Browse by People

Collapse authors list.
Bryois, Julien, Skene, Nathan G ORCID: 0000-0002-6807-3180, Hansen, Thomas Folkmann ORCID: 0000-0001-6703-7762, Kogelman, Lisette JA, Watson, Hunna J ORCID: 0000-0001-8405-381X, Liu, Zijing ORCID: 0000-0002-0189-7409, Eating Disorders Working Group of the Psychiatric Genomics Conso, , International Headache Genetics Consortium, , 23andMe Research Team, , Brueggeman, Leo et al (show 5 more authors) , Breen, Gerome ORCID: 0000-0003-2053-1792, Bulik, Cynthia M, Arenas, Ernest ORCID: 0000-0003-0197-6577, Hjerling-Leffler, Jens ORCID: 0000-0002-4539-1776 and Sullivan, Patrick F ORCID: 0000-0002-6619-873X (2020) Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. Nature genetics, 52 (5). pp. 482-493.

Collapse authors list.
Trpchevska, Natalia, Freidin, Maxim B, Broer, Linda, Oosterloo, Berthe C, Yao, Shuyang, Zhou, Yitian, Vona, Barbara, Bishop, Charles, Bizaki-Vallaskangas, Argyro, Canlon, Barbara et al (show 56 more authors) , Castellana, Fabio, Chasman, Daniel I, Cherny, Stacey, Christensen, Kaare, Concas, Maria Pina, Correa, Adolfo, Elkon, Ran, Mengel-From, Jonas, Gao, Yan, Giersch, Anne BS, Girotto, Giorgia, Gudjonsson, Alexander, Gudnason, Vilmundur, Heard-Costa, Nancy L, Hertzano, Ronna, v.B. Hjelmborg, Jacob, Hjerling-Leffler, Jens, Hoffman, Howard J, Kaprio, Jaakko, Kettunen, Johannes, Krebs, Kristi, Kahler, Anna K, Lallemend, Francois, Launer, Lenore J, Lee, I-Min, Leonard, Hampton, Li, Chuan-Ming, Lowenheim, Hubert, Magnusson, Patrik KE, van Meurs, Joyce, Milani, Lili, Morton, Cynthia C, Makitie, Antti, Nalls, Mike A, Nardone, Giuseppe Giovanni, Nygaard, Marianne, Palviainen, Teemu, Pratt, Sheila, Quaranta, Nicola, Ramo, Joel, Saarentaus, Elmo, Sardone, Rodolfo ORCID: 0000-0003-1383-1850, Satizabal, Claudia L, Schweinfurth, John M, Seshadri, Sudha, Shiroma, Eric, Shulman, Eldad, Simonsick, Eleanor, Spankovich, Christopher, Tropitzsch, Anke, Lauschke, Volker M, Sullivan, Patrick F, Goedegebure, Andre, Cederroth, Christopher R, Williams, Frances MK and Nagtegaal, Andries Paul (2022) Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss. AMERICAN JOURNAL OF HUMAN GENETICS, 109 (6). pp. 1077-1091.