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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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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 03, 2024
. (Total: 63769 Documents since 2012)
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Records 1 - 14 (of 14 Records)
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Targeted gene expression profiling predicts meningioma outcomes and radiotherapy responses.
William C Chen et al. Nat Med 2023
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Early-onset grade 2-3 diffuse gliomas and schwannomas increase the risk of central nervous system tumors among the patients' relatives.
Eljas Alanen et al. Neuro-oncology advances 2023 5(1) vdad008
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Molecular profile to guide personalized medicine in adult patients with primary brain tumors: results from the ProfiLER trial.
Bonneville-Levard Alice et al. Medical oncology (Northwood, London, England) 2021 39(1) 4
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Genomic Biomarkers of Meningioma: A Focused Review.
Pawloski Jacob A et al. International journal of molecular sciences 2021 22(19)
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Assessing the utility and attitudes toward molecular testing in neuro-oncology: a survey of the Society for Neuro-Oncology members.
Fortin Ensign Shannon et al. Neuro-oncology practice 2021 8(3) 310-316
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Associations of Meningioma Molecular Subgroup and Tumor Recurrence.
Youngblood Mark W et al. Neuro-oncology 2020 Oct
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Subsequent Neoplasm Risk Associated With Rare Variants in DNA Damage Response and Clinical Radiation Sensitivity Syndrome Genes in the Childhood Cancer Survivor Study.
Morton Lindsay M et al. JCO precision oncology 2020 4
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Neurofibromatosis 2 in children presenting during the first decade of life.
Gaudioso Cristina et al. Neurology 2019 93(10) e964-e967
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Families with BAP1-Tumor Predisposition Syndrome in The Netherlands: Path to Identification and a Proposal for Genetic Screening Guidelines.
Chau Cindy et al. Cancers 2019 Aug 11(8)
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CLINGEN Actionability Report for Tumor Predisposition Syndrome - BAP1
ClinGen Actionability Working Group
Genetic Severity Score predicts clinical phenotype in NF2.
Halliday Dorothy et al. Journal of medical genetics 2017 Aug
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Association of Genetic Predisposition With Solitary Schwannoma or Meningioma in Children and Young Adults.
Pathmanaban Omar N et al. JAMA neurology 2017 Jul
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Effect of a detailed family history of melanoma on risk for other tumors: a cohort study based on the nationwide Swedish Family-Cancer Database.
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Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO.
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 03, 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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