Published Erratum
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
1
, Micol Avenali
2
3
, Melina Ellis
4
5
, Anastasia Illarionova
6
, Ignacio J Keller Sarmiento
7
, Ai-Huey Tan
8
, Harutyun Madoev
1
, Caterina Galandra
2
9
, Johanna Junker
1
, Karisha Roopnarain
1
, Justin Solle
10
, Claire Wegel
11
, Zih-Hua Fang
6
, Peter Heutink
6
, Kishore R Kumar
12
13
, Shen-Yang Lim
8
, Enza Maria Valente
2
9
, Mike Nalls
14
15
16
, Cornelis Blauwendraat
15
17
, Andrew Singleton
15
16
, Niccolo Mencacci
7
, Katja Lohmann
1
, Christine Klein
18
; Global Parkinson’s Genetic Program (GP2)
Collaborators,
Affiliations
Collaborators
-
Global Parkinson’s Genetic Program (GP2):
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, Jifeng Guo, Piu Chan, Wei Luo, Gonzalo Arboleda, Jorge Orozco, Marlene Jimenez Del Rio, Alvaro Hernandez, Mohamed Salama, Walaa A Kamel, Yared Z Zewde, Alexis Brice, Jean-Christophe Corvol, Ana Westenberger, Anastasia Illarionova, Brit Mollenhauer, Christine Klein, Eva-Juliane Vollstedt, Franziska Hopfner, Günter Höglinger, Harutyun Madoev, Joanne Trinh, Johanna Junker, Katja Lohmann, Lara M Lange, Manu Sharma, Sergio Groppa, Thomas Gasser, Zih-Hua Fang, Albert Akpalu, Georgia Xiromerisiou, Georgios Hadjigorgiou, Ioannis Dagklis, Ioannis Tarnanas, Leonidas Stefanis, Maria Stamelou, Efthymios Dadiotis, Alex Medina, Germaine Hiu-Fai Chan, Nancy Ip, Nelson Yuk-Fai Cheung, Phillip Chan, Xiaopu Zhou, Asha Kishore, Divya Kp, Pramod Pal, Prashanth Lingappa Kukkle, Roopa Rajan, Rupam Borgohain, Mehri Salari, Andrea Quattrone, Enza Maria Valente, Lucilla Parnetti, Micol Avenali, Tommaso Schirinzi, Manabu Funayama, Nobutaka Hattori, Tomotaka Shiraishi, Altynay Karimova, Gulnaz Kaishibayeva, Cholpon Shambetova, Rejko Krüger, Ai Huey Tan, Azlina Ahmad-Annuar, Mohamed Ibrahim Norlinah, Nor Azian Abdul Murad, Norlinah Mohamed Ibrahim, Shahrul Azmin, Shen-Yang Lim, Wael Mohamed, Yi Wen Tay, Daniel Martinez-Ramirez, Mayela Rodriguez-Violante, Paula Reyes-Pérez, Bayasgalan Tserensodnom, Rajeev Ojha, Tim J Anderson, Toni L Pitcher, Arinola Sanyaolu, Njideka Okubadejo, Oluwadamilola Ojo, Jan O Aasly, Lasse Pihlstrøm, Manuela Tan, Shoaib Ur-Rehman, Mario Cornejo-Olivas, Maria Leila Doquenia, Raymond Rosales, Angel Vinuela, Elena Iakovenko, Bashayer Al Mubarak, Muhammad Umair, Eng-King Tan, Jia Nee Foo, Ferzana Amod, Jonathan Carr, Soraya Bardien, Beomseok Jeon, Yun Joong Kim, Esther Cubo, Ignacio Alvarez, Janet Hoenicka, Katrin Beyer, Maria Teresa Periñan, Pau Pastor, Sarah El-Sadig, Christiane Zweier, Krack Paul, Chin-Hsien Lin, Hsiu-Chuan Wu, Pin-Jui Kung, Ruey-Meei Wu, Serena Wu, Yihru Wu, Rim Amouri, Samia Ben Sassi, A Nazl Başak, Gencer Genc, Özgür Öztop Çakmak, Sibel Ertan, Alastair Noyce, Alejandro Martínez-Carrasco, Anette Schrag, Anthony Schapira, Camille Carroll, Claire Bale, Donald Grosset, Eleanor J Stafford, Henry Houlden, Huw R Morris, John Hardy, Kin Ying Mok, Mie Rizig, Nicholas Wood, Nigel Williams, Olaitan Okunoye, Patrick Alfryn Lewis, Rauan Kaiyrzhanov, Rimona Weil, Seth Love, Simon Stott, Simona Jasaitye, Sumit Dey, Vida Obese, Alberto Espay, Alyssa O'Grady, Andrew B Singleton, Andrew K Sobering, Bernadette Siddiqi, Bradford Casey, Brian Fiske, Cabell Jonas, Carlos Cruchaga, Caroline B Pantazis, Charisse Comart, Claire Wegel, Cornelis Blauwendraat, Dan Vitale, Deborah Hall, Dena Hernandez, Ejaz Shiamim, Ekemini Riley, Faraz Faghri, Geidy E Serrano, Hampton Leonard, Hirotaka Iwaki, Honglei Chen, Ignacio F Mata, Ignacio Juan Keller Sarmiento, Jared Williamson, Jonggeol Jeff Kim, Joseph Jankovic, Joshua Shulman, Justin C Solle, Kaileigh Murphy, Karen Nuytemans, Karl Kieburtz, Katerina Markopoulou, Kenneth Marek, Kristin S Levine, Lana M Chahine, Laurel Screven, Lauren Ruffrage, Lisa Shulman, Luca Marsili, Maggie Kuhl, Marissa Dean, Mary B Makarious, Mathew Koretsky, Miguel Inca-Martinez, Mike A Nalls, Naomi Louie, Niccolò Emanuele Mencacci, Roger Albin, Roy Alcalay, Ruth Walker, Sara Bandres-Ciga, Sohini Chowdhury, Sonya Dumanis, Steven Lubbe, Tao Xie, Tatiana Foroud, Thomas Beach, Todd Sherer, Yeajin Song, Duan Nguyen, Toan Nguyen, Masharip Atadzhanov
Affiliations
- 1 Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
- 2 IRCCS Mondino Foundation, Pavia, Italy.
- 3 Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
- 4 Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW, Australia.
- 5 Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
- 6 German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
- 7 Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
- 8 Division of Neurology, Department of Medicine, and the Mah Pooi Soo and Tan Chin Nam Centre for Parkinson's and Related Disorders, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
- 9 Department of Molecular Medicine, University of Pavia, Pavia, Italy.
- 10 Department of Clinical Research, Michael J. Fox Foundation for Parkinson's Research, New York City, NY, USA.
- 11 Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
- 12 Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
- 13 Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, The University of Sydney, Concord, NSW, Australia.
- 14 Data Tecnica International, Washington, DC, USA.
- 15 Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
- 16 Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
- 17 Integrative Genomics Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
- 18 Institute of Neurogenetics, University of Lübeck, Lübeck, Germany. christine.klein@neuro.uni-luebeck.de.
- PMID: 37704671
- PMCID: PMC10499986
- DOI: 10.1038/s41531-023-00560-7
Item in Clipboard
Published Erratum
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)
Lara M Lange et al.
NPJ Parkinsons Dis.
.
Display options
Format
doi: 10.1038/s41531-023-00560-7.
Authors
Lara M Lange
1
, Micol Avenali
2
3
, Melina Ellis
4
5
, Anastasia Illarionova
6
, Ignacio J Keller Sarmiento
7
, Ai-Huey Tan
8
, Harutyun Madoev
1
, Caterina Galandra
2
9
, Johanna Junker
1
, Karisha Roopnarain
1
, Justin Solle
10
, Claire Wegel
11
, Zih-Hua Fang
6
, Peter Heutink
6
, Kishore R Kumar
12
13
, Shen-Yang Lim
8
, Enza Maria Valente
2
9
, Mike Nalls
14
15
16
, Cornelis Blauwendraat
15
17
, Andrew Singleton
15
16
, Niccolo Mencacci
7
, Katja Lohmann
1
, Christine Klein
18
; Global Parkinson’s Genetic Program (GP2)
Collaborators
-
Global Parkinson’s Genetic Program (GP2):
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, Jifeng Guo, Piu Chan, Wei Luo, Gonzalo Arboleda, Jorge Orozco, Marlene Jimenez Del Rio, Alvaro Hernandez, Mohamed Salama, Walaa A Kamel, Yared Z Zewde, Alexis Brice, Jean-Christophe Corvol, Ana Westenberger, Anastasia Illarionova, Brit Mollenhauer, Christine Klein, Eva-Juliane Vollstedt, Franziska Hopfner, Günter Höglinger, Harutyun Madoev, Joanne Trinh, Johanna Junker, Katja Lohmann, Lara M Lange, Manu Sharma, Sergio Groppa, Thomas Gasser, Zih-Hua Fang, Albert Akpalu, Georgia Xiromerisiou, Georgios Hadjigorgiou, Ioannis Dagklis, Ioannis Tarnanas, Leonidas Stefanis, Maria Stamelou, Efthymios Dadiotis, Alex Medina, Germaine Hiu-Fai Chan, Nancy Ip, Nelson Yuk-Fai Cheung, Phillip Chan, Xiaopu Zhou, Asha Kishore, Divya Kp, Pramod Pal, Prashanth Lingappa Kukkle, Roopa Rajan, Rupam Borgohain, Mehri Salari, Andrea Quattrone, Enza Maria Valente, Lucilla Parnetti, Micol Avenali, Tommaso Schirinzi, Manabu Funayama, Nobutaka Hattori, Tomotaka Shiraishi, Altynay Karimova, Gulnaz Kaishibayeva, Cholpon Shambetova, Rejko Krüger, Ai Huey Tan, Azlina Ahmad-Annuar, Mohamed Ibrahim Norlinah, Nor Azian Abdul Murad, Norlinah Mohamed Ibrahim, Shahrul Azmin, Shen-Yang Lim, Wael Mohamed, Yi Wen Tay, Daniel Martinez-Ramirez, Mayela Rodriguez-Violante, Paula Reyes-Pérez, Bayasgalan Tserensodnom, Rajeev Ojha, Tim J Anderson, Toni L Pitcher, Arinola Sanyaolu, Njideka Okubadejo, Oluwadamilola Ojo, Jan O Aasly, Lasse Pihlstrøm, Manuela Tan, Shoaib Ur-Rehman, Mario Cornejo-Olivas, Maria Leila Doquenia, Raymond Rosales, Angel Vinuela, Elena Iakovenko, Bashayer Al Mubarak, Muhammad Umair, Eng-King Tan, Jia Nee Foo, Ferzana Amod, Jonathan Carr, Soraya Bardien, Beomseok Jeon, Yun Joong Kim, Esther Cubo, Ignacio Alvarez, Janet Hoenicka, Katrin Beyer, Maria Teresa Periñan, Pau Pastor, Sarah El-Sadig, Christiane Zweier, Krack Paul, Chin-Hsien Lin, Hsiu-Chuan Wu, Pin-Jui Kung, Ruey-Meei Wu, Serena Wu, Yihru Wu, Rim Amouri, Samia Ben Sassi, A Nazl Başak, Gencer Genc, Özgür Öztop Çakmak, Sibel Ertan, Alastair Noyce, Alejandro Martínez-Carrasco, Anette Schrag, Anthony Schapira, Camille Carroll, Claire Bale, Donald Grosset, Eleanor J Stafford, Henry Houlden, Huw R Morris, John Hardy, Kin Ying Mok, Mie Rizig, Nicholas Wood, Nigel Williams, Olaitan Okunoye, Patrick Alfryn Lewis, Rauan Kaiyrzhanov, Rimona Weil, Seth Love, Simon Stott, Simona Jasaitye, Sumit Dey, Vida Obese, Alberto Espay, Alyssa O'Grady, Andrew B Singleton, Andrew K Sobering, Bernadette Siddiqi, Bradford Casey, Brian Fiske, Cabell Jonas, Carlos Cruchaga, Caroline B Pantazis, Charisse Comart, Claire Wegel, Cornelis Blauwendraat, Dan Vitale, Deborah Hall, Dena Hernandez, Ejaz Shiamim, Ekemini Riley, Faraz Faghri, Geidy E Serrano, Hampton Leonard, Hirotaka Iwaki, Honglei Chen, Ignacio F Mata, Ignacio Juan Keller Sarmiento, Jared Williamson, Jonggeol Jeff Kim, Joseph Jankovic, Joshua Shulman, Justin C Solle, Kaileigh Murphy, Karen Nuytemans, Karl Kieburtz, Katerina Markopoulou, Kenneth Marek, Kristin S Levine, Lana M Chahine, Laurel Screven, Lauren Ruffrage, Lisa Shulman, Luca Marsili, Maggie Kuhl, Marissa Dean, Mary B Makarious, Mathew Koretsky, Miguel Inca-Martinez, Mike A Nalls, Naomi Louie, Niccolò Emanuele Mencacci, Roger Albin, Roy Alcalay, Ruth Walker, Sara Bandres-Ciga, Sohini Chowdhury, Sonya Dumanis, Steven Lubbe, Tao Xie, Tatiana Foroud, Thomas Beach, Todd Sherer, Yeajin Song, Duan Nguyen, Toan Nguyen, Masharip Atadzhanov
Affiliations
- 1 Institute of Neurogenetics, University of Lübeck, Lübeck, Germany.
- 2 IRCCS Mondino Foundation, Pavia, Italy.
- 3 Department of Brain and Behavioral Sciences, University of Pavia, Pavia, Italy.
- 4 Northcott Neuroscience Laboratory, ANZAC Research Institute, Concord, NSW, Australia.
- 5 Faculty of Medicine and Health, University of Sydney, Sydney, NSW, Australia.
- 6 German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
- 7 Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
- 8 Division of Neurology, Department of Medicine, and the Mah Pooi Soo and Tan Chin Nam Centre for Parkinson's and Related Disorders, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
- 9 Department of Molecular Medicine, University of Pavia, Pavia, Italy.
- 10 Department of Clinical Research, Michael J. Fox Foundation for Parkinson's Research, New York City, NY, USA.
- 11 Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA.
- 12 Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.
- 13 Molecular Medicine Laboratory and Neurology Department, Concord Repatriation General Hospital, The University of Sydney, Concord, NSW, Australia.
- 14 Data Tecnica International, Washington, DC, USA.
- 15 Center for Alzheimer's and Related Dementias (CARD), National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.
- 16 Molecular Genetics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
- 17 Integrative Genomics Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD, USA.
- 18 Institute of Neurogenetics, University of Lübeck, Lübeck, Germany. christine.klein@neuro.uni-luebeck.de.
- PMID: 37704671
- PMCID: PMC10499986
- DOI: 10.1038/s41531-023-00560-7
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Erratum for
-
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2).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; Global Parkinson’s Genetic Program (GP2). Lange LM, et al. NPJ Parkinsons Dis. 2023 Jun 27;9(1):100. doi: 10.1038/s41531-023-00526-9. NPJ Parkinsons Dis. 2023. PMID: 37369645 Free PMC article.
