Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

Authors

• Lara M. Lange, University of Lübeck
• Micol Avenali, IRCCS Fondazione Istituto Neurologico Casimiro Mondino - Pavia
• Melina Ellis, ANZAC Research Institute
• Anastasia Illarionova, German Center for Neurodegenerative Diseases
• Sarmiento IJ Keller
• Ai Huey Tan, University of Malaya
• Harutyun Madoev, University of Lübeck
• Caterina Galandra, IRCCS Fondazione Istituto Neurologico Casimiro Mondino - Pavia
• Johanna Junker, University of Lübeck
• Karisha Roopnarain, University of Lübeck
• Justin Solle, Michael J. Fox Foundation for Parkinson's Research
• Claire Wegel, Indiana University Bloomington
• Zih Hua Fang, German Center for Neurodegenerative Diseases
• Peter Heutink, German Center for Neurodegenerative Diseases
• Kishore R. Kumar, Garvan Institute of Medical Research
• Shen Yang Lim, University of Malaya
• Enza Maria Valente, IRCCS Fondazione Istituto Neurologico Casimiro Mondino - Pavia
• Mike Nalls, Data Tecnica International
• Cornelis Blauwendraat, National Institutes of Health
• Andrew Singleton, National Institutes of Health
• Niccolo Mencacci, Northwestern University
• Katja Lohmann, University of Lübeck
• Christine Klein, University of Lübeck
• Emilia M. Gatto, Sanatorio de la Trinidad
• Marcelo Kauffman, Hospital General de Agudos José María Ramos Mejía
• Samson Khachatryan, Somnus Neurology Clinic
• Zaruhi Tavadyan, Somnus Neurology Clinic
• Claire E. Shepherd, Neuroscience Research Australia
• Julie Hunter, ANZAC Research Institute
• Miguel E. Rentería, Queensland Institute of Medical Research

Abstract

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.

DOI Link

10.1038/s41531-023-00560-7

Publication Date

2023-09-13

Publication Title

npj Parkinson's Disease

Volume

9

Issue

1

Acceptance Date

2023-05-15

Deposit Date

2023-12-18

Embargo Period

2023-12-19

Recommended Citation

Lange, L., Avenali, M., Ellis, M., Illarionova, A., Keller, S., Tan, A., Madoev, H., Galandra, C., Junker, J., Roopnarain, K., Solle, J., Wegel, C., Fang, Z., Heutink, P., Kumar, K., Lim, S., Valente, E., Nalls, M., Blauwendraat, C., Singleton, A., Mencacci, N., Lohmann, K., Klein, C., Gatto, E., Kauffman, M., Khachatryan, S., Tavadyan, Z., Shepherd, C., Hunter, J., & Rentería, M. (2023) 'Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)', npj Parkinson's Disease, 9(1). Available at: 10.1038/s41531-023-00560-7