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1.
Garg, V.* et al.: Unlocking plant genetics with telomere-to-telomere genome assemblies. Nat. Genet., DOI: 10.1038/s41588-024-01830-7 (2024)
2.
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)
3.
Kentistou, K.A.* et al.: Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat. Genet., DOI: 10.1038/s41588-024-01857-w (2024)
4.
Kentistou, K.A.* et al.: Understanding the genetic complexity of puberty timing across the allele frequency spectrum. Nat. Genet. 56, 1397–1411 (2024)
5.
Meng, X.* et al.: Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nat. Genet. 56, 222-233 (2024)
6.
Schmidt, A.* et al.: 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/s41588-024-01836-1 (2024)
7.
Schormair, B. et al.: Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction. Nat. Genet. 56, 1090-1099 (2024)
8.
Shrine, N.* et al.: Author Correction: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Nat. Genet. 56, 1032-1033 (2024)
9.
An, U.* et al.: Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Nat. Genet. 55, 2269-2276 (2023)
10.
Dahl, A.* et al.: Phenotype integration improves power and preserves specificity in biobank-based genetic studies of major depressive disorder. Nat. Genet. 55, 2082-2093 (2023)
11.
Lagou, V.* et al.: GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Nat. Genet. 55, 1448-1461 (2023)
12.
Rahmioglu, N.* et al.: The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nat. Genet. 55, 423-436 (2023)
13.
Shrine, N.* et al.: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Nat. Genet. 55, 410-422 (2023)
14.
Shrine, N.* et al.: Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk (Nature Genetics, (2023), 55, 3, (410-422), 10.1038/s41588-023-01314-0). Nat. Genet. 55, 1778-1779 (2023)
15.
Wagner, N.* et al.: Aberrant splicing prediction across human tissues. Nat. Genet. 55, 861-870 (2023)
16.
Williamson, A.* et al.: Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Nat. Genet. 55, 973-983 (2023)
17.
Aragam, K.G.* et al.: Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Nat. Genet. 54, 1803-1815 (2022)
18.
Barc, J.* et al.: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat. Genet. 54, 232-239 (2022)
19.
Barc, J.* et al.: Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nat. Genet. 54:735 (2022)
20.
Bellenguez, C.* et al.: New insights into the genetic etiology of Alzheimer's disease and related dementias. Nat. Genet. 54, 412-436 (2022)
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