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21.
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)
22.
Rayner, N.W. ; Park, Y.-C. ; Fuchsberger, C.* ; Barysenska, A. & Zeggini, E.: Toward GDPR compliance with the Helmholtz Munich genotype imputation server. Nat. Genet., DOI: 10.1038/s41588-024-02012-1 (2024)
23.
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. 56, 1644–1653 (2024)
24.
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)
25.
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)
26.
An, U.* et al.: Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Nat. Genet. 55, 2269-2276 (2023)
27.
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)
28.
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)
29.
Rahmioglu, N.* et al.: The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Nat. Genet. 55, 423-436 (2023)
30.
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)
31.
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)
32.
Wagner, N.* et al.: Aberrant splicing prediction across human tissues. Nat. Genet. 55, 861-870 (2023)
33.
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)
34.
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)
35.
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)
36.
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)
37.
Bellenguez, C.* et al.: New insights into the genetic etiology of Alzheimer's disease and related dementias. Nat. Genet. 54, 412-436 (2022)
38.
Byun, J.* et al.: Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Nat. Genet. 54, 1167-1177 (2022)
39.
Hawe, J. et al.: Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function. Nat. Genet. 54, 18–29 (2022)
40.
Eumorphia Consortium (Hrabě de Angelis, M. ; Wurst, W. ; Abe, K. ; Beckers, J. ; Busch, D.H. ; Dalke, C. ; Gailus-Durner, V. ; Fuchs, H. ; Graw, J. ; Hölter, S.M. ; Kallnik, M. ; Lengger, C. ; Pedersen, V. ; Puk, O. ; Vogt Weisenhorn, D.M. ; Wagner, S.) & Quintanilla-Fend, L.: EMPReSS: Standardized phenotype screens for functional annotation of the mouse genome (vol 37, pg 1155, 2005). Nat. Genet. 54, 358-360 (2022)
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