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41.
Hsieh, T.C.* et al.: GestaltMatcher facilitates rare disease matching using facial phenotype descriptors. Nat. Genet. 54, 349-357 (2022)
42.
Hu, B.* et al.: Origin and function of activated fibroblast states during zebrafish heart regeneration. Nat. Genet. 54, 1227-1237 (2022)
43.
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)
44.
Nakatani, T. et al.: DNA replication fork speed underlies cell fate changes and promotes reprogramming. Nat. Genet. 54, 318–327 (2022)
45.
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)
46.
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)
47.
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)
48.
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)
49.
Birling, M.C.* et al.: A resource of targeted mutant mouse lines for 5,061 genes. Nat. Genet. 53, 416-419 (2021)
50.
Bonder, M.J.* et al.: Identification of rare and common regulatory variants in pluripotent cells using population-scale transcriptomics. Nat. Genet. 53, 313-321 (2021)
51.
Chen, J.* et al.: The trans-ancestral genomic architecture of glycemic traits. Nat. Genet. 53, 840-860 (2021)
52.
Cousin, M.A.* et al.: Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome. Nat. Genet. 53, 1006-1021 (2021)
53.
Lotta, L.A.* et al.: A cross-platform approach identifies genetic regulators of human metabolism and health. Nat. Genet. 53, 54-64 (2021)
54.
Rabanus-Wallace, M.T.* et al.: Chromosome-scale genome assembly provides insights into rye biology, evolution and agronomic potential. Nat. Genet. 53, 564-573 (2021)
55.
Rühlemann, M.C.* et al.: Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. Nat. Genet. 53, 147–155 (2021)
56.
Surendran, P.* et al.: Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals (Nature Genetics, (2020), 52, 12, (1314-1332), 10.1038/s41588-020-00713-x). Nat. Genet., DOI: 10.1038/s41588-021-00832-z (2021)
57.
Tadros, R.* et al.: Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Nat. Genet. 53, 128-134 (2021)
58.
Võsa, U.* et al.: Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nat. Genet. 53, 1300-1310 (2021)
59.
Bryois, J.* et al.: Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease. Nat. Genet. 52, 482-493 (2020)
60.
Cai, N. et al.: Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Nat. Genet. 52, 437-447 (2020)
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