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Author Details

Shruti Rao
Innovation Center for Biomedical Informatics, Georgetown University Medical Center
2013
30
12
PMIDPaper TitleJournal TitlePublished Year
36373660CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.Nucleic Acids Res2023
36373660CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.Nucleic Acids Res2023
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
36214808Culture-Independent Raman Spectroscopic Identification of Bacterial Pathogens from Clinical Samples Using Deep Transfer Learning.Anal Chem2022
35624339A community approach to the cancer-variant-interpretation bottleneck.Nat Cancer2022
35366592Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions.Cancer Genet2022
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
35366592Standardized evidence-based approach for assessment of oncogenic and clinical significance of NTRK fusions.Cancer Genet2022
35624339A community approach to the cancer-variant-interpretation bottleneck.Nat Cancer2022
36214808Culture-Independent Raman Spectroscopic Identification of Bacterial Pathogens from Clinical Samples Using Deep Transfer Learning.Anal Chem2022
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
32644817Collaborative, Multidisciplinary Evaluation of Cancer Variants Through Virtual Molecular Tumor Boards Informs Local Clinical Practices.JCO Clin Cancer Inform2020
31990579Evidence-Based Network Approach to Recommending Targeted Cancer Therapies.JCO Clin Cancer Inform2020
32644817Collaborative, Multidisciplinary Evaluation of Cancer Variants Through Virtual Molecular Tumor Boards Informs Local Clinical Practices.JCO Clin Cancer Inform2020
31990579Evidence-Based Network Approach to Recommending Targeted Cancer Therapies.JCO Clin Cancer Inform2020
31199921Dynamic Regulation of Caveolin-1 Phosphorylation and Caveolae Formation by Mammalian Target of Rapamycin Complex 2 in Bladder Cancer Cells.Am J Pathol2019
32025647A virtual molecular tumor board to improve efficiency and scalability of delivering precision oncology to physicians and their patients.JAMIA Open2019
31645350A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen).Cold Spring Harb Mol Case Stud2019
31779674Standard operating procedure for curation and clinical interpretation of variants in cancer.Genome Med2019
31199921Dynamic Regulation of Caveolin-1 Phosphorylation and Caveolae Formation by Mammalian Target of Rapamycin Complex 2 in Bladder Cancer Cells.Am J Pathol2019
31645350A case for expert curation: an overview of cancer curation in the Clinical Genome Resource (ClinGen).Cold Spring Harb Mol Case Stud2019
32025647A virtual molecular tumor board to improve efficiency and scalability of delivering precision oncology to physicians and their patients.JAMIA Open2019
31779674Standard operating procedure for curation and clinical interpretation of variants in cancer.Genome Med2019
29218886ClinGen Cancer Somatic Working Group - standardizing and democratizing access to cancer molecular diagnostic data to drive translational research.Pac Symp Biocomput2018
31930186Future of Evidence Synthesis in Precision Oncology: Between Systematic Reviews and Biocuration.JCO Precis Oncol2018
35135129Eye-Tracking Study to Enhance Usability of Molecular Diagnostics Reports in Cancer Precision Medicine.JCO Precis Oncol2018
30311370Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.Hum Mutat2018
29888062Standardizing And Democratizing Access To Cancer Molecular Diagnostic Test Data From Patients To Drive Translational Research.AMIA Jt Summits Transl Sci Proc2018
30576489iTextMine: integrated text-mining system for large-scale knowledge extraction from the literature.Database (Oxford)2018
29218886ClinGen Cancer Somatic Working Group - standardizing and democratizing access to cancer molecular diagnostic data to drive translational research.Pac Symp Biocomput2018
29545332Acquired Resistance to a MET Antibody <i>In Vivo</i> Can Be Overcome by the MET Antibody Mixture Sym015.Mol Cancer Ther2018
35135129Eye-Tracking Study to Enhance Usability of Molecular Diagnostics Reports in Cancer Precision Medicine.JCO Precis Oncol2018
31930186Future of Evidence Synthesis in Precision Oncology: Between Systematic Reviews and Biocuration.JCO Precis Oncol2018
29888062Standardizing And Democratizing Access To Cancer Molecular Diagnostic Test Data From Patients To Drive Translational Research.AMIA Jt Summits Transl Sci Proc2018
30576489iTextMine: integrated text-mining system for large-scale knowledge extraction from the literature.Database (Oxford)2018
30311370Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.Hum Mutat2018
29545332Acquired Resistance to a MET Antibody <i>In Vivo</i> Can Be Overcome by the MET Antibody Mixture Sym015.Mol Cancer Ther2018
27888622Quantification and expert evaluation of evidence for chemopredictive biomarkers to personalize cancer treatment.Oncotarget2017
29261751eGARD: Extracting associations between genomic anomalies and drug responses from text.PLoS One2017
27888622Quantification and expert evaluation of evidence for chemopredictive biomarkers to personalize cancer treatment.Oncotarget2017
29261751eGARD: Extracting associations between genomic anomalies and drug responses from text.PLoS One2017
27082433Discovery of Metabolic Biomarkers for Duchenne Muscular Dystrophy within a Natural History Study.PLoS One2016
27434074Correction: Discovery of Metabolic Biomarkers for Duchenne Muscular Dystrophy within a Natural History Study.PLoS One2016
27242035MET network in PubMed: a text-mined network visualization and curation system.Database (Oxford)2016
27082433Discovery of Metabolic Biomarkers for Duchenne Muscular Dystrophy within a Natural History Study.PLoS One2016
27589961Overview of the interactive task in BioCreative V.Database (Oxford)2016
27814769Somatic cancer variant curation and harmonization through consensus minimum variant level data.Genome Med2016
27589961Overview of the interactive task in BioCreative V.Database (Oxford)2016
27814769Somatic cancer variant curation and harmonization through consensus minimum variant level data.Genome Med2016
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