Wang, X., Walker, A., Revez, J. A., Ni, G., Adams, M. J., McIntosh, A. M. & Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium (2023).
Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability.
American Journal of Human Genetics,
110(7), 1207-1215.
https://doi.org/10.1016/j.ajhg.2023.06.006Rolland, T., Cliquet, F., Anney, R. J. L., Moreau, C., Traut, N., Mathieu, A., Huguet, G.
, Duan, J., Warrier, V., Portalier, S., Dry, L., Leblond, C. S., Douard, E., Amsellem, F., Malesys, S., Maruani, A., Toro, R.
, Børglum, A. D., Grove, J. ... Bourgeron, T. (2023).
Phenotypic effects of genetic variants associated with autism.
Nature Medicine,
29(7), 1671-1680.
https://doi.org/10.1038/s41591-023-02408-2Antaki, D., Guevara, J., Maihofer, A. X., Klein, M., Gujral, M.
, Grove, J., Carey, C. E., Hong, O., Arranz, M. J., Hervas, A., Corsello, C., Vaux, K. K., Muotri, A. R., Iakoucheva, L. M., Courchesne, E., Pierce, K., Gleeson, J. G., Robinson, E. B., Nievergelt, C. M. & Sebat, J. (2022).
Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.
Nature Genetics,
54(8), Article 1259.
https://doi.org/10.1038/s41588-022-01145-5
