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Pottinger, T. D., Motelow, J. E., Povysil, G., Moreno, C. A. M., Ren, Z., Phatnani, H., Harms, M. B., Kwan, J., Sareen, D., Wang, H.-I., Broach, J. R., Simmons, Z., Arcila-Londono, X., Parrott, S., Lee, E. B., Parrott, S., Deerlin, V. M. V., Fraenkel, E., … Ostrow, L. W. (2024). Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies ANTXR2 as a candidate in PLS. BMC Genomics, 25(1). https://doi.org/10.1186/s12864-024-10538-1

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Ghandhi, S. A., Morton, S. R., Shuryak, I., Lee, Y., Soni, R. K., Perrier, J. R., Bakke, J., Gahagan, J., Bujold, K., Authier, S., Amundson, S. A., Brenner, D. J., Nishita, D., Chang, P., & Turner, H. C. (2023). Longitudinal multi-omic changes in the transcriptome and proteome of peripheral blood cells after a 4 Gy total body radiation dose to Rhesus macaques. BMC Genomics, 24(1). https://doi.org/10.1186/s12864-023-09230-7

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

He, K. Y., Kelly, T. N., Wang, H., Liang, J., Zhu, L., Cade, B. E., Assimes, T. L., Becker, L. C., Beitelshees, A. L., Bielak, L. F., Bress, A. P., Brody, J. A., Chang, Y.-P. C., Chang, Y.-C., de Vries, P. S., Duggirala, R., Fox, E. R., Franceschini, N., Furniss, A. L., … Zhu, X. (2022). Rare coding variants in RCN3 are associated with blood pressure. BMC Genomics, 23(1). https://doi.org/10.1186/s12864-022-08356-4

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