Identify the genetic basis of myopathies
Subgroup Leader : Valérie BIANCALANA
We study rare and severe neuromuscular disorders caused by mutations in proteins controlling intracellular organization and dynamics. We aim to tackle the three main bottlenecks in this field:
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Identify the genetic basis of myopathies, myalgia and high athletic performances
Project leaders : Valérie BIANCALANA, Johann BOHM, Jocelyn LAPORTE
Understand and cure myotubular/centronuclear myopathies through gene modulation and pharmacology
Project leader : Jocelyn LAPORTE
Understand and cure tubular aggregates myopathy and Stormorken syndrome through gene modulation and pharmacology
Project leader : Johann BOHM
Subgroup Leader : Valérie BIANCALANA
Subgroup Leader : Jocelyn LAPORTE
Article in a journal
Human Molecular Genetics ; Volume: 26 ; Page: 3736-3748
Article in a journal
Ann Neurol ; Volume: 81 ; Page: 467-473
Article in a journal
Nature Communications ; Volume: 8 ; Page: 15661
Article in a journal
Brain - A Journal of Neurology ; Volume: 140 ; Page: 37-48
Article in a journal
American Journal of Human Genetics ; Volume: 99 ; Page: 1086-1105
Article in a journal
American Journal of Human Genetics ; Volume: 99 ; Page: 753 - 761
Article in a journal
Biochemical and Biophysical Research Communications ; Volume: 476 ; Page: 167-173
Article in a journal
Journal of Neuromuscular Diseases ; Volume: 3 ; Page: 111-114
Article in a journal
Nature ; Volume: 529 ; Page: 408-12
Article in a journal
Pediatric neurology ; Volume: 58 ; Page: 107-12
Current fundings:

Her work, supervised by Dr. Jocelyn Laporte, is entitled "New Therapeutic Approaches for Neuromuscular Diseases."
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On
12/102025
Follow our publications and latest research on Researchgate : www.researchgate.net/profile/Jocelyn-Laporte
Raw data for our study on Multi-omics comparisons of different forms of centronuclear myopathies and the effects of several therapeutic strategies. Mol Ther. 2021 Apr 30:S1525-0016(21)00247-1.
www.ncbi.nlm.nih.gov/geo/query/acc.cgi
www.sciencedirect.com/science/article/abs/pii/S1525001621002471
In the press: