Nature Genetics, Published online: 27 October 2025; doi:10.1038/s41588-025-02416-7
Author Correction: Prioritizing effector genes at trait-associated loci using multimodal evidence]]>Nature Genetics, Published online: 27 October 2025; doi:10.1038/s41588-025-02254-7
The transcription factors responsible for initiating embryonic genome activation (EGA) in humans remain largely unknown. A study now characterizes the role of the maternal factor OTX2 in kickstarting human EGA.]]>Nature Genetics, Published online: 27 October 2025; doi:10.1038/s41588-025-02331-x
Gene implication methods (GIMs) are crucial tools for analyzing genome-wide association studies, but are often ambiguous. We present the LocusCompare2 platform to incorporate six popular GIMs and hundreds of quantitative trait loci datasets, enabling validation across several GIMs and window settings to improve accuracy and reproducibility.]]>Nature Genetics, Published online: 27 October 2025; doi:10.1038/s41588-025-02378-w
This study presents 25 new maize genome assemblies and integrates them with 31 publicly available maize genomes to conduct a pangenome analysis that provides genetic insights into drought resistance.]]>Nature Genetics, Published online: 27 October 2025; doi:10.1038/s41588-025-02345-5
Integrated clinical and single-cell analysis of primary pancreatic tumor samples that later recur in the liver or lung shows that tumor cells at the primary site transcriptionally resemble the normal parenchymal epithelia of the liver or lung, respectively.]]>Nature Genetics, Published online: 27 October 2025; doi:10.1038/s41588-025-02350-8
OTX2 binds to and activates genes involved in embryonic genome activation, including TPRX1 and TPRX2. OTX2 knockdown impairs embryonic genome activation and early development, which can be partially rescued by overexpression of TPRX1 and TPRX2.]]>Nature Genetics, Published online: 22 October 2025; doi:10.1038/s41588-025-02394-w
Author Correction: An aberrant SREBP-dependent lipogenic program promotes metastatic prostate cancer]]>Nature Genetics, Published online: 22 October 2025; doi:10.1038/s41588-025-02361-5
Pathogenic variants in UNC13A underlie a novel neurodevelopmental syndrome, with three subtypes defined by distinct genotypes with varying clinical and functional impacts characterized in cellular and animal models.]]>