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Author Details
Full Name
Richard de Borja
Affiliation
The Hospital for Sick Children
ORCID
Career Start Year
2012
Papers
25
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36604421
Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis.
Nat Commun
2023
36912329
Coronavirus disease 2019 (COVID-19) outbreak on an in-patient medical unit associated with unrecognized exposures in common areas-Epidemiological and whole-genome sequencing investigation.
Infect Control Hosp Epidemiol
2023
35986021
Author Correction: Emergence of a mutation in the nucleocapsid gene of SARS-CoV-2 interferes with PCR detection in Canada.
Sci Rep
2022
35501919
Impact of neoadjuvant chemotherapy on somatic mutation status in high-grade serous ovarian carcinoma.
J Ovarian Res
2022
35760824
Emergence of a mutation in the nucleocapsid gene of SARS-CoV-2 interferes with PCR detection in Canada.
Sci Rep
2022
34535459
Diverse Oncogenic Fusions and Distinct Gene Expression Patterns Define the Genomic Landscape of Pediatric Papillary Thyroid Carcinoma.
Cancer Res
2021
36778585
CanDIG: Federated network across Canada for multi-omic and health data discovery and analysis.
Cell Genom
2021
35261998
Detection of the novel SARS-CoV-2 European lineage B.1.177 in Ontario, Canada.
J Clin Virol Plus
2021
32938641
Cancers from Novel <i>Pole</i>-Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint Blockade.
Cancer Res
2020
31990679
Cellular and molecular architecture of hematopoietic stem cells and progenitors in genetic models of bone marrow failure.
JCI Insight
2020
30665349
BPG: Seamless, automated and interactive visualization of scientific data.
BMC Bioinformatics
2019
31511937
Comparative toxicoproteogenomics of mouse and rat liver identifies TCDD-resistance genes.
Arch Toxicol
2019
31189997
Myxoid smooth muscle neoplasia of the uterus: comprehensive analysis by next-generation sequencing and nucleic acid hybridization.
Mod Pathol
2019
29488881
Explosive mutation accumulation triggered by heterozygous human Pol ε proofreading-deficiency is driven by suppression of mismatch repair.
Elife
2018
30166462
Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors.
Science
2018
28068672
Genomic hallmarks of localized, non-indolent prostate cancer.
Nature
2017
29056344
Comprehensive Analysis of Hypermutation in Human Cancer.
Cell
2017
27001570
Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair Deficiency.
J Clin Oncol
2016
25642631
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers.
Nat Genet
2015
26005866
Spatial genomic heterogeneity within localized, multifocal prostate cancer.
Nat Genet
2015
24154973
Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants.
Int J Cancer
2014
25240283
Hotspot activating PRKD1 somatic mutations in polymorphous low-grade adenocarcinomas of the salivary glands.
Nat Genet
2014
25173705
SeqControl: process control for DNA sequencing.
Nat Methods
2014
24445778
Robust global microRNA expression profiling using next-generation sequencing technologies.
Lab Invest
2014
23103869
Pancreatic cancer genomes reveal aberrations in axon guidance pathway genes.
Nature
2012
1 - 25 of 25
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row(s) 1 - 30 of 30
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University Health Network
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Lee Timms
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Eric Bouffet
The Hospital for Sick Children
Co-authored papers
4
Michelle Sam
Ontario Institute for Cancer Research
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Nicholas Buchner
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Kenneth C Chu
Ontario Institute for Cancer Research
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Daryl Waggott
Ontario Institute for Cancer Research
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Robert E Denroche
Ontario Institute for Cancer Research
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4
Jianxin Wang
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