BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Menzel M, Ossowski S, Kral S, et al. (2023) Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients. Npj Precision Oncology. 7: 106 |
Weisschuh N, Mazzola P, Zuleger T, et al. (2023) Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases. Journal of Medical Genetics |
Demidov G, Park J, Armeanu-Ebinger S, et al. (2021) Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data. Molecular Genetics & Genomic Medicine. e1807 |
Susak H, Serra-Saurina L, Demidov G, et al. (2021) Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation. Plos Computational Biology. 17: e1007784 |
Hilke FJ, Sinnberg T, Gschwind A, et al. (2020) Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients. Cancers. 12 |
Muyas F, Zapata L, Guigó R, et al. (2020) The rate and spectrum of mosaic mutations during embryogenesis revealed by RNA sequencing of 49 tissues. Genome Medicine. 12: 49 |
Oberhettinger P, Schüle L, Marschal M, et al. (2020) Description of sp. nov., isolated from human rectal swabs and stool samples. International Journal of Systematic and Evolutionary Microbiology |
Pogoda M, Hilke FJ, Lohmann E, et al. (2019) Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in Dystonia. Frontiers in Neurology. 10: 1332 |
Arcas-García A, Garcia-Prat M, Magallón-Lorenz M, et al. (2019) The IL2RG R328X nonsense mutation allows partial STAT5 phosphorylation and defines a critical region involved in leaky-SCID phenotype. Clinical and Experimental Immunology |
Zwirner K, Hilke FJ, Demidov G, et al. (2019) Radiogenomics in head and neck cancer: correlation of radiomic heterogeneity and somatic mutations in TP53, FAT1 and KMT2D. Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al] |