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Items where Author is "Blauwendraat, Cornelis"

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Number of items: 3.

Article

Lange, Lara M. and Levine, Kristin and Fox, Susan H. and Marras, Connie and Ahmed, Nazish and Kuznetsov, Nicole and Vitale, Dan and Iwaki, Hirotaka and Lohmann, Katja and Marsili, Luca and Espay, Alberto J. and Bauer, Peter and Beetz, Christian and Martin, Jessica and Factor, Stewart A. and Higginbotham, Lenora A. and Chen, Honglei and Leonard, Hampton and Nalls, Mike A. and Mencacci, Niccolo E. and Morris, Huw R. and Singleton, Andrew B. and Klein, Christine and Blauwendraat, Cornelis and Fang, Zih-Hua and Mohamed, Wael Mohamed Yousef (2025) The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population. npj Parkinson's Disease, 11 (1). pp. 1-10. E-ISSN 2373-8057

Ojo, Oluwadamilola Omolara and Bandres-Ciga, Sara and Makarious, Mary B. and Crea, Peter Wild and Hernandez, Dena G. and Houlden, Henry and Rizig, Mie and Singleton, Andrew B. and Noyce, Alastair J. and Nalls, Mike A. and Blauwendraat, Cornelis and Okubadejo, Njideka Ulunma and Mohamed, Wael Mohamed Yousef (2024) GBA1 rs3115534 is associated with REM sleep behavior disorder in Parkinson’s disease in Nigerians. Movements Disorders. pp. 1-6. ISSN 0885-3185 E-ISSN 1531-8257

Towns, Clodagh and Richer, Madeleine and Jasaityte, Simona and Mohamed, Wael Mohamed Yousef and Stafford, Eleanor J. and Joubert, Julie and Antar, Tarek and Martinez-Carrasco, Alejandro and Makarious, Mary B. and Casey, Bradford and Vitale, Dan and Levine, Kristin and Leonard, Hampton and Pantazis, Caroline B. and Screven, Laurel A. and Hernandez, Dena G. and Wegel, Claire E. and Solle, Justin and Nalls, Mike A. and Blauwendraat, Cornelis and Singleton, Andrew B. and Tan, Manuela M. X. and Iwaki, Hirotaka and Morris, Huw R. (2023) Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2). npj Parkinson's Disease, 9. pp. 1-6. E-ISSN 2373-8057

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