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Author Details
Full Name
John V Pearson
Affiliation
QIMR Berghofer Medical Research Institute
ORCID
Career Start Year
1996
Papers
101
H Index
46
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36757207
Efficient detection and monitoring of pediatric brain malignancies with liquid biopsy based on patient-specific somatic mutation screening.
Neuro Oncol
2023
36656928
Heritable defects in telomere and mitotic function selectively predispose to sarcomas.
Science
2023
37149669
Generalising uncertainty improves accuracy and safety of deep learning analytics applied to oncology.
Sci Rep
2023
36757207
Efficient detection and monitoring of pediatric brain malignancies with liquid biopsy based on patient-specific somatic mutation screening.
Neuro Oncol
2023
36868206
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.
Am J Hum Genet
2023
37149669
Generalising uncertainty improves accuracy and safety of deep learning analytics applied to oncology.
Sci Rep
2023
36656928
Heritable defects in telomere and mitotic function selectively predispose to sarcomas.
Science
2023
36868206
Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare.
Am J Hum Genet
2023
35012638
Patient-derived xenograft models capture genomic heterogeneity in endometrial cancer.
Genome Med
2022
36098958
Comparative Genomics Provides Etiologic and Biological Insight into Melanoma Subtypes.
Cancer Discov
2022
36291058
Identifying Candidate Circulating RNA Markers for Coronary Artery Disease by Deep RNA-Sequencing in Human Plasma.
Cells
2022
36095262
Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions.
Hum Mutat
2022
36222710
Gene-Expression Profiling of Mucinous Ovarian Tumors and Comparison with Upper and Lower Gastrointestinal Tumors Identifies Markers Associated with Adverse Outcomes.
Clin Cancer Res
2022
35637530
Comprehensive genomic and tumour immune profiling reveals potential therapeutic targets in malignant pleural mesothelioma.
Genome Med
2022
36332611
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.
Am J Hum Genet
2022
35355015
Anatomic position determines oncogenic specificity in melanoma.
Nature
2022
35849877
Comparison of actionable events detected in cancer genomes by whole-genome sequencing, in silico whole-exome and mutation panels.
ESMO Open
2022
36699384
qmotif: determination of telomere content from whole-genome sequence data.
Bioinform Adv
2022
35012638
Patient-derived xenograft models capture genomic heterogeneity in endometrial cancer.
Genome Med
2022
34951955
Multiomic profiling of checkpoint inhibitor-treated melanoma: Identifying predictors of response and resistance, and markers of biological discordance.
Cancer Cell
2022
35637530
Comprehensive genomic and tumour immune profiling reveals potential therapeutic targets in malignant pleural mesothelioma.
Genome Med
2022
35849877
Comparison of actionable events detected in cancer genomes by whole-genome sequencing, in silico whole-exome and mutation panels.
ESMO Open
2022
35355015
Anatomic position determines oncogenic specificity in melanoma.
Nature
2022
36699384
qmotif: determination of telomere content from whole-genome sequence data.
Bioinform Adv
2022
36332611
Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.
Am J Hum Genet
2022
36098958
Comparative Genomics Provides Etiologic and Biological Insight into Melanoma Subtypes.
Cancer Discov
2022
36095262
Analysis of hereditary cancer gene variant classifications from ClinVar indicates a need for regular reassessment of clinical assertions.
Hum Mutat
2022
36291058
Identifying Candidate Circulating RNA Markers for Coronary Artery Disease by Deep RNA-Sequencing in Human Plasma.
Cells
2022
36222710
Gene-Expression Profiling of Mucinous Ovarian Tumors and Comparison with Upper and Lower Gastrointestinal Tumors Identifies Markers Associated with Adverse Outcomes.
Clin Cancer Res
2022
34951955
Multiomic profiling of checkpoint inhibitor-treated melanoma: Identifying predictors of response and resistance, and markers of biological discordance.
Cancer Cell
2022
34579788
Deep learning in cancer diagnosis, prognosis and treatment selection.
Genome Med
2021
33811161
Radiomics Biomarkers Correlate with CD8 Expression and Predict Immune Signatures in Melanoma Patients.
Mol Cancer Res
2021
33514769
Verifying explainability of a deep learning tissue classifier trained on RNA-seq data.
Sci Rep
2021
33600021
Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a model.
Hum Mutat
2021
33917078
Tumor Signature Analysis Implicates Hereditary Cancer Genes in Endometrial Cancer Development.
Cancers (Basel)
2021
34579788
Deep learning in cancer diagnosis, prognosis and treatment selection.
Genome Med
2021
34732514
Ask the people: developing guidelines for genomic research with Aboriginal and Torres Strait Islander peoples.
BMJ Glob Health
2021
33600021
Considerations for using population frequency data in germline variant interpretation: Cancer syndrome genes as a model.
Hum Mutat
2021
33514769
Verifying explainability of a deep learning tissue classifier trained on RNA-seq data.
Sci Rep
2021
33811161
Radiomics Biomarkers Correlate with CD8 Expression and Predict Immune Signatures in Melanoma Patients.
Mol Cancer Res
2021
33917078
Tumor Signature Analysis Implicates Hereditary Cancer Genes in Endometrial Cancer Development.
Cancers (Basel)
2021
34732514
Ask the people: developing guidelines for genomic research with Aboriginal and Torres Strait Islander peoples.
BMJ Glob Health
2021
32384699
<i>APC</i> Mutation Marks an Aggressive Subtype of <i>BRAF</i> Mutant Colorectal Cancers.
Cancers (Basel)
2020
32415113
Whole genome landscapes of uveal melanoma show an ultraviolet radiation signature in iris tumours.
Nat Commun
2020
31935636
Alterations in signaling pathways that accompany spontaneous transition to malignancy in a mouse model of BRAF mutant microsatellite stable colorectal cancer.
Neoplasia
2020
32384699
<i>APC</i> Mutation Marks an Aggressive Subtype of <i>BRAF</i> Mutant Colorectal Cancers.
Cancers (Basel)
2020
32818150
Using whole-genome sequencing data to derive the homologous recombination deficiency scores.
NPJ Breast Cancer
2020
32917657
Tumor Mutation Burden and Structural Chromosomal Aberrations Are Not Associated with T-cell Density or Patient Survival in Acral, Mucosal, and Cutaneous Melanomas.
Cancer Immunol Res
2020
33067454
Whole-genome sequencing of acral melanoma reveals genomic complexity and diversity.
Nat Commun
2020
31935636
Alterations in signaling pathways that accompany spontaneous transition to malignancy in a mouse model of BRAF mutant microsatellite stable colorectal cancer.
Neoplasia
2020
1 - 50 of 202
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Ann-Marie Patch
QIMR Berghofer Medical Research Institute
Co-authored papers
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Co-authored papers
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Co-authored papers
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Co-authored papers
15
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Garvan Institute of Medical Research and The Kinghorn Cancer Centre
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13
Mark J Cowley
Children's Cancer Institute, Lowy Cancer Research Centre
Co-authored papers
12
Eric M Reiman
Banner Alzheimer's Institute
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Georgina V Long
Co-authored papers
10
Peter T Simpson
UQ Centre for Clinical Research, The University of Queensland
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9
Sunil R Lakhani
University of Queensland
Co-authored papers
8
Szabolcs Szelinger
College of American Pathologists
Co-authored papers
8
Nikolajs Zeps
Queensland University of Technology
Co-authored papers
8
Amanda B Spurdle
QIMR Berghofer Medical Research Institute
Co-authored papers
7
William A Robinson
National Centre for Asbestos Related Diseases, University of Western Australia
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David A Wheeler
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Paul Harnett
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