GP2: The Global Parkinson's Genetics Program

The Global Parkinson’s Genetics Program

doi:10.1002/mds.28494

GP2: The Global Parkinson's Genetics Program

The Global Parkinson’s Genetics Program

Neurology

Research output: Contribution to journal › Comment/debate › peer-review

76 Scopus citations

Original language	English (US)
Pages (from-to)	842-851
Number of pages	10
Journal	Movement Disorders
Volume	36
Issue number	4
DOIs	https://doi.org/10.1002/mds.28494
State	Published - Apr 2021

Funding

Dr. Singleton is supported by the Intramural Research Program of the National Institute on Aging and has received grant support from the Michael J. Fox Foundation for Parkinson's Research and the Aligning Science Across Parkinson's Initiative. He has received royalty payments related to a diagnostic for stroke. Dr. Blauwendraat is supported by the Intramural Research Program of the National Institute on Aging and has received grant support from the Michael J. Fox Foundation for Parkinson's Research and the Aligning Science Across Parkinson's Initiative. Relevant conflicts of interest/financial disclosures: This research was supported by the Aligning Science Across Parkinson's Initiative, the Intramural Research Program, National Institute on Aging, National Institutes of Health, Department of Health and Human Services, project ZO1 AG000949, and the Michael J. Fox Foundation for Parkinson's Research.

Keywords

Parkinson's disease
genetics
genome-wide association
mutation

ASJC Scopus subject areas

Neurology
Clinical Neurology

Access to Document

10.1002/mds.28494

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title = "GP2: The Global Parkinson's Genetics Program",

keywords = "Parkinson's disease, genetics, genome-wide association, mutation",

author = "{The Global Parkinson{\textquoteright}s Genetics Program} and Tan, {Ai Huey} and Alastair Noyce and Carrasco, {Alejandro Martinez} and Alexis Brice and Alyssa Reimer and Anastasia Illarionova and Andrew Singleton and Artur Schumacher-Schuh and Benjamin Stecher and Bernadette Siddiqi and Bradford Casey and Brian Fiske and Caroline Pantazis and Christine Klein and Claire Bale and Claire Wegel and Cornelis Blauwendraat and Dan Vitale and Dena Hernandez and Ekemini Riley and Emily Fisher and Valente, {Enza Maria} and Vollstedt, {Eva Juliane} and Faraz Faghri and Hampton Leonard and Hirotaka Iwaki and Huw Morris and Sarmiento, {Ignacio Juan Keller} and Ignacio Mata and Jeff Kim and John Hardy and Kaileigh Murphy and Katja Lohmann and Ken Marek and Kin Mok and Kishore Kumar and Lara Lange and Maggie Kuhl and Manu Sharma and Manuela Tan and Mary Makarious and Michelle Durborow and Micol Avenali and Mie Rizig and Mike Nalls and Niccolo Mencacci and Nicholas Wood and Nigel Williams and Njideka Okubadejo and Olaitan Okunoye",

year = "2021",

month = apr,

doi = "10.1002/mds.28494",

language = "English (US)",

volume = "36",

pages = "842--851",

journal = "Movement Disorders",

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AU - The Global Parkinson’s Genetics Program

AU - Tan, Ai Huey

AU - Noyce, Alastair

AU - Carrasco, Alejandro Martinez

AU - Brice, Alexis

AU - Reimer, Alyssa

AU - Illarionova, Anastasia

AU - Singleton, Andrew

AU - Schumacher-Schuh, Artur

AU - Stecher, Benjamin

AU - Siddiqi, Bernadette

AU - Casey, Bradford

AU - Fiske, Brian

AU - Pantazis, Caroline

AU - Klein, Christine

AU - Bale, Claire

AU - Wegel, Claire

AU - Blauwendraat, Cornelis

AU - Vitale, Dan

AU - Hernandez, Dena

AU - Riley, Ekemini

AU - Fisher, Emily

AU - Valente, Enza Maria

AU - Vollstedt, Eva Juliane

AU - Faghri, Faraz

AU - Leonard, Hampton

AU - Iwaki, Hirotaka

AU - Morris, Huw

AU - Sarmiento, Ignacio Juan Keller

AU - Mata, Ignacio

AU - Kim, Jeff

AU - Hardy, John

AU - Murphy, Kaileigh

AU - Lohmann, Katja

AU - Marek, Ken

AU - Mok, Kin

AU - Kumar, Kishore

AU - Lange, Lara

AU - Kuhl, Maggie

AU - Sharma, Manu

AU - Tan, Manuela

AU - Makarious, Mary

AU - Durborow, Michelle

AU - Avenali, Micol

AU - Rizig, Mie

AU - Nalls, Mike

AU - Mencacci, Niccolo

AU - Wood, Nicholas

AU - Williams, Nigel

AU - Okubadejo, Njideka

AU - Okunoye, Olaitan

PY - 2021/4

Y1 - 2021/4

KW - Parkinson's disease

KW - genetics

KW - genome-wide association

KW - mutation

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SN - 0885-3185

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SP - 842

EP - 851

JO - Movement Disorders

JF - Movement Disorders

IS - 4

ER -

GP2: The Global Parkinson's Genetics Program

Funding

Keywords

ASJC Scopus subject areas

Access to Document

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