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Author Details
Full Name
Mark J Routbort
Affiliation
University of Texas MD Anderson Cancer Center
ORCID
Career Start Year
1989
Papers
161
H Index
45
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37981812
<i>STAT5B</i> mutations in myeloid neoplasms differ by disease subtypes but characterize a subset of chronic myeloid neoplasms with eosinophilia and/or basophilia.
Haematologica
2024
37747438
Detection of clinically actionable gene fusions by next-generation sequencing-based RNA sequencing of non-small cell lung cancer cytology specimens: A single-center experience with comparison to fluorescence in situ hybridization.
Cancer Cytopathol
2024
36244574
Recommendations for the Use of in Silico Approaches for Next-Generation Sequencing Bioinformatic Pipeline Validation: A Joint Report of the Association for Molecular Pathology, Association for Pathology Informatics, and College of American Pathologists.
J Mol Diagn
2023
37547448
PTEN in triple-negative breast carcinoma: protein expression and genomic alteration in pretreatment and posttreatment specimens.
Ther Adv Med Oncol
2023
37322121
The NCI-MATCH trial: lessons for precision oncology.
Nat Med
2023
37154083
DDX41 mutations in patients with non-myeloid hematologic neoplasms.
Am J Hematol
2023
36755027
Efficacy and clinicogenomic correlates of response to immune checkpoint inhibitors alone or with chemotherapy in non-small cell lung cancer.
Nat Commun
2023
34775472
Myelodysplastic/myeloproliferative neoplasms-unclassifiable with isolated isochromosome 17q represents a distinct clinico-biologic subset: a multi-institutional collaborative study from the Bone Marrow Pathology Group.
Mod Pathol
2022
35353553
Actionable Tumor Alterations and Treatment Protocol Enrollment of Pediatric and Young Adult Patients With Refractory Cancers in the National Cancer Institute-Children's Oncology Group Pediatric MATCH Trial.
J Clin Oncol
2022
35504958
Immunohistochemical loss of enhancer of Zeste Homolog 2 (EZH2) protein expression correlates with EZH2 alterations and portends a worse outcome in myelodysplastic syndromes.
Mod Pathol
2022
35467000
Distinct Gene Mutations Are Associated With Clinicopathologic Features in Urachal Carcinoma.
Am J Clin Pathol
2022
35430388
Landscape of NOTCH1 mutations and co-occurring biomarker alterations in chronic lymphocytic leukemia.
Leuk Res
2022
35820397
Poziotinib for EGFR exon 20-mutant NSCLC: Clinical efficacy, resistance mechanisms, and impact of insertion location on drug sensitivity.
Cancer Cell
2022
35690645
Clinicopathologic spectrum of myeloid neoplasms with concurrent myeloproliferative neoplasm driver mutations and SRSF2 mutations.
Mod Pathol
2022
35390143
TP53 copy number and protein expression inform mutation status across risk categories in acute myeloid leukemia.
Blood
2022
36671709
Concurrent Mutations in <i>SF3B1</i> and <i>PHF6</i> in Myeloid Neoplasms.
Biology (Basel)
2022
36230473
Clinical Testing for Mismatch Repair in Neoplasms Using Multiple Laboratory Methods.
Cancers (Basel)
2022
35977347
Impact of Somatic Mutations on Survival Outcomes in Patients With Anaplastic Thyroid Carcinoma.
JCO Precis Oncol
2022
34903824
Correction to: Myelodysplastic/myeloproliferative neoplasms-unclassifiable with isolated isochromosome 17q represents a distinct clinico-biologic subset: a multi-institutional collaborative study from the Bone Marrow Pathology Group.
Mod Pathol
2022
34992253
Acquired WT1 mutations contribute to relapse of NPM1-mutated acute myeloid leukemia following allogeneic hematopoietic stem cell transplant.
Bone Marrow Transplant
2022
34989420
Non-coding NOTCH1 mutations in chronic lymphocytic leukemia negatively impact prognosis.
Am J Hematol
2022
32667737
Determination of immunophenotypic aberrancies provides better assessment of peripheral blood involvement by mycosis fungoides/Sézary syndrome than quantification of CD26- or CD7- CD4+ T-cells.
Cytometry B Clin Cytom
2021
33493304
Factors Impacting Clinically Relevant RNA Fusion Assays Using Next-Generation Sequencing.
Arch Pathol Lab Med
2021
33677472
Evolutionary action score identifies a subset of TP53 mutated myelodysplastic syndrome with favorable prognosis.
Blood Cancer J
2021
33585199
Next-Generation Sequencing of <i>DDX41</i> in Myeloid Neoplasms Leads to Increased Detection of Germline Alterations.
Front Oncol
2021
34161603
Only SF3B1 mutation involving K700E independently predicts overall survival in myelodysplastic syndromes.
Cancer
2021
33109741
Development and Validation of a Gene Signature Classifier for Consensus Molecular Subtyping of Colorectal Carcinoma in a CLIA-Certified Setting.
Clin Cancer Res
2021
33450747
An Overview of Characteristics of Clinical Next-Generation Sequencing-Based Testing for Hematologic Malignancies.
Arch Pathol Lab Med
2021
33119213
Utilization of cytology smears improves success rates of RNA-based next-generation sequencing gene fusion assays for clinically relevant predictive biomarkers.
Cancer Cytopathol
2021
32856987
Germline DNMT3A mutation in familial acute myeloid leukaemia.
Epigenetics
2021
31400013
Successful lenalidomide treatment in high risk myelodysplastic syndrome with germline DDX41 mutation.
Am J Hematol
2020
31986076
Proficiency Testing of Standardized Samples Shows High Interlaboratory Agreement for Clinical Next Generation Sequencing-Based Hematologic Malignancy Assays With Survey Material-Specific Differences in Variant Frequencies.
Arch Pathol Lab Med
2020
31922567
The Molecular Analysis for Therapy Choice (NCI-MATCH) Trial: Lessons for Genomic Trial Design.
J Natl Cancer Inst
2020
31804006
RAS and TP53 can predict survival in adults with T-cell lymphoblastic leukemia treated with hyper-CVAD.
Cancer Med
2020
32005111
Simplified molecular classification of lung adenocarcinomas based on EGFR, KRAS, and TP53 mutations.
BMC Cancer
2020
32848129
Clinicopathological characterization of chronic lymphocytic leukemia with MYD88 mutations: L265P and non-L265P mutations are associated with different features.
Blood Cancer J
2020
33022638
A Cryptic BCR-PDGFRB Fusion Resulting in a Chronic Myeloid Neoplasm With Monocytosis and Eosinophilia: A Novel Finding With Treatment Implications.
J Natl Compr Canc Netw
2020
32183953
Pan-Cancer Landscape and Analysis of ERBB2 Mutations Identifies Poziotinib as a Clinically Active Inhibitor and Enhancer of T-DM1 Activity.
Cancer Cell
2020
32112433
Outcomes of acute myeloid leukemia with myelodysplasia related changes depend on diagnostic criteria and therapy.
Am J Hematol
2020
32238878
Clinico-pathologic characteristics and outcomes of the World Health Organization (WHO) provisional entity de novo acute myeloid leukemia with mutated RUNX1.
Mod Pathol
2020
31211490
Low-Grade Myelodysplastic Syndromes with Preserved CD34+ B-Cell Precursors (CD34+ Hematogones).
Cytometry B Clin Cytom
2020
30508305
Targeted multigene deep sequencing of Bruton tyrosine kinase inhibitor-resistant chronic lymphocytic leukemia with disease progression and Richter transformation.
Cancer
2019
35100667
Validation of <i>HER2</i> Amplification as a Predictive Biomarker for Anti-Epidermal Growth Factor Receptor Antibody Therapy in Metastatic Colorectal Cancer.
JCO Precis Oncol
2019
31648317
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.
Blood Adv
2019
32914014
Germline Genetic Predisposition to Myeloid Neoplasia From <i>GATA2</i> Gene Mutations: Lessons Learned From Two Cases.
JCO Precis Oncol
2019
32923865
Targeting <i>ERBB2</i> (<i>HER2</i>) Amplification Identified by Next-Generation Sequencing in Patients With Advanced or Metastatic Solid Tumors Beyond Conventional Indications.
JCO Precis Oncol
2019
30171025
Persistent <i>IDH1/2</i> mutations in remission can predict relapse in patients with acute myeloid leukemia.
Haematologica
2019
31588020
Pan-Cancer Landscape and Analysis of ERBB2 Mutations Identifies Poziotinib as a Clinically Active Inhibitor and Enhancer of T-DM1 Activity.
Cancer Cell
2019
31243771
Association of gene mutations with time-to-first treatment in 384 treatment-naive chronic lymphocytic leukaemia patients.
Br J Haematol
2019
31497255
Correction: A feasibility study of returning clinically actionable somatic genomic alterations identified in a research laboratory.
Oncotarget
2019
1 - 50 of 161
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row(s) 1 - 30 of 30
Collaborators
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The University of Texas MD Anderson Cancer Center
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MD Anderson Cancer Center
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Courtney D DiNardo
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Farhad Ravandi
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Kenna R Mills Shaw
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Scott Kopetz
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Gordon B Mills
Knight Cancer Institute, Oregon Health and Sciences University
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13
Alexander J Lazar
The University of Texas MD Anderson Cancer Center
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Ken Chen
University of Texas MD Anderson Cancer Center
Co-authored papers
11
Kenneth Aldape
National Cancer Institute
Co-authored papers
10
Michael A Davies
The University of Texas MD Anderson Cancer Center
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Pei Lin
Co-authored papers
7
Jorge Cortes
Georgia Cancer Center
Co-authored papers
6
Rakesh Nagarajan
Current or past members of the College of American Pathologists
Co-authored papers
5
Elmer V Bernstam
The University of Texas Health Science Center at Houston
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Gautam Borthakur
MD Anderson Cancer Center
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Anthony J Iafrate
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Yuan Qi
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