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Doust, Catherine, Fontanillas, Pierre, Eising, Else, Gordon, Scott D, Wang, Zhengjun, Alagöz, Gökberk, Molz, Barbara, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth
et al (show 137 more authors) (2022) Discovery of 42 genome-wide significant loci associated with dyslexia. Nature Genetics, 54 (11). pp. 1621-1629.


Nalls, Mike A, Blauwendraat, Cornelis, Vallerga, Costanza L, Heilbron, Karl, Bandres-Ciga, Sara, Chang, Diana, Tan, Manuela, Kia, Demis A, Noyce, Alastair J, Xue, Angli
et al (show 260 more authors) (2019) Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet Neurology, 18 (12). pp. 1091-1102.


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) (2024) Multi-ancestry genome-wide association meta-analysis of Parkinson's disease. Nature genetics, 56 (1). pp. 27-36.

This list was generated on Sun Mar 24 12:57:22 2024 GMT.