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Author Details

Jaime M Guidry Auvil
National Cancer Institute
2013
30
21
PMIDPaper TitleJournal TitlePublished Year
37688579Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.J Natl Cancer Inst2024
37688579Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.J Natl Cancer Inst2024
36747619Germline pathogenic variants in 786 neuroblastoma patients.medRxiv2023
37584517Integrative Genomic Analyses Identify LncRNA Regulatory Networks across Pediatric Leukemias and Solid Tumors.Cancer Res2023
37267580The Childhood Cancer Data Initiative: Using the Power of Data to Learn From and Improve Outcomes for Every Child and Young Adult With Pediatric Cancer.J Clin Oncol2023
36747619Germline pathogenic variants in 786 neuroblastoma patients.medRxiv2023
37584517Integrative Genomic Analyses Identify LncRNA Regulatory Networks across Pediatric Leukemias and Solid Tumors.Cancer Res2023
37267580The Childhood Cancer Data Initiative: Using the Power of Data to Learn From and Improve Outcomes for Every Child and Young Adult With Pediatric Cancer.J Clin Oncol2023
36050548The genomic landscape of pediatric acute lymphoblastic leukemia.Nat Genet2022
36050548The genomic landscape of pediatric acute lymphoblastic leukemia.Nat Genet2022
34428097Cancer Informatics for Cancer Centers: Scientific Drivers for Informatics, Data Science, and Care in Pediatric, Adolescent, and Young Adult Cancer.JCO Clin Cancer Inform2021
34428097Cancer Informatics for Cancer Centers: Scientific Drivers for Informatics, Data Science, and Care in Pediatric, Adolescent, and Young Adult Cancer.JCO Clin Cancer Inform2021
34820660GA4GH Passport standard for digital identity and access permissions.Cell Genom2021
34820659The Data Use Ontology to streamline responsible access to human biomedical datasets.Cell Genom2021
35072136GA4GH: International policies and standards for data sharing across genomic research and healthcare.Cell Genom2021
35072136GA4GH: International policies and standards for data sharing across genomic research and healthcare.Cell Genom2021
34820660GA4GH Passport standard for digital identity and access permissions.Cell Genom2021
34820659The Data Use Ontology to streamline responsible access to human biomedical datasets.Cell Genom2021
32796005Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.Genome Res2020
32796005Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.Genome Res2020
30705421Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.Nat Med2019
30705421Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.Nat Med2019
29227476The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.Nat Med2018
30209392The genetic basis and cell of origin of mixed phenotype acute leukaemia.Nature2018
29489755Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.Nature2018
29227476The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.Nat Med2018
29634680Erratum: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.Nat Med2018
29784674Clinically Relevant Cytotoxic Immune Cell Signatures and Clonal Expansion of T-Cell Receptors in High-Risk <i>MYCN</i>-Not-Amplified Human Neuroblastoma.Clin Cancer Res2018
30209392The genetic basis and cell of origin of mixed phenotype acute leukaemia.Nature2018
29784674Clinically Relevant Cytotoxic Immune Cell Signatures and Clonal Expansion of T-Cell Receptors in High-Risk <i>MYCN</i>-Not-Amplified Human Neuroblastoma.Clin Cancer Res2018
29634680Erratum: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.Nat Med2018
29489755Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.Nature2018
28825729A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.Nat Genet2017
28825729A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.Nat Genet2017
28671688The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.Nat Genet2017
28671688The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.Nat Genet2017
26683771MYCN controls an alternative RNA splicing program in high-risk metastatic neuroblastoma.Cancer Lett2016
27143256CSF3R mutations have a high degree of overlap with CEBPA mutations in pediatric AML.Blood2016
26941285Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse.Cancer Res2016
26683771MYCN controls an alternative RNA splicing program in high-risk metastatic neuroblastoma.Cancer Lett2016
27702824Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group.Clin Cancer Res2016
27702824Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group.Clin Cancer Res2016
27143256CSF3R mutations have a high degree of overlap with CEBPA mutations in pediatric AML.Blood2016
26941285Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse.Cancer Res2016
25790293Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia.Nat Commun2015
25790293Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia.Nat Commun2015
26560027Genetic predisposition to neuroblastoma mediated by a LMO1 super-enhancer polymorphism.Nature2015
26121087Relapsed neuroblastomas show frequent RAS-MAPK pathway mutations.Nat Genet2015
26635203MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours.Nat Commun2015
26158413TCF21 hypermethylation in genetically quiescent clear cell sarcoma of the kidney.Oncotarget2015
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Collaborators

National Cancer Institute
Co-authored papers 21
National Cancer Institute
Co-authored papers 21
Changhai Hospital, Second Military Medical University
Co-authored papers 12
Children's Hospital of Philadelphia
Co-authored papers 10
St Jude Children's Research Hospital
Co-authored papers 9
Center for Cancer Research, National Cancer Institute
Co-authored papers 9
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University of British Columbia
Co-authored papers 9
Baylor College of Medicine
Co-authored papers 9
University of Pittsburgh
Co-authored papers 8
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Co-authored papers 8
Center for Cancer Research, National Cancer Institute
Co-authored papers 8
Co-authored papers 8
Children's Hospital of Philadelphia
Co-authored papers 8
Fred Hutchinson Cancer Research Centre
Co-authored papers 8
Children's Hospital of Philadelphia
Co-authored papers 7
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital
Co-authored papers 7
St. Jude Children's Research Hospital
Co-authored papers 7
Ann & Robert H. Lurie Children's Hospital of Chicago
Co-authored papers 6
Clinical Research Division, Fred Hutchinson Cancer Research Center
Co-authored papers 6
Keck School of Medicine, University of Southern California
Co-authored papers 6
University of Washington
Co-authored papers 5
Baylor College of Medicine
Co-authored papers 5
St Jude Children's Research Hospital
Co-authored papers 5
St Jude Children's Research Hospital
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St. Jude Children's Research Hospital
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Departments of Pharmaceutical Sciences.
Co-authored papers 4
Mayo Clinic
Co-authored papers 4
St. Jude Children's Research Hospital.
Co-authored papers 4