Browse by People

Collapse authors list.
Towns, Clodagh, Richer, Madeleine, Jasaityte, Simona, Stafford, Eleanor J, Joubert, Julie, Antar, Tarek, Martinez-Carrasco, Alejandro, Makarious, Mary B, Casey, Bradford, Vitale, Dan et al (show 14 more authors) , Levine, Kristin, Leonard, Hampton, Pantazis, Caroline B, Screven, Laurel A, Hernandez, Dena G, Wegel, Claire E, Solle, Justin, Nalls, Mike A, Blauwendraat, Cornelis, Singleton, Andrew B, Tan, Manuela MX, Iwaki, Hirotaka, Morris, Huw R and Global Parkinson’s Genetics Program (GP2), (2023) Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2). NPJ Parkinson's disease, 9 (1). p. 131.

Collapse authors list.
Kim, Jonggeol Jeffrey ORCID: 0000-0003-0738-0512, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, 23andMe Research Team, , Iwaki, Hirotaka, Lake, Julie ORCID: 0000-0002-3441-2455, Solsberg, Caroline Warly ORCID: 0000-0001-7049-6281, Leonard, Hampton et al (show 10 more authors) , Makarious, Mary B ORCID: 0000-0002-7978-1051, Tan, Eng-King ORCID: 0000-0003-2977-9743, Singleton, Andrew B, Bandres-Ciga, Sara, Noyce, Alastair J, Global Parkinson’s Genetics Program (GP2), , Blauwendraat, Cornelis ORCID: 0000-0001-9358-8111, Nalls, Mike A ORCID: 0000-0003-0319-4325, Foo, Jia Nee and Mata, Ignacio (2024) Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Nature genetics, 56 (1). pp. 27-36.