Moritz Gerstung

Latest

• Characterizing Genetic Intra-Tumor Heterogeneity across 2,658 Human Cancer Genomes
• Genomic Copy Number Predicts Esophageal Cancer Years before Transformation
• The Evolutionary History of 2,658 Cancers
• Genomic Landscape and Chronological Reconstruction of Driver Events in Multiple Myeloma
• Neutral Tumor Evolution?
• The Genomic Landscape of Structural Variations and Complex Events in Multiple Myeloma
• Classification and Personalized Prognosis in Myeloproliferative Neoplasms
• Analysis of Mutations and Structural Variants to Redefine the Genomic Landscape of Multiple Myeloma and Its Clinical Implications
• Abstract 3000: Pervasive Intra-Tumour Heterogeneity and Subclonal Selection across Cancer Types
• PO-329 Rejecting Neutral Tumour Evolution across Human Cancer Types
• 635 - Personalized Prognostic Predictions for Patients with Myeloproliferative Neoplasms through Integration of Comprehensive Genomic and Clinical Information
• The Genomic Landscape of Multiple Myeloma Complex Structural Variations
• Genomic Evolution of Breast Cancer Metastasis and Relapse
• Somatic Mutations Reveal Asymmetric Cellular Dynamics in the Early Human Embryo
• Analysis of Mutational Signatures Suggest That Aid Has an Early and Driver Role in Multiple Myeloma
• Landscape of Somatic Mutations in 560 Breast Cancer Whole-Genome Sequences
• Abstract B09: DNA Polymerase Mutations Trigger Rapid Onset of Ultra-Hypermutant Malignant Brain Tumors in Children with Biallelic Mismatch Repair Deficiency
• Subclonal Diversification of Primary Breast Cancer Revealed by Multiregion Sequencing
• High Burden and Pervasive Positive Selection of Somatic Mutations in Normal Human Skin
• Combined Hereditary and Somatic Mutations of Replication Error Repair Genes Result in Rapid Onset of Ultra-Hypermutated Cancers
• Extensive Transduction of Nonrepetitive DNA Mediated by L1 Retrotransposition in Cancer Genomes
• Genomic Heterogeneity in Primary Breast Cancer: Clinical Implications.
• Clinical and Biological Implications of Driver Mutations in Myelodysplastic Syndromes