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Public Health Genomics and Precision Health Knowledge Base (v7.9)

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Precision Health Database

Genomics & Health Impact Scan Database|Search|PHGKB

Neurological Disorders

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Records 1 - 19 (of 19 Records)

Query Trace: Epilepsy[original query]>>Evidence Synthesis [Product Type]
A systematic review on the cost effectiveness of pharmacogenomics in developing countries: implementation challenges. Sukri Asif et al. The pharmacogenomics journal 2022 Similar articles in PubMed
Genetic testing for the epilepsies: A systematic review. Sheidley Beth R et al. Epilepsia 2021 Similar articles in PubMed
Machine learning models for decision support in epilepsy management: A critical review. Smolyansky Eliot D et al. Epilepsy & behavior : E&B 2021 123108273 Similar articles in PubMed
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) Similar articles in PubMed
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 Similar articles in PubMed
Clinical sequencing yield in epilepsy, autism spectrum disorder, and intellectual disability: A systematic review and meta-analysis. Stefanski Arthur et al. Epilepsia 2020 Nov Similar articles in PubMed
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 Similar articles in PubMed
Customized multigene panels in epilepsy: the best things come in small packages. Pellacani Simona et al. Neurogenetics 2019 Dec Similar articles in PubMed
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 Similar articles in PubMed
Diagnostic yield of genetic tests in epilepsy: A meta-analysis and cost-effectiveness study. Sánchez Fernández Iván et al. Neurology 2019 Jan Similar articles in PubMed
SCN1A testing for epilepsy: application in clinical practice. Similar articles in PubMed

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