Selected Publications

(See the full list at Google Scholar)

Chen, C. Y.*, Chen, T. T., Feng, Y. A.*, Yu, M., Lin, S. C., Longchamps, R., Wang, S. H., Hsu, Y. H., Yang, H. I., Kuo, P. H., Daly, M. J., Chen, W. J., Huang, H.*, Ge, T.*, & Lin, Y. F.* (2023). Analysis across Taiwan Biobank, Biobank Japan and UK Biobank identifies hundreds of novel loci for 36 quantitative traits. Cell Genomics, 3(12):100436.

Campos, A. I., Namba, S., Lin, S. C., Nam, K., Sidorenko, J., Wang, H., Kamatani, Y., Biobank Japan Project, Wang, L. H., Lee, S., Lin, Y. F., Feng, Y. A., Okada, Y., Visscher, P., & Yengo, L. (2023). Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores. Nature Genetics, 55, 1769–1776.

International League Against Epilepsy Consortium on Complex Epilepsies (2023). GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Nature Genetics, 55, 1471-1482.

Feng, Y. A.*, Chen, C. Y., Chen, T. T., Kuo, P. H., Hsu, Y. H., Yang, H. I., Chen, W. J., Shen, C. Y., Ge, T., Huang, H., Lin, Y. F.* (2022). Taiwan Biobank: a rich biomedical research database of the Taiwanese population. Cell Genomics, 2(11): 100197.

Feng, Y. A.*, Stanaway, I. B., Connolly, J. J., Denny, J. C., Luo, Y., Weng, C., Wei, W.-Q., Weiss, S. T., Karlson, E. W., & Smoller, J. W.* (2022). Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach. BMC Genomics, 23(1), 385.

Ruan, Y., Lin, Y.-F., Feng, Y. A., Chen, C.-Y., Lam, M., Guo, Z., Stanley Global Asia Initiatives, He, L., Sawa, A., Martin, A. R., Qin, S., Huang, H., & Ge, T. (2022). Improving polygenic prediction in ancestrally diverse populations. Nature Genetics, 54(5), 573–580.

COVID-19 Host Genetics Initiative (2021). Mapping the human genetic architecture of COVID-19. Nature, 600(7889), 472-477.

Feng, Y. A.*, Guo, Y., Pain, L., Lathrop, G. M., Laprise, C., Moffatt, M. F., Cookson, W. O., & Liang, L.* (2021). Estimating cell-type-specific DNA methylation effects in heterogeneous cellular populations. Epigenomics, 13(2), 87–97.

Lee, P. H., Feng, Y. A., & Smoller, J. W. (2021). Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders. Biological Psychiatry, 89(1), 20-31.

Lee, P. H., Anttila, V., Won, H., Feng, Y. A., Rosenthal, J., Zhu, Z., ..., Smoller, J. W. (Cross-Disorder Group of the Psychiatric Genomics Consortium) (2019). Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell, 179(7), 1469-1482 e11.

Feng, Y. A., Howrigan, D. P., Abbott, L. E., Tashman, K., Cerrato, F., Singh, T., ..., Daly, M. J., Lander, E. S., Lowenstein, D. H., Goldstein, D., Lerche, H., Berkovic, S. F., & Neale, B. M. (Epi25 Collaborative) (2019). Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals. The American Journal of Human Genetics, 105(2), 267-282.

Ge, T., Chen, C.-Y., Ni, Y., Feng, Y. A., & Smoller, J. W. (2019). Polygenic prediction via Bayesian regression and continuous shrinkage priors. Nature Communications, 10(1), 1776.