Keisuke Hamada

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

Hirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi et al. · Nature Genetics · 2008 · 539 citations

Neurological Disorder, Genetic Disorder, Genetics +8

Structural basis of the membrane-targeting and unmasking mechanisms of the radixin FERM domain

Keisuke Hamada · The EMBO Journal · 2000 · 377 citations · Full text

Proteinlipid Interaction, Radixin Ferm Domain, Protein Secretion +9

Mutations in POLR3A and POLR3B Encoding RNA Polymerase III Subunits Cause an Autosomal-Recessive Hypomyelinating Leukoencephalopathy

Hirotomo Saitsu, Hitoshi Osaka, Masayuki Sasaki et al. · The American Journal of Human Genetics · 2011 · 169 citations · Full text

Autosomal-recessive Hypomyelinating Leukoencephalopathy, Neurological Disorder, Experimental Neuropathology +6

Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay

Hirotomo Saitsu, Jun Tohyama, Tatsuro Kumada et al. · The American Journal of Human Genetics · 2010 · 151 citations · Full text

Mendelian Disorder, Severe Cerebral Hypomyelination, Neurological Disorder +10

A Fast Loss and Temperature Simulation Method for Power Converters, Part I: Electrothermal Modeling and Validation

A.T. Bryant, N.-A. Parker-Allotey, Dean Hamilton et al. · IEEE Transactions on Power Electronics · 2011 · 71 citations

Engineering, Power Engineering, Energy Efficiency +21