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1.
Birk, S. et al.: Quantitative characterization of cell niches in spatially resolved omics data. Nat. Genet. 57, 897–909 (2025)
2.
Fatumo, S.* et al.: KidneyGenAfrica, a pan-African partnership to deliver research and training excellence in genomics of kidney disease. Nat. Genet. 57, 2079–2082 (2025)
3.
Guo, W.* et al.: A barley pan-transcriptome reveals layers of genotype-dependent transcriptional complexity. Nat. Genet. 57, 441-450 (2025)
4.
Lammi, V.* et al.: Genome-wide association study of long COVID. Nat. Genet., DOI: 10.1038/s41588-025-02100-w (2025)
5.
Lazarescu, O.* et al.: Human subcutaneous and visceral adipocyte atlases uncover classical and nonclassical adipocytes and depot-specific patterns. Nat. Genet. 57, 413-426 (2025)
6.
Nava, C.* et al.: Dominant variants in major spliceosome U4 and U5 small nuclear RNA genes cause neurodevelopmental disorders through splicing disruption. Nat. Genet., DOI: 10.1038/s41588-025-02184-4 (2025)
7.
Roselli, C.* et al.: Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases. Nat. Genet. 57, 539-547 (2025)
8.
Schmidt, A.* et al.: Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings. Nat. Genet., DOI: 10.1038/s41588-025-02271-6 (2025)
9.
Tejada Lapuerta, A. et al.: Causal machine learning for single-cell genomics. Nat. Genet. 57, 797–808 (2025)
10.
Tomaz da Silva, P.* et al.: Nucleotide dependency analysis of genomic language models detects functional elements. Nat. Genet. 57, 2589-2602 (2025)
11.
van der Laan, C.M.* et al.: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes. Nat. Genet. 57, 2427-2435 (2025)
12.
van der Laan, C.M.* et al.: Publisher Correction: Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes. Nat. Genet. 57:2604 (2025)
13.
Xu, Q.* et al.: An integrated transcriptomic cell atlas of human endoderm-derived organoids. Nat. Genet. 57, 1201–1212 (2025)
14.
Yépez, V.A.* et al.: The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease. Nat. Genet. 57, 2361-2370 (2025)
15.
Clarke, B.* et al.: Integration of variant annotations using deep set networks boosts rare variant association testing. Nat. Genet., DOI: 10.1038/s41588-024-01919-z (2024)
16.
García-Marín, L.M.* et al.: Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries. Nat. Genet. 56, 2333–2344 (2024)
17.
Garg, V.* et al.: Unlocking plant genetics with telomere-to-telomere genome assemblies. Nat. Genet., 1788–1799 (2024)
18.
Keaton, J.M.* et al.: Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits. Nat. Genet. 56, 778-791 (2024)
19.
Kentistou, K.A.* et al.: Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat. Genet. 56, 1763-1764 (2024)
20.
Kentistou, K.A.* et al.: Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat. Genet. 56, 1397–1411 (2024)
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