Giovanni Stevanin

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

Dagmar Nolte, Ulrich Müller, S. Pulst, 2006, Nature Genetics.

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

Yves Agid, Jean-Louis Mandel, Gaël Yvert, 1996, Nature Genetics.

Differential distribution of the normal and mutated forms of huntingtin in the human brain

Yves Agid, Laszlo Tora, E. Hirsch, 1997, Annals of neurology.

Spinocerebellar ataxia 3 and machado‐joseph disease: Clinical, molecular, and neuropathological features

Alexandra Durr, Charles Duyckaerts, Yves Agid, 1996, Annals of neurology.

Spectrin mutations cause spinocerebellar ataxia type 5

J. Rothstein, A. Dürr, A. Brice, 2006, Nature Genetics.

Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia.

Alexandra Durr, Chokri Mhiri, Stephan Züchner, 2013, American journal of human genetics.