Yao, M., Miller, G. W., Vardarajan, B. N., Baccarelli, A. A., Guo, Z., & Liu, Z. (2024). Deciphering proteins in Alzheimer’s disease: A new Mendelian randomization method integrated with AlphaFold3 for 3D structure prediction. Cell Genomics, 4(12), 100700. https://doi.org/10.1016/j.xgen.2024.100700

Tayran, H., Yilmaz, E., Bhattarai, P., Min, Y., Wang, X., Ma, Y., Wang, N., Jeong, I., Nelson, N., Kassara, N., Cosacak, M. I., Dogru, R. M., Reyes-Dumeyer, D., Stenersen, J. M., Reddy, J. S., Qiao, M., Flaherty, D., Gunasekaran, T. I., Yang, Z., … Kizil, C. (2024). ABCA7-dependent induction of neuropeptide Y is required for synaptic resilience in Alzheimer’s disease through BDNF/NGFR signaling. Cell Genomics, 4(9), 100642. https://doi.org/10.1016/j.xgen.2024.100642

Recinos, Y., Bao, S., Wang, X., Phillips, B. L., Yeh, Y.-T., Weyn-Vanhentenryck, S. M., Swanson, M. S., & Zhang, C. (2024). Lineage-specific splicing regulation of MAPT gene in the primate brain. Cell Genomics, 4(6), 100563. https://doi.org/10.1016/j.xgen.2024.100563

Gouveia Roque, C., Phatnani, H., & Hengst, U. (2024). The broken Alzheimer’s disease genome. Cell Genomics, 4(5), 100555. https://doi.org/10.1016/j.xgen.2024.100555

Wang, L., Babushkin, N., Liu, Z., & Liu, X. (2024). Trans-eQTL mapping in gene sets identifies network effects of genetic variants. Cell Genomics, 4(4), 100538. https://doi.org/10.1016/j.xgen.2024.100538

Xu, M., Feng, R., Liu, Z., Zhou, X., Chen, Y., Cao, Y., Valeri, L., Li, Z., Liu, Z., Cao, S.-M., Liu, Q., Xie, S.-H., Chang, E. T., Jia, W.-H., Shen, J., Yao, Y., Cai, Y.-L., Zheng, Y., Zhang, Z., … Lin, X. (2024). Host genetic variants, Epstein-Barr virus subtypes, and the risk of nasopharyngeal carcinoma: Assessment of interaction and mediation. Cell Genomics, 4(2), 100474. https://doi.org/10.1016/j.xgen.2023.100474

Li, T., Ferraro, N., Strober, B. J., Aguet, F., Kasela, S., Arvanitis, M., Ni, B., Wiel, L., Hershberg, E., Ardlie, K., Arking, D. E., Beer, R. L., Brody, J., Blackwell, T. W., Clish, C., Gabriel, S., Gerszten, R., Guo, X., Gupta, N., … Montgomery, S. B. (2023). The functional impact of rare variation across the regulatory cascade. Cell Genomics, 3(10), 100401. https://doi.org/10.1016/j.xgen.2023.100401

Brown, B. C., Wang, C., Kasela, S., Aguet, F., Nachun, D. C., Taylor, K. D., Tracy, R. P., Durda, P., Liu, Y., Johnson, W. C., Van Den Berg, D., Gupta, N., Gabriel, S., Smith, J. D., Gerzsten, R., Clish, C., Wong, Q., Papanicolau, G., Blackwell, T. W., … Lappalainen, T. (2023). Multiset correlation and factor analysis enables exploration of multi-omics data. Cell Genomics, 3(8), 100359. https://doi.org/10.1016/j.xgen.2023.100359

Kaivola, K., Chia, R., Ding, J., Rasheed, M., Fujita, M., Menon, V., Walton, R. L., Collins, R. L., Billingsley, K., Brand, H., Talkowski, M., Zhao, X., Dewan, R., Stark, A., Ray, A., Solaiman, S., Alvarez Jerez, P., Malik, L., Dawson, T. M., … Zinman, L. (2023). Genome-wide structural variant analysis identifies risk loci for non-Alzheimer’s dementias. Cell Genomics, 3(6), 100316. https://doi.org/10.1016/j.xgen.2023.100316

Santhanam, B., Oikonomou, P., & Tavazoie, S. (2023). Systematic assessment of prognostic molecular features across cancers. Cell Genomics, 3(3), 100262. https://doi.org/10.1016/j.xgen.2023.100262

Dolan, D. D., Lee, S. S.-J., & Cho, M. K. (2022). Three decades of ethical, legal, and social implications research: Looking back to chart a path forward. Cell Genomics, 2(7), 100150. https://doi.org/10.1016/j.xgen.2022.100150