Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Healthcare utilization and clinical characteristics of genetic epilepsy in electronic health records

1 Jan 2024

Abstract excerpt

Abstract Understanding the clinical characteristics and medical treatment of individuals affected by genetic epilepsies is instrumental in guiding selection for genetic testing, defining the phenotype range of these rare disorders, optimizing patient care pathways and pinpointing unaddressed medical need by quantifying healthcare resource utilization. To date, a matched longitudinal cohort study encompassing the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Epilepsy research and treatment
Share to Genetics and Neurodevelopmental Disorders
Share to Genomics and Rare Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 38524155
DOI: 10.1093/braincomms/fcae090

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Healthcare utilization and clinical characteristics of genetic epilepsy in electronic health recordsPMID 38524155Read ↗

Healthcare utilization and clinical characteristics of genetic epilepsy syndromes: a longitudinal case-control study of electronic health recordsSemantic proximity Read ↗

Clinical signatures of genetic epilepsy precede diagnosis in electronic medical records of 32,000 individualsSemantic proximity Read ↗

A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation.Semantic proximity Read ↗

Underutilization of Syndrome-Specific ICD-10 Codes for Genetic Epilepsies: Implications for Precision MedicineSemantic proximity Read ↗

An algorithm to identify patients with rare genetic disorders and its real-world data applicationSemantic proximity Read ↗

Evaluating Clinical Presentation and Long-Term Outcomes in Individuals with Genetic and Non-Genetic Epilepsy Treated with Epilepsy Surgery: A Single-Center StudySemantic proximity Read ↗

Genetic Testing in Adult Patients With Epilepsy: Genetic Risk Index for Seizure Etiology for Identifying Optimal Candidates.Semantic proximity Read ↗

Clinical signatures of genetic epilepsies precede diagnosis in electronic medical records of 32,000 individualsSemantic proximity Read ↗

Epilepsy panels in clinical practice: Yield, variants of uncertain significance, and treatment implications.Semantic proximity Read ↗

Multigene Panel Testing in a Large Cohort of Adults With EpilepsySemantic proximity Read ↗

Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical PracticeSemantic proximity Read ↗

Expansion of clinical genetic testing since the completion of the human genome projectSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.