Yoshio Ikeda

Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI

Mikio Shoji, Mitsunori Watanabe, Koichi Okamoto, 2000, Journal of the Neurological Sciences.

Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.

Koji Abe, Akio Koizumi, Hiroko Okuda, 2011, American journal of human genetics.

Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes

L. Ranum, Y. Ikeda, R. Daughters, 2008, The Cerebellum.

Spectrin mutations cause spinocerebellar ataxia type 5

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