K. Cao

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Aliases
K Cao, Kajia Cao
Publication record
78 papers · 3,179 citations · H-index 24

PAPERS

O11: Mutational spectra of >1000 pediatric acute leukemias and their clinical utility in prognosis, risk stratification, and precision medicine therapeutics
20250 citationsauthor #10
Leveraging genomic diagnostics for prognostics and therapeutics in pediatric acute leukemia
20250 citationsauthor #16
Advances in Inherited Bone Marrow Failure Syndromes
20250 citationsauthor #2
Genomic profiling of pediatric hematologic malignancies and diagnosis of cancer predisposition syndromes: tumor-only versus paired tumor-normal sequencing
20243 citationsauthor #21
P588: Identification of NF1-associated tumor mutations in plasma cfDNA and its clinical application
20230 citationsauthor #4
Uncovering the Genetic Etiology of Inherited Bone Marrow Failure Syndromes Using a Custom-designed Next Generation Sequencing Panel.
20234 citationsauthor #2
Model performance and interpretability of semi-supervised generative adversarial networks to predict oncogenic variants with unlabeled data
20237 citationsauthor #3
Comprehensive Gene Panel Testing for Hearing Loss in Children: Understanding Factors Influencing Diagnostic Yield.
202311 citationsauthor #19
Cancer Predisposition Genetic Testing Among Children with Hematologic Malignancies
20230 citationsauthor #16
134. Novel fusions in aggressive infant sarcomas: Expanding the scope of 'CIC-rearranged' sarcoma without CIC rearrangement
20220 citationsauthor #6
Correction: Model performance and interpretability of semi-supervised generative adversarial networks to predict oncogenic variants with unlabeled data
20220 citationsauthor #3
eP288: Genomic characterization of a TP53 tandem duplication in a pediatric patient with Li-Fraumeni syndrome
20220 citationsauthor #7
Abstract 5268: The spectrum of FGFR mutations in pediatric and young adult solid tumor
20220 citationsauthor #8
Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma
202211 citationsauthor #7
Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma
20222 citationsauthor #7
eP313: Too few or too many? Variant reporting burden and diagnostic comparisons of an extensive gene panel with exome-sequencing in immunodeficiency
20220 citationsauthor #2
A novel TP53 tandem duplication in a child with Li–Fraumeni syndrome
20223 citationsauthor #9
Molecular Diagnostic Outcomes from 700 Cases
20227 citationsauthor #11
CancerVar: An artificial intelligence–empowered platform for clinical interpretation of somatic mutations in cancer
202239 citationsauthor #3
Best Practice for Clinical Somatic Variant Interpretation and Reporting.
20221 citationsauthor #4
Genomic analysis of early-stage lung cancer reveals a role for TP53 mutations in distant metastasis
202216 citationsauthor #29
Genomic characterization of 747 pediatric hematological malignancies
20210 citationsauthor #10
Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease.
202114 citationsauthor #7
Clinical impact of genomic characterization of 15 patients with acute megakaryoblastic leukemia–related malignancies
20216 citationsauthor #4
29. When amplification meets gene fusion: Molecular characterization of PPP1CB-ALK fusion and amplification in pediatric HGG
20200 citationsauthor #8
Clinical significance of serial tumor next generation sequencing (NGS) in 155 pediatric cancer patients.
20201 citationsauthor #11
64. Characterization of BCOR ITD in pediatric solid tumors using targeted NGS panel and whole transcriptome sequencing
20200 citationsauthor #5
Genomic characterization of a PPP1CB-ALK fusion with fusion gene amplification in a congenital glioblastoma.
202010 citationsauthor #8
A germline PALB2 pathogenic variant identified in a pediatric high-grade glioma
20202 citationsauthor #6
Using Machine Learning to Identify True Somatic Variants from Next-Generation Sequencing
20199 citationsauthor #5
Variant Interpretation for Cancer (VIC): a computational tool for assessing clinical impacts of somatic variants
201944 citationsauthor #7
Development and Clinical Validation of a Large Fusion Gene Panel for Pediatric Cancers.
201950 citationsauthor #3
Use of a Dynamic Genetic Testing Approach for Childhood-Onset Epilepsy
201955 citationsauthor #5
Automated Clinical Exome Reanalysis Reveals Novel Diagnoses.
201978 citationsauthor #18
26. Uncovering the genetic etiology of inherited bone marrow failure syndromes using a custom-designed NGS panel
20190 citationsauthor #3
Clinical utility of custom-designed NGS panel testing in pediatric tumors
201998 citationsauthor #4
Famitinib in combination with concurrent chemoradiotherapy in patients with locoregionally advanced nasopharyngeal carcinoma: a phase 1, open-label, dose-escalation Study
201824 citationsauthor #25
Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data
20180 citationsauthor #3
Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach
201816 citationsauthor #7
Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data
20180 citationsauthor #3
22. Clinical utility of integrated genomic profiling in pediatric brain tumor
20180 citationsauthor #6
Correction: Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data
201815 citationsauthor #3
Development and validation of an endoscopic images-based deep learning model for detection with nasopharyngeal malignancies
201876 citationsauthor #11
Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data
201831 citationsauthor #3
AUDIOME: a tiered exome sequencing–based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss
201834 citationsauthor #3
Molecular Diagnosis of Mosaic Overgrowth Syndromes Using a Custom-Designed Next-Generation Sequencing Panel.
201742 citationsauthor #6
WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features.
201753 citationsauthor #11
Novel findings with reassessment of exome data: implications for validation testing and interpretation of genomic data
20170 citationsauthor #3
Clinical Utility of Integrated Genomic Profiling in Pediatric Leukemia
20170 citationsauthor #5
BCL 2 Translocation Defines a Unique Tumor Subset within the Germinal Center B-Cell-Like Diffuse Large B-Cell Lymphoma
201613 citationsauthor #9
Phenotypic predictors and final diagnoses in patients referred for RASopathy testing by targeted next-generation sequencing
201621 citationsauthor #5
Combination of 12-O-tetradecanoylphorbol-13-acetate with diethyldithiocarbamate markedly inhibits pancreatic cancer cell growth in 3D culture and in immunodeficient mice
20158 citationsauthor #2
Exome sequencing expands the mechanism of SOX5‐associated intellectual disability: A case presentation with review of sox‐related disorders
201539 citationsauthor #8
H3K36 methylation promotes longevity by enhancing transcriptional fidelity
2015203 citationsauthor #8
Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints
2014107 citationsauthor #5
Inactivation of yeast Isw2 chromatin remodeling enzyme mimics longevity effect of calorie restriction via induction of genotoxic stress response.
201477 citationsauthor #5
Mung Bean Nuclease Treatment Increases Capture Specificity of Microdroplet-PCR Based Targeted DNA Enrichment
20141 citationsauthor #2
Potent obatoclax cytotoxicity and activation of triple death mode killing across infant acute lymphoblastic leukemia.
201364 citationsauthor #7
Cellular, synaptic, and biochemical features of resilient cognition in Alzheimer's disease.
2013114 citationsauthor #3
Analysis of Nonlinear Gene Expression Progression Reveals Extensive Pathway and Age-Specific Transitions in Aging Human Brains
20136 citationsauthor #1
Lamin B1 depletion in senescent cells triggers large-scale changes in gene expression and the chromatin landscape
2013506 citationsauthor #6
Yeast Aging Proteome Unveiled a Novel Aging Regulation Pathway Mediated by the Chromatin Remodeling Complex ISW2
20120 citationsauthor #4
Quantification detection and clinical significance of plasma Epstein-Barr virus DNA in metastatic nasopharyngeal Carcinoma
20120 citationsauthor #2
Computational detection and analysis of sequences with duplex-derived interstrand G-quadruplex forming potential.
201221 citationsauthor #1
The microRNA miR-34 modulates aging and neurodegeneration in Drosophila
2012383 citationsauthor #3
Age-Correlated Gene Expression in Normal and Neurodegenerative Human Brain Tissues
201038 citationsauthor #1
Infant Acute Lymphoblastic Leukemias Are Pan-Sensitive to Obatoclax Across molecular/Cytogenetic Subtypes, Especially MLL-ENL, and gene Expression Profiles Determine Obatoclax IC50: A Report on the Children's Oncology Group (COG) P9407 Trial
20101 citationsauthor #8
Genome-Wide Double-Stranded RNA Sequencing Reveals the Functional Significance of Base-Paired RNAs in Arabidopsis
2010148 citationsauthor #7
An efficient algorithm for identification of real belief measures
20090 citationsauthor #2
Genomic analyses reveal global functional alterations that promote tumor growth and novel tumor suppressor genes in natural killer-cell malignancies
2009204 citationsauthor #10
Altered gene expression in the Werner and Bloom syndromes is associated with sequences having G-quadruplex forming potential
2009152 citationsauthor #2
Age Is the Strongest Determinant of Leukemia Blast Cell Gene Expression in MLL -Rearranged Infant ALL and MLL-AF4 Directs a Distinct Gene Expression Profile Related to CNS Disease.
20080 citationsauthor #2
Belief Combination for Uncertainty Reduction in Microarray Gene Expression Pattern Analysis
20073 citationsauthor #1
Integrative pattern recognition techniques and their applications to microarray gene profiling data analysis
20070 citationsauthor #1
A trend pattern assessment approach to microarray gene expression profiling data analysis
20072 citationsauthor #1
Algorithmic fusion of gene expression profiling for diffuse large B-cell lymphoma outcome prediction
200422 citationsauthor #3
On the Alleviation of Side Effect of Outliers to Fisher's Discriminate Criterion in Micro-Array Data Analysis
20040 citationsauthor #1
BCL2 translocation defines a unique tumor subset within the germinal center B-cell-like diffuse large B-cell lymphoma.
2004284 citationsauthor #9

TIMELINE

2004 306 citations

2007 5 citations

2008 0 citations

2009 356 citations

2010 187 citations

2012 404 citations

2013 690 citations

2014 185 citations

2015 250 citations

2016 34 citations

2017 95 citations

2018 196 citations

2019 334 citations

2020 13 citations

2021 20 citations

2022 79 citations

2023 22 citations

2024 3 citations

2025 0 citations

COAUTHOR MAP

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