Estrogen receptor status in breast cancer is associated with remarkably distinct gene expression patterns.

By Sofia Gruvberger, Markus Ringnér, Yidong Chen, Sujatha Panavally, L. Saal, Å. Borg, Mårten Fernö, Carsten O. Peterson, Paul S. Meltzer. Cancer Research, 2001

729 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/beebb981b045d9f23700b3334ca4405fed6136b1

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Citations in the corpus

Single-cell RNA-seq enables comprehensive tumour and immune cell profiling in primary breast cancer (2017, unknown): “Most carcinoma cells in all luminal tumours (BC01, BC02 and BC03) expressed high levels of ER and the canonical ER pathway genes 20,33,34 (Fig.”
Etiology of hormone receptor-defined breast cancer: a systematic review of the literature. (2004, background): “ER-positive and ER-negative tumors differ in the expression of many genes that do not seem to be controlled by hormones (75).”
Correcting Sample Selection Bias by Unlabeled Data (2006, methodology): “We study a very similar scenario on two breast cancer microar ray datasets from [4] and [19], measuring the expression levels of 2,166 common genes for norma l and cancer patients [18].”
BioArray Software Environment (BASE): a platform for comprehensive management and analysis of microarray data (2002, background): “Whereas microarrays have shed light on many biological processes and disease states, for us [7-10] and others, a significant bottle-neck remains the analysis of hybridization data in the context of biomaterial and reporter annotations.”
Coexpression analysis of human genes across many microarray data sets. (2004, unknown): “…(Golub et al. 1999) 72 5418 52283 (Tezak et al. 2002) 24 12057 12944 (Greenberg et al. 2002) 12 8243 5280 (Unpublished, GSE443) 60 5418 51286 (Gruvberger et al. 2001) 58 2756 24781 (Unpublished, GSE470) 85 8243 241088 (Hedenfalk et al. 2001) 22 2253 1265 (Unpublished, GSE474) 10 5418 7941…”