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Record W2904891280 · doi:10.1038/s41467-018-07524-z

Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies

2018· article· en· W2904891280 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenueNature Communications · 2018
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenomics and Rare Diseases
Canadian institutionsUniversité de Montréal
FundersNational Institute of Child Health and Human DevelopmentNational Institute of Neurological Disorders and StrokeStatens Serum InstitutNational Center for Advancing Translational SciencesMedical Research CouncilNational Institutes of HealthRoyal Melbourne Hospital Neuroscience FoundationChinese University of Hong KongEunice Kennedy Shriver National Institute of Child Health and Human DevelopmentUniversitair Medisch Centrum UtrechtScience Foundation IrelandHelmholtz Zentrum MünchenEuropean Regional Development FundBundesministerium für Bildung und ForschungNational Institute for Health and Care ResearchEuropean CommissionNationwide Children's HospitalDanish Cancer Society Research CenterWellcome TrustUniversité du LuxembourgNational Health and Medical Research CouncilChildren's Hospital of PhiladelphiaDeutsche ForschungsgemeinschaftEuropean Science FoundationEpilepsy SocietyUniversity of DundeeGlaxoSmithKline
KeywordsEpilepsyBiologyEpigeneticsGenome-wide association studyGeneticsGeneGenomeComputational biologyHeritabilitySNPGenetic associationEvolutionary biologyBioinformaticsSingle-nucleotide polymorphismNeuroscienceGenotype

Abstract

fetched live from OpenAlex

The epilepsies affect around 65 million people worldwide and have a substantial missing heritability component. We report a genome-wide mega-analysis involving 15,212 individuals with epilepsy and 29,677 controls, which reveals 16 genome-wide significant loci, of which 11 are novel. Using various prioritization criteria, we pinpoint the 21 most likely epilepsy genes at these loci, with the majority in genetic generalized epilepsies. These genes have diverse biological functions, including coding for ion-channel subunits, transcription factors and a vitamin-B6 metabolism enzyme. Converging evidence shows that the common variants associated with epilepsy play a role in epigenetic regulation of gene expression in the brain. The results show an enrichment for monogenic epilepsy genes as well as known targets of antiepileptic drugs. Using SNP-based heritability analyses we disentangle both the unique and overlapping genetic basis to seven different epilepsy subtypes. Together, these findings provide leads for epilepsy therapies based on underlying pathophysiology.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.414
Threshold uncertainty score0.300

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.020
GPT teacher head0.283
Teacher spread0.264 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it