M. Muglia

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Stephan Züchner, Irina Mersiyanova, M. Muglia et al. · Nature Genetics · 2004 · 1.5K citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Mitochondrial Function +9

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2

Alessandra Bolino, M. Muglia, F. L. Conforti et al. · Nature Genetics · 2000 · 457 citations

Myotubularin-related Protein-2, Mendelian Disorder, Genetic Disorder +7

Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity

Luca Passamonti, Francesco Saverio Fera, A. Magariello et al. · Biological Psychiatry · 2005 · 168 citations

Neuropsychology, Psychiatry, Neural Correlates +14

Loss-of-function mutations in the<i>SIGMAR1</i>gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca²⁺signalling

Elisa Gregianin, Giorgia Pallafacchina, Sofia Zanin et al. · Human Molecular Genetics · 2016 · 93 citations · Full text

Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis

F. L. Conforti, Rossella Spataro, William Sproviero et al. · Neurology · 2012 · 85 citations · Full text