Peter J Campbell

Latest

• The Architecture of Clonal Expansions in Morphologically Normal Tissue from Cancerous and Non-Cancerous Prostates
• Clonal Diversification and Histogenesis of Malignant Germ Cell Tumours
• Changes in Clonal Architecture Inform MPN Disease Course in Advance of Phenotypic Manifestations
• Multi-Site Clonality Analysis Uncovers Pervasive Heterogeneity across Melanoma Metastases
• Embryonal Precursors of Wilms Tumor
• Genomic Landscape and Chronological Reconstruction of Driver Events in Multiple Myeloma
• Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis
• 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
• Genomic Patterns of Progression in Smoldering Multiple Myeloma
• Timing the Landmark Events in the Evolution of Clear Cell Renal Cell Cancer: TRACERx Renal
• Pan-Cancer Analysis of Whole Genomes Reveals Driver Rearrangements Promoted by LINE-1 Retrotransposition in Human Tumours
• The Genomic Landscape of Multiple Myeloma Complex Structural Variations
• Pan-Cancer Analysis of Homozygous Deletions in Primary Tumours Uncovers Rare Tumour Suppressors
• Genomic Evolution of Breast Cancer Metastasis and Relapse
• Recurrent Mutation of IGF Signalling Genes and Distinct Patterns of Genomic Rearrangement in Osteosarcoma
• Somatic Mutations Reveal Asymmetric Cellular Dynamics in the Early Human Embryo
• ascatNgs: Identifying Somatically Acquired Copy-Number Alterations from Whole-Genome Sequencing Data
• 651 - Whole Genome Sequencing of Unique Paired Smm-Mgus Progressing to Mm Samples Reveals a Genomic Landscape with Diverse Evolutionary Pattern
• Analysis of Mutational Signatures Suggest That Aid Has an Early and Driver Role in Multiple Myeloma
• The Complex Landscape of Rearrangements in Smoldering and Symptomatic Multiple Myeloma Revealed By Whole-Genome Sequencing
• Mutational Signatures of Ionizing Radiation in Second Malignancies
• Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer
• 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
• Clock-like Mutational Processes in Human Somatic Cells
• DNMT3A Mutations Occur Early or Late in Patients with Myeloproliferative Neoplasms and Mutation Order Influences Phenotype
• Subclonal Diversification of Primary Breast Cancer Revealed by Multiregion Sequencing
• High Burden and Pervasive Positive Selection of Somatic Mutations in Normal Human Skin
• The Evolutionary History of Lethal Metastatic Prostate Cancer
• Analysis of the Genetic Phylogeny of Multifocal Prostate Cancer Identifies Multiple Independent Clonal Expansions in Neoplastic and Morphologically Normal Prostate Tissue
• Combined Hereditary and Somatic Mutations of Replication Error Repair Genes Result in Rapid Onset of Ultra-Hypermutated Cancers
• Diagnostic Value of H3F3A Mutations in Giant Cell Tumour of Bone Compared to Osteoclast-Rich Mimics
• Differential and Limited Expression of Mutant Alleles in Multiple Myeloma
• Spatial and Temporal Diversity in Genomic Instability Processes Defines Lung Cancer Evolution
• Intratumor Heterogeneity in Non-Small Cell Lung Cancer Inferred by Multi-Region Exome Sequencing
• Evolution of the Genomic Landscape in Non-Small Cell Lung Cancer
• Extensive Transduction of Nonrepetitive DNA Mediated by L1 Retrotransposition in Cancer Genomes
• Genome Sequencing of Normal Cells Reveals Developmental Lineages and Mutational Processes
• Myelodysplastic Syndromes Are Propagated by Rare and Distinct Human Cancer Stem Cells in Vivo
• Genomic Heterogeneity in Primary Breast Cancer: Clinical Implications.
• Association of a Germline Copy Number Polymorphism of APOBEC3A and APOBEC3B with Burden of Putative APOBEC-Dependent Mutations in Breast Cancer
• Recurrent PTPRB and PLCG1 Mutations in Angiosarcoma
• Transmissible Dog Cancer Genome Reveals the Origin and History of an Ancient Cell Lineage
• Heterogeneity of Genomic Evolution and Mutational Profiles in Multiple Myeloma
• RAG-Mediated Recombination Is the Predominant Driver of Oncogenic Rearrangement in ETV6-RUNX1 Acute Lymphoblastic Leukemia
• Somatic CALR Mutations in Myeloproliferative Neoplasms with Nonmutated JAK2
• The Genetic Heterogeneity and Mutational Burden of Engineered Melanomas in Zebrafish Models
• Clinical and Biological Implications of Driver Mutations in Myelodysplastic Syndromes
• 651 - Whole Exome Sequencing Of Multiple Myeloma Reveals An Heterogeneous Clonal Architecture and Genomic Evolution
• The Genomic Landscape of Myeloproliferative Neoplasms: Somatic Calr Mutations in the Majority of JAK2-Wildtype Patients
• Distinct H3F3A and H3F3B Driver Mutations Define Chondroblastoma and Giant Cell Tumor of Bone
• Signatures of Mutational Processes in Human Cancer
• Whole Exome Sequencing of Adenoid Cystic Carcinoma
• Frequent Mutation of the Major Cartilage Collagen Gene COL2A1 in Chondrosarcoma
• ETV6-RUNX1 ALL, INSIGHTS FROM INTEGRATIVE GENOMIC ANALYSIS
• Deciphering Signatures of Mutational Processes Operative in Human Cancer
• 604 Cancer Genomics, Epigenetics and Genomic Instability. Mutational Processes Shaping the Genomes of Twenty-One Breast Cancers
• Mutational Processes Molding the Genomes of 21 Breast Cancers
• The Life History of 21 Breast Cancers
• The Landscape of Cancer Genes and Mutational Processes in Breast Cancer
• Exploring the Subclonal Architecture of Breast Cancer
• Genome Sequencing and Analysis of the Tasmanian Devil and Its Transmissible Cancer
• Tandem Duplication of Chromosomal Segments Is Common in Ovarian and Breast Cancer Genomes