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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)
Last data update: Apr 18, 2024
. (Total: 63623 Documents since 2012)
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Epilepsy[original query]>>Evidence Synthesis [Product Type]
Integrating real-world data in cost-effectiveness analysis of universal HLA-B*15:02 screening in Malaysia.
Huey Yi Chong et al. Br J Clin Pharmacol 2023
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KCNQ2 - Related Epilepsy: geno - phenotype relationship with tailorized anti seizures medication (ASM): Systematic review.
Raffaele Falsaperla et al. Neuropediatrics 2023
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Impact of Genetic polymorphisms on the risk of epilepsy amongst patients with acute brain injury: a systematic review.
Shubham Misra et al. European journal of neurology 2023
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ndividualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual participant data meta-analysis
R Stevelink et al, EBiomedicine, November 11, 2022
Early cost-utility analysis of genetically-guided therapy for patients with drug-resistant epilepsy.
Gordon Louisa G et al. Epilepsia 2022
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A systematic review on the cost effectiveness of pharmacogenomics in developing countries: implementation challenges.
Sukri Asif et al. The pharmacogenomics journal 2022
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Genetic testing for the epilepsies: A systematic review.
Sheidley Beth R et al. Epilepsia 2021
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Machine learning models for decision support in epilepsy management: A critical review.
Smolyansky Eliot D et al. Epilepsy & behavior : E&B 2021 123108273
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Genetic Neonatal-Onset Epilepsies and Developmental/Epileptic Encephalopathies with Movement Disorders: A Systematic Review.
Spagnoli Carlotta et al. International journal of molecular sciences 2021 22(8)
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Cost-effectiveness analysis of genotyping for HLA-B*15:02 in Indonesian patients with epilepsy using a generic model.
Yuliwulandari Rika et al. The pharmacogenomics journal 2021
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Clinical sequencing yield in epilepsy, autism spectrum disorder, and intellectual disability: A systematic review and meta-analysis.
Stefanski Arthur et al. Epilepsia 2020 Nov
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Systematic Review of the Genetics of Sudden Unexpected Death in Epilepsy: Potential Overlap With Sudden Cardiac Death and Arrhythmia-Related Genes.
Chahal C Anwar A et al. Journal of the American Heart Association 2020 Jan 9(1) e012264
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Customized multigene panels in epilepsy: the best things come in small packages.
Pellacani Simona et al. Neurogenetics 2019 Dec
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CLINGEN Actionability Report for Phenylketonuria (PKU) - PAH
ClinGen Actionability Working Group
CLINGEN Actionability Report for Glutaric Acidemia I - GCDH
ClinGen Actionability Working Group
CLINGEN Actionability Report for Basal Cell Nevus Syndrome (BCNS) - PTCH1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Neurofibromatosis type 1 - NF1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Tuberous Sclerosis Complex (TSC)-TSC1, TSC2
ClinGen Actionability Working Group
CLINGEN Actionability Report for Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukocenphalopathy, type 1 - NOTCH3
ClinGen Actionability Working Group
CLINGEN Actionability Report for Gaucher Disease - GBA
ClinGen Actionability Working Group
CLINGEN Actionability Report for Cerebral cavernous malformations 1, 2, and 3 - KRIT1, CCM2, PDCD10
ClinGen Actionability Working Group
Cost-effectiveness of screening for HLA-B*1502 prior to initiation of carbamazepine in epilepsy patients of Asian ancestry in the United States.
Choi Hyunmi et al. Epilepsia 2019 Jun
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Diagnostic yield of genetic tests in epilepsy: A meta-analysis and cost-effectiveness study.
Sánchez Fernández Iván et al. Neurology 2019 Jan
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SCN1A testing for epilepsy: application in clinical practice.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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