Yasumasa Kokubo

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study

Manabu Funayama, Kenji Ohe, Taku Amo et al. · The Lancet Neurology · 2015 · 346 citations

Neurodegenerative Diseases, Chchd2 Mutations, Mendelian Disorder +10

Familial amyotrophic lateral sclerosis and parkinsonism‐dementia complex of the Kii peninsula of Japan: Clinical and neuropathological study and tau analysis

Shigeki Kuzuhara, Yasumasa Kokubo, Ryogen Sasaki et al. · Annals of Neurology · 2001 · 115 citations

Pathology, Neurobiology Of Disease, Alzheimer's Disease +19

C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan

Hiroyuki Ishiura, Yuji Takahashi, Jun Mitsui et al. · Archives of Neurology · 2012 · 101 citations

Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS

Kotaro Ogaki, Yuanzhe Li, Masashi Takanashi et al. · Parkinsonism & Related Disorders · 2012 · 93 citations · Full text

Mendelian Disorder, C9orf72 Mutations, Medicine +8

<i>VPS35</i> mutation in Japanese patients with typical Parkinson's disease

Maya Ando, Manabu Funayama, Yuanzhe Li et al. · Movement Disorders · 2012 · 82 citations · Full text