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Frontiers in Genetics|June 29, 2026
Correction: Clinical variant interpretation comparing two saturation genome editing-based functional studies for BRCA2Ju Hyeon Shin, Kyung Sun Park, Young-Gon Kim, et al.Frontiers in Genetics|April 30, 2019
Network Medicine in the Age of Biomedical Big DataAbhijeet R Sonawane, Scott T Weiss, Kimberly Glass, et al.Frontiers in Genetics|December 28, 2020
Rapid Transmission of a Hyper-Virulent Meningococcal Clone Due to High Effective Contact Numbers and Super SpreadersJonathan C Holmes, Luke R Green, Neil J Oldfield, et al.Frontiers in Genetics|December 11, 2023
Unlocking the potential of RNA-based therapeutics in the lung: current status and future directionsH S Jeffrey Man, Vaneeza A Moosa, Anand Singh, et al.Frontiers in Genetics|May 30, 2023
Ethical and legal challenges in nanomedical innovations: a scoping reviewSophia Wasti, Il Ho Lee, Sumin Kim, et al.Frontiers in Genetics|June 30, 2022
You Can't Have AI Both Ways: Balancing Health Data Privacy and Access FairlyMarieke Bak, Vince Istvan Madai, Marie-Christine Fritzsche, et al.Frontiers in Genetics|July 13, 2026
WTAP-mediated m6A methylation of SOX2 affects lung adenocarcinoma malignancy via Wnt/β-catenin pathwayNa Li, Xiangbo Zeng, Hong Xie, et al.Frontiers in Genetics|July 13, 2026
Epigenetic silencing of PHYHD1 in hepatocellular carcinoma revealed by integrated multi-omics analysisTianfu Guo, Yafei Li, Tiansheng He, et al.Frontiers in Genetics|July 14, 2026
Correction: The impact of X chromosome inactivation on human healthJunyi Gu, Qian ChenFrontiers in Genetics|July 10, 2026
Correction: Editorial: Unraveling GI cancer heterogeneity through single-cell multi-omics approachesRick J Jansen, Roberta Bardini, Elena GrassiPageof 1,604