Florence Kyndt - Publications

From outflow tract development to ventriculo-arterial discordance - Developmental and genetic mechanisms of d-TGA and ccTGA.

Journal: FEBS letters

Published: April 09, 2026

Etiologic Diagnosis of Neuropathies Based on First-Line Screening of TTR Gene Mutations.

Journal: Journal of the peripheral nervous system : JPNS

Published: April 20, 2025

Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiology.

Journal: medRxiv : the preprint server for health sciences

Published: November 01, 2024

Non-juvenile familial form of life-threatening arrhythmias caused by the Ryanodine Receptor type 2 c.13823 G>A, p.(Arg4608Gln) pathogenic variant: Atypical catecholaminergic polymorphic ventricular Tachycardia or misdiagnosis?

Journal: Forensic science international. Genetics

Published: October 30, 2024

Late outcomes of congenital and childhood non-immune, isolated atrioventricular block: a French nationwide retrospective cohort study.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: September 08, 2024

Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome.

Journal: Heart rhythm

Published: August 19, 2024

Phenotypic spectrum of cardiac conduction disturbance and cardiomyopathy linked to titin canonical splice-site variants.

Journal: Cardiovascular research

Published: June 11, 2024

Generation of a patient-specific induced pluripotent stem cell line carrying the DES p.R406W mutation, an isogenic control and a DES p.R406W knock-in line.

Journal: Stem cell research

Published: February 02, 2024

Filamin A heart valve disease as a genetic cause of inherited bicuspid and tricuspid aortic valve disease.

Journal: Heart (British Cardiac Society)

Published: September 22, 2023

Type 3 long QT syndrome: Is the effectiveness of treatment with beta-blockers population-specific?

Journal: Heart rhythm

Published: September 01, 2023

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.

Journal: Nature communications

Published: February 17, 2023

Functional Epicardial Conduction Disturbances Due to a SCN5A Variant Associated With Brugada Syndrome.

Journal: JACC. Clinical electrophysiology

Published: February 03, 2023