Kenya Nishioka

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

Genomic investigation of α‐synuclein multiplication and parkinsonism

Owen A. Ross, Adam Braithwaite, Lisa Skipper et al. · Annals of Neurology · 2008 · 339 citations · Full text

Plasma endothelin concentrations in patients with pulmonary hypertension associated with congenital heart defects. Evidence for increased production of endothelin in pulmonary circulation.

Muneo Yoshibayashi, Kenya Nishioka, Kazuwa Nakao et al. · Circulation · 1991 · 334 citations · Full text

Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease

Kenya Nishioka, Shin Hayashi, Matthew J. Farrer et al. · Annals of Neurology · 2005 · 311 citations

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell et al. · The American Journal of Human Genetics · 2011 · 299 citations · Full text

Familial Parkinson Disease, Mendelian Disorder, Genetic Disorder +5