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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
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Last data update: May 20, 2024
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Current practice of cancer predisposition testing in pediatric patients with CNS tumors in the United States.
Baylee Roy et al. Pediatr Blood Cancer 2023 e30725
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Next-generation Sequencing of Cerebrospinal Fluid for Clinical Molecular Diagnostics in Pediatric, Adolescent and Young Adult (AYA) Brain Tumor Patients.
Miller Alexandra M et al. Neuro-oncology 2022
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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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Retrospective investigation of hereditary syndromes in patients with medulloblastoma in a single institution.
Wang Ying et al. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2020 Sep
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Prognostic significance of molecular subgroups of medulloblastoma in young children receiving irradiation-sparing regimens.
Yeo Kee Kiat et al. Journal of neuro-oncology 2019 Oct
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Pediatric Brain Tumor Genetics: What Radiologists Need to Know.
AlRayahi Jehan et al. Radiographics : a review publication of the Radiological Society of North America, Inc 38(7) 2102-2122
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Indian Society of Neuro-Oncology consensus guidelines for the contemporary management of medulloblastoma.
Gupta Tejpal et al. Neurology India 65(2) 315-332
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CLINGEN Actionability Report for Basal Cell Nevus Syndrome (BCNS) - PTCH1
ClinGen Actionability Working Group
Simplified Molecular Subtyping of Medulloblastoma for Reduced Cost and Improved Turnaround Time.
Shuangshoti Somruetai et al. Applied immunohistochemistry & molecular morphology : AIMM 2019 Jul
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Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort.
Waszak Sebastian M et al. The Lancet. Oncology 2018 19(6) 785-798
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Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial.
Goschzik Tobias et al. The Lancet. Oncology 2018 Nov
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The next frontier in the battle against childhood cancer: Genetics and genomics
N Blanton, Baylor Medicine, Blog, October 9, 2018
Clinical and pre-clinical utility of genomics in medulloblastoma.
Nör Carolina et al. Expert review of neurotherapeutics 2018 Jul
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Targeted next-generation sequencing of pediatric neuro-oncology patients improves diagnosis, identifies pathogenic germline mutations, and directs targeted therapy.
Kline Cassie N et al. Neuro-oncology 2017 19(5) 699-709
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ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).
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Dissecting the genomic complexity underlying medulloblastoma.
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 20, 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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