ArticleEpilepsy currents2011
Genetic testing in epilepsy: what should you be doing?
Article in Epilepsy currents, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
16 citing papers in PubMed.
- Tracking Multifocal Epilepsy With Automated Electric Source Imaging in a Patient With Triple-X Syndrome.Journal of clinical neurology (Seoul, Korea) · 2022Article
- Multimodal Analysis ofFrontiers in neurology · 2019Article
- ExACtly zero or once: A clinically helpful guide to assessing genetic variants in mild epilepsies.Neurology. Genetics · 2017Article
- Unexplained Early Infantile Epileptic Encephalopathy in Han Chinese Children: Next-Generation Sequencing and Phenotype Enriching.Scientific reports · 2017Article
- Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes.PloS one · 2017Article
- Parents' interest in genetic testing of their offspring in multiplex epilepsy families.Epilepsia · 2016Article
- Precision medicine is here, break out your wallet.Applied & translational genomics · 2015Article
- Genetic testing preferences in families containing multiple individuals with epilepsy.Epilepsia · 2014Article
- Genotype & Phenotype of Ohtahara Syndrome-What's SCN2A Got to Do With It? A Clinician's Read.Epilepsy currents · 2014Article
- Genomic biomarkers of SUDEP in brain and heart.Epilepsy & behavior : E&B · 2014Review
- Genetic testing in the epilepsies-developments and dilemmas.Nature reviews. Neurology · 2014Review
- Seizures and X-linked intellectual disability.European journal of medical genetics · 2012Review
- Epilepsy and autism: is there a special relationship?Epilepsy & behavior : E&B · 2012Review
- Alphabet Soup: Recurrent De Novo Mutations in Novel Genes Causing Developmental and Epileptic Encephalopathies.Epilepsy currentsArticle
- Attitudes Toward Epilepsy Genetics Testing Among Adult and Pediatric Epileptologists-Results of a Q-PULSE Survey.Epilepsy currentsArticle
- Genetic Testing in the Presurgical Evaluation of Drug-Resistant Epilepsy: Bells and Whistles or Nuts and Bolts?Epilepsy currentsArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
With the burgeoning array of molecular tests available in the epilepsies, the clinician needs to know which tests to order for each patient. Epileptic encephalopathies are the most important clinical group for genetic testing with an increasing number of distinctive epilepsy syndromes being recognized. Identification of the causative mutation affects treatment as well as prognostic and genetic counseling.
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.