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Author Details
Full Name
Curtis Gumbs
Affiliation
The University of Texas MD Anderson Cancer Center
ORCID
Career Start Year
1995
Papers
66
H Index
36
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37068116
Comparative Tumor Microenvironment Analysis of Primary and Recurrent Ovarian Granulosa Cell Tumors.
Mol Cancer Res
2023
37593416
Complete loss of <i>TP53</i> and <i>RB1</i> is associated with complex genome and low immune infiltrate in pleomorphic rhabdomyosarcoma.
HGG Adv
2023
37443196
T-prolymphocytic leukemia: TCL1 or MTCP1 rearrangement is not mandatory to establish diagnosis.
Leukemia
2023
35132195
Genetic correlates in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia treated with Hyper-CVAD plus dasatinib or ponatinib.
Leukemia
2022
35512188
Lenalidomide promotes the development of TP53-mutated therapy-related myeloid neoplasms.
Blood
2022
35411096
Correction: Genetic correlates in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia treated with Hyper-CVAD plus dasatinib or ponatinib.
Leukemia
2022
35546239
Immunogenomic intertumor heterogeneity across primary and metastatic sites in a patient with lung adenocarcinoma.
J Exp Clin Cancer Res
2022
35379887
Multi-site desmoplastic small round cell tumors are genetically related and immune-cold.
NPJ Precis Oncol
2022
32856987
Germline DNMT3A mutation in familial acute myeloid leukaemia.
Epigenetics
2021
33552049
Distinct Immunophenotypes of T Cells in Bronchoalveolar Lavage Fluid From Leukemia Patients With Immune Checkpoint Inhibitors-Related Pulmonary Complications.
Front Immunol
2021
34873156
The histologic phenotype of lung cancers is associated with transcriptomic features rather than genomic characteristics.
Nat Commun
2021
34789716
Cold and heterogeneous T cell repertoire is associated with copy number aberrations and loss of immune genes in small-cell lung cancer.
Nat Commun
2021
33980839
Author Correction: Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinoma.
Nat Commun
2021
34115096
Clonal dynamics and clinical implications of postremission clonal hematopoiesis in acute myeloid leukemia.
Blood
2021
33976164
Immune evolution from preneoplasia to invasive lung adenocarcinomas and underlying molecular features.
Nat Commun
2021
33972555
Author Correction: Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics.
Nat Commun
2021
33323402
Cross-Site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms for the CIMAC-CIDC Network.
Clin Cancer Res
2021
33096269
Neoadjuvant Chemotherapy Increases Cytotoxic T Cell, Tissue Resident Memory T Cell, and B Cell Infiltration in Resectable NSCLC.
J Thorac Oncol
2021
32304704
T-Cell Repertoire in Combination with T-Cell Density Predicts Clinical Outcomes in Patients with Merkel Cell Carcinoma.
J Invest Dermatol
2020
32001676
Comprehensive T cell repertoire characterization of non-small cell lung cancer.
Nat Commun
2020
31678224
Immune 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 Phys
2020
33214561
Publisher Correction: Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics.
Nat Commun
2020
32816946
Evolution of Genomic and T-cell Repertoire Heterogeneity of Malignant Pleural Mesothelioma Under Dasatinib Treatment.
Clin Cancer Res
2020
30651532
Late relapse in acute myeloid leukemia (AML): clonal evolution or therapy-related leukemia?
Blood Cancer J
2019
31278276
Multi-region exome sequencing reveals genomic evolution from preneoplasia to lung adenocarcinoma.
Nat Commun
2019
29610390
Genomic profiling of dedifferentiated liposarcoma compared to matched well-differentiated liposarcoma reveals higher genomic complexity and a common origin.
Cold Spring Harb Mol Case Stud
2018
29991687
Integrative genomic analysis of adult mixed phenotype acute leukemia delineates lineage associated molecular subtypes.
Nat Commun
2018
29950560
KMT2D/MLL2 inactivation is associated with recurrence in adult-type granulosa cell tumors of the ovary.
Nat Commun
2018
29702001
Clearance of Somatic Mutations at Remission and the Risk of Relapse in Acute Myeloid Leukemia.
J Clin Oncol
2018
29358183
Clinical implications of cancer gene mutations in patients with chronic lymphocytic leukemia treated with lenalidomide.
Blood
2018
27923552
Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study.
Lancet Oncol
2017
28251903
Integrated molecular analysis of tumor biopsies on sequential CTLA-4 and PD-1 blockade reveals markers of response and resistance.
Sci Transl Med
2017
29296745
Copy number alterations detected as clonal hematopoiesis of indeterminate potential.
Blood Adv
2017
28819565
Genomic and immune heterogeneity are associated with differential responses to therapy in melanoma.
NPJ Genom Med
2017
28733428
TCR Repertoire Intratumor Heterogeneity in Localized Lung Adenocarcinomas: An Association with Predicted Neoantigen Heterogeneity and Postsurgical Recurrence.
Cancer Discov
2017
26871476
Clinical implications of TP53 mutations in myelodysplastic syndromes treated with hypomethylating agents.
Oncotarget
2016
24633157
Recurrent PTPRB and PLCG1 mutations in angiosarcoma.
Nat Genet
2014
25301631
Intratumor heterogeneity in localized lung adenocarcinomas delineated by multiregion sequencing.
Science
2014
22842232
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
Nat Genet
2012
22939633
Using ERDS to infer copy-number variants in high-coverage genomes.
Am J Hum Genet
2012
22863191
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.
Am J Hum Genet
2012
22863189
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Am J Hum Genet
2012
21199653
Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase function.
Gastroenterology
2011
20398883
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet
2010
20838461
The characterization of twenty sequenced human genomes.
PLoS Genet
2010
20577567
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
PLoS Genet
2010
20205591
Host determinants of HIV-1 control in African Americans.
J Infect Dis
2010
20173735
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.
Nature
2010
19812560
CCL3L1 and HIV/AIDS susceptibility.
Nat Med
2009
20041166
Common genetic variation and the control of HIV-1 in humans.
PLoS Genet
2009
1 - 50 of 66
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Elizabeth T Cirulli
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Co-authored papers
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Duke University School of Medicine and Duke Health System
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Jacques Fellay
Ecole Polytechnique Federale de Lausanne
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Alexander J Lazar
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Andrew Berchuck
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