Gene-expression profiles to predict distant metastasis of lymph-node-negative primary breast cancer.
By Yixin Wang, J. Klijn, Yi Zhang, Anieta M. Sieuwerts, M. Look, Fei Yang, D. Talantov, M. Timmermans, M. M. Meijer-van Gelder, Jack Yu and 4 more. The Lancet, 2005
2,816 citations recorded by the source corpus.
Subfields: Cancer Research, Genetics, Pathology and Forensic Medicine
View Paper: https://www.semanticscholar.org/paper/73d6948a5fb62bd8c3fbbd612b1064003bcb2222
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In Cancer Research
- Balázs Győrffy
- J. Massagué
- H. Horlings
- Yibin Kang
- Douglas B. Kell
- K. Polyak
- Trey Ideker
- Adrian L. Harris
In Genetics
- Frank Dudbridge
- Naomi R. Wray
- Sang Hong Lee
- A. Vinkhuyzen
- C. Middeldorp
- D. Mehta
- Jason S. Carroll
- Douglas B. Kell
In Pathology and Forensic Medicine
Citations in the corpus
- A New Molecular Predictor of Distant Recurrence in ER-Positive, HER2-Negative Breast Cancer Adds Independent Information to Conventional Clinical Risk Factors (2011, background): “Recently, several molecular tests for prediction of breast cancer prognosis have been developed in order to aid clinical decision making (3-5).”
- Carcinoma-associated fibroblast-like differentiation of human mesenchymal stem cells. (2008, background): “June 1, 2008 ( 30 ) revealed that 25% of the TCM-exposed hMSC markers are up-regulated in the basals, 15% are up-regulated in luminals, and <5% are up-regulated in the HER2+ subtype of human breast”
- Genome-wide analysis of estrogen receptor binding sites (2006, neutral): “dtd" [ ]> Recent work has focused on identifying gene expression signatures in breast cancer subtypes that predict response to specific treatment regimes and improved disease outcom”
- Improved classification of breast cancer by analysis of genetic alterations and gene expression profiling (2011, methodology): “Many of these signatures have also been shown to be prognostic factors and identify patients at increased risk of developing distant metastases [45, 46], including a 70gene prognosis signature [1, 44], a 76 gene prognosis signature [47] and a 21-gene classifier for paraffin-embedded tissues (Oncotyp”
- L1 Penalized Estimation in the Cox Proportional Hazards Model (2009, positive): “We used four large and well-known gene expression data sets with a survival response: Van de Vijver (Van de Vijver et al., 2002, 295 80 J. J. Goeman: L1 penalized estimation r 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim www.biometrical-journal.com subjects, 79 events and 4919 covariates), Rosenw”
- Statistical strategies for avoiding false discoveries in metabolomics and related experiments (2007, result): “A comparison of two studies using hundreds of samples found respectively 76 (Wang et al., 2005) and 70 (van 't Veer et al., 2002; van de Vijver et al., 2002) 'significant' genes, but only 3 of them were in fact the same (Ein-Dor et al., 2006 )!”
- Identification of diagnostic subnetwork markers for cancer in human protein-protein interaction network (2010, methodology): “We obtained two independent breast cancer datasets from the large-scale expression studies in Wang et al. [10] (referred as the USA dataset) and van ’ t Veer et al. [9] (referred as the Netherlands dataset).”
- Gene expression profiling and histopathological characterization of triple-negative/basal-like breast carcinomas (2007, methodology): “have identified a 16-gene signature associated with distant metastasis in ER-negative breast carcinomas [14].”
- Latent bone metastasis in breast cancer tied to Src-dependent survival signals (2009, background): “Approximately twothirds of these cases were lymph node negative at diagnosis, and were not subject to adjuvant therapy after primary tumor resection (Wang et al., 2005; Yu et al., 2007).”
- GOBO: Gene Expression-Based Outcome for Breast Cancer Online (2011, neutral): “A multitude of microarray-based gene signatures have been derived stratifying breast cancer into subtypes [1,2,24], identifying patients at risk [5,6,8,9,11,12], and predicting response to therapeutic agents [3,4].”
- Research review: Polygenic methods and their application to psychiatric traits. (2014, background): “The genomics era has allowed good progress in subtyping of cancers (e.g. ER +ve/ER – ve and over-expression of HER2 as a breast-cancer subtype (Wang et al., 2005; Slamon et al., 1987) or K-ras mutations in colorectal cancer and EGFR mutations in lung cancer, reviewed in (Ferraldeschi & Newman,…”