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Author Details

Dmitriy Sonkin
National Cancer Institute
2008
33
19
PMIDPaper TitleJournal TitlePublished Year
37550087Targeted Investigational Oncology Agents in the NCI-60: A Phenotypic Systems-based Resource.Mol Cancer Ther2023
37550087Targeted Investigational Oncology Agents in the NCI-60: A Phenotypic Systems-based Resource.Mol Cancer Ther2023
35101336Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
35796744Response to Mehta et al.Genet Med2022
36063163Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
35101336Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
35796744Response to Mehta et al.Genet Med2022
36063163Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
34446762TP53 isoform junction reads based analysis in malignant and normal contexts.Sci Rep2021
33600011MutSpliceDB: A database of splice sites variants with RNA-seq based evidence on effects on splicing.Hum Mutat2021
34446762TP53 isoform junction reads based analysis in malignant and normal contexts.Sci Rep2021
33600011MutSpliceDB: A database of splice sites variants with RNA-seq based evidence on effects on splicing.Hum Mutat2021
31502173Bioinformatics Tools and Resources for Cancer Immunotherapy Study.Methods Mol Biol2020
32246132A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.Nat Genet2020
32586373Epigenome-wide DNA methylation analysis of small cell lung cancer cell lines suggests potential chemotherapy targets.Clin Epigenetics2020
31502173Bioinformatics Tools and Resources for Cancer Immunotherapy Study.Methods Mol Biol2020
32586373Epigenome-wide DNA methylation analysis of small cell lung cancer cell lines suggests potential chemotherapy targets.Clin Epigenetics2020
32246132A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.Nat Genet2020
30559381Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.Nature2019
31645891Are neuroendocrine negative small cell lung cancer and large cell neuroendocrine carcinoma with WT RB1 two faces of the same entity?Lung Cancer Manag2019
31779674Standard operating procedure for curation and clinical interpretation of variants in cancer.Genome Med2019
30559381Addendum: The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.Nature2019
31068700Next-generation characterization of the Cancer Cell Line Encyclopedia.Nature2019
31645891Are neuroendocrine negative small cell lung cancer and large cell neuroendocrine carcinoma with WT RB1 two faces of the same entity?Lung Cancer Manag2019
31779674Standard operating procedure for curation and clinical interpretation of variants in cancer.Genome Med2019
31068700Next-generation characterization of the Cancer Cell Line Encyclopedia.Nature2019
29218886ClinGen Cancer Somatic Working Group - standardizing and democratizing access to cancer molecular diagnostic data to drive translational research.Pac Symp Biocomput2018
30311370Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.Hum Mutat2018
30311369Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes.Hum Mutat2018
29888062Standardizing And Democratizing Access To Cancer Molecular Diagnostic Test Data From Patients To Drive Translational Research.AMIA Jt Summits Transl Sci Proc2018
30355619The NCI Transcriptional Pharmacodynamics Workbench: A Tool to Examine Dynamic Expression Profiling of Therapeutic Response in the NCI-60 Cell Line Panel.Cancer Res2018
29218886ClinGen Cancer Somatic Working Group - standardizing and democratizing access to cancer molecular diagnostic data to drive translational research.Pac Symp Biocomput2018
29888062Standardizing And Democratizing Access To Cancer Molecular Diagnostic Test Data From Patients To Drive Translational Research.AMIA Jt Summits Transl Sci Proc2018
30311370Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.Hum Mutat2018
30311369Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes.Hum Mutat2018
30355619The NCI Transcriptional Pharmacodynamics Workbench: A Tool to Examine Dynamic Expression Profiling of Therapeutic Response in the NCI-60 Cell Line Panel.Cancer Res2018
28762582Detection of homozygous deletions in tumor-suppressor genes ranging from dozen to hundreds nucleotides in cancer models.Hum Mutat2017
28766886Small cell lung carcinoma cell line screen of etoposide/carboplatin plus a third agent.Cancer Med2017
28762582Detection of homozygous deletions in tumor-suppressor genes ranging from dozen to hundreds nucleotides in cancer models.Hum Mutat2017
28766886Small cell lung carcinoma cell line screen of etoposide/carboplatin plus a third agent.Cancer Med2017
26864072Integrative modeling of multi-omics data to identify cancer drivers and infer patient-specific gene activity.BMC Syst Biol2016
27247353Small Cell Lung Cancer Screen of Oncology Drugs, Investigational Agents, and Gene and microRNA Expression.J Natl Cancer Inst2016
27328919TP53 Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data.Hum Mutat2016
26864072Integrative modeling of multi-omics data to identify cancer drivers and infer patient-specific gene activity.BMC Syst Biol2016
27814769Somatic cancer variant curation and harmonization through consensus minimum variant level data.Genome Med2016
27814769Somatic cancer variant curation and harmonization through consensus minimum variant level data.Genome Med2016
27328919TP53 Variations in Human Cancers: New Lessons from the IARC TP53 Database and Genomics Data.Hum Mutat2016
27247353Small Cell Lung Cancer Screen of Oncology Drugs, Investigational Agents, and Gene and microRNA Expression.J Natl Cancer Inst2016
25524945The identification and characterization of a STAT5 gene signature in hematologic malignancies.Cancer Biomark2015
25524945The identification and characterization of a STAT5 gene signature in hematologic malignancies.Cancer Biomark2015
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Collaborators

Baylor College of Medicine
Co-authored papers 9
Innovation Center for Biomedical Informatics, Georgetown University Medical Center
Co-authored papers 8
Washington University
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Centene Center for Health Transformation, Centene Corporation
Co-authored papers 7
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Memorial Sloan Kettering Cancer Center
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Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis
Co-authored papers 5
Children's Hospital Los Angeles
Co-authored papers 5
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Washington University School of Medicine
Co-authored papers 5
McDonnell Genome Institute, Washington University in St Louis School of Medicine
Co-authored papers 4
Vanderbilt Ingram Cancer Center, Vanderbilt University Medical Center
Co-authored papers 4
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Baylor College of Medicine
Co-authored papers 4
Texas Children's Hospital and Baylor College of Medicine
Co-authored papers 4
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Broad Institute
Co-authored papers 3
German Cancer Consortium and German Cancer Research Center
Co-authored papers 3
Institute of Genetics and Cancer, University of Edinburgh
Co-authored papers 3
Broad Institute of Harvard and MIT
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Icahn School of Medicine
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Mayo Clinic
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Mayo Clinic
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University of California San Diego
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