Prediction of BRCA1 Status in Patients with Breast Cancer Using Estrogen Receptor and Basal Phenotype
By S. Lakhani, J. Reis-Filho, L. Fulford, F. Penault-Llorca, M. van der Vijver, S. Parry, T. Bishop, J. Benítez, C. Rivas, Y. Bignon and 26 more. Clinical Cancer Research, 2005
669 citations recorded by the source corpus.
Subfields: Cancer Research, Genetics
View Paper: https://www.semanticscholar.org/paper/59e46f8e29c9649a5e6bbe6066999751326f3f36
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- J. Reis-Filho
- Olivier Elemento
- Alan Ashworth
- M. J. van de Vijver
- Lisa A. Carey
- Andrew Tutt
- Jane E. Visvader
In Genetics
Citations in the corpus
- Triple-negative breast cancer--current status and future directions. (2009, background): “Additional characteristics of BLBC are frequent metaplastic elements and medullary/atypical medullary features [28,29,34,35].”
- BRCA1 basal-like breast cancers originate from luminal epithelial progenitors and not from basal stem cells. (2010, background): “Strikingly, the majority of breast tumors arising in carriers of germline mutations in BRCA1 have the basal-like phenotype (Lakhani et al., 2005; Palacios et al., 2005).”
- BRCA1 dysfunction in sporadic basal-like breast cancer (2007, background): “We hypothesized that the phenotypic overlap of BRCA1 familial cancers and sporadic basal-like cancers (Foulkes et al., 2003; Sorlie et al., 2003; Lakhani et al., 2005) implied that sporadic basal-like cancers might have an underlying defect in BRCA1-related pathways (Turner et al., 2004).”
- Gene expression profiling and histopathological characterization of triple-negative/basal-like breast carcinomas (2007, background): “Specific subgroups of triple-negative tumors may be formed by medullary and atypical medullary cancers [12,37-39].”
- Deep Convolutional Neural Networks Enable Discrimination of Heterogeneous Digital Pathology Images (2017, background): “Furthermore, the minimum mis-classification is related to the score 3 and EGFR marker which is a well known basal marker for breast cancer therapy (Lakhani et al., 2005).”
- Triple-negative breast cancer: disease entity or title of convenience? (2010, background): “TNBC and the BRCA1 pathway The majority of tumors in BRCA1 mutation carriers are triple negative and show morphological and immunohistochemical similarities to BLBCs”
- Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene (2010, background): “Despite the fact that five of the seven ovarian cancers presented as pT3 tumors, only two had lymph node involvement, again indicating distinct features compared to BRCA1 -associated ovarian cancers, the majority of which are poorly differentiated invasive serous adenocarcinoma”
- Keeping abreast of the mammary epithelial hierarchy and breast tumorigenesis. (2009, background): “However, ERa is expressed on about one-third of luminal progenitor cells; furthermore, not all BRCA1 tumors are negative for ERa, with up to 30% expressing variable levels of this receptor (Lakhani et al. 2005).”