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Prashant Bavi

Researcher at Ontario Institute for Cancer Research

Publications -  90
Citations -  6870

Prashant Bavi is an academic researcher from Ontario Institute for Cancer Research. The author has contributed to research in topics: Cancer & Diffuse large B-cell lymphoma. The author has an hindex of 36, co-authored 81 publications receiving 5005 citations. Previous affiliations of Prashant Bavi include University Health Network & University of Toronto.

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Pan-cancer analysis of whole genomes

Peter J. Campbell, +1332 more
- 06 Feb 2020 - 
TL;DR: The flagship paper of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium describes the generation of the integrative analyses of 2,658 whole-cancer genomes and their matching normal tissues across 38 tumour types, the structures for international data sharing and standardized analyses, and the main scientific findings from across the consortium studies.
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International validation of the consensus Immunoscore for the classification of colon cancer: a prognostic and accuracy study

Franck Pagès, +120 more
- 26 May 2018 - 
TL;DR: The immunoscore provides a reliable estimate of the risk of recurrence in patients with colon cancer and supports the implementation of the consensus Immunoscore as a new component of a TNM-Immune classification of cancer.
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Association of Distinct Mutational Signatures With Correlates of Increased Immune Activity in Pancreatic Ductal Adenocarcinoma

TL;DR: Signatures were faithfully propagated from primaries to matched metastases, implying their stability during carcinogenesis, and signature-based subtyping may guide personalized therapy of PDAC in the context of biomarker-driven prospective trials.
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Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature

TL;DR: Clinical and genetic findings suggest that ADAMTS17 plays a role in crystalline lens zonules and connective tissue formation and that mutations in ADAM TS17 are sufficient to produce some of the main features typically described in Weill-Marchesani syndrome.