matsumoto ayumi

Faculty
Job titleAssistant ProfessorWeb site

Profile

Research Keywords

    Human Genetics, pediatric neurology

Academic Societies

  • JAPAN PEDIATRIC SOCIETY
  • THE JAPANESE SOCIETY OF CHILD NEUROLOGY
  • THE JAPAN SOCIETY OF HUMAN GENETICS
  • JAPAN EPILEPSY SOCIETY
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Academic Societiesclose
  • JAPAN PEDIATRIC SOCIETY
  • THE JAPANESE SOCIETY OF CHILD NEUROLOGY
  • THE JAPAN SOCIETY OF HUMAN GENETICS
  • JAPAN EPILEPSY SOCIETY

Research Activities

Papers(paper)

  • Morphological characterization of Class III phosphoinositide 3-kinase during mouse brain development.
    Inaguma Y, Ito H, Iwamoto I, Matsumoto A, Yamagata T, Tabata H, Nagata KI
    Medical molecular morphology 49(1) 28-33 Aug. 2015
  • Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients.
    Yang Z, Matsumoto A, Nakayama K, Jimbo EF, Kojima K, Nagata KI, Iwamoto S, Yamagata T
    Brain & development 38(1) 99 May 2015
  • Morphological characterization of mammalian timeless in the mouse brain development.
    Inaguma Y, Ito H, Hara A, Iwamoto I, Matsumoto A, Yamagata T, Tabata H, Nagata K
    Neuroscience research 92 21-28 Mar. 2015
  • Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders.
    Mizuno M, Matsumoto A, Hamada N, Ito H, Miyauchi A, Jimbo EF, Momoi MY, Tabata H, Yamagata T, Nagata KI
    Journal of neurochemistry 132(1) 61-69 Sep. 2014
  • [Genetic analysis and genes relating synaptic function for autism spectrum disorder].
    Yamagata T, Matsumoto A, Nagata K
    No to hattatsu. Brain and development 46 125-130 Mar. 2014
  • MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus.
    Saito M, Yamagata T, Matsumoto A, Shiba Y, Nagashima M, Taniguchi S, Jimbo E, Momoi MY
    Brain & development 36(1) 64-69 Jan. 2014
  • LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome.
    Matsumoto A, Mizuno M, Hamada N, Nozaki Y, Jimbo EF, Momoi MY, Nagata K, Yamagata T
    PloS one 9(3) 2014
  • An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities.
    Matsumoto A, Kuwajima M, Miyake K, Kojima K, Nakashima N, Jimbo EF, Kubota T, Momoi MY, Yamagata T
    Journal of human genetics 58(11) 755-757 Nov. 2013
  • Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.
    Kato M, Yamagata T, Kubota M, Arai H, Yamashita S, Nakagawa T, Fujii T, Sugai K, Imai K, Uster T, Chitayat D, Weiss S, Kashii H, Kusano R, Matsumoto A, Nakamura K, Oyazato Y, Maeno M, Nishiyama K, Kodera H, Nakashima M, Tsurusaki Y, Miyake N, Saito K, Hayasaka K, Matsumoto N, Saitsu H
    Epilepsia 54(7) 1282-1287 Jul. 2013
  • Contiguous ABCD1 DXS1357E deletion syndrome: report of an autopsy case.
    Iwasa M, Yamagata T, Mizuguchi M, Itoh M, Matsumoto A, Hironaka M, Honda A, Momoi MY, Shimozawa N
    Neuropathology : official journal of the Japanese Society of Neuropathology 33(3) 292-298 Jun. 2013
Display all
Papers(paper)close
  • Morphological characterization of Class III phosphoinositide 3-kinase during mouse brain development.
    Inaguma Y, Ito H, Iwamoto I, Matsumoto A, Yamagata T, Tabata H, Nagata KI
    Medical molecular morphology 49(1) 28-33 Aug. 2015
  • Circadian-relevant genes are highly polymorphic in autism spectrum disorder patients.
    Yang Z, Matsumoto A, Nakayama K, Jimbo EF, Kojima K, Nagata KI, Iwamoto S, Yamagata T
    Brain & development 38(1) 99 May 2015
  • Morphological characterization of mammalian timeless in the mouse brain development.
    Inaguma Y, Ito H, Hara A, Iwamoto I, Matsumoto A, Yamagata T, Tabata H, Nagata K
    Neuroscience research 92 21-28 Mar. 2015
  • Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders.
    Mizuno M, Matsumoto A, Hamada N, Ito H, Miyauchi A, Jimbo EF, Momoi MY, Tabata H, Yamagata T, Nagata KI
    Journal of neurochemistry 132(1) 61-69 Sep. 2014
  • [Genetic analysis and genes relating synaptic function for autism spectrum disorder].
    Yamagata T, Matsumoto A, Nagata K
    No to hattatsu. Brain and development 46 125-130 Mar. 2014
  • MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus.
    Saito M, Yamagata T, Matsumoto A, Shiba Y, Nagashima M, Taniguchi S, Jimbo E, Momoi MY
    Brain & development 36(1) 64-69 Jan. 2014
  • LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome.
    Matsumoto A, Mizuno M, Hamada N, Nozaki Y, Jimbo EF, Momoi MY, Nagata K, Yamagata T
    PloS one 9(3) 2014
  • An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities.
    Matsumoto A, Kuwajima M, Miyake K, Kojima K, Nakashima N, Jimbo EF, Kubota T, Momoi MY, Yamagata T
    Journal of human genetics 58(11) 755-757 Nov. 2013
  • Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation.
    Kato M, Yamagata T, Kubota M, Arai H, Yamashita S, Nakagawa T, Fujii T, Sugai K, Imai K, Uster T, Chitayat D, Weiss S, Kashii H, Kusano R, Matsumoto A, Nakamura K, Oyazato Y, Maeno M, Nishiyama K, Kodera H, Nakashima M, Tsurusaki Y, Miyake N, Saito K, Hayasaka K, Matsumoto N, Saitsu H
    Epilepsia 54(7) 1282-1287 Jul. 2013
  • Contiguous ABCD1 DXS1357E deletion syndrome: report of an autopsy case.
    Iwasa M, Yamagata T, Mizuguchi M, Itoh M, Matsumoto A, Hironaka M, Honda A, Momoi MY, Shimozawa N
    Neuropathology : official journal of the Japanese Society of Neuropathology 33(3) 292-298 Jun. 2013
  • Role of Class III phosphoinositide 3-kinase in the brain development: possible involvement in specific learning disorders.
    Inaguma Y, Matsumoto A, Noda M, Tabata H, Maeda A, Goto M, Usui D, Jimbo EF, Kikkawa K, Ohtsuki M, Momoi MY, Osaka H, Yamagata T, Nagata KI
    Journal of neurochemistry 245-255 Oct. 2016
  • Role of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders.
    Goto M, Mizuno M, Matsumoto A, Yang Z, Jimbo EF, Tabata H, Yamagata T, Nagata KI
    Scientific reports 7 43945 Mar. 2017
  • The presence of diminished white matter and corpus callosal thinning in a case with a SOX9 mutation.
    Matsumoto A, Imagawa E, Miyake N, Ikeda T, Kobayashi M, Goto M, Matsumoto N, Yamagata T, Osaka H
    Brain & development 40(4) 325-329 Apr. 2018


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