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Lista de obras de Andrew Mungall

A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.

artículo científico publicado en 2017

A Gene Map of the Human Genome

artículo científico publicado en 1996

A Hematogenous Route for Medulloblastoma Leptomeningeal Metastases

artículo científico publicado en 2018

A Hematogenous Route for Medulloblastoma Leptomeningeal Metastases.

artículo científico publicado en 2018

A clinically validated diagnostic second-generation sequencing assay for detection of hereditary BRCA1 and BRCA2 mutations.

artículo científico publicado en 2013

A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation

artículo científico publicado en 2008

A somatic reference standard for cancer genome sequencing

artículo científico publicado en 2016

A transgenic mouse model demonstrating the oncogenic role of mutations in the polycomb-group gene EZH2 in lymphomagenesis

article

Altered Gene Expression along the Glycolysis-Cholesterol Synthesis Axis Is Associated with Outcome in Pancreatic Cancer

artículo científico publicado en 2019

Alternative splicing, genomic structure, and fine chromosome localization of REV3L.

artículo científico publicado en 1998

An exon splice enhancer primes IGF2:IGF2R binding site structure and function evolution

artículo científico publicado en 2012

An imprinted locus associated with transient neonatal diabetes mellitus

article

An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobin

artículo científico publicado en 2000

An opportune moment to sequence an opportunistic pathogen

artículo científico publicado en 2000

Analysis of FOXO1 mutations in diffuse large B-cell lymphoma

artículo científico publicado en 2013

Analysis of Normal Human Mammary Epigenomes Reveals Cell-Specific Active Enhancer States and Associated Transcription Factor Networks

artículo científico publicado en 2016

Analysis of Ugandan cervical carcinomas identifies human papillomavirus clade-specific epigenome and transcriptome landscapes

artículo científico publicado en 2020

Application of a Neural Network Whole Transcriptome-Based Pan-Cancer Method for Diagnosis of Primary and Metastatic Cancers

artículo científico publicado en 2019

Application of genomics to identify therapeutic targets in recurrent pediatric papillary thyroid carcinoma.

artículo científico publicado en 2018

Array for cancer prognostics

artículo científico publicado en 2002

Assembling the 20 Gb white spruce (Picea glauca) genome from whole-genome shotgun sequencing data

artículo científico publicado en 2013

Assessment of Capture and Amplicon-Based Approaches for the Development of a Targeted Next-Generation Sequencing Pipeline to Personalize Lymphoma Management.

artículo científico publicado en 2018

Automated high throughput nucleic acid purification from formalin-fixed paraffin-embedded tissue samples for next generation sequence analysis. ⬇️

artículo científico publicado en 2017

Barnacle: detecting and characterizing tandem duplications and fusions in transcriptome assemblies

artículo científico publicado en 2013

Base excision repair deficiency signatures implicate germline and somatic MUTYH aberrations in pancreatic ductal adenocarcinoma and breast cancer oncogenesis

artículo científico publicado en 2019

Before and After: Comparison of Legacy and Harmonized TCGA Genomic Data Commons' Data

artículo científico publicado en 2019

BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data

artículo científico publicado en 2012

CSF3R mutations have a high degree of overlap with CEBPA mutations in pediatric AML

artículo científico publicado en 2016

Characterization of 6q deletions in mature B cell lymphomas and childhood acute lymphoblastic leukemia

artículo científico publicado en 2008

Characterization of clustered MHC-linked olfactory receptor genes in human and mouse

artículo científico publicado en 2001

Characterization of the human thyroid epigenome.

artículo científico

Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing

artículo científico publicado en 2019

Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors

artículo científico

Cloning and characterization of two overlapping genes in a subregion at 6q21 involved in replicative senescence and schizophrenia

artículo científico publicado en 2000

Comparison of human genetic and sequence-based physical maps

scientific article published in Nature

Complete Chloroplast Genome Sequence of a White Spruce (Picea glauca, Genotype WS77111) from Eastern Canada

artículo científico publicado en 2019

Complete Chloroplast Genome Sequence of an Engelmann Spruce (Picea engelmannii, Genotype Se404-851) from Western Canada

artículo científico publicado en 2019

Complete MHC haplotype sequencing for common disease gene mapping

artículo científico publicado en 2004

Complete genomic landscape of a recurring sporadic parathyroid carcinoma ⬇️

artículo científico publicado el 1 de julio de 2013

Comprehensive Analysis of Alternative Splicing Across Tumors from 8,705 Patients

artículo científico

Comprehensive Characterization of Cancer Driver Genes and Mutations

article

Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma

artículo científico publicado en 2015

Comprehensive Pan-Genomic Characterization of Adrenocortical Carcinoma

article

Comprehensive characterization of pediatric AML reveals diverse fusion oncoproteins and age-specific mutational interactions

Comprehensive characterization of programmed death ligand structural rearrangements in B-cell non-Hodgkin lymphomas.

artículo científico publicado en 2016

Comprehensive miRNA sequence analysis reveals survival differences in diffuse large B-cell lymphoma patients

artículo científico publicado en 2015

Concurrent CIC mutations, IDH mutations, and 1p/19q loss distinguish oligodendrogliomas from other cancers

artículo científico publicado en 2011

Conservation of the H19 noncoding RNA and H19-IGF2 imprinting mechanism in therians

artículo científico publicado en 2008

Correction: miR-509-3p is clinically significant and strongly attenuates cellular migration and multi-cellular spheroids in ovarian cancer

artículo científico publicado en 2017

Corrigendum: Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline :c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcinoma

scholarly article published in Cold Spring Harbor molecular case studies

Cyclin D3 is a target gene of t(6;14)(p21.1;q32.3) of mature B-cell malignancies

article

DNA hypomethylation within specific transposable element families associates with tissue-specific enhancer landscape

artículo científico publicado en 2013

Delving into Early Onset Pancreatic Ductal Adenocarcinoma: How Does Age Fit In?

scientific article published on 21 September 2020

Divergent clonal selection dominates medulloblastoma at recurrence

artículo científico publicado en 2016

Divergent modes of clonal spread and intraperitoneal mixing in high-grade serous ovarian cancer

artículo científico publicado en 2016

Dynamics of genomic clones in breast cancer patient xenografts at single-cell resolution.

artículo científico publicado en 2014

Endogenous retrovirus transcript levels are associated with immunogenic signatures in multiple metastatic cancer types

artículo científico publicado en 2020

Epigenetic and transcriptional determinants of the human breast

artículo científico publicado en 2015

Erratum: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions

scholarly article published in Nature Medicine

Fate mapping of human glioblastoma reveals an invariant stem cell hierarchy.

artículo científico publicado en 2017

Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

artículo científico publicado en 2011

From long range mapping to sequence-ready contigs on human chromosome 6

article

Genome and transcriptome biomarkers of response to immune checkpoint inhibitors in advanced solid tumours

artículo científico publicado en 2020

Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma

artículo científico publicado en 2019

Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma

Genome-wide discovery of somatic regulatory variants in diffuse large B-cell lymphoma

artículo científico publicado en 2018

Genomic analyses identify recurrent MEF2D fusions in acute lymphoblastic leukaemia

artículo científico publicado en 2016

Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia

artículo científico publicado en 2013

Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes

artículo científico publicado en 2017

High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes

article

High-resolution architecture and partner genes of rearrangements in lymphoma with DLBCL morphology

artículo científico

Histological Transformation and Progression in Follicular Lymphoma: A Clonal Evolution Study

artículo científico publicado en 2016

Homologous Recombination Deficiency and Platinum-Based Therapy Outcomes in Advanced Breast Cancer

artículo científico publicado en 2017

Identification and Analyses of Extra-Cranial and Cranial Rhabdoid Tumor Molecular Subgroups Reveal Tumors with Cytotoxic T Cell Infiltration

scientific article published on 07 November 2019

Identification of candidate tumor-suppressor genes in 6q27 by combined deletion mapping and electronic expression profiling in lymphoid neoplasms

artículo científico publicado en 2003

Immunogenicity of recurrent mutations in MYD88 and EZH2 in non-Hodgkin lymphomas.

artículo científico publicado en 2015

Increasing quality, throughput and speed of sample preparation for strand-specific messenger RNA sequencing

artículo científico publicado en 2017

Initial sequencing and analysis of the human genome

artículo científico publicado en 2001

Integrated Molecular Characterization of Testicular Germ Cell Tumors

article by Hui Shen et al published 12 June 2018 in Cell Reports

Integrative genomic analysis identifies key pathogenic mechanisms in primary mediastinal large B-cell lymphoma

artículo científico publicado en 2019

Integrative genomic analysis of ghost cell odontogenic carcinoma

artículo científico publicado en 2015

Intratumoral Genetic and Functional Heterogeneity in Pediatric Glioblastoma

artículo científico publicado en 2019

It's okay to be green: Draft genome of the North American bullfrog (Rana [Lithobates] catesbeiana)

Large-scale profiling of microRNAs for The Cancer Genome Atlas.

artículo científico publicado en 2015

Lessons learned from the application of whole-genome analysis to the treatment of patients with advanced cancers

artículo científico publicado en 2015

Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6q.

artículo científico publicado en 1999

MAVIS: merging, annotation, validation, and illustration of structural variants

scholarly article by Caralyn Reisle published in July 2018

MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours.

artículo científico publicado en 2015

Mapping the human T cell repertoire to recurrent driver mutations in MYD88 and EZH2 in lymphoma

artículo científico publicado en 2017

Meeting review: Epigenetics in Development and Disease

artículo científico publicado en 2002

MicroRNA Expression-Based Model Indicates Event-Free Survival in Pediatric Acute Myeloid Leukemia

artículo científico publicado en 2017

Molecular characterisation of metastatic pancreatic neuroendocrine tumours (PNETs) using whole genome and transcriptome sequencing.

artículo científico publicado en 2017

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss

artículo científico publicado en 2005

Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma

artículo científico publicado en 2013

Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing

artículo científico publicado en 2013

Mutations in EZH2 cause Weaver syndrome

artículo científico publicado en 2011

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

artículo científico publicado en 1998

NRG1 Gene Fusions Are Recurrent, Clinically Actionable Gene Rearrangements in KRAS Wild-Type Pancreatic Ductal Adenocarcinoma

scientific article published on 08 May 2019

National Cancer Institute Biospecimen Evidence-Based Practices: Harmonizing Procedures for Nucleic Acid Extraction from Formalin-Fixed, Paraffin-Embedded Tissue

artículo científico publicado en 2018

Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.

artículo científico publicado en 2002

Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma

artículo científico publicado en 2018

Personalized oncogenomic analysis of metastatic adenoid cystic carcinoma: using whole-genome sequencing to inform clinical decision-making

artículo científico publicado en 2018

Physical Mapping of Chromosome 6: A Strategy for the Rapid Generation of Sequence-Ready Contigs

Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer

artículo científico publicado en 2002

Putative BRAF activating fusion in a medullary thyroid cancer.

artículo científico publicado en 2016

Pyruvate Kinase Inhibits Proliferation during Postnatal Cerebellar Neurogenesis and Suppresses Medulloblastoma Formation.

artículo científico publicado en 2017

Quiescent sox2(+) cells drive hierarchical growth and relapse in sonic hedgehog subgroup medulloblastoma

artículo científico publicado en 2014

RPS6KA2, a putative tumour suppressor gene at 6q27 in sporadic epithelial ovarian cancer

artículo científico publicado en 2007

Recurrent DGCR8, DROSHA, and SIX homeodomain mutations in favorable histology Wilms tumors.

artículo científico publicado en 2015

Recurrent genomic rearrangements in primary testicular lymphoma.

artículo científico

Recurrent targets of aberrant somatic hypermutation in lymphoma

artículo científico publicado en 2012

Replication timing of human chromosome 6.

artículo científico publicado en 2005

Report of the Fourth International Chromosome 6 Workshop 1999. 10-12 June 1999. Cambridge, UK. Abstracts

artículo científico publicado en 2000

Response to angiotensin blockade with irbesartan in a patient with metastatic colorectal cancer.

artículo científico publicado en 2016

Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group.

artículo científico publicado en 2016

Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

artículo científico publicado en 2010

Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation

artículo científico publicado en 2010

Spatial heterogeneity in medulloblastoma

artículo científico publicado en 2017

Subgroup-specific structural variation across 1,000 medulloblastoma genomes

artículo científico publicado en 2012

Subtype-discordant pancreatic ductal adenocarcinoma tumors show intermediate clinical and molecular characteristics

scientific article published on 13 October 2020

TBL1XR1/TP63: a novel recurrent gene fusion in B-cell non-Hodgkin lymphoma

artículo científico publicado en 2012

TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma

scientific article published on 24 February 2020

The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma

article

The Chromosome 6 database at the Sanger Centre

The DNA sequence and analysis of human chromosome 6

artículo científico publicado en 2003

The E3 ubiquitin ligase UBR5 is recurrently mutated in mantle cell lymphoma.

artículo científico publicado en 2013

The Genome of the Beluga Whale (Delphinapterus leucas).

artículo científico publicado en 2017

The Genome of the North American Brown Bear or Grizzly: Ursus arctos ssp. horribilis

article

The Genome of the Northern Sea Otter (Enhydra lutris kenyoni).

artículo científico publicado en 2017

The Genome of the Steller Sea Lion (Eumetopias jubatus)

artículo científico publicado en 2019

The North American bullfrog draft genome provides insight into hormonal regulation of long noncoding RNA.

artículo científico publicado en 2017

The evolution of imprinting: chromosomal mapping of orthologues of mammalian imprinted domains in monotreme and marsupial mammals

artículo científico publicado en 2007

The evolution of the DLK1-DIO3 imprinted domain in mammals

artículo científico publicado en 2008

The expression level of small non-coding RNAs derived from the first exon of protein-coding genes is predictive of cancer status.

artículo científico publicado en 2014

The genomic and transcriptomic landscape of anaplastic thyroid cancer: implications for therapy.

artículo científico publicado en 2015

The genomic structure and promoter region of the human parkin gene

artículo científico publicado en 2001

The human homologue of unc-93 maps to chromosome 6q27 - characterisation and analysis in sporadic epithelial ovarian cancer

artículo científico publicado en 2002

The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.

artículo científico publicado en 2017

The organization of the gamma-glutamyl transferase genes and other low copy repeats in human chromosome 22q11.

artículo científico publicado en 1997

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X

artículo científico publicado en 2001

The transcriptional landscape of Shh medulloblastoma

artículo científico publicado en 2021

The whole-genome landscape of medulloblastoma subtypes

artículo científico publicado en 2017

Tumor necrosis factor overcomes immune evasion in p53-mutant medulloblastoma

artículo científico publicado en 2020

Uncovering Clinically Relevant Gene Fusions with Integrated Genomic and Transcriptomic Profiling of Metastatic Cancers

scientific article published on 04 November 2020

Validation and calibration of next-generation sequencing to identify Epstein-Barr virus-positive gastric cancer in The Cancer Genome Atlas

artículo científico publicado en 2015

Vanin genes are clustered (human 6q22-24 and mouse 10A2B1) and encode isoforms of pantetheinase ectoenzymes

artículo científico publicado en 2001

Whole genome and whole transcriptome genomic profiling of a metastatic eccrine porocarcinoma.

artículo científico publicado en 2018

Whole-genome and transcriptome profiling of a metastatic thyroid-like follicular renal cell carcinoma

artículo científico publicado en 2018

Whole-slide laser microdissection for tumour enrichment

scientific article published on 02 November 2020

miR-509-3p is clinically significant and strongly attenuates cellular migration and multi-cellular spheroids in ovarian cancer.

scientific article published on 27 March 2016

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