Lenaers, Guy

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

Delettre, C., Lenaers, G., Griffoin, J.-M., Gigarel, N., Lorenzo, C., Belenguer, P., Pelloquin, L., Grosgeorge, J., Turc-Carel, C., Perret, E., et al. (2000) · Nature Genetics

Mitochondrial Function and PathologyHereditary Neurological Disorders

Cited by 1,446

Loss of OPA1 Perturbates the Mitochondrial Inner Membrane Structure and Integrity, Leading to Cytochrome c Release and Apoptosis

Olichon, A., Baricault, L., Gas, N., Guillou, E., Valette, A., Belenguer, P., & Lenaers, G. (2003) · Journal of Biological Chemistry

Mitochondrial Function and PathologyCell death mechanisms and regulation

Cited by 1,168

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

Amati-Bonneau, P., Valentino, M. L., Reynier, P., Gallardo, M. E., Bornstein, B., Boissiere, A., Campos, Y., Rivera, H., de la Aleja, J. G., Carroccia, R., et al. (2008) · Brain

Mitochondrial Function and PathologyHereditary Neurological Disorders

Cited by 520

Mitochondrial fusion is frequent in skeletal muscle and supports excitation–contraction coupling

Eisner, V., Lenaers, G., & Hajnóczky, G. (2014) · Journal of Cell Biology

Mitochondrial Function and PathologyMuscle Physiology and Disorders

Cited by 177

A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium

Meunier, I., Lenaers, G., Bocquet, B., Baudoin, C., Piro-Megy, C., Cubizolle, A., Quilès, M., Jean-Charles, A., Cohen, S. Y., Merle, H., et al. (2016) · Human Molecular Genetics

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 16