Author

C. Dina

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Open access Oct 2026

Convergent genetic and functional evidence implicate KCND3 in Brugada Syndrome

Background: Dysfunction of the KCND3-encoded Kv4.3 channel, which carries the transient outward potassium current (Ito), has long been suspected to contribute to the pathophysiology of Brugada Syndrome (BrS). Although recent genome-wide association studies (GWAS) have implicated KCND3, the role of rare variation in thi...

H. Liu, A. Verkerk, P. Lindenbaum et al. · medRxiv · 0 citations

Open access Sep 2026

Clinical and multi-omics characterisation of early neurodevelopmental disorders associated with critical congenital heart disease: the prospective cohort CATAMARAN neonatal study protocol

This study aims to evaluate early neurodevelopmental status in infants with prenatally diagnosed critical CHD and to determine how intrinsic susceptibility, prenatal and postnatal factors are functionally associated with developmental delay in this population.

Oscar Werner, Véronique Ferchaud-Roucher, Matilde Karakachoff et al. · BMJ Open · 0 citations

Open access Aug 2026

Genomic meta-analyses of binge-eating behavior and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes

A genomic meta-analysis of case–control studies of binge-eating behavior and analyses of anorexia nervosa and its subtypes, alongside analyses of AN, identified six BE-associated loci and eight areas that are associated with anorexia nervosa, in people of European ancestry.

Jet D. Termorshuizen, Helena L. Davies, Sang-Hyuck Lee et al. · Nature Mental Health · 1 citation