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21.
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)
22.
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)
23.
Wagner, N.* et al.: Aberrant splicing prediction across human tissues. Nat. Genet. 55, 861-870 (2023)
24.
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)
25.
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)
26.
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)
27.
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)
28.
Bellenguez, C.* et al.: New insights into the genetic etiology of Alzheimer's disease and related dementias. Nat. Genet. 54, 412-436 (2022)
29.
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)
30.
Hawe, J. et al.: Genetic variation influencing DNA methylation provides insights into molecular mechanisms regulating genomic function. Nat. Genet. 54, 18–29 (2022)
31.
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)
32.
Hsieh, T.C.* et al.: GestaltMatcher facilitates rare disease matching using facial phenotype descriptors. Nat. Genet. 54, 349-357 (2022)
33.
Hu, B.* et al.: Origin and function of activated fibroblast states during zebrafish heart regeneration. Nat. Genet. 54, 1227-1237 (2022)
34.
Mahajan, A.* et al.: Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Nat. Genet. 54, 560-572 (2022)
35.
Nakatani, T. et al.: DNA replication fork speed underlies cell fate changes and promotes reprogramming. Nat. Genet. 54, 318–327 (2022)
36.
Okbay, A.* et al.: Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Nat. Genet. 54, 437-449 (2022)
37.
Schork, A.J.* ; Peterson, R.E.* ; Dahl, A.* ; Cai, N. & Kendler, K.S.*: Indirect paths from genetics to education. Nat. Genet. 54, 372-373 (2022)
38.
Schork, A.J.* ; Peterson, R.E.* ; Dahl, A.* ; Cai, N. & Kendler, K.S.*: Author Correction: Indirect paths from genetics to education (Nature Genetics, (2022), 54, 4, (372-373), 10.1038/s41588-021-00999-5). Nat. Genet., DOI: 10.1038/s41588-022-01092-1 (2022)
39.
Wang, Z.* et al.: Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Nat. Genet. 54, 1332–1344 (2022)
40.
Birling, M.C.* et al.: A resource of targeted mutant mouse lines for 5,061 genes. Nat. Genet. 53, 416-419 (2021)
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