Camille Laberthonnière

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 5

Top Venues

Biomedicines

Journal of cachexia, sarcopenia and muscle

Neurology. Genetics

International journal of molecular sciences

Marseille Medical Genetics

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

Affiliation History

Marseille Medical Genetics

France

PhD Candidate :: Epigenetics, Chromatin and Disease Modeling

Publications

Julian A Arts, Camille Laberthonnière, Dulce Lima Cunha, Huiqing Zhou
Single-Cell RNA Sequencing: Opportunities and Challenges for Studies on Corneal Biology in Health and Disease. Cells 12 (13) (2023)
María Del Carmen Ortuño-Costela, Victoria Cerrada, Ana Moreno-Izquierdo, Inés García-Consuegra, Camille Laberthonnière, Mégane Delourme, Rafael Garesse, Joaquín Arenas, Carla Fuster-García, Gema García-García, José María Millán, Frédérique Magdinier, María Esther Gallardo
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology. International journal of molecular sciences 23 (22) (2022)
Camille Laberthonnière, Elva Maria Novoa-Del-Toro, Raphaël Chevalier, Natacha Broucqsault, Vanitha Venkoba Rao, Jean Philippe Trani, Karine Nguyen, Shifeng Xue, Bruno Reversade, Jérôme D Robin, Anaïs Baudot, Frédérique Magdinier
AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia Syndrome. Biomedicines 9 (7) (2021)
Camille Laberthonnière, Elva-Maria Novoa-Del-Toro, Mégane Delourme, Raphaël Chevalier, Natacha Broucqsault, Kilian Mazaleyrat, Nathalie Streichenberger, Véronique Manel, Rafaëlle Bernard, Emmanuelle Salort Campana, Shahram Attarian, Karine Nguyen, Jérôme D Robin, Anais Baudot, Frédérique Magdinier
Facioscapulohumeral dystrophy weakened sarcomeric contractility is mimicked in induced pluripotent stem cells-derived innervated muscle fibres. Journal of cachexia, sarcopenia and muscle (2021)
Stéphane Roche, Camille Dion, Natacha Broucqsault, Camille Laberthonnière, Marie-Cécile Gaillard, Jérôme D Robin, Arnaud Lagarde, Francesca Puppo, Catherine Vovan, Charlene Chaix, Emmanuelle Salort Campana, Shahram Attarian, Marc Bartoli, Rafaelle Bernard, Karine Nguyen, Frédérique Magdinier
Methylation hotspots evidenced by deep sequencing in patients with facioscapulohumeral dystrophy and mosaicism. Neurology. Genetics 5 (6) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Camille Laberthonnière