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Author Details
Full Name
Erica K Barnell
Affiliation
McDonnell Genome Institute, Washington University School of Medicine
ORCID
Career Start Year
2014
Papers
22
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36251745
Distinct clonal identities of B-ALLs arising after lenolidomide therapy for multiple myeloma.
Blood Adv
2023
36373660
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebase.
Nucleic Acids Res
2023
36273232
Personalized ctDNA micro-panels can monitor and predict clinical outcomes for patients with triple-negative breast cancer.
Sci Rep
2022
35568002
Genomic and transcriptomic somatic alterations of hepatocellular carcinoma in non-cirrhotic livers.
Cancer Genet
2022
35624339
A community approach to the cancer-variant-interpretation bottleneck.
Nat Cancer
2022
33397681
Correction: Neoadjuvant and Adjuvant Pembrolizumab in Resectable Locally Advanced, Human Papillomavirus-unrelated Head and Neck Cancer: A Multicenter, Phase II Trial.
Clin Cancer Res
2021
35611186
<i>In silico</i> epitope prediction analyses highlight the potential for distracting antigen immunodominance with allogeneic cancer vaccines.
Cancer Res Commun
2021
33547198
Yap1 Mediates Trametinib Resistance in Head and Neck Squamous Cell Carcinomas.
Clin Cancer Res
2021
34036230
Impact of a 40-Gene Targeted Panel Test on Physician Decision Making for Patients With Acute Myeloid Leukemia.
JCO Precis Oncol
2021
34029233
Multitarget Stool RNA Test for Noninvasive Detection of Colorectal Neoplasias in a Multicenter, Prospective, and Retrospective Cohort.
Clin Transl Gastroenterol
2021
32665297
Neoadjuvant and Adjuvant Pembrolizumab in Resectable Locally Advanced, Human Papillomavirus-Unrelated Head and Neck Cancer: A Multicenter, Phase II Trial.
Clin Cancer Res
2020
30287923
Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samples.
Genet Med
2019
31779674
Standard operating procedure for curation and clinical interpretation of variants in cancer.
Genome Med
2019
31390566
A Spontaneous Aggressive ERα+ Mammary Tumor Model Is Driven by Kras Activation.
Cell Rep
2019
31618044
Open-Sourced CIViC Annotation Pipeline to Identify and Annotate Clinically Relevant Variants Using Single-Molecule Molecular Inversion Probes.
JCO Clin Cancer Inform
2019
30311370
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.
Hum Mutat
2018
30134176
Oral Cavity Squamous Cell Carcinoma Xenografts Retain Complex Genotypes and Intertumor Molecular Heterogeneity.
Cell Rep
2018
30397337
A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data.
Nat Genet
2018
28874413
A Phase II Trial of Neoadjuvant MK-2206, an AKT Inhibitor, with Anastrozole in Clinical Stage II or III <i>PIK3CA</i>-Mutant ER-Positive and HER2-Negative Breast Cancer.
Clin Cancer Res
2017
28138153
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancer.
Nat Genet
2017
26973864
Environmental Enteric Dysfunction Includes a Broad Spectrum of Inflammatory Responses and Epithelial Repair Processes.
Cell Mol Gastroenterol Hepatol
2015
24662296
Growth and HIV-free survival of HIV-exposed infants in Malawi: a randomized trial of two complementary feeding interventions in the context of maternal antiretroviral therapy.
J Acquir Immune Defic Syndr
2014
1 - 22 of 22
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Co-authored papers
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7
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The Ohio State University
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5
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