Gilles Millat (G Millat)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 17

Top Topics

Hypertrophic Cardiomyopathy

African American

Intellectual Disability

Top Venues

Clinical genetics

Circulation. Genomic and precision medicine

Molecular diagnosis & therapy

This page only lists publications with an associated author ORCID identifier.

Publications

Flavie Ader, Guillaume Jedraszak, Alexandre Janin, Clarisse Billon, Nathalie Roux Buisson, Adrien Bloch, Meriem Bensalah, Anachiara De Sandre-Giovannoli, Adeline Goudal, Luisa Marsili, Cécile Cazeneuve, Philippe Charron, Gilles Millat, Pascale Richard, null null
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical genetics 105 (6) (2024)
Zangbéwendé Guy Ouedraogo, Caroline Janel, Alexandre Janin, Gilles Millat, Sarah Langlais, Bénédicte Pontier, Marie Biard, Mathis Lepage, Christine Francannet, Fanny Laffargue, Isabelle Creveaux
Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report. Genes 15 (2) (2024)
Zangbéwendé Guy Ouedraogo, Caroline Janel, Alexandre Janin, Gilles Millat, Sarah Langlais, Bénédicte Pontier, Marie Biard, Mathis Lepage, Christine Francannet, Fanny Laffargue, Isabelle Creveaux
Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report. Genes 15 (2) (2024)
Flavie Ader, Guillaume Jedraszak, Alexandre Janin, Clarisse Billon, Nathalie Roux Buisson, Adrien Bloch, Meriem Bensalah, Anachiara De Sandre-Giovannoli, Adeline Goudal, Luisa Marsili, Cécile Cazeneuve, Philippe Charron, Gilles Millat, Pascale Richard, null null
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical genetics (2024)
Zangbéwendé Guy Ouedraogo, Caroline Janel, Alexandre Janin, Gilles Millat, Sarah Langlais, Bénédicte Pontier, Marie Biard, Mathis Lepage, Christine Francannet, Fanny Laffargue, Isabelle Creveaux
Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report. Genes 15 (2) (2024)
Zangbéwendé Guy Ouedraogo, Caroline Janel, Alexandre Janin, Gilles Millat, Sarah Langlais, Bénédicte Pontier, Marie Biard, Mathis Lepage, Christine Francannet, Fanny Laffargue, Isabelle Creveaux
Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report. Genes 15 (2) (2024)
Zangbéwendé Guy Ouedraogo, Caroline Janel, Alexandre Janin, Gilles Millat, Sarah Langlais, Bénédicte Pontier, Marie Biard, Mathis Lepage, Christine Francannet, Fanny Laffargue, Isabelle Creveaux
Relevance of Extending FGFR3 Gene Analysis in Osteochondrodysplasia to Non-Coding Sequences: A Case Report. Genes 15 (2) (2024)
Flavie Ader, Guillaume Jedraszak, Alexandre Janin, Clarisse Billon, Nathalie Roux Buisson, Adrien Bloch, Meriem Bensalah, Anachiara De Sandre-Giovannoli, Adeline Goudal, Luisa Marsili, Cécile Cazeneuve, Philippe Charron, Gilles Millat, Pascale Richard, null null
Prevalence and phenotypes associated with ALPK3 null variants in a large French multicentric cohort: Confirming its involvement in hypertrophic cardiomyopathy. Clinical genetics 105 (6) (2024)
Alexis Hermida, Flavie Ader, Gilles Millat, Guillaume Jedraszak, Philippe Maury, Romain Cador, Pierre Antoine Catalan, Gaël Clerici, Nicolas Combes, Pascal De Groote, Delphine Dupin-Deguine, Romain Eschalier, Laurence Olivier-Faivre, Patricia Garcia, Benoit Guillon, Alexandre Janin, Beatrice Kugener, Marylin Lackmy, Mikael Laredo, Xavier Maximin Le Guillou Horn, François Lesaffre, Hugues Lucron, Antoine Milhem, Gwenaël Nadeau, Karine Nguyen, Asurélien Palmyre, Elodie Perdreau, François Picard, Nicolas Rebotier, Pascale Richard, Caroline Rooryck, Julien Seitz, Alain Verloes, Agathe Vernier, Pierre Winum, Grace-A-Dieu Yabeta, Océane Bouchot, Philippe Chevalier, Philippe Charron, Estelle Gandjbakhch
NEXN Gene in Cardiomyopathies and Sudden Cardiac Deaths: Prevalence, Phenotypic Expression, and Prognosis. Circulation. Genomic and precision medicine (2023)
Antoine Delinière, Christelle Haddad, C Herrera Siklody, Alexis Hermida, Etienne Pruvot, Sabrina Bressieux-Degueldre, Gilles Millat, Alexandre Janin, Jean-Sylvain Hermida, Babken Asatryan, Philippe Chevalier
Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant. Circulation. Genomic and precision medicine (2023)
Alexandre Janin, Evan Gouy, Audrey Putoux, Thomas Perouse-de-Monclos, Philippe Chevalier, Adèle Faucherre, Jourdano Mancilla Abaroa, Chris Jopling, Sophie Collardeau Frachon, Jelena Radojevic, Salima El Chehadeh, Gilles Millat
Biallelic PRKAG2 Truncating Variants Are Associated with Severe Neonatal Cardiomyopathies. Circulation. Genomic and precision medicine (2023)
Alexandre Janin, Thomas Perouse de Montclos, Karine Nguyen, Emilie Consolino, Gwenael Nadeau, Gaelle Rey, Océane Bouchot, Patricia Blanchet, Quentin Sabbagh, Cécile Cazeneuve, Rajae El-Malti, Elodie Morel, Antoine Delinière, Philippe Chevalier, Gilles Millat
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. Molecular diagnosis & therapy 26 (5) (2022)
Alexandre Janin, Louis Januel, Cécile Cazeneuve, Antoine Delinière, Philippe Chevalier, Gilles Millat
Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 Years. Molecular diagnosis & therapy 25 (3) (2021)
Oriane Marmontel, Pierre Antoine Rollat-Farnier, Anne-Sophie Wozny, Sybil Charrière, Xavier Vanhoye, Thomas Simonet, Nicolas Chatron, Delphine Collin-Chavagnac, Séverine Nony, Sabrina Dumont, Muriel Mahl, Chantal Jacobs, Alexandre Janin, Cyrielle Caussy, Pierre Poinsot, Igor Tauveron, Claire Bardel, Gilles Millat, Noël Peretti, Philippe Moulin, Christophe Marçais, Mathilde Di Filippo
Development of a new expanded next-generation sequencing panel for genetic diseases involved in dyslipidemia. Clinical genetics 98 (6) (2020)
Pauline Renaudin, Alexandre Janin, Gilles Millat, Philippe Chevalier
A Novel Missense Mutation p.Gly162Glu of the Gene MYL2 Involved in Hypertrophic Cardiomyopathy: A Pedigree Analysis of a Proband. Molecular diagnosis & therapy 22 (2) (2018)
Oriane Marmontel, S Charrière, T Simonet, V Bonnet, S Dumont, M Mahl, C Jacobs, S Nony, K Chabane, D Bozon, Alexandre Janin, N Peretti, A Lachaux, C Bardel, Gilles Millat, P Moulin, C Marçais, M Di Filippo
Single, short in-del, and copy number variations detection in monogenic dyslipidemia using a next-generation sequencing strategy. Clinical genetics 94 (1) (2018)
A Janin, K N'Guyen, G Habib, C Dauphin, V Chanavat, P Bouvagnet, R Eschalier, N Streichenberger, P Chevalier, Gilles Millat
Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy. Clinical genetics 92 (6) (2017)