Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
Date
2023-09-13Author
Lange, Lara Mariah
Avenali, M
Ellis, M
Illarionova, Anastasia
Keller Sarmiento, IJ
TAN, AI HUEY
Madoev, H
Galandra, C
Junker, J
Roopnarain, K
Solle, J
Wegel, C
Fang, Zih-Hua
Heutink, Peter
Kumar, Kishore Raj
Lim, S-Y
Valente, Enza Maria
Nalls, M
Blauwendraat, Cornelis
Singleton, Andrew
Mencacci, N
Lohmann, K
Klein, Christine
Gatto, EM
Kauffman, M
Khachatryan, S
Tavadyan, Z
Shepherd, CE
Hunter, J
Kumar, K
Ellis, M
Rentería, 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
Höglinger, 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
Chan, P
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
Krüger, R
Tan, AH
Ahmad-Annuar, A
Norlinah, MI
Murad, NAA
Ibrahim, NM
Azmin, S
Lim, S-Y
Mohamed, W
Tay, YW
Martinez-Ramirez, D
Rodriguez-Violante, M
Reyes-Pérez, P
Tserensodnom, B
Ojha, R
Anderson, TJ
Pitcher, TL
Sanyaolu, A
Okubadejo, N
Ojo, O
Aasly, JO
Pihlstrøm, 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
Periñan, MT
Pastor, P
El-Sadig, S
Zweier, C
Paul, K
Lin, C-H
Wu, H-C
Kung, P-J
Wu, R-M
Wu, S
Wu, Y
Amouri, R
Sassi, SB
Başak, AN
Genc, G
Çakmak, ÖÖ
Ertan, S
Noyce, A
Martínez-Carrasco, A
Schrag, A
Schapira, A
Carroll, Camille
Bale, C
Grosset, D
Stafford, EJ
Houlden, H
Morris, HR
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
Singleton, AB
Sobering, AK
Siddiqi, B
Casey, B
Fiske, B
Jonas, C
Cruchaga, C
Pantazis, CB
Comart, C
Wegel, C
Blauwendraat, C
Vitale, D
Hall, D
Hernandez, D
Shiamim, E
Riley, E
Faghri, F
Serrano, GE
Leonard, H
Iwaki, H
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
Screven, L
Ruffrage, L
Shulman, L
Marsili, L
Kuhl, M
Dean, M
Makarious, MB
Koretsky, M
Inca-Martinez, M
Nalls, MA
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
Subject
Global Parkinson’s Genetic Program (GP2)
Metadata
Show full item recordAbstract
Correction to: s41531-023-00526-9 npj Parkinson’s Disease, published online 27 June 2023 In this article the Global Parkinson’s Genetics Program (GP2) members names and affiliations were missing in the main author list of the Original article which are listed in the below.
Collections
Publisher
Springer Science and Business Media LLC
Place of Publication
United States
Journal
npj Parkinson's Disease
Volume
9
Issue
1
Pagination
133-
Author URL
Number
133
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