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Author Details

Elaine R Mardis
The Ohio State University
1988
427
128
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
35801295EGFR internal tandem duplications in fusion-negative congenital and neonatal spindle cell tumors.Genes Chromosomes Cancer2023
35716171Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case-based review.Genes Chromosomes Cancer2023
37672882Supervised Risk Predictor of Breast Cancer Based on Intrinsic Subtypes.J Clin Oncol2023
37583388Oncolytic virus-driven immune remodeling revealed in mouse medulloblastomas at single cell resolution.Mol Ther Oncolytics2023
36585450Multiomics in primary and metastatic breast tumors from the AURORA US network finds microenvironment and epigenetic drivers of metastasis.Nat Cancer2023
36827605Correspondence comprehensive characterization of a brainstem aggregoma (light and heavy chain deposition disease).Brain Pathol2023
36583990Manufacture and Characterization of Good Manufacturing Practice-Compliant SARS-COV-2 Cytotoxic T Lymphocytes.J Infect Dis2023
36508930Myeloid cell heterogeneity in the tumor microenvironment and therapeutic implications for childhood central nervous system (CNS) tumors.J Neuroimmunol2023
37400526Genetic characterization of primary and metastatic high-grade serous ovarian cancer tumors reveals distinct features associated with survival.Commun Biol2023
37013636A novel transcriptional signature identifies T-cell infiltration in high-risk paediatric cancer.Genome Med2023
36631516Single-nuclei transcriptomics enable detection of somatic variants in patient brain tissue.Sci Rep2023
36871221Single-cell RNA sequencing reveals immunosuppressive myeloid cell diversity during malignant progression in a murine model of glioma.Cell Rep2023
36869713DIS3 Variants are Associated With Primary Ovarian Insufficiency: Importance of Transcription/Translation in Oogenesis.J Clin Endocrinol Metab2023
36932243Accurate diagnosis of pediatric brain cancers.Nat Med2023
36539618Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.Nat Genet2023
37169845A chance encounter leads into immunogenomics.Nat Cancer2023
36782065Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.Nat Genet2023
37583388Oncolytic virus-driven immune remodeling revealed in mouse medulloblastomas at single cell resolution.Mol Ther Oncolytics2023
37672882Supervised Risk Predictor of Breast Cancer Based on Intrinsic Subtypes.J Clin Oncol2023
35801295EGFR internal tandem duplications in fusion-negative congenital and neonatal spindle cell tumors.Genes Chromosomes Cancer2023
35716171Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case-based review.Genes Chromosomes Cancer2023
37013636A novel transcriptional signature identifies T-cell infiltration in high-risk paediatric cancer.Genome Med2023
37169845A chance encounter leads into immunogenomics.Nat Cancer2023
37400526Genetic characterization of primary and metastatic high-grade serous ovarian cancer tumors reveals distinct features associated with survival.Commun Biol2023
36782065Author Correction: Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.Nat Genet2023
36585450Multiomics in primary and metastatic breast tumors from the AURORA US network finds microenvironment and epigenetic drivers of metastasis.Nat Cancer2023
36583990Manufacture and Characterization of Good Manufacturing Practice-Compliant SARS-COV-2 Cytotoxic T Lymphocytes.J Infect Dis2023
36539618Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries.Nat Genet2023
36871221Single-cell RNA sequencing reveals immunosuppressive myeloid cell diversity during malignant progression in a murine model of glioma.Cell Rep2023
36508930Myeloid cell heterogeneity in the tumor microenvironment and therapeutic implications for childhood central nervous system (CNS) tumors.J Neuroimmunol2023
36869713DIS3 Variants are Associated With Primary Ovarian Insufficiency: Importance of Transcription/Translation in Oogenesis.J Clin Endocrinol Metab2023
36932243Accurate diagnosis of pediatric brain cancers.Nat Med2023
36827605Correspondence comprehensive characterization of a brainstem aggregoma (light and heavy chain deposition disease).Brain Pathol2023
36631516Single-nuclei transcriptomics enable detection of somatic variants in patient brain tissue.Sci Rep2023
34718612Causal and Candidate Gene Variants in a Large Cohort of Women With Primary Ovarian Insufficiency.J Clin Endocrinol Metab2022
35912263Molecular Heterogeneity in Pediatric Malignant Rhabdoid Tumors in Patients With Multi-Organ Involvement.Front Oncol2022
35712307Salivary miRNA Expression in Children With Persistent Post-concussive Symptoms.Front Public Health2022
35590059Acute lymphoblastic leukemia displays a distinct highly methylated genome.Nat Cancer2022
35967098An unusual case of atypical teratoid/rhabdoid tumor, initially diagnosed as atypical pituitary adenoma in a 13-year-old male patient.Neurooncol Adv2022
36033525Risk of secondary malignant neoplasms in children following proton therapy vs. photon therapy for primary CNS tumors: A systematic review and meta-analysis.Front Oncol2022
35962045Author Correction: Comparative and demographic analysis of orang-utan genomes.Nature2022
35568002Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.Cancer Genet2022
35687047Detection of brain somatic variation in epilepsy-associated developmental lesions.Epilepsia2022
35624339A community approach to the cancer-variant-interpretation bottleneck.Nat Cancer2022
35617766Pediatric CNS cancer genomics and immunogenomics.Curr Opin Genet Dev2022
35418131LINC00355 regulates p27<sup>KIP</sup> expression by binding to MENIN to induce proliferation in late-stage relapse breast cancer.NPJ Breast Cancer2022
36325690The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission.Mol Cancer Ther2022
36325685The AACR Journals: Advancing Progress Toward the AACR's 115-Year Mission.Mol Cancer Res2022
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Collaborators

The Ohio State University
Co-authored papers 176
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 92
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Co-authored papers 76
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Co-authored papers 75
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McDonnell Genome Institute, Washington University School of Medicine
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Washington University
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McDonnell Genome Institute, Washington University in St. Louis
Co-authored papers 37
Changhai Hospital, Second Military Medical University
Co-authored papers 34
Massachusetts General Hospital
Co-authored papers 29
Co-authored papers 28
College of Medicine, The Ohio State University
Co-authored papers 28
Harvard T.H. Chan School of Public Health
Co-authored papers 28
Washington University School of Medicine
Co-authored papers 28
McDonnell Genome Institute, Washington University School of Medicine
Co-authored papers 27
St Jude Children's Research Hospital
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Washington University School of Medicine
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University of Washington
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Nationwide Children's Hospital
Co-authored papers 26
Washington University School of Medicine in St. Louis
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St. Jude Children's Research Hospital
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University of Texas MD Anderson Cancer Center
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McDonnell Genome Institute, Washington University
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