Kenji Yokochi

Mutations in the integrin α7 gene cause congenital myopathy

Yukiko Hayashi, Fan-Li Chou, Eva Engvall et al. · Nature Genetics · 1998 · 357 citations

Genetic Disorder, Immunodeficiencies, Genetics +3

Phenotypic Spectrum of <i>COL4A1</i> Mutations: Porencephaly to Schizencephaly

Yuriko Yoneda, Kazuhiro Haginoya, Mitsuhiro Kato et al. · Annals of Neurology · 2012 · 171 citations

Genotype–phenotype correlations in alternating hemiplegia of childhood

Masayuki Sasaki, Atsushi Ishii, Yoshiaki Saito et al. · Neurology · 2014 · 118 citations

Magnetic Resonance Imaging Children with Spastic Diplegia: Correlation with the Severity of their Motor and Mental Abnormality

Kenji Yokochi, Kumi Aiba, Masayo Horie et al. · Developmental Medicine & Child Neurology · 1991 · 114 citations

De Novo and Inherited Mutations in COL4A2, Encoding the Type IV Collagen α2 Chain Cause Porencephaly

Yuriko Yoneda, Kazuhiro Haginoya, Hiroshi Arai et al. · The American Journal of Human Genetics · 2011 · 96 citations

Developmental Biology, Medicine, Cell Biology +3