Skip to Main Content

Author Details

Andrew J Mungall
1996
192
63
PMIDPaper TitleJournal TitlePublished Year
37918557SETD1A variant-associated psychosis: A systematic review of the clinical literature and description of two new cases.Prog Neuropsychopharmacol Biol Psychiatry2024
36982943Immune Activation following Irbesartan Treatment in a Colorectal Cancer Patient: A Case Study.Int J Mol Sci2023
36302166Molecular determinants of clinical outcomes in a real-world diffuse large B-cell lymphoma population.Blood2023
37875130Assembly and annotation of the black spruce genome provide insights on spruce phylogeny and evolution of stress response.G3 (Bethesda)2023
37961641Genomic structures and regulation patterns at HPV integration sites in cervical cancer.bioRxiv2023
37551834A high-throughput pipeline for DNA/RNA/small RNA purification from tissue samples for sequencing.Biotechniques2023
37084389Genetic subdivisions of follicular lymphoma defined by distinct coding and noncoding mutation patterns.Blood2023
37455852The genome sequence of the Loggerhead sea turtle, <i>Caretta caretta</i> Linnaeus 1758.F1000Res2023
36797466Defining the heterogeneity of unbalanced structural variation underlying breast cancer susceptibility by nanopore genome sequencing.Eur J Hum Genet2023
34907396Retraction Note: Tumor necrosis factor overcomes immune evasion in p53-mutant medulloblastoma.Nat Neurosci2022
35691590Whole-genome and transcriptome analysis enhances precision cancer treatment options.Ann Oncol2022
36209277Integrative analysis of KRAS wildtype metastatic pancreatic ductal adenocarcinoma reveals mutation and expression-based similarities to cholangiocarcinoma.Nat Commun2022
35789009Spruce giga-genomes: structurally similar yet distinctive with differentially expanding gene families and rapidly evolving genes.Plant J2022
34687784Optimization of magnetic bead-based nucleic acid extraction for SARS-CoV-2 testing using readily available reagents.J Virol Methods2022
35257510The impact of whole genome and transcriptome analysis (WGTA) on predictive biomarker discovery and diagnostic accuracy of advanced malignancies.J Pathol Clin Res2022
34644566Proteotranscriptomic classification and characterization of pancreatic neuroendocrine neoplasms.Cell Rep2021
33741928The transcriptional landscape of Shh medulloblastoma.Nat Commun2021
34163070Clonal fitness inferred from time-series modelling of single-cell cancer genomes.Nature2021
34149808A Scalable Strand-Specific Protocol Enabling Full-Length Total RNA Sequencing From Single Cells.Front Genet2021
33931648A clinical transcriptome approach to patient stratification and therapy selection in acute myeloid leukemia.Nat Commun2021
33372414Tumor infiltrating neutrophils and gland formation predict overall survival and molecular subgroups in pancreatic ductal adenocarcinoma.Cancer Med2021
33148671Uncovering Clinically Relevant Gene Fusions with Integrated Genomic and Transcriptomic Profiling of Metastatic Cancers.Clin Cancer Res2021
32817292Molecular attributes underlying central nervous system and systemic relapse in diffuse large B-cell lymphoma.Haematologica2021
33135777Whole-slide laser microdissection for tumour enrichment.J Pathol2021
33020056Genome and Transcriptome Biomarkers of Response to Immune Checkpoint Inhibitors in Advanced Solid Tumors.Clin Cancer Res2021
32958704Delving into Early-onset Pancreatic Ductal Adenocarcinoma: How Does Age Fit In?Clin Cancer Res2021
33120427The impact of MYC and BCL2 structural variants in tumors of DLBCL morphology and mechanisms of false-negative MYC IHC.Blood2021
33051307Subtype-Discordant Pancreatic Ductal Adenocarcinoma Tumors Show Intermediate Clinical and Molecular Characteristics.Clin Cancer Res2021
34700376Modulation of the Host Cell Transcriptome and Epigenome by Fusobacterium nucleatum.mBio2021
31481506Altered Gene Expression along the Glycolysis-Cholesterol Synthesis Axis Is Associated with Outcome in Pancreatic Cancer.Clin Cancer Res2020
32424282Tumor necrosis factor overcomes immune evasion in p53-mutant medulloblastoma.Nat Neurosci2020
31837431Sample Tracking Using Unique Sequence Controls.J Mol Diagn2020
32160292Coding and noncoding drivers of mantle cell lymphoma identified through exome and genome sequencing.Blood2020
32094924TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma.Nat Med2020
32972944Complete Chloroplast Genome Sequence of a Black Spruce (Picea mariana) from Eastern Canada.Microbiol Resour Announc2020
32747824Analysis of Ugandan cervical carcinomas identifies human papillomavirus clade-specific epigenome and transcriptome landscapes.Nat Genet2020
32518206Endogenous Retrovirus Transcript Levels Are Associated with Immunogenic Signatures in Multiple Metastatic Cancer Types.Mol Cancer Ther2020
32577165Tumor microRNA profile and prognostic value for lymph node metastasis in oral squamous cell carcinoma patients.Oncotarget2020
32624572Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing.Genet Med2020
32677466Epigenomic programming in early fetal brain development.Epigenomics2020
33335541A Distributed Whole Genome Sequencing Benchmark Study.Front Genet2020
35121966Pan-cancer analysis of advanced patient tumors reveals interactions between therapy and genomic landscapes.Nat Cancer2020
31196920Complete Chloroplast Genome Sequence of an Engelmann Spruce (<i>Picea engelmannii</i>, Genotype Se404-851) from Western Canada.Microbiol Resour Announc2019
31623682Dissociation of solid tumor tissues with cold active protease for single-cell RNA-seq minimizes conserved collagenase-associated stress responses.Genome Biol2019
31671154Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA.PLoS One2019
31708418Identification and Analyses of Extra-Cranial and Cranial Rhabdoid Tumor Molecular Subgroups Reveal Tumors with Cytotoxic T Cell Infiltration.Cell Rep2019
35100702Therapeutic Implication of Genomic Landscape of Adult Metastatic Sarcoma.JCO Precis Oncol2019
30514790Clinical outcomes after whole-genome sequencing in patients with metastatic non-small-cell lung cancer.Cold Spring Harb Mol Case Stud2019
30016509MAVIS: merging, annotation, validation, and illustration of structural variants.Bioinformatics2019
30418619Sources of erroneous sequences and artifact chimeric reads in next generation sequencing of genomic DNA from formalin-fixed paraffin-embedded samples.Nucleic Acids Res2019
  • 1 - 50 of 192

Recommended Authors

Collaborators

University of British Columbia
Co-authored papers 129
Co-authored papers 110
University of British Columbia
Co-authored papers 103
Co-authored papers 57
Canada British Columbia Cancer Research Centre, University of British Columbia
Co-authored papers 47
Co-authored papers 33
Simon Fraser University
Co-authored papers 26
Co-authored papers 24
Canada British Columbia Cancer Research Centre, University of British Columbia
Co-authored papers 22
European Bioinformatics Institute (EMBL-EBI)
Co-authored papers 22
University of British Columbia
Co-authored papers 22
University of British Columbia
Co-authored papers 21
BC Cancer Research Centre.
Co-authored papers 20
BC Cancer Research Institute
Co-authored papers 19
Co-authored papers 18
The Hospital for Sick Children
Co-authored papers 17
Co-authored papers 16
Memorial Sloan Kettering Cancer Center
Co-authored papers 14
Cumming School of Medicine, University of Calgary
Co-authored papers 13
Co-authored papers 13
University of British Columbia
Co-authored papers 13
National Cancer Institute
Co-authored papers 12
University of British Columbia
Co-authored papers 12
University of British Columbia
Co-authored papers 11
Ontario Institute for Cancer Research
Co-authored papers 11
University of British Columbia
Co-authored papers 11
Co-authored papers 10
Co-authored papers 10
UCL Cancer Institute, University College London
Co-authored papers 10
Co-authored papers 10