Physician
Pathology
Dr. Mark J. Routbort, MD
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Mark Routbort practices Pathology. He attended Duke University School of Medicine. Duke University School of Medicine is a top medical university. Duke University School of Medicine is ranked 8 in research and 29 in primary care medicine He received 8 awards: "Best Scientific Session Project", "Best Postgraduate Student Project", "Ruth K. Broad Biomedical Research Fellowship", "Alpha Omega Alpha Elected President", "Duke Medical Scientist Training Program Fellow", "Phi Beta Kappa", "Full Tuition Merit Scholarship" and "National Merit Scholar". Dr. Mark J. Routbort is also published. He has 38 publications published. The lastest publication: "Selective inhibition of kindling development by intraventricular administration of TrkB receptor body.' Mark Routbort is registered with Medicare and accepts Medicare payments.
Publications
- Prognostic Factors of Hepatosplenic T-cell Lymphoma: Clinicopathologic Study of 28 Cases.
- Principles of analytical validation of next-generation sequencing based mutational analysis for hematologic neoplasms in a CLIA-certified laboratory.
- Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS.
- IDH1 and IDH2 mutations in myelodysplastic syndromes and role in Disease progression.
- Comparison of Next-generation Sequencing Mutation Profiling With BRAF and IDH1 Mutation-specific Immunohistochemistry.
- Clinical Actionability Enhanced through Deep Targeted Sequencing of Solid Tumors.
- The clinical significance of negative flow cytometry immunophenotypic results in a morphologically scored positive bone marrow in patients following treatment for acut...
- Mutational profiling of therapy-related myelodysplastic syndromes and Acute myeloid leukemia by next generation sequencing, a comparison with de novo diseases.
- Hotspot mutation panel testing reveals clonal evolution in a study of 265 paired primary and metastatic tumors.
- Beyond BRAF(V600): clinical mutation panel testing by next-generation sequencing in advanced melanoma.
- Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours.
- Flow Cytometry Immunophenotypic Findings in Chronic Myelomonocytic Leukemia and Its Utility in Monitoring Treatment Response.
- Quantitative assessment of mutant allele burden in solid tumors by semiconductor-based next-generation sequencing.
- Next-generation sequencing-based multigene mutational screening for Acute myeloid leukemia using MiSeq: applicability for diagnostics and disease monitoring.
- BRAF kinase domain mutations are present in a subset of chronic myelomonocytic Leukemia with wild-type RAS.
- Clinical validation of a next-generation sequencing screen for mutational hotspots in 46 cancer-related genes.
- TET2 mutations, Myelodysplastic features, and a distinct immunoprofile characterize blastic plasmacytoid dendritic cell neoplasm in the bone marrow.
- Next-generation sequencing-based multi-gene mutation profiling of solid tumors using fine needle aspiration samples: promises and challenges for routine clinical diagn...
- Absence of terminal deoxynucleotidyl transferase expression identifies a subset of high-risk adult T-lymphoblastic Leukemia/lymphoma.
- Low rates of hepatitis B virus screening at the onset of chemotherapy.
- Prognostic value of MYC rearrangement in cases of B-cell Lymphoma, unclassifiable, with features intermediate between diffuse large B-cell Lymphoma and Burkitt Lymphoma.
- Tolerance testing of passive radio frequency identification tags for solvent, temperature, and pressure conditions encountered in an anatomic pathology or biorepositor...
- The p53 tumor suppressor network in cancer and the therapeutic modulation of cell death.
- Lymphomas involving the breast: a study of 106 cases comparing localized and disseminated neoplasms.
- Primary adrenal natural killer/T-cell nasal type Lymphoma: first case report in adults.
- Pancreatic and bile duct brushing cytology in 1000 cases: review of findings and comparison of preparation methods.
- Primary pancreatic Lymphoma evaluated by fine-needle aspiration: findings in 14 cases.
- Real-time process "defect" collection within the anatomic pathology laboratory to facilitate informatics driven workflow optimization.
- High frequency of NPM1 gene mutations in Acute myeloid leukemia with prominent nuclear invaginations ("cuplike" nuclei).
- Posttransplant lymphoproliferative disorder after umbilical cord blood transplantation in children.
- Polyclonal IgM anti-GM1 ganglioside antibody in patients with motor neuron Disease and variants.
- Neurovirulence determinants of genetically engineered Theiler viruses.
- Theiler's murine encephalomyelitis virus neutralization escape mutants have a change in Disease phenotype.
- Selective inhibition of kindling development by intraventricular administration of TrkB receptor body.
- Immunohistochemical evidence of seizure-induced activation of trk receptors in the mossy fiber pathway of adult rat hippocampus.
- Seizures, cell death, and mossy fiber sprouting in kainic acid-treated organotypic hippocampal cultures.
- Dyspoietic changes associated with hepatosplenic T-cell Lymphoma are not a manifestation of a myelodysplastic syndrome: analysis of 25 patients.
Schools
Duke University
Conditions Treated
- Acute Leukemia
- Anemia
- Chronic Myeloid Leukemia (CML)
- Deep Vein Thrombosis (DVT)
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Doctors Specialties
- Hematology
- Hematopathology
- Pathology
Accepted Insurances
Awards
- Best Scientific Session Project
- Best Postgraduate Student Project
- Ruth K. Broad Biomedical Research Fellowship
- Alpha Omega Alpha Elected President
- Duke Medical Scientist Training Program Fellow
- Phi Beta Kappa
- Full Tuition Merit Scholarship
- National Merit Scholar
Education
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Duke University Hospital -
Duke University School of Medicine
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1699849133 |
| Last Name Of The Provider | ROUTBORT |
| First Name Of The Provider | MARK |
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