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

The Epilepsy Phenome/Genome Project (EPGP) informatics platform.

International journal of medical informatics - 1 Apr 2013

Nesbitt Gerry, McKenna Kevin, Mays Vickie, Carpenter Alan, Miller Kevin, Williams Michael

Abstract excerpt

BACKGROUND: The Epilepsy Phenome/Genome Project (EPGP) is a large-scale, multi-institutional, collaborative network of 27 epilepsy centers throughout the U.S., Australia, and Argentina, with the objective of collecting detailed phenotypic and genetic data on a large number of epilepsy participants. The goals of EPGP are (1) to perform detailed phenotyping on 3750 participants with specific forms of non-acquired...

Read the complete abstract on PubMed

Topics

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

Share to Argentina
Share to Australia
Share to Databases, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electroencephalography

Share to Epilepsy

Share to Internet

Share to Specimen Handling

Share to United States

Source

Open in PubMed Open full text

Identifiers

PMID: 22579394
DOI: 10.1016/j.ijmedinf.2012.03.004
PMCID: PMC3655424

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The Epilepsy Phenome/Genome Project (EPGP) informatics platform.PMID 22579394Read ↗

The epilepsy phenome/genome project.Semantic proximity Read ↗

Individualised human phenotype ontology gene panels improve clinical whole exome and genome sequencing analytical efficacy in a cohort of developmental and epileptic encephalopathies.Semantic proximity Read ↗

Accessibility, availability and common practices regarding genetic testing for epilepsy across Europe: A survey of the European Reference Network EpiCARESemantic proximity Read ↗

Computation of longitudinal phenotypes in 466 individuals with a developmental and epileptic encephalopathy enables clinical trial readinessSemantic proximity Read ↗

The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning systemSemantic proximity Read ↗

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

Healthcare utilization and clinical characteristics of genetic epilepsy in electronic health recordsSemantic proximity Read ↗

Using Phecodes for Research with the Electronic Health Record: From PheWAS to PheRS.Semantic proximity Read ↗

pyPheWAS: A Phenome-Disease Association Tool for Electronic Medical Record Analysis.Semantic proximity Read ↗

Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable.Semantic proximity Read ↗

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

Clinical Characteristics and Treatment Experience of Individuals with SCN8A Developmental and Epileptic Encephalopathy (SCN8A-DEE): Findings from an Online Caregiver SurveySemantic proximity Read ↗

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