Rchr
J-GLOBAL ID:201001041745594791
Update date: Feb. 06, 2024
Aleksic Branko
Aleksic Branko
Affiliation and department:
Job title:
Designated associate professor
Homepage URL (2):
https://profs.provost.nagoya-u.ac.jp/html/100001548_ja.html
,
https://profs.provost.nagoya-u.ac.jp/html/100001548_en.html
Research field (3):
Neuroscience - general
, Medical biochemistry
, Basic brain sciences
Research keywords (5):
cognitive genetics
, resequencing
, CNV
, genetics
, Schizophrenia
Research theme for competitive and other funds (7):
- 2021 - 2024 Long read sequencing to expand the accessible genetic architecture of autism
- 2018 - 2021 NGS of multiple onset schizophrenia families
- 2015 - 2018 Exome sequencing of schizophrenia using families with multiple affected members
- 2015 - 2018 次世代シーケンサーを用いた統合失調症多発家系の遺伝子解析と病因・病態解明
- 2013 - 2016 Identification of rare genetic variants associated with bipolar disorder and comprehensive analysis to elucidate its pathophysiology
- 2010 - 2012 Genome-wide association study of schizophrenia in a Japanese population and follow-up study
- 2010 - 2012 日本人における統合失調症のゲノムワイド関連研究およびそのフォローアップ
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Papers (162):
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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
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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
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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
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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
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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
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MISC (43):
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池田 匡志, 高橋 篤, 鎌谷 洋一郎, 桃沢 幸秀, 齋藤 竹生, 近藤 健治, 島崎 愛夕, 川瀬 康平, 作佐部 太也, 岩山 佳美, et al. Genome-wide association study detected novel susceptibility genes for schizophrenia and shared trans-populations/diseases genetic effect(和訳中). 日本臨床精神神経薬理学会・日本神経精神薬理学会合同年会プログラム・抄録集. 2019. 29回・49回. 124-124
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山本真江里, EPIFANIO Bagarinao, 久島周, 久島周, 高橋努, 笹林大樹, 鈴木道雄, ALEKSIC Branko, 稲田俊也, 稲田俊也, et al. MRI構造画像を用いたサポートベクターマシンによる統合失調症患者と健常者の判別法の検討. 日本生物学的精神医学会(Web). 2019. 41st
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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
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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
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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
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Books (1):
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Genetics in Pediatric Consultation-Liaison Psychiatry and Multidisciplinary Management of Complex Conditions
Springer 2018 ISBN:9783319894881
Education (2):
- 2005 - 2009 Nagoya University Graduate School of Medicine Doctoral course (Child psychiatry)
- 1994 - 2001 Belgrade University School of Medicine Undergraduate course (MD)
Professional career (3):
- MD (セルビア共和国ベオグラード大学医学部)
- PhD (Nagoya University)
- MD (University of Belgrade, School of Medicine)
Work history (8):
- 2018/04/01 - 現在 Nagoya University Graduate School of Medicine International Collaborative Program in Comprehensive Medical Science between Nagoya University and University of Adelaide Designated associate professor
- 2016/03/01 - 2018/03/31 Nagoya University Administrative Support Organizations International Education & Exchange International Education & Exchange Center Department of International Program Designated associate professor
- 2013/10/01 - 2016/02/29 Nagoya University Administrative Support Organizations International Education & Exchange International Education & Exchange Center Division of Foreign Students Designated associate professor
- 2012/01/01 - 2013/09/30 Nagoya University Administrative Support Organizations International Exchange and Cooperation Headquarters Designated associate professor
- 2009/04/01 - 2011/12/31 Nagoya University Graduate School of Medicine COE designated assistant professor
- 2008/04 - 2010/03 Fujita Health University
- 2003/12/01 - 2005/03/31 Institute of Mental Health
- 2002/04/01 - 2003/11/30 Clinical Center of Serbia
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Association Membership(s) (4):
Serbian Medical Chamber
, Serbian Medical Society
, The International Society of Psychiatric Genetics
, American Psychiatric Association/International Member
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