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Author Details
Full Name
John D McPherson
Affiliation
Ontario Institute for Cancer Research
ORCID
Career Start Year
1986
Papers
153
H Index
67
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37337105
Transcriptomic classes of BCR-ABL1 lymphoblastic leukemia.
Nat Genet
2023
31435024
Cryptic genomic lesions in adverse-risk acute myeloid leukemia identified by integrated whole genome and transcriptome sequencing.
Leukemia
2020
32686686
Landscape of somatic single nucleotide variants and indels in colorectal cancer and impact on survival.
Nat Commun
2020
30478095
Future Promises and Concerns of Ubiquitous Next-Generation Sequencing.
Cold Spring Harb Perspect Med
2019
35100692
Identification of Distinct Prognostic Groups: Implications for Patient Selection to Targeted Therapies Among Anti-Endocrine Therapy-Resistant Early Breast Cancers.
JCO Precis Oncol
2019
31511937
Comparative toxicoproteogenomics of mouse and rat liver identifies TCDD-resistance genes.
Arch Toxicol
2019
31591588
Genome-wide germline correlates of the epigenetic landscape of prostate cancer.
Nat Med
2019
30837567
Regional perturbation of gene transcription is associated with intrachromosomal rearrangements and gene fusion transcripts in high grade ovarian cancer.
Sci Rep
2019
30923040
Activation of hedgehog signaling associates with early disease progression in chronic lymphocytic leukemia.
Blood
2019
30478097
Next-Generation Sequencing Technologies.
Cold Spring Harb Perspect Med
2019
30429608
Sensitive tumour detection and classification using plasma cell-free DNA methylomes.
Nature
2018
35135130
Minimally Invasive Real-Time Detection of Actionable Mutations in Patients With Metastatic Solid Tumors Using Fine-Needle and Liquid Biopsies.
JCO Precis Oncol
2018
29988082
Prediction of acute myeloid leukaemia risk in healthy individuals.
Nature
2018
29954844
Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line.
Genome Res
2018
27750381
Molecular heterogeneity of non-small cell lung carcinoma patient-derived xenografts closely reflect their primary tumors.
Int J Cancer
2017
31015706
Microscopy with ultraviolet surface excitation for rapid slide-free histology.
Nat Biomed Eng
2017
28481342
Recurrent noncoding regulatory mutations in pancreatic ductal adenocarcinoma.
Nat Genet
2017
28273451
Interrogation of Functional Cell-Surface Markers Identifies CD151 Dependency in High-Grade Serous Ovarian Cancer.
Cell Rep
2017
28939825
Mitochondrial mutations drive prostate cancer aggression.
Nat Commun
2017
28659176
ISOWN: accurate somatic mutation identification in the absence of normal tissue controls.
Genome Med
2017
28658204
Tracing the origins of relapse in acute myeloid leukaemia to stem cells.
Nature
2017
27851734
Erratum: A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns.
Nature
2017
27768182
Association of Distinct Mutational Signatures With Correlates of Increased Immune Activity in Pancreatic Ductal Adenocarcinoma.
JAMA Oncol
2017
28068672
Genomic hallmarks of localized, non-indolent prostate cancer.
Nature
2017
28067867
Germline BRCA2 mutations drive prostate cancers with distinct evolutionary trajectories.
Nat Commun
2017
26859458
Truncating Erythropoietin Receptor Rearrangements in Acute Lymphoblastic Leukemia.
Cancer Cell
2016
26546047
Candidate DNA repair susceptibility genes identified by exome sequencing in high-risk pancreatic cancer.
Cancer Lett
2016
26541609
Distinct routes of lineage development reshape the human blood hierarchy across ontogeny.
Science
2016
26590902
Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci.
Carcinogenesis
2016
27732578
A renewed model of pancreatic cancer evolution based on genomic rearrangement patterns.
Nature
2016
27184599
Coming of age: ten years of next-generation sequencing technologies.
Nat Rev Genet
2016
26005866
Spatial genomic heterogeneity within localized, multifocal prostate cancer.
Nat Genet
2015
26647970
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.
Nat Commun
2015
26708082
A cancer cell-line titration series for evaluating somatic classification.
BMC Res Notes
2015
25889765
GLI2 inhibition abrogates human leukemia stem cell dormancy.
J Transl Med
2015
25888698
Optimization of miRNA-seq data preprocessing.
Brief Bioinform
2015
24154973
Identification of genes expressed by immune cells of the colon that are regulated by colorectal cancer-associated variants.
Int J Cancer
2014
25264775
A defining decade in DNA sequencing.
Nat Methods
2014
25240283
Hotspot activating PRKD1 somatic mutations in polymorphous low-grade adenocarcinomas of the salivary glands.
Nat Genet
2014
25049390
Next-generation sequencing identifies rare variants associated with Noonan syndrome.
Proc Natl Acad Sci U S A
2014
25173705
SeqControl: process control for DNA sequencing.
Nat Methods
2014
24825849
Genomic support for a moa-tinamou clade and adaptive morphological convergence in flightless ratites.
Mol Biol Evol
2014
24962202
Genomic testing in cancer: patient knowledge, attitudes, and expectations.
Cancer
2014
24522528
Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia.
Nature
2014
24551080
Use of Sequenom sample ID Plus® SNP genotyping in identification of FFPE tumor samples.
PLoS One
2014
24511469
Antioxidant supplementation reduces genomic aberrations in human induced pluripotent stem cells.
Stem Cell Reports
2014
24728235
A two-dimensional pooling strategy for rare variant detection on next-generation sequencing platforms.
PLoS One
2014
24646301
ShatterProof: operational detection and quantification of chromothripsis.
BMC Bioinformatics
2014
24445778
Robust global microRNA expression profiling using next-generation sequencing technologies.
Lab Invest
2014
24192544
WaveCNV: allele-specific copy number alterations in primary tumors and xenograft models from next-generation sequencing.
Bioinformatics
2014
1 - 50 of 153
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