Gilles Millat
12PUBLICATIONS
61CO-AUTHORS
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Publications (12)
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|Jan 17, 2025
RBM20 Gene in Patients With Cardiomyopathy: Phenotypic Expression for Loss-of-Function Versus Hotspot Variants.Alexis Hermida, Flavie Ader, Gilles Millat
|Feb 24, 2024
Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report.Zangbéwendé Guy Ouedraogo, Caroline Janel, Alexandre Janin
|Feb 15, 2024
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy.Flavie Ader, Guillaume Jedraszak, Alexandre Janin
|Dec 07, 2023
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis.Alexis Hermida, Flavie Ader, Gilles Millat
|Apr 04, 2023
Biallelic PRKAG2 Truncating Variants Are Associated with Severe Neonatal Cardiomyopathies.Alexandre Janin, Evan Gouy, Audrey Putoux
|Apr 03, 2023
Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant.Antoine Delinière, Christelle Haddad, Claudia Herrera-Siklódy
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Frequent Collaborators
7 joint publications
Alexandre Janin
4 joint publications
Philippe Chevalier
3 joint publications
Pascale Richard
3 joint publications
Alexis Hermida
3 joint publications
Flavie Ader
2 joint publications
Oriane Marmontel
2 joint publications
Aurélien Palmyre
2 joint publications
Pascal De Groote
2 joint publications
Phillipe Maury
2 joint publications
Guillaume Jedraszak
