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Junker, Johanna and Lange, Lara M. and Vollstedt, Eva-Juliane and Roopnarain, Karisha and Doquenia, Maria Leila M. and Annuar, Azlina Ahmad and Avenali, Micol and Bardien, Soraya and Bahr, Natascha and Ellis, Melina and Galandra, Caterina and Gasser, Thomas and Heutink, Peter and Illarionova, Anastasia and Kanana, Yuliia and Sarmiento, Ignacio J. Keller and Kumar, Kishore R. and Lim, Shen-Yang and Madoev, Harutyun and Mata, Ignacio F. and Mencacci, Niccolo E. and Nalls, Mike A. and Padmanabhan, Shalini and Shambetova, Cholpon and Solle, J. C. and Tan, Ai-Huey and Trinh, Joanne and Valente, Enza Maria and Singleton, Andrew and Blauwendraat, Cornelis and Lohmann, Katja and Fang, Zih-Hua and Klein, Christine (2024) Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale. Movement Disorders, 39 (10). pp. 1868-1873. ISSN 0885-3185, DOI https://doi.org/10.1002/mds.29925.
Lange, Lara and Avenali, Micol and Ellis, Melina and Illarionova, Anastasia J. and Sarmiento, Ignacio Keller and Tan, Ai-Huey and Madoev, Harutyun and Galandra, Caterina and Junker, Johanna and Roopnarain, Karisha and Solle, Justin and Wegel, Claire and Fang, Zih-Hua and Heutink, Peter R. and Kumar, Kishore and Lim, Shen-Yang and Valente, Enza Maria and Nalls, Mike and Blauwendraat, Cornelis and Singleton, Andrew and Mencacci, Niccolo and Lohmann, Katja and Klein, Christine and Program, Global Parkinsons Genetic (2023) Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2). NPJ Parkinson's Disease, 9 (1). ISSN 2373-8057, DOI https://doi.org/10.1038/s41531-023-00526-9.
