Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)

Lara M. Lange; Micol Avenali; Melina Ellis; Anastasia Illarionova; Ignacio J. Keller Sarmiento; 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 Kumar; Melina Ellis; Miguel E. Rentería; Sulev Koks; Alexander Zimprich; Artur F. Schumacher-Schuh; Carlos Rieder; Paula Saffie Awad; Vitor Tumas; Sarah Camargos; Edward A. Fon; Oury Monchi; Ted Fon; Benjamin Pizarro Galleguillos; Marcelo Miranda; Maria Leonor Bustamante; Patricio Olguin; Pedro Chana; Beisha Tang; Huifang Shang; Rejko Krüger; the Global Parkinson’s Genetic Program (GP2)

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) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)

Lara M. Lange
, Micol Avenali
, Melina Ellis
, Anastasia Illarionova
, Ignacio J. Keller Sarmiento
, 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 Kumar, Melina Ellis, Miguel E. Rentería, Sulev Koks, Alexander Zimprich, Artur F. Schumacher-Schuh, Carlos Rieder, Paula Saffie Awad, Vitor Tumas, Sarah Camargos, Edward A. Fon, Oury Monchi, Ted Fon, Benjamin Pizarro Galleguillos, Marcelo Miranda, Maria Leonor Bustamante, Patricio Olguin, Pedro Chana, Beisha Tang, Huifang Shang, Rejko Krüger, the Global Parkinson’s Genetic Program (GP2)

^*Corresponding author for this work

Research output: Contribution to journal › Correction

1 Citation (Scopus)

Abstract

Correction to: 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
Article number	133
Journal	npj Parkinson's Disease
Volume	9
Issue number	1
DOIs	https://doi.org/10.1038/s41531-023-00560-7
Publication status	Published - 13 Sept 2023
Externally published	Yes

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Lange, L. M., Avenali, M., Ellis, M., Illarionova, A., Keller Sarmiento, I. J., 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., ... the Global Parkinson’s Genetic Program (GP2) (2023). Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9). npj Parkinson's Disease, 9(1), Article 133. https://doi.org/10.1038/s41531-023-00560-7

@article{0ec967f81a3c4c439e5fdb3e833c4ee2,

title = "Author Correction: Elucidating causative gene variants in hereditary Parkinson{\textquoteright}s disease in the Global Parkinson{\textquoteright}s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)",

abstract = "Correction to: 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\}, \{Ignacio J.\} 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 Kishore Kumar 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 Fon, \{Edward A.\} and Oury Monchi and Ted 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 Rejko Kr{\"u}ger and \{the Global Parkinson{\textquoteright}s Genetic Program (GP2)\}",

note = "Publisher Copyright: {\textcopyright} 2023, Springer Nature Limited.",

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",

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Lange, LM, Avenali, M, Ellis, M, Illarionova, A, Keller Sarmiento, IJ, 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, 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, Krüger, R & the Global Parkinson’s Genetic Program (GP2) 2023, 'Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)', npj Parkinson's Disease, vol. 9, no. 1, 133. https://doi.org/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) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9). / Lange, Lara M.; Avenali, Micol; Ellis, Melina et al.
In: npj Parkinson's Disease, Vol. 9, No. 1, 133, 13.09.2023.

Research output: Contribution to journal › Correction

TY - JOUR

T1 - Author Correction

T2 - Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)

AU - Lange, Lara M.

AU - Avenali, Micol

AU - Ellis, Melina

AU - Illarionova, Anastasia

AU - Keller Sarmiento, Ignacio J.

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

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, Edward A.

AU - Monchi, Oury

AU - Fon, Ted

AU - Galleguillos, Benjamin Pizarro

AU - Miranda, Marcelo

AU - Bustamante, Maria Leonor

AU - Olguin, Patricio

AU - Chana, Pedro

AU - Tang, Beisha

AU - Shang, Huifang

AU - Krüger, Rejko

AU - the Global Parkinson’s Genetic Program (GP2)

PY - 2023/9/13

Y1 - 2023/9/13

N2 - Correction to: 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: 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://www.scopus.com/pages/publications/85171453011

UR - https://pubmed.ncbi.nlm.nih.gov/37704671

U2 - 10.1038/s41531-023-00560-7

DO - 10.1038/s41531-023-00560-7

M3 - Correction

C2 - 37704671

AN - SCOPUS:85171453011

SN - 2373-8057

VL - 9

JO - npj Parkinson's Disease

JF - npj Parkinson's Disease

IS - 1

M1 - 133

ER -

Lange LM, Avenali M, Ellis M, Illarionova A, Keller Sarmiento IJ, Tan AH et al. Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9). npj Parkinson's Disease. 2023 Sept 13;9(1):133. 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) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)

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