Yengo, L and Vedantam, S and Marouli, E and Sidorenko, J and Bartell, E and Sakaue, S and Graff, M and Eliasen, AU and Jiang, AU and Raghavan, S and Miao, J and Arias, JD and Graham, SE and Mukamel, RE and Spracklen, CN and Yin, X and Chen, SH and Ferreira, T and Highland, HH and Ji, Y and Karaderi, T and Lin, K and Lull, K and Medina-Gomez, C and Machado, M and Moore, A and Rueger, S and Sim, X and Vrieze, S and Ahluwalia, TS and Akiyama, M and Allison, MA and Alvarez, M and Andersen, MK and Ani, A and Appadurai, V and Arbeeva, L and Bhaskar, S and Bielak, LF and Bollepalli, S and Bonnycastle, LL and Bork-Jensen, J and Bradfield, JP and Bradford, Y and Braund, PS and Brody, JA and Burgdorf, KS and Cade, BE and Cai, H and Cai, Q and Campbell, A and Campbell, M and Catamo, E and Chai, JF and Chai, X and Chang, LC and Chang, YC and Chen, CH and Chesi, A and Choi, SH and Chung, RH and Cocca, M and Concas, MP and Couture, C and Cuellar-Partida, G and Danning, R and Daw, EW and Degenhard, F and Delgado, GE and Delitala, A and Demirkan, A and Deng, X and Devineni, P and Dietl, A and Dimitriou, M and Dimitrov, L and Dorajoo, R and Ekici, AB and Engmann, JE and Fairhurst-Hunter, Z and Faul, JD and Fernandez-Lopez, JC and Forer, L and Francescatto, M and Freitag-Wolf, S and Fuchsberger, C and Galesloot, TE and Gao, Y and Gao, Z and Geller, F and Giannakopoulou, O and Giulianini, F and Gjesing, AP and Goel, A and Goel, SD and Gorski, M and Grove, J and Hewitt, AW, 23andMe Research Team; VA Million Veteran Program; DiscovEHR (DiscovEHR and MyCode Community Health Initiative); eMERGE (Electronic Medical Records and Genomics Network); Lifelines Cohort Study; PRACTICAL Consortium; Understanding Society Scientific, “A saturated map of common genetic variants associated with human height”, Nature, 610 pp. 704-712. ISSN 0028-0836 (2022) [Refereed Article] |