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Author Details
Full Name
Ultan McDermott
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
1993
Papers
119
H Index
59
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36219477
Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma.
J Pathol
2023
35086954
Functional Genomic Identification of Predictors of Sensitivity and Mechanisms of Resistance to Multivalent Second-Generation TRAIL-R2 Agonists.
Mol Cancer Ther
2022
35351890
Knowledge graph-based recommendation framework identifies drivers of resistance in EGFR mutant non-small cell lung cancer.
Nat Commun
2022
36969743
Pharmaceutical Reactivation of Attenuated Apoptotic Pathways Leads to Elimination of Osimertinib Drug-Tolerant Cells.
Cancer Res Commun
2022
32690604
Image-based consensus molecular subtype (imCMS) classification of colorectal cancer using deep learning.
Gut
2021
34021238
Genome-wide CRISPR/Cas9 deletion screen defines mitochondrial gene essentiality and identifies routes for tumour cell viability in hypoxia.
Commun Biol
2021
33028592
In-depth Clinical and Biological Exploration of DNA Damage Immune Response as a Biomarker for Oxaliplatin Use in Colorectal Cancer.
Clin Cancer Res
2021
32554709
ctDNA monitoring using patient-specific sequencing and integration of variant reads.
Sci Transl Med
2020
35121986
Genomics-guided pre-clinical development of cancer therapies.
Nat Cancer
2020
31743054
Molecular Evolution of <i>IDH</i> Wild-Type Glioblastomas Treated With Standard of Care Affects Survival and Design of Precision Medicine Trials: A Report From the EORTC 1542 Study.
J Clin Oncol
2020
33334013
Targeting Acid Ceramidase to Improve the Radiosensitivity of Rectal Cancer.
Cells
2020
33205120
Identification of Intrinsic Drug Resistance and Its Biomarkers in High-Throughput Pharmacogenomic and CRISPR Screens.
Patterns (N Y)
2020
32878980
A YAP/FOXM1 axis mediates EMT-associated EGFR inhibitor resistance and increased expression of spindle assembly checkpoint components.
Sci Transl Med
2020
32990596
Genome-wide CRISPR screens of oral squamous cell carcinoma reveal fitness genes in the Hippo pathway.
Elife
2020
30849372
Characterizing Mutational Signatures in Human Cancer Cell Lines Reveals Episodic APOBEC Mutagenesis.
Cell
2019
30218636
A lentiviral vector-based insertional mutagenesis screen identifies mechanisms of resistance to MAPK inhibitors in melanoma.
Pigment Cell Melanoma Res
2019
30224339
NOTCH1 Represses MCL-1 Levels in GSI-resistant T-ALL, Making them Susceptible to ABT-263.
Clin Cancer Res
2019
31127149
Imipridone ONC212 activates orphan G protein-coupled receptor GPR132 and integrated stress response in acute myeloid leukemia.
Leukemia
2019
31097696
Functional linkage of gene fusions to cancer cell fitness assessed by pharmacological and CRISPR-Cas9 screening.
Nat Commun
2019
30852338
Large-scale compound screens and pharmacogenomic interactions in cancer.
Curr Opin Genet Dev
2019
29170471
Steps forward for cancer precision medicine.
Nat Rev Drug Discov
2018
30166531
Circulating tumor DNA in patients with colorectal adenomas: assessment of detectability and genetic heterogeneity.
Cell Death Dis
2018
30202034
An integrated genomic analysis of anaplastic meningioma identifies prognostic molecular signatures.
Sci Rep
2018
30139972
The germline genetic component of drug sensitivity in cancer cell lines.
Nat Commun
2018
30262817
Cancer cell lines as patient avatars for drug response prediction.
Nat Genet
2018
30286710
XenofilteR: computational deconvolution of mouse and human reads in tumor xenograft sequence data.
BMC Bioinformatics
2018
30299440
Corrigendum: High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer.
Sci Data
2018
29634948
The Origins and Vulnerabilities of Two Transmissible Cancers in Tasmanian Devils.
Cancer Cell
2018
29662167
Sequencing of prostate cancers identifies new cancer genes, routes of progression and drug targets.
Nat Genet
2018
29713020
Pathway-based dissection of the genomic heterogeneity of cancer hallmarks' acquisition with SLAPenrich.
Sci Rep
2018
29061644
Comprehensive Pharmacogenomic Profiling of Malignant Pleural Mesothelioma Identifies a Subgroup Sensitive to FGFR Inhibition.
Clin Cancer Res
2018
29157092
Single agent and synergistic combinatorial efficacy of first-in-class small molecule imipridone ONC201 in hematological malignancies.
Cell Cycle
2018
29345617
Loss of functional BAP1 augments sensitivity to TRAIL in cancer cells.
Elife
2018
27740635
A novel signalling screen demonstrates that CALR mutations activate essential MAPK signalling and facilitate megakaryocyte differentiation.
Leukemia
2017
28495283
Molecular diagnoses of century-old childhood tumours.
Lancet Oncol
2017
28179366
Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer genome and identification of drug resistance mutations.
Genome Res
2017
28092685
Precision oncology for acute myeloid leukemia using a knowledge bank approach.
Nat Genet
2017
28945760
Appraising the relevance of DNA copy number loss and gain in prostate cancer using whole genome DNA sequence data.
PLoS Genet
2017
28972570
High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer.
Sci Data
2017
28854368
Genomic Determinants of Protein Abundance Variation in Colorectal Cancer Cells.
Cell Rep
2017
28643781
Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma.
Nat Commun
2017
28767654
Cancer stem cell-related gene expression as a potential biomarker of response for first-in-class imipridone ONC201 in solid tumors.
PLoS One
2017
28865260
Societal challenges of precision medicine: Bringing order to chaos.
Eur J Cancer
2017
28736238
The Pursuit of Therapeutic Biomarkers with High-Throughput Cancer Cell Drug Screens.
Cell Chem Biol
2017
26923330
Targeting the RB-E2F pathway in breast cancer.
Oncogene
2016
27615322
Mutational signatures of ionizing radiation in second malignancies.
Nat Commun
2016
27876821
Logic models to predict continuous outputs based on binary inputs with an application to personalized cancer therapy.
Sci Rep
2016
27760321
A CRISPR Dropout Screen Identifies Genetic Vulnerabilities and Therapeutic Targets in Acute Myeloid Leukemia.
Cell Rep
2016
27804975
Corrigendum: A DERL3-associated defect in the degradation of SLC2A1 mediates the Warburg effect.
Nat Commun
2016
27397505
A Landscape of Pharmacogenomic Interactions in Cancer.
Cell
2016
1 - 50 of 119
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Collaborators
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Wellcome Sanger Institute
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Michael R Stratton
Wellcome Sanger Institute
Co-authored papers
18
Cyril H Benes
Co-authored papers
16
Peter J Campbell
Wellcome Sanger Institute
Co-authored papers
16
Adam Butler
Wellcome Sanger Institute
Co-authored papers
14
Ludmil B Alexandrov
Moores Cancer Center, university of california san diego
Co-authored papers
12
Patrick S Tarpey
Wellcome Trust Sanger Institute
Co-authored papers
12
Gunes Gundem
Memorial Sloan Kettering Cancer Center
Co-authored papers
12
Peter Van Loo
The Francis Crick Institute
Co-authored papers
11
David C Wedge
Manchester Cancer Research Centre, University of Manchester
Co-authored papers
11
Phillip A Futreal
The University of Texas MD Anderson Cancer Center
Co-authored papers
11
Inigo Martincorena
Wellcome Sanger Institute
Co-authored papers
11
Serena Nik-Zainal
Early Cancer Institute, University of Cambridge
Co-authored papers
10
Julio Saez-Rodriguez
Institute of Computational Biomedicine, Heidelberg University
Co-authored papers
10
Colin S Cooper
Norwich Medical School, University of East Anglia
Co-authored papers
10
David E Neal
University of Oxford, John Radcliffe Hospital
Co-authored papers
9
Lodewyk F A Wessels
University Medical Centre Mannheim, University of Heidelberg
Co-authored papers
9
Christopher S Foster
The Institute of Cancer Research
Co-authored papers
9
Jon Teague
Wellcome Sanger Institute
Co-authored papers
9
Rosalind A Eeles
The Institute of Cancer Research
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9
Keiran Raine
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Sarah O'Meara
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8
Andrew Menzies
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