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Sharip, A., Rakhimova, S., Molkenov, A., Ashenova, A., Kozhamkulov, U., Akhmetollayev, I., Zinovyev, A., Zhukov, Y., Omarov, M., Tuleutaev, M., Rakhmetova, V., Terwilliger, J. D., Lee, J. H., Zhumadilov, Z., Akilzhanova, A., & Kairov, U. (2024). Transcriptome profiling and analysis of patients with esophageal squamous cell carcinoma from Kazakhstan. Frontiers in Genetics, 15. https://doi.org/10.3389/fgene.2024.1249751

DeWan, A. T., Cahill, M. E., Cornejo-Sanchez, D. M., Li, Y., Dong, Z., Fabiha, T., Sun, H., Wang, G., & Leal, S. M. (2023). Variants in JAZF1 are associated with asthma, type 2 diabetes, and height in the United Kingdom biobank population. Frontiers in Genetics, 14. https://doi.org/10.3389/fgene.2023.1129389

Awah, C. U., Glemaud, Y., Levine, F., Yang, K., Ansary, A., Dong, F., Ash, L., Zhang, J., & Ogunwobi, O. O. (2023). Destabilized 3’UTR elements therapeutically degrade ERBB2 mRNA in drug-resistant ERBB2+ cancer models. Frontiers in Genetics, 14. https://doi.org/10.3389/fgene.2023.1184600

Becerra, C. Y., Wells, R. K., Kunihiro, B. P., Lee, R. H., Umeda, L., Allan, N. P., Rubas, N. C., McCracken, T. A., Nunokawa, C. K. L., Lee, M.-H., Pidlaoan, F. G. S., Phankitnirondorn, K., Dye, C. K., Yamamoto, B. Y., Peres, R., Juarez, R., & Maunakea, A. K. (2023). Examining the immunoepigenetic-gut microbiome axis in the context of self-esteem among Native Hawaiians and other Pacific Islanders. Frontiers in Genetics, 14. https://doi.org/10.3389/fgene.2023.1125217

Cossu, G., Tonlorenzi, R., Brunelli, S., Sampaolesi, M., Messina, G., Azzoni, E., Benedetti, S., Biressi, S., Bonfanti, C., Bragg, L., Camps, J., Cappellari, O., Cassano, M., Ciceri, F., Coletta, M., Covarello, D., Crippa, S., Cusella-De Angelis, M. G., De Angelis, L., … Ugarte, G. (2023). Mesoangioblasts at 20: From the embryonic aorta to the patient bed. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.1056114

Chen, Z., Zhang, B., Gong, F., Wan, L., & Ma, L. (2023). RobustTree: An adaptive, robust PCA algorithm for embedded tree structure recovery from single-cell sequencing data. Frontiers in Genetics, 14. https://doi.org/10.3389/fgene.2023.1110899

Naderi, E., Cornejo-Sanchez, D. M., Li, G., Schrauwen, I., Wang, G. T., Dewan, A. T., & Leal, S. M. (2023). The genetic contribution of the X chromosome in age-related hearing loss. Frontiers in Genetics, 14. https://doi.org/10.3389/fgene.2023.1106328

Greising, S. M., Weiner, J. I., Garry, D. J., Sachs, D. H., & Garry, M. G. (2022). Human muscle in gene edited pigs for treatment of volumetric muscle loss. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.948496

Ahn, J., Lee, J., Kim, D.-H., Hwang, I.-S., Park, M.-R., Cho, I.-C., Hwang, S., & Lee, K. (2022). Loss of Monoallelic Expression of IGF2 in the Adult Liver Via Alternative Promoter Usage and Chromatin Reorganization. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.920641

Dharmadhikari, A. V., Pereira, E. M., Andrews, C. C. ., Macera, M., Harkavy, N., Wapner, R., Jobanputra, V., Levy, B., Ganapathi, M., & Liao, J. (2022). Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.906077

Kairov, U., Molkenov, A., Sharip, A., Rakhimova, S., Seidualy, M., Rhie, A., Kozhamkulov, U., Zhabagin, M., Kim, J.-I., Lee, J. H., Terwilliger, J. D., Seo, J.-S., Zhumadilov, Z., & Akilzhanova, A. (2022). Whole-Genome Sequencing and Genomic Variant Analysis of Kazakh Individuals. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.902804

Deyssenroth, M. A., Peng, S., Hao, K., Marsit, C. J., & Chen, J. (2022). Placental Gene Transcript Proportions are Altered in the Presence of In Utero Arsenic and Cadmium Exposures, Genetic Variants, and Birth Weight Differences. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.865449

Guo, J., Riley, K. W., Durham, T., Margolis, A. E., Wang, S., Perera, F., & Herbstman, J. B. (2022). Association Studies of Environmental Exposures, DNA Methylation and Children’s Cognitive, Behavioral, and Mental Health Problems. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.871820

Aguiar, T., Teixeira, A., Scliar, M. O., Sobral de Barros, J., Lemes, R. B., Souza, S., Tolezano, G., Santos, F., Tojal, I., Cypriano, M., Caminada de Toledo, S. R., Valadares, E., Borges Pinto, R., Pinto Artigalas, O. A., Caetano de Aguirre Neto, J., Novak, E., Cristofani, L. M., Miura Sugayama, S. M., Odone, V., … Krepischi, A. (2022). Unraveling the Genetic Architecture of Hepatoblastoma Risk: Birth Defects and Increased Burden of Germline Damaging Variants in Gastrointestinal/Renal Cancer Predisposition and DNA Repair Genes. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.858396

Li, Z., Wang, D., Liao, H., Zhang, S., Guo, W., Chen, L., Lu, L., Huang, T., & Cai, Y.-D. (2022). Exploring the Genomic Patterns in Human and Mouse Cerebellums Via Single-Cell Sequencing and Machine Learning Method. Frontiers in Genetics, 13. https://doi.org/10.3389/fgene.2022.857851