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Author Details
Full Name
Daniela S Gerhard
Affiliation
National Cancer Institute
ORCID
Career Start Year
2009
Papers
36
H Index
28
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37688579
Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.
J Natl Cancer Inst
2024
37688579
Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.
J Natl Cancer Inst
2024
36747619
Germline pathogenic variants in 786 neuroblastoma patients.
medRxiv
2023
36747619
Germline pathogenic variants in 786 neuroblastoma patients.
medRxiv
2023
35106508
A community challenge for a pancancer drug mechanism of action inference from perturbational profile data.
Cell Rep Med
2022
36050548
The genomic landscape of pediatric acute lymphoblastic leukemia.
Nat Genet
2022
35106508
A community challenge for a pancancer drug mechanism of action inference from perturbational profile data.
Cell Rep Med
2022
36050548
The genomic landscape of pediatric acute lymphoblastic leukemia.
Nat Genet
2022
34007079
Author Correction: The NCI Genomic Data Commons.
Nat Genet
2021
34007079
Author Correction: The NCI Genomic Data Commons.
Nat Genet
2021
33619384
The NCI Genomic Data Commons.
Nat Genet
2021
33619384
The NCI Genomic Data Commons.
Nat Genet
2021
32796005
Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.
Genome Res
2020
33028839
Framework for quality assessment of whole genome cancer sequences.
Nat Commun
2020
32747824
Analysis of Ugandan cervical carcinomas identifies human papillomavirus clade-specific epigenome and transcriptome landscapes.
Nat Genet
2020
32796005
Somatic structural variation targets neurodevelopmental genes and identifies <i>SHANK2</i> as a tumor suppressor in neuroblastoma.
Genome Res
2020
33028839
Framework for quality assessment of whole genome cancer sequences.
Nat Commun
2020
32747824
Analysis of Ugandan cervical carcinomas identifies human papillomavirus clade-specific epigenome and transcriptome landscapes.
Nat Genet
2020
30617194
Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma.
Blood
2019
30617194
Genome-wide discovery of somatic coding and noncoding mutations in pediatric endemic and sporadic Burkitt lymphoma.
Blood
2019
30705421
Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Nat Med
2019
30705421
Publisher Correction: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Nat Med
2019
29227476
The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Nat Med
2018
30209392
The genetic basis and cell of origin of mixed phenotype acute leukaemia.
Nature
2018
30543698
A 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 One
2018
29489755
Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.
Nature
2018
29227476
The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Nat Med
2018
29634680
Erratum: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Nat Med
2018
29784674
Clinically Relevant Cytotoxic Immune Cell Signatures and Clonal Expansion of T-Cell Receptors in High-Risk <i>MYCN</i>-Not-Amplified Human Neuroblastoma.
Clin Cancer Res
2018
30209392
The genetic basis and cell of origin of mixed phenotype acute leukaemia.
Nature
2018
30543698
A 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 One
2018
29784674
Clinically Relevant Cytotoxic Immune Cell Signatures and Clonal Expansion of T-Cell Receptors in High-Risk <i>MYCN</i>-Not-Amplified Human Neuroblastoma.
Clin Cancer Res
2018
29634680
Erratum: The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Nat Med
2018
29489755
Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours.
Nature
2018
28825729
A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.
Nat Genet
2017
28825729
A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor.
Nat Genet
2017
28671688
The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.
Nat Genet
2017
29068783
MicroRNA Expression-Based Model Indicates Event-Free Survival in Pediatric Acute Myeloid Leukemia.
J Clin Oncol
2017
29068783
MicroRNA Expression-Based Model Indicates Event-Free Survival in Pediatric Acute Myeloid Leukemia.
J Clin Oncol
2017
28671688
The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.
Nat Genet
2017
26977886
Genome-Wide Profiles of Extra-cranial Malignant Rhabdoid Tumors Reveal Heterogeneity and Dysregulated Developmental Pathways.
Cancer Cell
2016
26977886
Genome-Wide Profiles of Extra-cranial Malignant Rhabdoid Tumors Reveal Heterogeneity and Dysregulated Developmental Pathways.
Cancer Cell
2016
27143256
CSF3R mutations have a high degree of overlap with CEBPA mutations in pediatric AML.
Blood
2016
26941285
Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse.
Cancer Res
2016
27702824
Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group.
Clin Cancer Res
2016
27702824
Significance of TP53 Mutation in Wilms Tumors with Diffuse Anaplasia: A Report from the Children's Oncology Group.
Clin Cancer Res
2016
27143256
CSF3R mutations have a high degree of overlap with CEBPA mutations in pediatric AML.
Blood
2016
26941285
Genomic Profiling of Pediatric Acute Myeloid Leukemia Reveals a Changing Mutational Landscape from Disease Diagnosis to Relapse.
Cancer Res
2016
25468567
A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults.
Blood
2015
25790293
Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia.
Nat Commun
2015
1 - 50 of 72
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Steven C Clifford
Wolfson Childhood Cancer Research Centre, Newcastle University Centre for Cancer
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1994
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Kyoto University
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1993
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McGill University Health Centre (MUHC), Montreal Children's Hospital (MCH)
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Collaborators
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National Cancer Institute
Co-authored papers
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St Jude Children's Research Hospital
Co-authored papers
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Changhai Hospital, Second Military Medical University
Co-authored papers
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13
Yussanne Ma
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Andrew J Mungall
Co-authored papers
12
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Children's Hospital of Philadelphia
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12
Julie M Gastier-Foster
Baylor College of Medicine
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11
Tanja M Davidsen
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Richard A Moore
Co-authored papers
11
Meenakshi Devidas
St Jude Children's Research Hospital
Co-authored papers
11
Mignon L Loh
University of Washington
Co-authored papers
10
Leandro C Hermida
University of Pittsburgh
Co-authored papers
8
Soheil Meshinchi
Fred Hutchinson Cancer Research Centre
Co-authored papers
8
John M Maris
Children's Hospital of Philadelphia
Co-authored papers
7
Javed Khan
Center for Cancer Research, National Cancer Institute
Co-authored papers
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Rhonda E Ries
Clinical Research Division, Fred Hutchinson Cancer Research Center
Co-authored papers
7
Yu Liu
Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital
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Xiaotu Ma
St. Jude Children's Research Hospital
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Elizabeth J Perlman
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