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Author Details

Curtis Gumbs
The University of Texas MD Anderson Cancer Center
1995
66
36
PMIDPaper TitleJournal TitlePublished Year
37068116Comparative Tumor Microenvironment Analysis of Primary and Recurrent Ovarian Granulosa Cell Tumors.Mol Cancer Res2023
37593416Complete loss of <i>TP53</i> and <i>RB1</i> is associated with complex genome and low immune infiltrate in pleomorphic rhabdomyosarcoma.HGG Adv2023
37443196T-prolymphocytic leukemia: TCL1 or MTCP1 rearrangement is not mandatory to establish diagnosis.Leukemia2023
35132195Genetic correlates in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia treated with Hyper-CVAD plus dasatinib or ponatinib.Leukemia2022
35512188Lenalidomide promotes the development of TP53-mutated therapy-related myeloid neoplasms.Blood2022
35411096Correction: Genetic correlates in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia treated with Hyper-CVAD plus dasatinib or ponatinib.Leukemia2022
35546239Immunogenomic intertumor heterogeneity across primary and metastatic sites in a patient with lung adenocarcinoma.J Exp Clin Cancer Res2022
35379887Multi-site desmoplastic small round cell tumors are genetically related and immune-cold.NPJ Precis Oncol2022
32856987Germline DNMT3A mutation in familial acute myeloid leukaemia.Epigenetics2021
33552049Distinct Immunophenotypes of T Cells in Bronchoalveolar Lavage Fluid From Leukemia Patients With Immune Checkpoint Inhibitors-Related Pulmonary Complications.Front Immunol2021
34873156The histologic phenotype of lung cancers is associated with transcriptomic features rather than genomic characteristics.Nat Commun2021
34789716Cold and heterogeneous T cell repertoire is associated with copy number aberrations and loss of immune genes in small-cell lung cancer.Nat Commun2021
33980839Author Correction: Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinoma.Nat Commun2021
34115096Clonal dynamics and clinical implications of postremission clonal hematopoiesis in acute myeloid leukemia.Blood2021
33976164Immune evolution from preneoplasia to invasive lung adenocarcinomas and underlying molecular features.Nat Commun2021
33972555Author Correction: Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics.Nat Commun2021
33323402Cross-Site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms for the CIMAC-CIDC Network.Clin Cancer Res2021
33096269Neoadjuvant Chemotherapy Increases Cytotoxic T Cell, Tissue Resident Memory T Cell, and B Cell Infiltration in Resectable NSCLC.J Thorac Oncol2021
32304704T-Cell Repertoire in Combination with T-Cell Density Predicts Clinical Outcomes in Patients with Merkel Cell Carcinoma.J Invest Dermatol2020
32001676Comprehensive T cell repertoire characterization of non-small cell lung cancer.Nat Commun2020
31678224Immune and Circulating Tumor DNA Profiling After Radiation Treatment for Oligometastatic Non-Small Cell Lung Cancer: Translational Correlatives from a Mature Randomized Phase II Trial.Int J Radiat Oncol Biol Phys2020
33214561Publisher Correction: Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics.Nat Commun2020
32816946Evolution of Genomic and T-cell Repertoire Heterogeneity of Malignant Pleural Mesothelioma Under Dasatinib Treatment.Clin Cancer Res2020
30651532Late relapse in acute myeloid leukemia (AML): clonal evolution or therapy-related leukemia?Blood Cancer J2019
31278276Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinoma.Nat Commun2019
29610390Genomic profiling of dedifferentiated liposarcoma compared to matched well-differentiated liposarcoma reveals higher genomic complexity and a common origin.Cold Spring Harb Mol Case Stud2018
29991687Integrative genomic analysis of adult mixed phenotype acute leukemia delineates lineage associated molecular subtypes.Nat Commun2018
29950560KMT2D/MLL2 inactivation is associated with recurrence in adult-type granulosa cell tumors of the ovary.Nat Commun2018
29702001Clearance of Somatic Mutations at Remission and the Risk of Relapse in Acute Myeloid Leukemia.J Clin Oncol2018
29358183Clinical implications of cancer gene mutations in patients with chronic lymphocytic leukemia treated with lenalidomide.Blood2018
27923552Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study.Lancet Oncol2017
28251903Integrated molecular analysis of tumor biopsies on sequential CTLA-4 and PD-1 blockade reveals markers of response and resistance.Sci Transl Med2017
29296745Copy number alterations detected as clonal hematopoiesis of indeterminate potential.Blood Adv2017
28819565Genomic and immune heterogeneity are associated with differential responses to therapy in melanoma.NPJ Genom Med2017
28733428TCR Repertoire Intratumor Heterogeneity in Localized Lung Adenocarcinomas: An Association with Predicted Neoantigen Heterogeneity and Postsurgical Recurrence.Cancer Discov2017
26871476Clinical implications of TP53 mutations in myelodysplastic syndromes treated with hypomethylating agents.Oncotarget2016
24633157Recurrent PTPRB and PLCG1 mutations in angiosarcoma.Nat Genet2014
25301631Intratumor heterogeneity in localized lung adenocarcinomas delineated by multiregion sequencing.Science2014
22842232De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.Nat Genet2012
22939633Using ERDS to infer copy-number variants in high-coverage genomes.Am J Hum Genet2012
22863191Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.Am J Hum Genet2012
22863189Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.Am J Hum Genet2012
21199653Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase function.Gastroenterology2011
20398883Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.Am J Hum Genet2010
20838461The characterization of twenty sequenced human genomes.PLoS Genet2010
20577567Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.PLoS Genet2010
20205591Host determinants of HIV-1 control in African Americans.J Infect Dis2010
20173735ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.Nature2010
19812560CCL3L1 and HIV/AIDS susceptibility.Nat Med2009
20041166Common genetic variation and the control of HIV-1 in humans.PLoS Genet2009
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Collaborators

The University of Texas MD Anderson Cancer Center
Co-authored papers 46
University of Texas MD Anderson Cancer Center
Co-authored papers 28
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Co-authored papers 18
Institute for Genomic Medicine, Columbia University Irving Medical Center
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Co-authored papers 13
University of Texas M.D. Anderson Cancer Center
Co-authored papers 12
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UT MD Anderson Cancer Center
Co-authored papers 10
Duke University
Co-authored papers 8
Imperial College London
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Co-authored papers 7
Duke University School of Medicine and Duke Health System
Co-authored papers 7
Ecole Polytechnique Federale de Lausanne
Co-authored papers 7
The University of Texas MD Anderson Cancer Center
Co-authored papers 6
Duke School of Medicine
Co-authored papers 6
University of North Carolina at Chapel Hill.
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Eshelman School of Pharmacy, University of North Carolina
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Georgia Cancer Center
Co-authored papers 5
UCL Institute of Neurology
Co-authored papers 5
Foundation Medicine
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University of Texas M.D. Anderson Cancer Center
Co-authored papers 4
Hopital Universitaire de Bruxelles - Hopital Erasme
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Frederick National Laboratory for Cancer Research, National Cancer Institute
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