Showing 1 - 8 results of 8 for search ' 23andMe Research Team', query time: 0.03s
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1
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. by Bryois, J, Skene, NG, Hansen, TF, Kogelman, LJA, Watson, HJ, Liu, Z, Eating Disorders Working Group of the Psychiatric Genomics Consortium, International Headache Genetics Consortium, 23andMe Research Team, Brueggeman, L, Breen, G, Bulik, CM, Arenas, E, Hjerling-Leffler, J, Sullivan, PF
Published 2020Journal article -
2
Genome-wide study identifies association between HLA-B∗55:01 and self-reported penicillin allergy by Krebs, K, Bovijn, J, Zheng, N, Lepamets, M, Censin, JC, Jürgenson, T, Särg, D, Abner, E, Laisk, T, Luo, Y, Skotte, L, Geller, F, Feenstra, B, Wang, W, Auton, A, 23andMe Research Team, Raychaudhuri, S, Esko, T, Metspalu, A, Laur, S, Roden, DM, Wei, W-Q, Holmes, MV, Lindgren, CM, Phillips, EJ, Mägi, R, Milani, L, Fadista, J
Published 2020Journal article -
3
Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis by Gallagher, C, Makinen, N, Harris, H, Uimari, O, Cook, J, Shigesi, N, Rahmioglu, N, Ferreira, T, Velez-Edwards, D, Edwards, T, Ruhioglu, Z, Day, F, Becker, C, Karhunen, V, Martikainen, H, Jarvelin, M, Cantor, R, Ridker, P, Terry, K, Buring, J, Gordon, S, Medland, S, Montgomery, G, Nyholt, D, Hinds, D, Tung, J, Perry, J, Lind, P, Painter, J, Martin, N, Morris, A, Chasman, D, Missmer, S, Zondervan, K, Morton, C, 23andMe Research Team
Published 2018Journal article -
4
Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color by Simcoe, M, Valdes, A, Liu, F, Furlotte, NA, Evans, DM, Hemani, G, Ring, SM, Smith, GD, Duffy, DL, Zhu, G, Gordon, SD, Medland, SE, Vuckovic, D, Girotto, G, Sala, C, Catamo, E, Concas, MP, Brumat, M, Gasparini, P, Toniolo, D, Cocca, M, Robino, A, Yazar, S, Hewitt, A, Wu, W, Kraft, P, Hammond, CJ, Shi, Y, Chen, Y, Zeng, C, Klaver, CCW, Uitterlinden, AG, Ikram, MA, Hamer, MA, van Duijn, CM, Nijsten, T, Han, J, Mackey, DA, Martin, NG, Cheng, C-Y, 23andMe Research Team, International Visible Trait Genetics Consortium, Hinds, DA, Spector, TD, Kayser, M, Hysi, PG
Published 2021Journal article -
5
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals by Lee, JJ, Wedow, R, Okbay, A, Kong, E, Maghzian, O, Zacher, M, Nguyen-Viet, TA, Bowers, P, Sidorenko, J, Linnér, R, Fontana, MA, Kundu, T, Lee, C, Li, H, Li, R, Royer, R, Timshel, PN, Walters, RK, Willoughby, EA, Yengo, L, 23andMe Research Team, COGENT (Cognitive Genomics Consortium), Social Science Genetic Association Consortium, Alver, M, Bao, Y, Clark, DW, Day, FR, Furlotte, NA, Joshi, PK, Kemper, KE, Kleinman, A, Langenberg, C, Mägi, R, Trampush, JW, Verma, SS, Wu, Y, Lam, M, Zhao, JH, Zheng, Z, Boardman, JD, Campbell, H, Freese, J, Harris, KM, Hayward, C, Herd, P, Kumari, M, Lencz, T, Luan, J, Malhotra, AK, Metspalu, A, Milani, L, Ong, KK, Perry, JRB, Porteous, DJ, Ritchie, MD, Smart, MC, Smith, BH, Tung, JY, Wareham, NJ, Wilson, JF, Beauchamp, JP, Conley, DC, Esko, T, Lehrer, SF, Magnusson, PKE, Oskarsson, S, Pers, TH, Robinson, MR, Thom, K, Watson, C, Chabris, CF, Meyer, MN, Laibson, DI, Yang, J, Johannesson, M, Koellinger, PD, Turley, P, Visscher, PM, Benjamin, DJ, Cesarini, D
Published 2018Journal article -
6
A saturated map of common genetic variants associated with human height by Yengo, L, Vedantam, S, Marouli, E, Ferreira, T, Karaderi, T, Malden, DE, Fairhurst-Hunter, Z, Goel, A, Lin, K, Liu, J, Mahajan, A, Millwood, I, Rayner, NW, Chen, Z, Karpe, F, Neville, MJ, van Duijn, CM, Watkins, H, McCarthy, MI, Lindgren, CM, Walters, RG
Published 2022Other Authors: “…23andMe Research Team…”
Journal article -
7
Genome-wide association analysis and replication in 810,625 individuals identifies novel therapeutic targets for varicose veins by Ahmed, WULR, Wiberg, A, Ng, M, Wang, W, Auton, A, Lee, R, Handa, A, Zondervan, KT, Furniss, D
Published 2021Other Authors: “… 23andMe Research Team…”
Conference item -
8
Discovery of 42 genome-wide significant loci associated with dyslexia by Doust, C, Fontanillas, P, Eising, E, Gordon, SD, Wang, Z, Alagöz, G, Molz, B, Pourcain, BS, Francks, C, Marioni, RE, Zhao, J, Paracchini, S, Talcott, JB, Monaco, AP, Stein, JF, Gruen, JR, Olson, RK, Willcutt, EG, DeFries, JC, Pennington, BF, Smith, SD, Wright, MJ, Martin, NG, Auton, A, Bates, TC, Fisher, SE, Luciano, M
Published 2022Other Authors: “…23andMe Research Team…”
Journal article