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Ian O. Ellis
Researcher at University of Nottingham
Publications - 1071
Citations - 84964
Ian O. Ellis is an academic researcher from University of Nottingham. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 126, co-authored 1051 publications receiving 75435 citations. Previous affiliations of Ian O. Ellis include Mansoura University & Curie Institute.
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Histological grade of invasive carcinoma of the breast assessed on needle core biopsy - modifications to mitotic count assessment to improve agreement with surgical specimens.
TL;DR: O’Shea A‐M, Rakha E A, Hodi Z, Ellis I O & Lee A H S’(2011) Histopathology59, 543–548.
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Redox protein expression predicts radiotherapeutic response in early-stage invasive breast cancer patients.
Caroline M. Woolston,Ahmad Al-Attar,Sarah J. Storr,Ian O. Ellis,David L Morgan,Stewart G. Martin +5 more
TL;DR: The results support the use of redox protein expression, namely glutathione S-transferase-θ and glutathion peroxidase 3, to predict the response to radiotherapy in early-stage breast cancer patients.
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Papillary carcinoma of the breast: diagnostic agreement and management implications
TL;DR: Assessment of the diagnostic agreement regarding PC among reporting breast pathologists found that there is little agreement on the diagnostic categorization of PC as in‐situ and invasive disease.
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Primary malignant mesenchymal tumour of the liver in an elderly female.
Ian O. Ellis,R. E. Cotton +1 more
TL;DR: A case of primary malignant mesenchymal tumour of the liver occurring in an 86‐year‐old woman described, which was large, rapidly growing though well circumscribed and extensively necrotic.
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Biological and clinical implications of nicastrin expression in invasive breast cancer
Aleksandra Filipovic,Julian H. Gronau,Andrew R. Green,Jayson Wang,Sabari Vallath,Dongmin Shao,Sabeena Rasul,Ian O. Ellis,Ernesto Yagüe,Justin Sturge,R. Charles Coombes +10 more
TL;DR: Data indicate that nicastrin can function to maintain epithelial to mesenchymal transition during BC progression, and supports the hypothesis that a Nicastrin blocking antibody could be used to limit metastatic dissemination in invasive BC.