Ray, N. R., Bradley, J., Yilmaz, E., Kizil, C., Kurup, J. T., Martin, E. R., Klein, H.-U., Kunkle, B. W., Bennett, D. A., De Jager, P. L., Beecham, G. W., Cruchaga, C., & Reitz, C. (2025). Local genetic covariance analysis with lipid traits identifies novel loci for early-onset Alzheimer’s Disease. PLOS Genetics, 21(3), e1011631. https://doi.org/10.1371/journal.pgen.1011631

Dominy, J., Bai, J., Koch, C., Zaman Khan, M., Khalid, S., Chung, J. H., Panditrao, M., Liu, L., Zhang, Q., Jahanzaib, M., Mian, M. R., Liaqat, M. B., Raza, S. S., Sultana, R., Jalal, A., Saeed, M. H., Abbas, S., Memon, F. R., Ishaq, M., … Saleheen, D. (2025). Human CD33 deficiency is associated with mild alteration of circulating white blood cell counts. PLOS Genetics, 21(3), e1011600. https://doi.org/10.1371/journal.pgen.1011600

Ahn, J., Hwang, I.-S., Park, M.-R., Rosa-Velazquez, M., Cho, I.-C., Relling, A. E., Hwang, S., & Lee, K. (2025). Evolutionary lineage-specific genomic imprinting at the ZNF791 locus. PLOS Genetics, 21(1), e1011532. https://doi.org/10.1371/journal.pgen.1011532

Bravo, J. I., Mizrahi, C. R., Kim, S., Zhang, L., Suh, Y., & Benayoun, B. A. (2024). An eQTL-based approach reveals candidate regulators of LINE-1 RNA levels in lymphoblastoid cells. PLOS Genetics, 20(6), e1011311. https://doi.org/10.1371/journal.pgen.1011311

Dugger, S. A., Dhindsa, R. S., Sampaio, G. D. A., Ressler, A. K., Rafikian, E. E., Petri, S., Letts, V. A., Teoh, J., Ye, J., Colombo, S., Peng, Y., Yang, M., Boland, M. J., Frankel, W. N., & Goldstein, D. B. (2023). Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency. PLOS Genetics, 19(10), e1010952. https://doi.org/10.1371/journal.pgen.1010952

Morgante, F., Carbonetto, P., Wang, G., Zou, Y., Sarkar, A., & Stephens, M. (2023). A flexible empirical Bayes approach to multivariate multiple regression, and its improved accuracy in predicting multi-tissue gene expression from genotypes. PLOS Genetics, 19(7), e1010539. https://doi.org/10.1371/journal.pgen.1010539

Yi, J., Zhao, X., Noell, C. R., Helmer, P., Solmaz, S. R., & Vallee, R. B. (2023). Role of Nesprin-2 and RanBP2 in BICD2-associated brain developmental disorders. PLOS Genetics, 19(3), e1010642. https://doi.org/10.1371/journal.pgen.1010642

Dapas, M., Thompson, E. E., Wentworth-Sheilds, W., Clay, S., Visness, C. M., Calatroni, A., Sordillo, J. E., Gold, D. R., Wood, R. A., Makhija, M., Khurana Hershey, G. K., Sherenian, M. G., Gruchalla, R. S., Gill, M. A., Liu, A. H., Kim, H., Kattan, M., Bacharier, L. B., Rastogi, D., … Ober, C. (2023). Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings. PLOS Genetics, 19(1), e1010594. https://doi.org/10.1371/journal.pgen.1010594

Chernoff, M. B., Delgado, D., Tong, L., Chen, L., Oliva, M., Tamayo, L. I., Best, L. G., Cole, S., Jasmine, F., Kibriya, M. G., Nelson, H., Huang, L., Haack, K., Kent, J., Umans, J. G., Graziano, J., Navas-Acien, A., Karagas, M. R., Ahsan, H., & Pierce, B. L. (2023). Sequencing-based fine-mapping and in silico functional characterization of the 10q24.32 arsenic metabolism efficiency locus across multiple arsenic-exposed populations. PLOS Genetics, 19(1), e1010588. https://doi.org/10.1371/journal.pgen.1010588

Wattacheril, J. J., Raj, S., Knowles, D. A., & Greally, J. M. (2023). Using epigenomics to understand cellular responses to environmental influences in diseases. PLOS Genetics, 19(1), e1010567. https://doi.org/10.1371/journal.pgen.1010567

Butler-Laporte, G., Povysil, G., Kosmicki, J. A., Cirulli, E. T., Drivas, T., Furini, S., Saad, C., Schmidt, A., Olszewski, P., Korotko, U., Quinodoz, M., Çelik, E., Kundu, K., Walter, K., Jung, J., Stockwell, A. D., Sloofman, L. G., Jordan, D. M., Thompson, R. C., … Richards, J. B. (2022). Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. PLOS Genetics, 18(11), e1010367. https://doi.org/10.1371/journal.pgen.1010367

Ketcham, A., Freddolino, P. L., & Tavazoie, S. (2022). Intracellular acidification is a hallmark of thymineless death in E. coli. PLOS Genetics, 18(10), e1010456. https://doi.org/10.1371/journal.pgen.1010456

Choi, J., Kong, M., Gallagher, D. N., Li, K., Bronk, G., Cao, Y., Greene, E. C., & Haber, J. E. (2022). Repair of mismatched templates during Rad51-dependent Break-Induced Replication. PLOS Genetics, 18(9), e1010056. https://doi.org/10.1371/journal.pgen.1010056

Peart, N. J., Johnson, T. A., Lee, S., Sears, M. J., Yang, F., Quesnel-Vallières, M., Feng, H., Recinos, Y., Barash, Y., Zhang, C., Hermann, B. P., Wang, P. J., Geyer, C. B., & Carstens, R. P. (2022). The germ cell-specific RNA binding protein RBM46 is essential for spermatogonial differentiation in mice. PLOS Genetics, 18(9), e1010416. https://doi.org/10.1371/journal.pgen.1010416

Scales, M. K., Velez-Delgado, A., Steele, N. G., Schrader, H. E., Stabnick, A. M., Yan, W., Mercado Soto, N. M., Nwosu, Z. C., Johnson, C., Zhang, Y., Salas-Escabillas, D. J., Menjivar, R. E., Maurer, H. C., Crawford, H. C., Bednar, F., Olive, K. P., Pasca di Magliano, M., & Allen, B. L. (2022). Combinatorial Gli activity directs immune infiltration and tumor growth in pancreatic cancer. PLOS Genetics, 18(7), e1010315. https://doi.org/10.1371/journal.pgen.1010315

Zou, Y., Carbonetto, P., Wang, G., & Stephens, M. (2022). Fine-mapping from summary data with the “Sum of Single Effects” model. PLOS Genetics, 18(7), e1010299. https://doi.org/10.1371/journal.pgen.1010299

Rajabli, F., Beecham, G. W., Hendrie, H. C., Baiyewu, O., Ogunniyi, A., Gao, S., Kushch, N. A., Lipkin-Vasquez, M., Hamilton-Nelson, K. L., Young, J. I., Dykxhoorn, D. M., Nuytemans, K., Kunkle, B. W., Wang, L., Jin, F., Liu, X., Feliciano-Astacio, B. E., Schellenberg, G. D., … Vance, J. M. (2022). A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer’s Disease in African Ancestry. PLOS Genetics, 18(7), e1009977. https://doi.org/10.1371/journal.pgen.1009977

Diez, S., Hydorn, M., Whalen, A., & Dworkin, J. (2022). Crosstalk between guanosine nucleotides regulates cellular heterogeneity in protein synthesis during nutrient limitation. PLOS Genetics, 18(5), e1009957. https://doi.org/10.1371/journal.pgen.1009957

Gurtan, A., Dominy, J., Khalid, S., Vong, L., Caplan, S., Currie, T., Richards, S., Lamarche, L., Denning, D., Shpektor, D., Gurinovich, A., Rasheed, A., Hameed, S., Saeed, S., Saleem, I., Jalal, A., Abbas, S., Sultana, R., Rasheed, S. Z., … Saleheen, D. (2022). Analyzing human knockouts to validate GPR151 as a therapeutic target for reduction of body mass index. PLOS Genetics, 18(4), e1010093. https://doi.org/10.1371/journal.pgen.1010093

Zernant, J., Lee, W., Wang, J., Goetz, K., Ullah, E., Nagasaki, T., Su, P.-Y., Fishman, G. A., Tsang, S. H., Tumminia, S. J., Brooks, B. P., Hufnagel, R. B., Chen, R., & Allikmets, R. (2022). Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease. PLOS Genetics, 18(3), e1010129. https://doi.org/10.1371/journal.pgen.1010129

Bao, K., Shan, C.-M., Chen, X., Raiymbek, G., Monroe, J. G., Fang, Y., Toda, T., Koutmou, K. S., Ragunathan, K., Lu, C., Berchowitz, L. E., & Jia, S. (2022). The cAMP signaling pathway regulates Epe1 protein levels and heterochromatin assembly. PLOS Genetics, 18(2), e1010049. https://doi.org/10.1371/journal.pgen.1010049

Flynn, E. D., Tsu, A. L., Kasela, S., Kim-Hellmuth, S., Aguet, F., Ardlie, K. G., Bussemaker, H. J., Mohammadi, P., & Lappalainen, T. (2022). Transcription factor regulation of eQTL activity across individuals and tissues. PLOS Genetics, 18(1), e1009719. https://doi.org/10.1371/journal.pgen.1009719