%22">Hong S</searchLink>; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Leonard+HL%22">Leonard HL</searchLink>; DataTecnica, Washington, District of Columbia, USA.; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Makarious+MB%22">Makarious MB</searchLink>; DataTecnica, Washington, District of Columbia, USA.<br /><searchLink fieldCode="AU" term="%22Lange+LM%22">Lange LM</searchLink>; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Solomonson+M%22">Solomonson M</searchLink>; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.<br /><searchLink fieldCode="AU" term="%22Heutink+P%22">Heutink P</searchLink>; Global Parkinson's Genetics Program, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Dilliott+AA%22">Dilliott AA</searchLink>; Parkinson's Foundation, New York, New York, USA.<br /><searchLink fieldCode="AU" term="%22Galvelis+KG%22">Galvelis KG</searchLink>; Parkinson's Foundation, New York, New York, USA.<br /><searchLink fieldCode="AU" term="%22Nalls+MA%22">Nalls MA</searchLink>; DataTecnica, Washington, District of Columbia, USA.; Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Singleton+AB%22">Singleton AB</searchLink>; Global Parkinson's Genetics Program, Bethesda, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Blauwendraat+C%22">Blauwendraat C</searchLink>; Global Parkinson's Genetics Program, Bethesda, Maryland, USA.; Coalition for Aligning Science, Chevy Chase, Maryland, USA. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22Global+Parkinson's+Genetics+Program+%28GP2%29%22">Global Parkinson's Genetics Program (GP2)</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] 2026 Apr 19. <i>Date of Electronic Publication: </i>2026 Apr 19. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – 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=42003207 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/mds.70309 Languages: – Code: eng Text: English Titles: – TitleFull: The Global Parkinson's Disease Genetics (GP2) Genome Browser. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Fang ZH – PersonEntity: Name: NameFull: Grant RH – PersonEntity: Name: NameFull: Vitale D – PersonEntity: Name: NameFull: Hernandez CF – PersonEntity: Name: NameFull: Hong S – PersonEntity: Name: NameFull: Leonard HL – PersonEntity: Name: NameFull: Makarious MB – PersonEntity: Name: NameFull: Lange LM – PersonEntity: Name: NameFull: Solomonson M – PersonEntity: Name: NameFull: Heutink P – PersonEntity: Name: NameFull: Dilliott AA – PersonEntity: Name: NameFull: Galvelis KG – PersonEntity: Name: NameFull: Nalls MA – PersonEntity: Name: NameFull: Singleton AB – PersonEntity: Name: NameFull: Blauwendraat C IsPartOfRelationships: – BibEntity: Dates: – D: 19 M: 04 Text: 2026 Apr 19 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1531-8257 Titles: – TitleFull: Movement disorders : official journal of the Movement Disorder Society Type: main |
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