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

Lara M. Lange; Micol Avenali; Melina Ellis; Anastasia Illarionova; Sarmiento IJ Keller; Ai Huey Tan; Harutyun Madoev; Caterina Galandra; Johanna Junker; Karisha Roopnarain; Justin Solle; Claire Wegel; Zih Hua Fang; Peter Heutink; Kishore R. Kumar; Shen Yang Lim; Enza Maria Valente; Mike Nalls; Cornelis Blauwendraat; Andrew Singleton; Niccolo Mencacci; Katja Lohmann; Christine Klein; Emilia M. Gatto; Marcelo Kauffman; Samson Khachatryan; Zaruhi Tavadyan; Claire E. Shepherd; Julie Hunter; Kishore R. Kumar; Melina Ellis; Miguel E. Rentería; Sulev Koks; Alexander Zimprich; Artur F. Schumacher-Schuh; Carlos Rieder; Paula Saffie Awad; Vitor Tumas; Sarah Camargos; EA Fon; Oury Monchi; T Fon; Benjamin Pizarro Galleguillos; Marcelo Miranda; Maria Leonor Bustamante; Patricio Olguin; Pedro Chana; Beisha Tang; Huifang Shang; Jifeng Guo; Piu Chan; W Luo; G Arboleda; J Orozco; Rio MJ del; A Hernandez; M Salama; WA Kamel; YZ Zewde; A Brice; J-C Corvol; A Westenberger; Anastasia Illarionova; B Mollenhauer; Christine Klein; E-J Vollstedt; F Hopfner; G Höglinger; Harutyun Madoev; J Trinh; Johanna Junker; Katja Lohmann; Lara M. Lange; M Sharma; S Groppa; T Gasser; Zih Hua Fang; A Akpalu; G Xiromerisiou; G Hadjigorgiou; I Dagklis; I Tarnanas; L Stefanis; M Stamelou; E Dadiotis; A Medina; Piu Chan; N Ip; NY-F Cheung; Piu Chan; Camille Carroll

doi:10.1038/s41531-023-00560-7

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

Lara M. Lange
, Micol Avenali
, Melina Ellis
, Anastasia Illarionova
, Sarmiento IJ Keller
, Ai Huey Tan
, Harutyun Madoev
, Caterina Galandra
, Johanna Junker
, Karisha Roopnarain
, Justin Solle
, Claire Wegel
, Zih Hua Fang
, Peter Heutink
, Kishore R. Kumar
, Shen Yang Lim
, Enza Maria Valente
, Mike Nalls
, Cornelis Blauwendraat
, Andrew Singleton

Niccolo Mencacci, Katja Lohmann, Christine Klein^*, Emilia M. Gatto, Marcelo Kauffman, Samson Khachatryan, Zaruhi Tavadyan, Claire E. Shepherd, Julie Hunter, Kishore R. Kumar, Melina Ellis, Miguel E. Rentería, Sulev Koks, Alexander Zimprich, Artur F. Schumacher-Schuh, Carlos Rieder, Paula Saffie Awad, Vitor Tumas, Sarah Camargos, EA Fon, Oury Monchi, T Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, Maria Leonor Bustamante, Patricio Olguin, Pedro Chana, Beisha Tang, Huifang Shang, Jifeng Guo, Piu Chan, W Luo, G Arboleda, J Orozco, Rio MJ del, A Hernandez, M Salama, WA Kamel, YZ Zewde, A Brice, J-C Corvol, A Westenberger, Anastasia Illarionova, B Mollenhauer, Christine Klein^*, E-J Vollstedt, F Hopfner, G Höglinger, Harutyun Madoev, J Trinh, Johanna Junker, Katja Lohmann, Lara M. Lange, M Sharma, S Groppa, T Gasser, Zih Hua Fang, A Akpalu, G Xiromerisiou, G Hadjigorgiou, I Dagklis, I Tarnanas, L Stefanis, M Stamelou, E Dadiotis, A Medina, Piu Chan, N Ip, NY-F Cheung, Piu Chan, Camille Carroll

^*Corresponding author for this work

Peninsula Medical School

University of Lübeck
IRCCS Fondazione Istituto Neurologico Casimiro Mondino - Pavia
University of Pavia
ANZAC Research Institute
Concord Repatriation General Hospital
University of Sydney
German Center for Neurodegenerative Diseases
University of Malaya
Michael J. Fox Foundation for Parkinson's Research
Indiana University Bloomington
Garvan Institute of Medical Research
Data Tecnica International
National Institutes of Health
Northwestern University
Sanatorio de la Trinidad
Hospital General de Agudos José María Ramos Mejía
Somnus Neurology Clinic
Neuroscience Research Australia
Queensland Institute of Medical Research
Murdoch University
University of Vienna
Universidade Federal do Rio Grande do Sul
Universidade Federal de Ciências da Saúde de Porto Alegre
Universidade de São Paulo
Universidade Federal de Minas Gerais
University of Montreal
Universidad de Chile
Fundación Diagnosis
CETRAM
Central South University
Sichuan University
Capital Medical University

Research output: Contribution to journal › Article › peer-review

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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.

Original language	English
Number of pages	0
Journal	npj Parkinson's Disease
Volume	9
Issue number	1
Early online date	13 Sept 2023
DOIs	https://doi.org/10.1038/s41531-023-00560-7
Publication status	Published - 13 Sept 2023

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Lange, L. M., Avenali, M., Ellis, M., Illarionova, A., Keller, S. IJ., Tan, A. H., Madoev, H., Galandra, C., Junker, J., Roopnarain, K., Solle, J., Wegel, C., Fang, Z. H., Heutink, P., Kumar, K. R., Lim, S. Y., Valente, E. M., Nalls, M., Blauwendraat, C., ... Carroll, C. (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). https://doi.org/10.1038/s41531-023-00560-7

@article{0c233219133a4b76821f9e7ebd019e4c,

title = "Author Correction: Elucidating causative gene variants in hereditary Parkinson{\textquoteright}s disease in the Global Parkinson{\textquoteright}s Genetics Program (GP2)",

abstract = "Correction to: s41531-023-00526-9 npj Parkinson{\textquoteright}s Disease, published online 27 June 2023 In this article the Global Parkinson{\textquoteright}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.",

author = "Lange, \{Lara M.\} and Micol Avenali and Melina Ellis and Anastasia Illarionova and Keller, \{Sarmiento IJ\} and Tan, \{Ai Huey\} and Harutyun Madoev and Caterina Galandra and Johanna Junker and Karisha Roopnarain and Justin Solle and Claire Wegel and Fang, \{Zih Hua\} and Peter Heutink and Kumar, \{Kishore R.\} and Lim, \{Shen Yang\} and Valente, \{Enza Maria\} and Mike Nalls and Cornelis Blauwendraat and Andrew Singleton and Niccolo Mencacci and Katja Lohmann and Christine Klein and Gatto, \{Emilia M.\} and Marcelo Kauffman and Samson Khachatryan and Zaruhi Tavadyan and Shepherd, \{Claire E.\} and Julie Hunter and Kumar, \{Kishore R.\} and Melina Ellis and Renter{\'i}a, \{Miguel E.\} and Sulev Koks and Alexander Zimprich and Schumacher-Schuh, \{Artur F.\} and Carlos Rieder and Awad, \{Paula Saffie\} and Vitor Tumas and Sarah Camargos and EA Fon and Oury Monchi and T Fon and Galleguillos, \{Benjamin Pizarro\} and Marcelo Miranda and Bustamante, \{Maria Leonor\} and Patricio Olguin and Pedro Chana and Beisha Tang and Huifang Shang and Jifeng Guo and Piu Chan and W Luo and G Arboleda and J Orozco and del, \{Rio MJ\} and A Hernandez and M Salama and WA Kamel and YZ Zewde and A Brice and J-C Corvol and A Westenberger and Anastasia Illarionova and B Mollenhauer and Christine Klein and E-J Vollstedt and F Hopfner and G H{\"o}glinger and Harutyun Madoev and J Trinh and Johanna Junker and Katja Lohmann and Lange, \{Lara M.\} and M Sharma and S Groppa and T Gasser and Fang, \{Zih Hua\} and A Akpalu and G Xiromerisiou and G Hadjigorgiou and I Dagklis and I Tarnanas and L Stefanis and M Stamelou and E Dadiotis and A Medina and Piu Chan and N Ip and NY-F Cheung and Piu Chan and Camille Carroll",

year = "2023",

month = sep,

day = "13",

doi = "10.1038/s41531-023-00560-7",

language = "English",

volume = "9",

journal = "npj Parkinson's Disease",

issn = "2373-8057",

publisher = "Nature Research",

number = "1",

}

Lange, LM, Avenali, M, Ellis, M, Illarionova, A, Keller, SIJ, Tan, AH, Madoev, H, Galandra, C, Junker, J, Roopnarain, K, Solle, J, Wegel, C, Fang, ZH, Heutink, P, Kumar, KR, Lim, SY, Valente, EM, Nalls, M, Blauwendraat, C, Singleton, A, Mencacci, N, Lohmann, K, Klein, C, Gatto, EM, Kauffman, M, Khachatryan, S, Tavadyan, Z, Shepherd, CE, Hunter, J, Kumar, KR, 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, RMJ, 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, ZH, Akpalu, A, Xiromerisiou, G, Hadjigorgiou, G, Dagklis, I, Tarnanas, I, Stefanis, L, Stamelou, M, Dadiotis, E, Medina, A, Chan, P, Ip, N, Cheung, NY-F, Chan, P & Carroll, C 2023, 'Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)', npj Parkinson's Disease, vol. 9, no. 1. https://doi.org/10.1038/s41531-023-00560-7

TY - JOUR

T1 - Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

AU - Lange, Lara M.

AU - Avenali, Micol

AU - Ellis, Melina

AU - Illarionova, Anastasia

AU - Keller, Sarmiento IJ

AU - Tan, Ai Huey

AU - Madoev, Harutyun

AU - Galandra, Caterina

AU - Junker, Johanna

AU - Roopnarain, Karisha

AU - Solle, Justin

AU - Wegel, Claire

AU - Fang, Zih Hua

AU - Heutink, Peter

AU - Kumar, Kishore R.

AU - Lim, Shen Yang

AU - Valente, Enza Maria

AU - Nalls, Mike

AU - Blauwendraat, Cornelis

AU - Singleton, Andrew

AU - Mencacci, Niccolo

AU - Lohmann, Katja

AU - Klein, Christine

AU - Gatto, Emilia M.

AU - Kauffman, Marcelo

AU - Khachatryan, Samson

AU - Tavadyan, Zaruhi

AU - Shepherd, Claire E.

AU - Hunter, Julie

AU - Kumar, Kishore R.

AU - Ellis, Melina

AU - Rentería, Miguel E.

AU - Koks, Sulev

AU - Zimprich, Alexander

AU - Schumacher-Schuh, Artur F.

AU - Rieder, Carlos

AU - Awad, Paula Saffie

AU - Tumas, Vitor

AU - Camargos, Sarah

AU - Fon, EA

AU - Monchi, Oury

AU - Fon, T

AU - Galleguillos, Benjamin Pizarro

AU - Miranda, Marcelo

AU - Bustamante, Maria Leonor

AU - Olguin, Patricio

AU - Chana, Pedro

AU - Tang, Beisha

AU - Shang, Huifang

AU - Guo, Jifeng

AU - Chan, Piu

AU - Luo, W

AU - Arboleda, G

AU - Orozco, J

AU - del, Rio MJ

AU - Hernandez, A

AU - Salama, M

AU - Kamel, WA

AU - Zewde, YZ

AU - Brice, A

AU - Corvol, J-C

AU - Westenberger, A

AU - Illarionova, Anastasia

AU - Mollenhauer, B

AU - Klein, Christine

AU - Vollstedt, E-J

AU - Hopfner, F

AU - Höglinger, G

AU - Madoev, Harutyun

AU - Trinh, J

AU - Junker, Johanna

AU - Lohmann, Katja

AU - Lange, Lara M.

AU - Sharma, M

AU - Groppa, S

AU - Gasser, T

AU - Fang, Zih Hua

AU - Akpalu, A

AU - Xiromerisiou, G

AU - Hadjigorgiou, G

AU - Dagklis, I

AU - Tarnanas, I

AU - Stefanis, L

AU - Stamelou, M

AU - Dadiotis, E

AU - Medina, A

AU - Chan, Piu

AU - Ip, N

AU - Cheung, NY-F

AU - Chan, Piu

AU - Carroll, Camille

PY - 2023/9/13

Y1 - 2023/9/13

N2 - 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.

AB - 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.

UR - https://pearl.plymouth.ac.uk/pms-research/1679/

U2 - 10.1038/s41531-023-00560-7

DO - 10.1038/s41531-023-00560-7

M3 - Article

SN - 2373-8057

VL - 9

JO - npj Parkinson's Disease

JF - npj Parkinson's Disease

IS - 1

ER -

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

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