Unraveling the role of non-coding rare variants in epilepsy.
The discovery of new variants has leveled off in recent years in epilepsy studies, despite the use of very large cohorts. Consequently, most of the heritability is still unexplained. Rare non-coding variants have been largely ignored in studies on epilepsy, although non-coding single nucleotide vari...
Main Authors: | Alexandre Girard, Claudia Moreau, Jacques L Michaud, Berge Minassian, Patrick Cossette, Simon L Girard |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2023-01-01
|
Series: | PLoS ONE |
Online Access: | https://doi.org/10.1371/journal.pone.0291935 |
Similar Items
-
Unraveling the role of non-coding rare variants in epilepsy
by: Alexandre Girard, et al.
Published: (2023-01-01) -
P607: Identification of pathogenic genetic variants using whole genome sequencing in patients with epilepsy
by: Oleksandr Olifir, et al.
Published: (2024-01-01) -
The role of common genetic variation in presumed monogenic epilepsies
by: Ciarán Campbell, et al.
Published: (2022-07-01) -
Progressive Myoclonus Epilepsy: A Scoping Review of Diagnostic, Phenotypic and Therapeutic Advances
by: Vincent Zimmern, et al.
Published: (2024-01-01) -
Rare Coding Variants in Patients with Non-Syndromic Vestibular Dysfunction
by: Angelo Augusto M. Sumalde, et al.
Published: (2023-03-01)