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Paper Details

Germline pathogenic variants in neuroblastoma patients are enriched in BARD1 and predict worse survival.
J Natl Cancer Inst
3
2024
BARD1, CNVs, CPG, Germline DNA, Neuroblastoma, P, P-LP variants, Patients, cancer, cancer predisposition gene (CPG) P-LP variants, children, embryonal cancer of the developing sympathetic nervous system, germline, germline DNA array, germline P-LP variant, germline variants, neuroblastoma, patients, tumor, tumor DNA
Author NameAffiliation
Jung KimClinical Genetics Branch, National Cancer Institute
Jung KimClinical Genetics Branch, National Cancer Institute
Zalman VaksmanChildren's Hospital of Philadelphia
Zalman VaksmanDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Zalman VaksmanChildren's Hospital of Philadelphia
Zalman VaksmanDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Gonzalo L??pezDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Gonzalo L??pezDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Belynda HicksNational Cancer Institute
Belynda HicksNational Cancer Institute
Jaime M Guidry AuvilNational Cancer Institute
Jaime M Guidry AuvilNational Cancer Institute
Daniela S GerhardNational Cancer Institute
Daniela S GerhardNational Cancer Institute
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia
Hakon HakonarsonPerelman School of Medicine, University of Pennsylvania
Hakon HakonarsonCenter for Applied Genomics, Children's Hospital of Philadelphia
Hakon HakonarsonPerelman School of Medicine, University of Pennsylvania
Kristina A ColeDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Kristina A ColePerelman School of Medicine, University of Pennsylvania
Kristina A ColeDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Kristina A ColePerelman School of Medicine, University of Pennsylvania
Kristopher R BosseDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Kristopher R BossePerelman School of Medicine, University of Pennsylvania
Kristopher R BosseAbramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania
Javed KhanCenter for Cancer Research, National Cancer Institute
Javed KhanCenter for Cancer Research, National Cancer Institute
Jun S WeiCenter for Cancer Research, National Cancer Institute
Jun S WeiCenter for Cancer Research, National Cancer Institute
John M MarisDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
John M MarisPerelman School of Medicine, University of Pennsylvania
John M MarisAbramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania
John M MarisDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
John M MarisAbramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania
John M MarisPerelman School of Medicine, University of Pennsylvania
Douglas R StewartClinical Genetics Branch, National Cancer Institute
Douglas R StewartClinical Genetics Branch, National Cancer Institute
Sharon J DiskinChildren's Hospital of Philadelphia
Sharon J DiskinDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Sharon J DiskinAbramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania
Sharon J DiskinPerelman School of Medicine, University of Pennsylvania
Sharon J DiskinChildren's Hospital of Philadelphia
Sharon J DiskinDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia
Sharon J DiskinAbramson Family Cancer Research Institute, Perelman School of Medicine, University of Pennsylvania
Sharon J DiskinPerelman School of Medicine, University of Pennsylvania
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