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Institution

John Radcliffe Hospital

HealthcareOxford, Oxfordshire, United Kingdom
About: John Radcliffe Hospital is a healthcare organization based out in Oxford, Oxfordshire, United Kingdom. It is known for research contribution in the topics: Population & Antigen. The organization has 14491 authors who have published 23670 publications receiving 1459015 citations.


Papers
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Journal ArticleDOI
TL;DR: Epoetin alfa safely and effectively ameliorates anemia and significantly improves QOL in cancer patients receiving nonplatinum chemotherapy in patients with solid or nonmyeloid hematologic malignancies.
Abstract: PURPOSE: This randomized, double-blind, placebo-controlled clinical trial assessed the effects of epoetin alfa on transfusion requirements, hematopoietic parameters, quality of life (QOL), and safety in anemic cancer patients receiving nonplatinum chemotherapy. The study also explored a possible relationship between increased hemoglobin and survival. PATIENTS AND METHODS: Three hundred seventy-five patients with solid or nonmyeloid hematologic malignancies and hemoglobin levels ≤ 10.5 g/dL, or greater than 10.5 g/dL but ≤ 12.0 g/dL after a hemoglobin decrease of ≥ 1.5 g/dL per cycle since starting chemotherapy, were randomized 2:1 to epoetin alfa 150 to 300 IU/kg (n = 251) or placebo (n = 124) three times per week subcutaneously for 12 to 24 weeks. The primary end point was proportion of patients transfused; secondary end points were change in hemoglobin and QOL. The protocol was amended before unblinding to prospectively collect and assess survival data 12 months after the last patient completed the stud...

985 citations

Journal ArticleDOI
TL;DR: The potential value of using statistical interaction effects to model electrophysiological responses to crossmodal stimuli in order to identify possible sites of multisensory integration in the human brain is highlighted.
Abstract: Modern brain imaging techniques have now made it possible to study the neural sites and mechanisms underlying crossmodal processing in the human brain. This paper reviews positron emission tomography, functional magnetic resonance imaging (fMRI), event-related potential and magnetoencephalographic studies of crossmodal matching, the crossmodal integration of content and spatial information, and crossmodal learning. These investigations are beginning to produce some consistent findings regarding the neuronal networks involved in these distinct crossmodal operations. Increasingly, specific roles are being defined for the superior temporal sulcus, the inferior parietal sulcus, regions of frontal cortex, the insula cortex and claustrum. The precise network of brain areas implicated in any one study, however, seems to be heavily dependent on the experimental paradigms used, the nature of the information being combined and the particular combination of modalities under investigation. The different analytic strategies adopted by different groups may also be a significant factor contributing to the variability in findings. In this paper, we demonstrate the impact of computing intersections, conjunctions and interaction effects on the identification of audiovisual integration sites using existing fMRI data from our own laboratory. This exercise highlights the potential value of using statistical interaction effects to model electrophysiological responses to crossmodal stimuli in order to identify possible sites of multisensory integration in the human brain.

983 citations

Journal ArticleDOI
TL;DR: This independent validation confirmed the performance of the 76-gene signature and adds to the growing evidence that gene expression signatures are of clinical relevance, especially for identifying patients at high risk of early distant metastases.
Abstract: Purpose: Recently, a 76-gene prognostic signature able to predict distant metastases in lymph node–negative (N − ) breast cancer patients was reported. The aims of this study conducted by TRANSBIG were to independently validate these results and to compare the outcome with clinical risk assessment. Experimental Design: Gene expression profiling of frozen samples from 198 N − systemically untreated patients was done at the Bordet Institute, blinded to clinical data and independent of Veridex. Genomic risk was defined by Veridex, blinded to clinical data. Survival analyses, done by an independent statistician, were done with the genomic risk and adjusted for the clinical risk, defined by Adjuvant! Online. Results: The actual 5- and 10-year time to distant metastasis were 98% (88-100%) and 94% (83-98%), respectively, for the good profile group and 76% (68-82%) and 73% (65-79%), respectively, for the poor profile group. The actual 5- and 10-year overall survival were 98% (88-100%) and 87% (73-94%), respectively, for the good profile group and 84% (77-89%) and 72% (63-78%), respectively, for the poor profile group. We observed a strong time dependence of this signature, leading to an adjusted hazard ratio of 13.58 (1.85-99.63) and 8.20 (1.10-60.90) at 5 years and 5.11 (1.57-16.67) and 2.55 (1.07-6.10) at 10 years for time to distant metastasis and overall survival, respectively. Conclusion: This independent validation confirmed the performance of the 76-gene signature and adds to the growing evidence that gene expression signatures are of clinical relevance, especially for identifying patients at high risk of early distant metastases.

982 citations

Journal ArticleDOI
William J. Astle, Heather Elding1, Heather Elding2, Tao Jiang3, Dave Allen4, Dace Ruklisa4, Dace Ruklisa3, Alice L. Mann1, Daniel Mead1, Heleen J. Bouman1, Fernando Riveros-Mckay1, Myrto Kostadima4, Myrto Kostadima3, Myrto Kostadima5, John J. Lambourne3, John J. Lambourne4, Suthesh Sivapalaratnam3, Suthesh Sivapalaratnam6, Kate Downes3, Kate Downes4, Kousik Kundu1, Kousik Kundu3, Lorenzo Bomba1, Kim Berentsen7, John Bradley3, John Bradley2, Louise C. Daugherty3, Louise C. Daugherty4, Olivier Delaneau8, Kathleen Freson9, Stephen F. Garner3, Stephen F. Garner4, Luigi Grassi4, Luigi Grassi3, Jose A. Guerrero3, Jose A. Guerrero4, Matthias Haimel3, Eva M. Janssen-Megens7, Anita Kaan7, Mihir A Kamat3, Bowon Kim7, Amit Mandoli7, Jonathan Marchini10, Jonathan Marchini11, Joost H.A. Martens7, Stuart Meacham3, Stuart Meacham4, Karyn Megy3, Karyn Megy4, Jared O'Connell10, Jared O'Connell11, Romina Petersen3, Romina Petersen4, Nilofar Sharifi7, S.M. Sheard, James R Staley3, Salih Tuna3, Martijn van der Ent7, Klaudia Walter1, Shuang-Yin Wang7, Eleanor Wheeler1, Steven P. Wilder5, Valentina Iotchkova5, Valentina Iotchkova1, Carmel Moore3, Jennifer G. Sambrook3, Jennifer G. Sambrook4, Hendrik G. Stunnenberg7, Emanuele Di Angelantonio3, Emanuele Di Angelantonio2, Emanuele Di Angelantonio12, Stephen Kaptoge3, Stephen Kaptoge2, Taco W. Kuijpers13, Enrique Carrillo-de-Santa-Pau, David Juan, Daniel Rico14, Alfonso Valencia, Lu Chen3, Lu Chen1, Bing Ge15, Louella Vasquez1, Tony Kwan15, Diego Garrido-Martín16, Stephen Watt1, Ying Yang1, Roderic Guigó16, Stephan Beck17, Dirk S. Paul3, Dirk S. Paul17, Tomi Pastinen15, David Bujold15, Guillaume Bourque15, Mattia Frontini4, Mattia Frontini12, Mattia Frontini3, John Danesh, David J. Roberts18, David J. Roberts19, Willem H. Ouwehand, Adam S. Butterworth3, Adam S. Butterworth12, Adam S. Butterworth2, Nicole Soranzo 
17 Nov 2016-Cell
TL;DR: A genome-wide association analysis in the UK Biobank and INTERVAL studies is performed, providing evidence of shared genetic pathways linking blood cell indices with complex pathologies, including autoimmune diseases, schizophrenia, and coronary heart disease and evidence suggesting previously reported population associations betweenBlood cell indices and cardiovascular disease may be non-causal.

982 citations

Journal ArticleDOI
10 Aug 1989-Nature
TL;DR: A cell in which association of a major histocompatibility complex class I heavy chain with β2-microglobulin is induced by a peptide derived from influenza nucleoprotein is described.
Abstract: We describe a cell in which association of a major histocompatibility complex class I heavy chain with beta 2-microglobulin is induced by a peptide derived from influenza nucleoprotein. Association of antigenic peptides with the binding site of class I molecules may be required for correct folding of the heavy chain, association with beta 2-microglobulin and transport of the antigen-MHC complex to the cell surface.

982 citations


Authors

Showing all 14542 results

NameH-indexPapersCitations
Douglas G. Altman2531001680344
Salim Yusuf2311439252912
David J. Hunter2131836207050
Mark I. McCarthy2001028187898
Stuart H. Orkin186715112182
Richard Peto183683231434
Ralph M. Steinman171453121518
Adrian L. Harris1701084120365
Rory Collins162489193407
Nicholas J. White1611352104539
David W. Johnson1602714140778
David Cella1561258106402
Edmund T. Rolls15361277928
Martin A. Nowak14859194394
Kypros H. Nicolaides147130287091
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202311
202252
20211,048
20201,013
2019916
2018773