Jocelyn Laporte

36PUBLICATIONS
153CO-AUTHORS
Craniofacial biologyMechanobiologyNeurology and neuromuscular diseasesMedical mycologyMicroelectromechanical systems (MEMS)
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Publications (36)

|Sep 23, 2026
DNM2-Charcot-Marie-Tooth neuropathy stems from disrupted Schwann cell function and shows limited therapeutic reversibility.

|Aug 25, 2026
BIN1 overexpression rescues cardiac but not skeletal muscle defects in a mouse model of caveolinopathy.

|Aug 18, 2026
Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

|Jul 03, 2026
Circulating MYOM3 fragments reflect disease severity and therapeutic efficacy in tubular aggregate myopathy and Stormorken syndrome.

|Feb 13, 2026
Muscle-Specific DNM2 Overexpression Improves Charcot-Marie-Tooth Disease In Vivo and Reveals a Narrow Therapeutic Window in Skeletal Muscle.

Marie Goret, Gwenaelle Piccolo, Jocelyn Laporte

|Dec 29, 2025
Tamoxifen treatment fails to improve muscle dysfunction in a model of recessive RYR1-linked centronuclear myopathy.

Charlotte Gineste, David Reiss, Jocelyn Laporte

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Frequent Collaborators

10 joint publications

Johann Böhm

4 joint publications

Belinda S Cowling

3 joint publications

Marie Goret

3 joint publications

Roberto Silva-Rojas