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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)

Title:	Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
Authors:	Towns C; Richer M; Jasaityte S; Stafford EJ; Joubert J; Antar T; Martinez-Carrasco A; Makarious MB; Casey B; Vitale D; Levine K; Leonard H; Pantazis CB; Screven LA; Hernandez DG; Wegel CE; Solle J; Nalls MA; Blauwendraat C; Singleton AB; Tan MMX; Iwaki H; Morris HR; Gatto EM; Kauffman M; Khachatryan S; Tavadyan Z; Shepherd CE; Hunter J; Kumar K; Ellis M; Renteria ME; Koks S; Zimprich A; Schumacher-Schuh AF; Rieder C; Awad PS; Tumas V; Camargos S; Fon EA; Monchi O; Fon T; Galleguillos BP; Miranda M; Bustamante ML; Olguin P; Chana P; Tang B; Shang H; Guo J; Chan P; Luo W; Arboleda G; Orozco J; del Rio MJ; Hernandez A; Salama M; Kamel WA; Zewde YZ; Brice A; Corvol J-C; Westenberger A; Illarionova A; Mollenhauer B; Klein C; Vollstedt E-J; Hopfner F; Hoglinger G; Madoev H; Trinh J; Junker J; Lohmann K; Lange LM; Sharma M; Groppa S; Gasser T; Fang Z-H; Akpalu A; Xiromerisiou G; Hadjigorgiou G; Dagklis I; Tarnanas I; Stefanis L; Stamelou M; Dadiotis E; Medina A; Chan GH-F; Ip N; Cheung NY-F; Zhou X; Kishore A; Kp D; Pal P; Kukkle PL; Rajan R; Borgohain R; Salari M; Quattrone A; Valente EM; Parnetti L; Avenali M; Schirinzi T; Funayama M; Hattori N; Shiraishi T; Karimova A; Kaishibayeva G; Shambetova C; Kruger R; Tan AH; Ahmad-Annuar A; Norlinah MI; Murad NAA; Azmin S; Lim S-Y; Mohamed W; Tay YW; Martinez-Ramirez D; Rodriguez-Violante M; Reyes-Perez P; Tserensodnom B; Ojha R; Anderson TJ; Pitcher TL; Sanyaolu A; Okubadejo N; Ojo O; Aasly JO; Pihlstrom L; Tan M; Ur-Rehman S; Cornejo-Olivas M; Doquenia ML; Rosales R; Vinuela A; Iakovenko E; Mubarak BA; Umair M; Tan E-K; Foo JN; Amod F; Carr J; Bardien S; Jeon B; Kim YJ; Cubo E; Alvarez I; Hoenicka J; Beyer K; Perinan MT; Pastor P; El-Sadig S; Zweier C; Krack P; Lin C-H; Wu H-C; Kung P-J; Wu R-M; Wu Y; Amouri R; Sassi SB; Basak AN; Genc G; Cakmak OO; Ertan S; Noyce A; Schrag A; Schapira A; Carroll C; Bale C; Grosset D; Houlden H; Hardy J; Mok KY; Rizig M; Wood N; Williams N; Okunoye O; Lewis PA; Kaiyrzhanov R; Weil R; Love S; Stott S; Jasaitye S; Dey S; Obese V; Espay A; O'Grady A; Sobering AK; Siddiqi B; Fiske B; Jonas C; Cruchaga C; Comart C; Wegel C; Hall D; Hernandez D; Shiamim E; Riley E; Faghri F; Serrano GE; Chen H; Mata IF; Sarmiento IJK; Williamson J; Kim JJ; Jankovic J; Shulman J; Solle JC; Murphy K; Nuytemans K; Kieburtz K; Markopoulou K; Marek K; Levine KS; Chahine LM; Ibanez L; Screven L; Ruffrage L; Shulman L; Marsili L; Kuhl M; Dean M; Koretsky M; Puckelwartz MJ; Inca-Martinez M; Louie N; Mencacci NE; Albin R; Alcalay R; Walker R; Bandres-Ciga S; Chowdhury S; Dumanis S; Lubbe S; Xie T; Foroud T; Beach T; Sherer T; Song Y; Nguyen D; Nguyen T; Atadzhanov M
Source:	npj Parkinson's Disease, December 2023
Publisher Information:	Springer Nature
Publication Year:	2023
Collection:	Newcastle University Library ePrints Service
Description:	© 2023, Springer Nature Limited. The Global Parkinson’s Genetics Program (GP2) will genotype over 150,000 participants from around the world, and integrate genetic and clinical data for use in large-scale analyses to dramatically expand our understanding of the genetic architecture of PD. This report details the workflow for cohort integration into the complex arm of GP2, and together with our outline of the monogenic hub in a companion paper, provides a generalizable blueprint for establishing large scale collaborative research consortia.
Document Type:	article in journal/newspaper
File Description:	application/pdf
Language:	unknown
Relation:	https://eprints.ncl.ac.uk/296408; https://eprints.ncl.ac.uk/fulltext.aspx?url=296408/89F98935-6A85-4E35-9CBF-AC9D9C9C2D43.pdf&pub_id=296408
Availability:	https://eprints.ncl.ac.uk/296408
Rights:	https://creativecommons.org/licenses/by/4.0/
Accession Number:	edsbas.78D3F326
Database:	BASE