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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: May 01, 2024
. (Total: 63728 Documents since 2012)
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Mathematical modeling of neuroblastoma associates evolutionary patterns with outcomes
G Caravagna, Nature Genetics, March 27, 2023
Supratentorial CNS-PNETs in children; a Swedish population-based study with molecular re-evaluation and long-term follow-up.
Elizabeth Schepke et al. Clinical epigenetics 2023 15(1) 40
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Germline pathogenic variants in 786 neuroblastoma patients.
Jung Kim et al. medRxiv : the preprint server for health sciences 2023
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Impact of Genomic and Clinical Factors on Outcome of Children ≥18 Months of Age with Stage 3 Neuroblastoma with Unfavorable Histology without MYCN Amplification.
Navin Pinto et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2023
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Medical guidelines for Li-Fraumeni syndrome 2019, version 1.1.
Kumamoto Tadashi et al. International journal of clinical oncology 2021
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The genomics and epigenetics of olfactory neuroblastoma: A systematic review.
Kaur Raman Preet et al. Laryngoscope investigative otolaryngology 2021 6(4) 721-728
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Differential Impact of ALK Mutations in Neuroblastoma.
O'Donohue Tara et al. JCO precision oncology 2021 5
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The MicroRNA Landscape of MYCN-Amplified Neuroblastoma.
Misiak Danny et al. Frontiers in oncology 2021 11647737
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A Targeted Gene Panel for Circulating Tumor DNA Sequencing in Neuroblastoma.
Cimmino Flora et al. Frontiers in oncology 2020 10596191
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Metastatic Burden Defines Clinically and Biologically Distinct Subgroups of Stage 4 High-Risk Neuroblastoma.
Seo Eun Seop et al. Journal of clinical medicine 2020 Aug 9(9)
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Genomic co-amplification of CDK4/MDM2/FRS2 is associated with very poor prognosis and atypical clinical features in neuroblastoma patients.
Amoroso Loredana et al. Genes, chromosomes & cancer 2019 Nov
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Tandem Transplant for High-Risk Neuroblastoma: Next Steps in the Era of Precision Medicine.
Bagatell Rochelle, et al. JAMA 2019 0 0. (8) 729-731
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CLINGEN Actionability Report for Retinoblastoma-RB1
ClinGen Actionability Working Group
Study reveals elevated cancer risk in children with birth defects,
EurekAlert, June 25, 2019
Predicting clinical outcomes in neuroblastoma with genomic data integration.
Baali Ilyes et al. Biology direct 2018 13(1) 20
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Germline SDHA mutations in children and adults with cancer.
Dubard Gault Marianne et al. Cold Spring Harbor molecular case studies 2018 4(4)
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The Childhood Cancer Data Initiative: Why Data Sharing Is Essential to Progress
D Lowy, NCI Director Blog, June 12, 2019
Molecularly Targeted Therapy for Neuroblastoma.
Greengard Emily G et al. Children (Basel, Switzerland) 2018 Oct 5(10)
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Clinical Impact of Tumor Mutational Burden in Neuroblastoma.
Hwang William L et al. Journal of the National Cancer Institute 2018 Oct
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Hotspot Mutations Detectable by Next-generation Sequencing in Exhaled Breath Condensates from Patients with Lung Cancer.
Youssef Omar et al. Anticancer research 2018 Oct 38(10) 5627-5634
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NCI-led research team develops predictor for immunotherapy response in melanoma
NCI, August 20, 2018
Retrospective evaluation of a decision-support algorithm (MIPOGG) for genetic referrals for children with neuroblastic tumors.
Goudie Catherine et al. Pediatric blood & cancer 2018 Aug e27390
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Mendelian randomization studies of cancer risk: a literature review.
Pierce Brandon L et al. Current epidemiology reports 2018 Jun 5(2) 184-196
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The genomic landscape of pediatric cancers
MassGenomics, Blog Mar 2018
Integrating Genomics Into Clinical Pediatric Oncology Using the Molecular Tumor Board at the Memorial Sloan Kettering Cancer Center.
Ortiz Michael V et al. Pediatric blood & cancer 2016 63(8) 1368-74
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Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.
et al. JAMA oncology 2017 Feb
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How can precision medicine help children with cancer?
By Srivani Ravoori, Cancer Research Catalyst Blog, Jul 29
Selective HDAC1/HDAC2 inhibitors induce neuroblastoma differentiation.
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Segmental chromosomal alterations have prognostic impact in neuroblastoma: a report from the INRG project.
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Prognostic significance of promoter DNA methylation in patients with childhood neuroblastoma.
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 01, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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