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Communications Biology|April 9, 2022
Rearrangement processes and structural variations show evidence of selection in oesophageal adenocarcinomasAlvin Wei Tian Ng, Gianmarco Contino, Sarah Killcoyne, et al.
Breast Cancer Research : BCR|January 8, 2021
NRG1 fusions in breast cancerKaren D Howarth, Tashfina Mirza, Susanna L Cooke, et al.
BMC Genomics|December 25, 2012
Structural analysis of the genome of breast cancer cell line ZR-75-30 identifies twelve expressed fusion genesIna Schulte, Elizabeth M Batty, Jessica C M Pole, et al.
Genes, Chromosomes & Cancer|June 12, 2003
A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 geneJosé Adélaïde, Huai-En Huang, Anne Murati, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2012
Tumor initiating but differentiated luminal-like breast cancer cells are highly invasive in the absence of basal-like activityJiyoung Kim, René Villadsen, Therese Sørlie, et al.
Cancer Research|October 7, 2004
A recurrent chromosome breakpoint in breast cancer at the NRG1/neuregulin 1/heregulin geneHuai-En Huang, Suet-Feung Chin, Christophe Ginestier, et al.
Nature|March 9, 2017
Complex multi-enhancer contacts captured by genome architecture mappingRobert A Beagrie, Antonio Scialdone, Markus Schueler, et al.
Genome Research|August 7, 2007
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolutionGraham R Bignell, Thomas Santarius, Jessica C M Pole, et al.
EMBO Molecular Medicine|May 10, 2023
Comparison of tumor-informed and tumor-naïve sequencing assays for ctDNA detection in breast cancerAngela Santonja, Wendy N Cooper, Matthew D Eldridge, et al.
Nature Genetics|September 6, 2016
Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevanceMaria Secrier, Xiaodun Li, Nadeera de Silva, et al.
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