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Author Details
Full Name
Cyriac Kandoth
Affiliation
University of California los angeles
ORCID
Career Start Year
2008
Papers
42
H Index
32
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35148171
Genome Nexus: A Comprehensive Resource for the Annotation and Interpretation of Genomic Variants in Cancer.
JCO Clin Cancer Inform
2022
34103301
Recurrent Mutations in Cyclin D3 Confer Clinical Resistance to FLT3 Inhibitors in Acute Myeloid Leukemia.
Clin Cancer Res
2021
31763684
Poor survival after resection of early gastric cancer: extremes of survivorship analysis reveal distinct genomic profile.
Br J Surg
2020
30537484
GNAQ Mutations in Diffuse and Solitary Choroidal Hemangiomas.
Ophthalmology
2019
30427539
Regional differences in gallbladder cancer pathogenesis: Insights from a multi-institutional comparison of tumor mutations.
Cancer
2019
29316429
Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.
Cancer Cell
2018
30053901
Integrative omics analyses broaden treatment targets in human cancer.
Genome Med
2018
30205045
The Genomic Landscape of Endocrine-Resistant Advanced Breast Cancers.
Cancer Cell
2018
30064973
Genetic and epigenetic evolution as a contributor to WT1-mutant leukemogenesis.
Blood
2018
29625050
Oncogenic Signaling Pathways in The Cancer Genome Atlas.
Cell
2018
29625057
Tumor Evolution and Drug Response in Patient-Derived Organoid Models of Bladder Cancer.
Cell
2018
29596782
Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.
Cell Syst
2018
29247016
Accelerating Discovery of Functional Mutant Alleles in Cancer.
Cancer Discov
2018
28810145
Integrative Analysis Identifies Four Molecular and Clinical Subsets in Uveal Melanoma.
Cancer Cell
2017
26619011
Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.
Nat Biotechnol
2016
25592567
Integrative genome-wide analysis of the determinants of RNA splicing in kidney renal clear cell carcinoma.
Pac Symp Biocomput
2015
26647970
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing.
Nat Commun
2015
26451490
Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer.
Cell
2015
26689913
Patterns and functional implications of rare germline variants across 12 cancer types.
Nat Commun
2015
26158448
Genome Modeling System: A Knowledge Management Platform for Genomics.
PLoS Comput Biol
2015
26147940
Transcriptomic Responses of the Heart and Brain to Anoxia in the Western Painted Turtle.
PLoS One
2015
24448499
Integrated analysis of germline and somatic variants in ovarian cancer.
Nat Commun
2014
25109877
Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin.
Cell
2014
23222849
Somatic neurofibromatosis type 1 (NF1) inactivation characterizes NF1-associated pilocytic astrocytoma.
Genome Res
2013
24132290
Mutational landscape and significance across 12 major cancer types.
Nature
2013
24071850
Enabling transparent and collaborative computational analysis of 12 tumor types within The Cancer Genome Atlas.
Nat Genet
2013
24084849
Comprehensive identification of mutational cancer driver genes across 12 tumor types.
Sci Rep
2013
24220575
Identification of a pan-cancer oncogenic microRNA superfamily anchored by a central core seed motif.
Nat Commun
2013
23636398
Integrated genomic characterization of endometrial carcinoma.
Nature
2013
23634996
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia.
N Engl J Med
2013
23443460
Clonal diversity of recurrently mutated genes in myelodysplastic syndromes.
Leukemia
2013
23583981
Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas.
Nat Genet
2013
23537068
The western painted turtle genome, a model for the evolution of extreme physiological adaptations in a slowly evolving lineage.
Genome Biol
2013
22563071
BreakFusion: targeted assembly-based identification of gene fusions in whole transcriptome paired-end sequencing data.
Bioinformatics
2012
22759861
MuSiC: identifying mutational significance in cancer genomes.
Genome Res
2012
22722193
Whole-genome analysis informs breast cancer response to aromatase inhibition.
Nature
2012
22817890
The origin and evolution of mutations in acute myeloid leukemia.
Cell
2012
21415852
Recurrent DNMT3A mutations in patients with myelodysplastic syndromes.
Leukemia
2011
21498403
PathScan: a tool for discerning mutational significance in groups of putative cancer genes.
Bioinformatics
2011
20946604
A framework for automated enrichment of functionally significant inverted repeats in whole genomes.
BMC Bioinformatics
2010
21067377
DNMT3A mutations in acute myeloid leukemia.
N Engl J Med
2010
18793465
Validation of an NSP-based (negative selection pattern) gene family identification strategy.
BMC Bioinformatics
2008
1 - 42 of 42
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David E Larson
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