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Author Details
Full Name
Susanna L Cooke
Affiliation
Institute of Cancer Sciences, University of Glasgow
ORCID
Career Start Year
2006
Papers
41
H Index
30
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35363872
Molecular subclusters of follicular lymphoma: a report from the United Kingdom's Haematological Malignancy Research Network.
Blood Adv
2022
33413557
NRG1 fusions in breast cancer.
Breast Cancer Res
2021
34562502
Genomic characterization of hepatoid tumors: context matters.
Hum Pathol
2021
32187361
Targeted sequencing in DLBCL, molecular subtypes, and outcomes: a Haematological Malignancy Research Network report.
Blood
2020
33144218
Defining the clinical genomic landscape for real-world precision oncology.
Genomics
2020
32675551
Precision Oncology in Surgery: Patient Selection for Operable Pancreatic Cancer.
Ann Surg
2020
31586074
Genetic modification of primary human B cells to model high-grade lymphoma.
Nat Commun
2019
31665210
Reasons to be testing: the dawn of complex molecular profiling in routine oncology practice.
Ann Oncol
2019
28643781
Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma.
Nat Commun
2017
28954785
The Driver Mutational Landscape of Ovarian Squamous Cell Carcinomas Arising in Mature Cystic Teratoma.
Clin Cancer Res
2017
25833184
Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process.
J Math Biol
2016
27615322
Mutational signatures of ionizing radiation in second malignancies.
Nat Commun
2016
27498871
Direct Transcriptional Consequences of Somatic Mutation in Breast Cancer.
Cell Rep
2016
25730763
Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
Nat Genet
2015
26018901
Corrigendum: analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
Nat Genet
2015
25710373
Spatial and temporal heterogeneity in high-grade serous ovarian cancer: a phylogenetic analysis.
PLoS Med
2015
24413735
RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia.
Nat Genet
2014
25030888
C. elegans whole-genome sequencing reveals mutational signatures related to carcinogens and DNA repair deficiency.
Genome Res
2014
25082706
Mobile DNA in cancer. Extensive transduction of nonrepetitive DNA mediated by L1 retrotransposition in cancer genomes.
Science
2014
24633157
Recurrent PTPRB and PLCG1 mutations in angiosarcoma.
Nat Genet
2014
24714652
Processed pseudogenes acquired somatically during cancer development.
Nat Commun
2014
23770606
Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma.
Nat Genet
2013
24162739
Distinct H3F3A and H3F3B driver mutations define chondroblastoma and giant cell tumor of bone.
Nat Genet
2013
23630320
Single-cell paired-end genome sequencing reveals structural variation per cell cycle.
Nucleic Acids Res
2013
22183581
The role of tandem duplicator phenotype in tumour evolution in high-grade serous ovarian cancer.
J Pathol
2012
23260012
Structural analysis of the genome of breast cancer cell line ZR-75-30 identifies twelve expressed fusion genes.
BMC Genomics
2012
22505352
Clinically significant copy number alterations and complex rearrangements of MYB and NFIB in head and neck adenoid cystic carcinoma.
Genes Chromosomes Cancer
2012
22527501
Circulating DNA and next-generation sequencing.
Recent Results Cancer Res
2012
22514011
Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes.
J Pathol
2012
22608084
Mutational processes molding the genomes of 21 breast cancers.
Cell
2012
22608083
The life history of 21 breast cancers.
Cell
2012
21063398
Intra-tumour genetic heterogeneity and poor chemoradiotherapy response in cervical cancer.
Br J Cancer
2011
21742554
Evolution of platinum resistance in high-grade serous ovarian cancer.
Lancet Oncol
2011
20581869
Genomic analysis of genetic heterogeneity and evolution in high-grade serous ovarian carcinoma.
Oncogene
2010
19956657
The specificity of the FOXL2 c.402C>G somatic mutation: a survey of solid tumors.
PLoS One
2009
18084325
Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes.
Oncogene
2008
18840272
High-resolution array CGH clarifies events occurring on 8p in carcinogenesis.
BMC Cancer
2008
18302246
Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement.
Am J Med Genet A
2008
17973251
Arylamine N-acetyltransferase 1 expression in breast cancer cell lines: a potential marker in estrogen receptor-positive tumors.
Genes Chromosomes Cancer
2008
17285574
Co-amplification of 8p12 and 11q13 in breast cancers is not the result of a single genomic event.
Genes Chromosomes Cancer
2007
16636668
High-resolution analysis of chromosome rearrangements on 8p in breast, colon and pancreatic cancer reveals a complex pattern of loss, gain and translocation.
Oncogene
2006
1 - 41 of 41
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David Jones
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