Feng, Y.-C. 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). https://doi.org/10.1186/s12864-022-08600-x

Hsiao, C. J., Dumeny, L., Bress, A. P., Johnson, D. A., Shimbo, D., Cavallari, L. H., & Mulligan, C. J. (2022). Identification of a SGCD × Discrimination Interaction Effect on Systolic Blood Pressure in African American Adults in the Jackson Heart Study. American Journal of Hypertension, 35(11), 938–947. https://doi.org/10.1093/ajh/hpac098

Lahti, J., Tuominen, S., Yang, Q., Pergola, G., Ahmad, S., Amin, N., Armstrong, N. J., Beiser, A., Bey, K., Bis, J. C., Boerwinkle, E., Bressler, J., Campbell, A., Campbell, H., Chen, Q., Corley, J., Cox, S. R., Davies, G., De Jager, P. L., … Räikkönen, K. (2022). Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Molecular Psychiatry, 27(11), 4419–4431. https://doi.org/10.1038/s41380-022-01710-8

Kim, M. S., Naidoo, D., Hazra, U., Quiver, M. H., Chen, W. C., Simonti, C. N., Kachambwa, P., Harlemon, M., Agalliu, I., Baichoo, S., Fernandez, P., Hsing, A. W., Jalloh, M., Gueye, S. M., Niang, L., Diop, H., Ndoye, M., Snyper, N. Y., Adusei, B., … Lachance, J. (2022). Testing the generalizability of ancestry-specific polygenic risk scores to predict prostate cancer in sub-Saharan Africa. Genome Biology, 23(1). https://doi.org/10.1186/s13059-022-02766-z

Manzali, S. B., Yu, E., Ravona-Springer, R., Livny, A., Golan, S., Ouyang, Y., Lesman-Segev, O., Liu, L., Ganmore, I., Alkelai, A., Gan-Or, Z., Lin, H.-M., Heymann, A., Schnaider Beeri, M., & Greenbaum, L. (2022). Alzheimer’s Disease Polygenic Risk Score Is Not Associated With Cognitive Decline Among Older Adults With Type 2 Diabetes. Frontiers in Aging Neuroscience, 14. https://doi.org/10.3389/fnagi.2022.853695

Tahir, U. A., Katz, D. H., Avila-Pachecho, J., Bick, A. G., Pampana, A., Robbins, J. M., Yu, Z., Chen, Z.-Z., Benson, M. D., Cruz, D. E., Ngo, D., Deng, S., Shi, X., Zheng, S., Eisman, A. S., Farrell, L., Hall, M. E., Correa, A., Tracy, R. P., … Gerszten, R. E. (2022). Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-32275-3

Eissman, J. M., Dumitrescu, L., Mahoney, E. R., Smith, A. N., Mukherjee, S., Lee, M. L., Scollard, P., Choi, S. E., Bush, W. S., Engelman, C. D., Lu, Q., Fardo, D. W., Trittschuh, E. H., Mez, J., Kaczorowski, C. C., Hernandez Saucedo, H., Widaman, K. F., Buckley, R. F., Properzi, M. J., … Hohman, T. J. (2022). Sex differences in the genetic architecture of cognitive resilience to Alzheimer’s disease. Brain, 145(7), 2541–2554. https://doi.org/10.1093/brain/awac177

Hu, X., Qiao, D., Kim, W., Moll, M., Balte, P. P., Lange, L. A., Bartz, T. M., Kumar, R., Li, X., Yu, B., Cade, B. E., Laurie, C. A., Sofer, T., Ruczinski, I., Nickerson, D. A., Muzny, D. M., Metcalf, G. A., Doddapaneni, H., Gabriel, S., … Manichaikul, A. (2022). Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program. The American Journal of Human Genetics, 109(5), 857–870. https://doi.org/10.1016/j.ajhg.2022.03.007

Lee, W., de Prisco, N., & Gennarino, V. A. (2022). Identifying patients and assessing variant pathogenicity for an autosomal dominant disease-driving gene. STAR Protocols, 3(1), 101150. https://doi.org/10.1016/j.xpro.2022.101150

Joo, Y. Y., Moon, S.-Y., Wang, H.-H., Kim, H., Lee, E.-J., Kim, J. H., Posner, J., Ahn, W.-Y., Choi, I., Kim, J.-W., & Cha, J. (2022). Association of Genome-Wide Polygenic Scores for Multiple Psychiatric and Common Traits in Preadolescent Youths at Risk of Suicide. JAMA Network Open, 5(2), e2148585. https://doi.org/10.1001/jamanetworkopen.2021.48585

Storm, C. S., Kia, D. A., Almramhi, M. M., Bandres-Ciga, S., Finan, C., Noyce, A. J., Kaiyrzhanov, R., Middlehurst, B., Tan, M., Houlden, H., Morris, H. R., Plun-Favreau, H., Holmans, P., Hardy, J., Trabzuni, D., Quinn, J., Bubb, V., Mok, K. Y., … Wood, N. W. (2021). Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome. Nature Communications, 12(1). https://doi.org/10.1038/s41467-021-26280-1

Zoghbi, A. W., Dhindsa, R. S., Goldberg, T. E., Mehralizade, A., Motelow, J. E., Wang, X., Alkelai, A., Harms, M. B., Lieberman, J. A., Markx, S., & Goldstein, D. B. (2021). High-impact rare genetic variants in severe schizophrenia. Proceedings of the National Academy of Sciences, 118(51). https://doi.org/10.1073/pnas.2112560118

Davis, E. J., Solsberg, C. W., White, C. C., Miñones-Moyano, E., Sirota, M., Chibnik, L., Bennett, D. A., De Jager, P. L., Yokoyama, J. S., & Dubal, D. B. (2021). Sex-Specific Association of the X Chromosome With Cognitive Change and Tau Pathology in Aging and Alzheimer Disease. JAMA Neurology, 78(10), 1249. https://doi.org/10.1001/jamaneurol.2021.2806

Liu, C., Zeinomar, N., Chung, W. K., Kiryluk, K., Gharavi, A. G., Hripcsak, G., Crew, K. D., Shang, N., Khan, A., Fasel, D., Manolio, T. A., Jarvik, G. P., Rowley, R., Justice, A. E., Rahm, A. K., Fullerton, S. M., Smoller, J. W., Larson, E. B., Crane, P. K., … Weng, C. (2021). Generalizability of Polygenic Risk Scores for Breast Cancer Among Women With European, African, and Latinx Ancestry. JAMA Network Open, 4(8), e2119084. https://doi.org/10.1001/jamanetworkopen.2021.19084