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David S. Wishart
Researcher at University of Alberta
Publications - 564
Citations - 93527
David S. Wishart is an academic researcher from University of Alberta. The author has contributed to research in topics: Metabolomics & Medicine. The author has an hindex of 108, co-authored 523 publications receiving 76652 citations. Previous affiliations of David S. Wishart include La Trobe University & International Agency for Research on Cancer.
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Journal ArticleDOI
Comprehensive Targeted Metabolomic Assay for Urine Analysis.
TL;DR: This targeted metabolomic assay has been successfully applied to the analysis of large numbers of human urine samples, with results closely matching those reported in the literature as well as those obtained from orthogonal analysis via NMR spectroscopy.
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Urinary Metabolomics for Noninvasive Detection of Antibody-Mediated Rejection in Children After Kidney Transplantation.
Tom Blydt-Hansen,Atul Sharma,Ian W. Gibson,David S. Wishart,Rupasri Mandal,Julie Ho,Peter Nickerson,David N. Rush +7 more
TL;DR: The preliminary findings identify a urine metabolic classifier for AMR, which was associated with the presence of donor-specific antibodies, biopsy indication, Banff ct, t, ah and cg scores, and retained accuracy when applied to subclinical cases.
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Correction: Accurate, Fully-Automated NMR Spectral Profiling for Metabolomics.
Siamak Ravanbakhsh,Philip K. Liu,Trent C. Bjorndahl,Rupasri Mandal,Jason R. Grant,Michael R. Wilson,Roman Eisner,Igor Sinelnikov,Xiaoyu Hu,Claudio Luchinat,Russell Greiner,David S. Wishart +11 more
TL;DR: An accurate, Fully-Automated NMR Spectral Profiling for Metabolomics and its applications in medicine andabolomics is presented.
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Genomic sequence and activity of KS10, a transposable phage of the Burkholderia cepacia complex
Amanda D Goudie,Karlene H Lynch,Kimberley D. Seed,Paul Stothard,Savita Shrivastava,David S. Wishart,Jonathan J. Dennis +6 more
TL;DR: KS10 is a novel phage with a genomic organization that differs from most phages in that its capsid genes are not aligned into one module but rather separated by approximately 11 kb, giving evidence of one or more prior genetic rearrangements.
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Improved synthetic methods for the selective deuteration of aromatic amino acids : applications of selective protonation towards the identification of protein folding intermediates through nuclear magnetic resonance
TL;DR: The utility of this approach to isotopic editing is demonstrated with the identification of a transient folding intermediate of Escherichia coli thioredoxin which is undetectable by standard 2-D NMR techniques.