Tzuyao Lo, Itaru Kushima, Hiroki Kimura, Branko Aleksic, Takashi Okada, Hidekazu Kato, Toshiya Inada, Yoshihiro Nawa, Youta Torii, Maeri Yamamoto, et al. Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case-control study. Neuropsychopharmacology reports. 2023
Hiroki Kimura, Itaru Kushima, Masahiro Banno, Toshiya Inada, Akira Yoshimi, Branko Aleksic, Norio Ozaki. Clinical characterization of patients with schizophrenia and 16p13.11 duplication: A case series. Neuropsychopharmacology reports. 2023. 43. 2. 267-271
Yuko Arioka, Yu Hayashi, Hiroki Okumura, Itaru Kushima, Daisuke Mori, Tzuyao Lo, Gantsooj Otgonbayar, Hidekazu Kato, Yoshihiro Nawa, Hiroki Kimura, et al. Analysis of human neuronal cells carrying ASTN2 deletion: A cross-disorder risk variant of schizophrenia, autism spectrum disorder, and bipolar disorder. 2023
Hiroki Kimura, Masahiro Nakatochi, Branko Aleksic, James Guevara, Miho Toyama, Yu Hayashi, Hidekazu Kato, Itaru Kushima, Mako Morikawa, Kanako Ishizuka, et al. Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes. Translational Psychiatry. 2022. 12. 1
Tzuyao Lo, Itaru Kushima, Branko Aleksic, Akira Yoshimi, Toshiyuki Someya, Yuichiro Watanabe, Norio Ozaki. Clinical manifestations of schizophrenia in four patients with variants in voltage-gated calcium channel-encoding genes: a case series. Psychiatry and clinical neurosciences. 2022. 77. 1. 57-59
George Kirov, Anthony Isles, Andres Ingason, Chelsea Lowther, James Walters, Anne Bassett, Gregory Costain, Douglas Levinson, Micha Gawlick, Franziska Degenhardt, et al. CLINICALLY RELEVANT GENETIC VARIANTS: MODELS FOR UNDERSTANDING SCHIZOPHRENIA AND OTHER NEUROPSYCHIATRIC DISORDERS DUPLICATIONS AT 15Q11-Q13 IN SCHIZOPHRENIA AND NEURODEVELOPMENTAL DISORDERS. EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2017. 27. S277-S277
Chenyao Wang, Hiroki Kimura, Jingrui Xing, Kanoko Ishizuka, Itaru Kushima, Yuko Arioka, Akira Yoshimi, Yukako Nakamura, Yomoko Shiino, Yuko Oya, et al. IDENTIFICATION OF RARE DISRUPTIVE VARIANTS IN VOLTAGE-GATED CHANNEL GENES (CACNA1C, CACNA1D, CACNA1S, CACNA1I) IN JAPANESE SAMPLES OF SCHIZOPHRENIA AND AUTISM SPECTRUM DISORDER USING ION TORRENT PGM PLATFORM. EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2017. 27. S341-S342
Kanako Ishizuka, Chenyao Wang, Hiroki Kimura, Jingrui Xing, Itaru Kushima, Yuko Arioka, Akira Yoshimi, Yukako Nakamura, Tomoko Oya-Ito, Yuto Takasaki, et al. MUTATION SCREENING OF THE PCDH15 GENE IN PATIENTS SUFFERING FROM AUTISM SPECTRUM DISORDERS AND SCHIZOPHRENIA. EUROPEAN NEUROPSYCHOPHARMACOLOGY. 2017. 27. S162-S163
2003/12/01 - 2005/03/31 Institute of Mental Health, ベオグラード、セルビア共和国
2002/04/01 - 2003/11/30 セルビア共和国ベオグラードClinical Center of Serbia
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所属学会 (4件):
Serbian Medical Chamber
, Serbian Medical Society
, The International Society of Psychiatric Genetics
, American Psychiatric Association/International Member