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1.
Cao, X.* et al.: Analysis of 3760 hematologic malignancies reveals rare transcriptomic aberrations of driver genes. Genome Med. 16:70 (2024)
2.
Curion, F. & Theis, F.J.: Machine learning integrative approaches to advance computational immunology. Genome Med. 16:80 (2024)
3.
Mueller, S.H.* et al.: Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry. Genome Med. 15:7 (2023)
4.
Dorling, L.* et al.: Breast cancer risks associated with missense variants in breast cancer susceptibility genes. Genome Med. 14:51 (2022)
5.
Hawe, J. et al.: Network reconstruction for trans acting genetic loci using multi-omics data and prior information. Genome Med. 14:125 (2022)
6.
Yépez, V.A.* et al.: Clinical implementation of RNA sequencing for Mendelian disease diagnostics. Genome Med. 14:38 (2022)
7.
Chakaroun, R.M.* et al.: Circulating bacterial signature is linked to metabolic disease and shifts with metabolic alleviation after bariatric surgery. Genome Med. 13:105 (2021)
8.
Yap, Z.Y.* et al.: Functional interpretation of ATAD3A variants in neuro-mitochondrial phenotypes. Genome Med. 13:55 (2021)
9.
Binyamin, D.* et al.: The aging mouse microbiome has obesogenic characteristics. Genome Med. 12:87 (2020)
10.
Di Maio, S.* et al.: Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals. Genome Med. 12:74 (2020)
11.
Gudmundsdottir, V.* et al.: Whole blood co-expression modules associate with metabolic traits and type 2 diabetes: An IMI-DIRECT study. Genome Med. 12:109 (2020)
12.
Keller, M. et al.: DNA methylation signature in blood mirrors successful weight-loss during lifestyle interventions: The CENTRAL trial. Genome Med. 12:97 (2020)
13.
de Oliveira, K.A.* et al.: A roadmap of constitutive NF-κB activity in Hodgkin lymphoma: Dominant roles of p50 and p52 revealed by genome-wide analyses. Genome Med. 8:28 (2016)
14.
Klopstock, T.* ; Klopstock, B.* & Prokisch, H.: Mitochondrial replacement approaches: Challenges for clinical implementation. Genome Med. 8:126 (2016)
15.
Kirschner, M.* et al.: Implementing systems medicine within healthcare. Genome Med. 7:102 (2015)
16.
Köferle, A.* ; Stricker, S.H. & Beck, S.*: Brave new epigenomes: The dawn of epigenetic engineering. Genome Med. 7:59 (2015)
17.
Köferle, A.* ; Stricker, S.H. & Beck, S.*: Erratum to: Brave new epigenomes: The dawn of epigenetic engineering. Genome Med. 7:75 (2015)
18.
Shin, S.-Y.* et al.: Interrogating causal pathways linking genetic variants, small molecule metabolites and circulating lipids. Genome Med. 6:25 (2014)
19.
Vogt, I. ; Prinz, J. & Campillos, M.: Molecularly and clinically related drugs and diseases are enriched in phenotypically similar drug-disease pairs. Genome Med. 6:52 (2014)
20.
Raffler, J. et al.: Identification and MS-assisted interpretation of genetically influenced NMR signals in human plasma. Genome Med. 5:13 (2013)
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