Gilles Millat

12PUBLICATIONS
61CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)NeonatologyNeurology and neuromuscular diseasesGene mappingCardiology (incl. cardiovascular diseases)
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Publications (12)

|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

|Jul 15, 2022
Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants.

Alexandre Janin, Thomas Perouse de Montclos, Karine Nguyen

|May 06, 2021
Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 Years.

Alexandre Janin, Louis Januel, Cécile Cazeneuve

|Oct 28, 2020
Development of a new expanded next-generation sequencing panel for genetic diseases involved in dyslipidemia.

Oriane Marmontel, Pierre Antoine Rollat-Farnier, Anne-Sophie Wozny

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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