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Author Details
Full Name
Ryan D Morin
Affiliation
Simon Fraser University
ORCID
Career Start Year
2005
Papers
128
H Index
53
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36302166
Molecular determinants of clinical outcomes in a real-world diffuse large B-cell lymphoma population.
Blood
2023
37598282
Exploiting the fibroblast growth factor receptor-1 vulnerability to therapeutically restrict the MYC-EZH2-CDKN1C axis-driven proliferation in Mantle cell lymphoma.
Leukemia
2023
37595057
Comparison of MHG and DZsig reveals shared biology and a core overlap group with inferior prognosis in DLBCL.
Blood Adv
2023
37190862
Long non-coding RNAs associated with transcriptomic signatures and treatment outcome in diffuse large B-cell lymphoma.
Br J Haematol
2023
37319384
Relapse Timing Is Associated With Distinct Evolutionary Dynamics in Diffuse Large B-Cell Lymphoma.
J Clin Oncol
2023
37084389
Genetic subdivisions of follicular lymphoma defined by distinct coding and noncoding mutation patterns.
Blood
2023
36945587
Relapse timing is associated with distinct evolutionary dynamics in DLBCL.
medRxiv
2023
37333387
Multiomic Analysis Identifies a High-Risk Metabolic and TME Depleted Signature that Predicts Early Clinical Failure in DLBCL.
medRxiv
2023
36745874
Emerging roles for heterogeneous ribonuclear proteins in normal and malignant B cells.
Biochem Cell Biol
2023
36701129
PeptideRanger: An R Package to Optimize Synthetic Peptide Selection for Mass Spectrometry Applications.
J Proteome Res
2023
36302254
Concerning data inconsistencies in Burkitt lymphoma genome study.
Blood
2023
34467527
Molecular profiling in diffuse large B-cell lymphoma: why so many types of subtypes?
Br J Haematol
2022
35794478
Super-enhancer hypermutation alters oncogene expression in B cell lymphoma.
Nature
2022
35571031
Combinatorial and Machine Learning Approaches for Improved Somatic Variant Calling From Formalin-Fixed Paraffin-Embedded Genome Sequence Data.
Front Genet
2022
35359007
Shared and distinct genetic features in human and canine B-cell lymphomas.
Blood Adv
2022
36001803
Genomic profiling for clinical decision making in lymphoid neoplasms.
Blood
2022
35963941
Molecular determinants of outcomes in relapsed or refractory mantle cell lymphoma treated with ibrutinib or temsirolimus in the MCL3001 (RAY) trial.
Leukemia
2022
36351924
Single-cell profiling reveals a memory B cell-like subtype of follicular lymphoma with increased transformation risk.
Nat Commun
2022
36219881
Minimal information for reporting a genomics experiment.
Blood
2022
36253470
Author Correction: Super-enhancer hypermutation alters oncogene expression in B cell lymphoma.
Nature
2022
35039569
Mutated RAS-associating proteins and ERK activation in relapse/refractory diffuse large B cell lymphoma.
Sci Rep
2022
32817292
Molecular attributes underlying central nervous system and systemic relapse in diffuse large B-cell lymphoma.
Haematologica
2021
33684939
Characterization of DLBCL with a PMBL gene expression signature.
Blood
2021
33904892
Treating lymphoma is now a bit EZ-er.
Blood Adv
2021
33777047
Mast Cell and Eosinophil Activation Are Associated With COVID-19 and TLR-Mediated Viral Inflammation: Implications for an Anti-Siglec-8 Antibody.
Front Immunol
2021
34644566
Proteotranscriptomic classification and characterization of pancreatic neuroendocrine neoplasms.
Cell Rep
2021
34759290
Indigenous sex-selective salmon harvesting demonstrates pre-contact marine resource management in Burrard Inlet, British Columbia, Canada.
Sci Rep
2021
34704593
Evolutionary conservation of systemic and reversible amyloid aggregation.
J Cell Sci
2021
34625792
Frequent mutations of FBXO11 highlight BCL6 as a therapeutic target in Burkitt lymphoma.
Blood Adv
2021
34323958
Prognostic significance of FCGR2B expression for the response of DLBCL patients to rituximab or obinutuzumab treatment.
Blood Adv
2021
33120427
The impact of MYC and BCL2 structural variants in tumors of DLBCL morphology and mechanisms of false-negative MYC IHC.
Blood
2021
32160292
Coding and noncoding drivers of mantle cell lymphoma identified through exome and genome sequencing.
Blood
2020
32094924
TMEM30A loss-of-function mutations drive lymphomagenesis and confer therapeutically exploitable vulnerability in B-cell lymphoma.
Nat Med
2020
33392514
PRPS-ST: A protocol-agnostic self-training method for gene expression-based classification of blood cancers.
Blood Cancer Discov
2020
32636395
IgCaller for reconstructing immunoglobulin gene rearrangements and oncogenic translocations from whole-genome sequencing in lymphoid neoplasms.
Nat Commun
2020
32619424
TBL1XR1 Mutations Drive Extranodal Lymphoma by Inducing a Pro-tumorigenic Memory Fate.
Cell
2020
32589730
Genetic and evolutionary patterns of treatment resistance in relapsed B-cell lymphoma.
Blood Adv
2020
32724107
Evaluating the quantity, quality and size distribution of cell-free DNA by multiplex droplet digital PCR.
Sci Rep
2020
32151517
Integration of Whole-Genome Sequencing With Circulating Tumor DNA Analysis Captures Clonal Evolution and Tumor Heterogeneity in Non-V600 BRAF Mutant Colorectal Cancer.
Clin Colorectal Cancer
2020
32407529
DLBCL subclassification: divide and conquer?
Blood
2020
32289277
A Probabilistic Classification Tool for Genetic Subtypes of Diffuse Large B Cell Lymphoma with Therapeutic Implications.
Cancer Cell
2020
30472330
A Novel Multiplex Droplet Digital PCR Assay to Identify and Quantify KRAS Mutations in Clinical Specimens.
J Mol Diagn
2019
31671154
Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA.
PLoS One
2019
31527075
The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH.
Blood
2019
31236944
Integrative genomic analysis of matched primary and metastatic pediatric osteosarcoma.
J Pathol
2019
31510674
Collaborative intra-tumor heterogeneity detection.
Bioinformatics
2019
30779047
Ultrasensitive Detection of Circulating Tumor DNA in Lymphoma via Targeted Hybridization Capture and Deep Sequencing of Barcoded Libraries.
Methods Mol Biol
2019
30744412
A high-throughput protocol for isolating cell-free circulating tumor DNA from peripheral blood.
Biotechniques
2019
30705065
Molecular and Genetic Characterization of MHC Deficiency Identifies EZH2 as Therapeutic Target for Enhancing Immune Recognition.
Cancer Discov
2019
30768166
SUBSTRA: Supervised Bayesian Patient Stratification.
Bioinformatics
2019
1 - 50 of 128
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Marco A Marra
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University of British Columbia
Co-authored papers
38
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University of British Columbia
Co-authored papers
30
Andrew J Mungall
Co-authored papers
26
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University of British Columbia
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Canada British Columbia Cancer Research Centre, University of British Columbia
Co-authored papers
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Sohrab P Shah
Memorial Sloan Kettering Cancer Center
Co-authored papers
20
Bruno M Grande
Simon Fraser University
Co-authored papers
19
Richard A Moore
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Robert A Holt
BC Cancer Research Institute
Co-authored papers
10
Malachi Griffith
Washington University
Co-authored papers
9
Lauren C Chong
University of British Columbia
Co-authored papers
9
Ali Bashashati
University of British Columbia
Co-authored papers
8
Samuel Aparicio
University of British Columbia
Co-authored papers
8
Kostiantyn Dreval
Simon Fraser University
Co-authored papers
8
Jacqueline E Schein
Canada British Columbia Cancer Research Centre, University of British Columbia
Co-authored papers
7
Tesa M Severson
Oncode Institute, The Netherlands Cancer Institute
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7
David G Huntsman
University of British Columbia
Co-authored papers
6
Louis M Staudt
National Cancer Institute, National Institutes of Health
Co-authored papers
6
Obi L Griffith
Washington University
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Trevor J Pugh
Princess Margaret Cancer Centre, University Health Network
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