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Author Details

Daniela S Gerhard
National Cancer Institute
2009
36
28
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
36747619Germline pathogenic variants in 786 neuroblastoma patients.medRxiv2023
35106508A community challenge for a pancancer drug mechanism of action inference from perturbational profile data.Cell Rep Med2022
36050548The genomic landscape of pediatric acute lymphoblastic leukemia.Nat Genet2022
35106508A community challenge for a pancancer drug mechanism of action inference from perturbational profile data.Cell Rep Med2022
36050548The genomic landscape of pediatric acute lymphoblastic leukemia.Nat Genet2022
34007079Author Correction: The NCI Genomic Data Commons.Nat Genet2021
34007079Author Correction: The NCI Genomic Data Commons.Nat Genet2021
33619384The NCI Genomic Data Commons.Nat Genet2021
33619384The NCI Genomic Data Commons.Nat Genet2021
32796005Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.Genome Res2020
33028839Framework for quality assessment of whole genome cancer sequences.Nat Commun2020
32747824Analysis of Ugandan cervical carcinomas identifies human papillomavirus clade-specific epigenome and transcriptome landscapes.Nat Genet2020
32796005Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.Genome Res2020
33028839Framework for quality assessment of whole genome cancer sequences.Nat Commun2020
32747824Analysis of Ugandan cervical carcinomas identifies human papillomavirus clade-specific epigenome and transcriptome landscapes.Nat Genet2020
30617194Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma.Blood2019
30617194Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma.Blood2019
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
30543698A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group study.PLoS One2018
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
30543698A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group study.PLoS One2018
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
29068783MicroRNA Expression-Based Model Indicates Event-Free Survival in Pediatric Acute Myeloid Leukemia.J Clin Oncol2017
29068783MicroRNA Expression-Based Model Indicates Event-Free Survival in Pediatric Acute Myeloid Leukemia.J Clin Oncol2017
28671688The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.Nat Genet2017
26977886Genome-Wide Profiles of Extra-cranial Malignant Rhabdoid Tumors Reveal Heterogeneity and Dysregulated Developmental Pathways.Cancer Cell2016
26977886Genome-Wide Profiles of Extra-cranial Malignant Rhabdoid Tumors Reveal Heterogeneity and Dysregulated Developmental Pathways.Cancer Cell2016
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
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
25468567A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults.Blood2015
25790293Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia.Nat Commun2015
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