Kyoko Hirasawa

<i>STXBP1</i> mutations cause not only Ohtahara syndrome but also West syndrome—Result of Japanese cohort study

Motoko Otsuka, Hirokazu Oguni, Jao‐Shwann Liang et al. · Epilepsia · 2010 · 115 citations

Medicine, Genetics, Molecular Genetics +15

CDKL5 alterations lead to early epileptic encephalopathy in both genders

Jao‐Shwann Liang, Keiko Shimojima, Rumiko Takayama et al. · Epilepsia · 2011 · 69 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Microarray analysis of 50 patients reveals the critical chromosomal regions responsible for 1p36 deletion syndrome-related complications

Shino Shimada, Keiko Shimojima, Nobuhiko Okamoto et al. · Brain and Development · 2014 · 65 citations

Life Sciences, Genetics, Molecular Genetics +16

Hemodynamic responses to visual stimulation in occipital and frontal cortex of newborn infants: a near-infrared optical topography study

Gentaro Taga, Kayo Asakawa, Kyoko Hirasawa et al. · Early Human Development · 2003 · 57 citations

Life Sciences, Neurobiology, Neuroscience +17

Clinical manifestations of Xq28 functional disomy involving <i>MECP2</i> in one female and two male patients

Shino Shimada, Nobuhiko Okamoto, Kyoko Hirasawa et al. · American Journal of Medical Genetics Part A · 2013 · 55 citations

Life Sciences, Genetics, Molecular Genetics +17