Journal article
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy
C Leu, S Balestrini, B Maher, L Hernández-Hernández, P Gormley, E Hämäläinen, K Heggeli, N Schoeler, J Novy, J Willis, V Plagnol, R Ellis, E Reavey, M O'Regan, WO Pickrell, RH Thomas, SK Chung, N Delanty, JM McMahon, S Malone Show all
Ebiomedicine | Published : 2015
Open access
Abstract
Sudden unexpected death in epilepsy (SUDEP) represents the most severe degree of the spectrum of epilepsy severity and is the commonest cause of epilepsy-related premature mortality. The precise pathophysiology and the genetic architecture of SUDEP remain elusive. Aiming to elucidate the genetic basis of SUDEP, we analysed rare, protein-changing variants from whole-exome sequences of 18 people who died of SUDEP, 87 living people with epilepsy and 1479 non-epilepsy disease controls. Association analysis revealed a significantly increased genome-wide polygenic burden per individual in the SUDEP cohort when compared to epilepsy (P=5.7×10-3) and non-epilepsy disease controls (P=1.2×10-3). The po..
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Awarded by Dravet Syndrome UK