Ken Inoue

Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations

Ken Inoue, Mehrdad Khajavi, Tomoko Ohyama et al. · Nature Genetics · 2004 · 417 citations

Neurodegenerative Diseases, Allelic Variant, Molecular Neuroscience +12

The 1.4-Mb CMT1A Duplication/HNPP Deletion Genomic Region Reveals Unique Genome Architectural Features and Provides Insights into the Recent Evolution of New Genes

Ken Inoue, Ken Dewar, Nicholas Katsanis et al. · Genome Research · 2001 · 182 citations · Full text

Myelin deficiencies in both the central and the peripheral nervous systems associated with aSOX10 mutation

Ken Inoue, Yuzo Tanabe, James R. Lupski · Annals of Neurology · 1999 · 173 citations

Neurological Disorder, Genetics, Unique Patient +20

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

Genomic Rearrangements Resulting in PLP1 Deletion Occur by Nonhomologous End Joining and Cause Different Dysmyelinating Phenotypes in Males and Females

Ken Inoue, Hitoshi Osaka, Virginia C. Thurston et al. · The American Journal of Human Genetics · 2002 · 159 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +8