Gilles Millat

Centre De Biologie Et Pathologie Est, CHU De Lyon HCL GH Est
Lyon, France

Last Updated: 09/26/2026

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Found 64 publications

Long-read Oxford Nanopore sequencing enables rapid, cost-effective, and comprehensive TTR genetic testing for hereditary transthyretin amyloidosis.

Long-read Oxford Nanopore sequencing enables rapid, cost-effective, and comprehensive TTR genetic testing for hereditary transthyretin amyloidosis.

Journal: Clinical chemistry and laboratory medicine

Published: April 08, 2026

Caenorhabditis elegans as an in vivo model system for human inherited primary arrhythmia syndromes.

Caenorhabditis elegans as an in vivo model system for human inherited primary arrhythmia syndromes.

Journal: The Journal of physiology

Published: July 29, 2025

How to approach multiple arrhythmias in a young athlete with SCN5A mutation.

How to approach multiple arrhythmias in a young athlete with SCN5A mutation.

Journal: HeartRhythm case reports

Published: June 09, 2025

Prognosis for loss-of-function vs hot-spot variants in RBM20-related cardiomyopathy.

Prognosis for loss-of-function vs hot-spot variants in RBM20-related cardiomyopathy.

Journal: Heart rhythm

Published: April 17, 2025

Dilated cardiomyopathy in patients with PRDM16 haploinsufficiency.

Dilated cardiomyopathy in patients with PRDM16 haploinsufficiency.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: February 24, 2025

RBM20 Gene in Patients With Cardiomyopathy: Phenotypic Expression for Loss-of-Function Versus Hotspot Variants.

RBM20 Gene in Patients With Cardiomyopathy: Phenotypic Expression for Loss-of-Function Versus Hotspot Variants.

Journal: Circulation. Heart failure

Published: January 17, 2025

Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategies.

Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategies.

Journal: Orphanet journal of rare diseases

Published: June 10, 2024

Cardiogenetics and uncertainty: Evaluation of professional vulnerability in France.

Cardiogenetics and uncertainty: Evaluation of professional vulnerability in France.

Journal: European journal of medical genetics

Published: April 21, 2024

Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report.

Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report.

Journal: Genes

Published: December 20, 2023

NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.

NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.

Journal: Circulation. Genomic and precision medicine

Published: December 07, 2023

Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy.

Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy.

Journal: Clinical genetics

Published: December 06, 2023

Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome.

Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome.

Journal: Gene

Published: September 29, 2023

Showing 1-12 of 64

Last Updated: 09/26/2026