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Clinicopathogenomic analysis of mismatch repair proficient colorectal adenocarcinoma uncovers novel prognostic subgroups with differing patterns of genetic evolution
David R. Braxton
, Ray Zhang
, Jennifer D. Morrissette
, Arturo Loaiza-Bonilla
, Emma E. Furth
Division of Laboratory and Genomic Medicine
Research output
:
Contribution to journal
›
Article
›
peer-review
16
Scopus citations
Overview
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Dive into the research topics of 'Clinicopathogenomic analysis of mismatch repair proficient colorectal adenocarcinoma uncovers novel prognostic subgroups with differing patterns of genetic evolution'. Together they form a unique fingerprint.
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Keyphrases
Genetic Evolution
100%
Mismatch Repair
100%
Colorectal Adenocarcinoma
100%
Prognostic Groups
100%
FBXW7
60%
PIK3CA
40%
ErbB2
40%
Mutational Event
40%
Tumor
20%
Clinical Outcomes
20%
Clinical Significance
20%
TP53 mutation
20%
Metastasis
20%
Amplicon
20%
Median Progression-free Survival
20%
SMAD4
20%
Hierarchical Clustering
20%
KRAS mutation
20%
Clinical Specimens
20%
Clinicopathologic Data
20%
Neoadjuvant Therapy
20%
Cox Model
20%
FMS-like Tyrosine Kinase 3 (FLT3)
20%
Illumina
20%
Clonal Diversity
20%
Intratumoral Heterogeneity
20%
Somatic Genetics
20%
PIK3CA mutation
20%
APC mutation
20%
Molecular Subtypes
20%
Spatiotemporal Heterogeneity
20%
Late Events
20%
TP53 mutant
20%
TruSeq
20%
Biochemistry, Genetics and Molecular Biology
Genetics
100%
DNA Mismatch Repair
100%
FBXW7
75%
Mitogen-Activated Protein Kinase
50%
Amplicon
25%
KRAS
25%
Progression Free Survival
25%