Rchr
J-GLOBAL ID：201801021183047286
Update date: Aug. 21, 2024
Masaki Tanaka
タナカ マサキ | Masaki Tanaka
Affiliation and department：
Research field (2)：
Neurology
, Genomics
Research keywords (2)：
ゲノム医科学
, 神経内科学
Research theme for competitive and other funds (5)：
- 2024 - 2029 The history of the relationship between rice and minor cereals: the use and evolution of cereals from the Jomon to early modern times, as deciphered by palaeogenomic analysis.
- 2022 - 2025 comprehensive search for expanded repeats in neurodegenerative diseaess
- 2019 - 2022 Exploring rare variants associated with Alzheimer disease
- 2017 - 2021 Research on the molecular mechanism of intracranial calcification and novel therapies
- 2015 - 2019 Investigating autoimmune inflammatory mechanism through transcriptome analysis of intramuscular CD8 T cells
Papers (38)：
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Kenta Orimo, Jun Mitsui, Takashi Matsukawa, Masaki Tanaka, Junko Nomoto, Hiroyuki Ishiura, Yosuke Omae, Yosuke Kawai, Katsushi Tokunaga, Hatsue Ishibashi-Ueda, et al. Association study of GBA1 variants with MSA based on comprehensive sequence analysis -Pitfalls in short-read sequence analysis depending on the human reference genome-. Journal of Human Genetics. 2024
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Akari Nagashima, Sohshi Morimura, Toshihisa Hamada, Takayuki Shiomi, Ichiro Mori, Naoko Sato, Junko Nomoto, Masaki Tanaka, Shoji Tsuji, Makoto Sugaya. Whole-Exome Sequencing Revealed a Pathogenic Germline Variant in the Fumarate Hydratase Gene, Leading to the Diagnosis of Hereditary Leiomyomatosis and Renal Cell Cancer. Diagnostics. 2024. 14. 12. 1279-1279
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Jun Mitsui, Takashi Matsukawa, Yukari Uemura, Takuya Kawahara, Ayaka Chikada, Kristine Joyce L Porto, Hiroya Naruse, Masaki Tanaka, Hiroyuki Ishiura, Tatsushi Toda, et al. High-dose ubiquinol supplementation in multiple-system atrophy: a multicentre, randomised, double-blinded, placebo-controlled phase 2 trial. EClinicalMedicine. 2023. 59. 101920-101920
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Orimo Kenta, Mitsutake Akihiko, Tanaka Masaki, Satake Shunya, Ishiura Hiroyuki, Itaya Sakiko, Inaba Akira, Orimo Satoshi, Shiio Yasushi, Matsukawa Takashi, et al. 特発性大脳基底核石灰化症における白質病変(White matter lesions in idiopathic basal ganglia calcification). 臨床神経学. 2022. 62. Suppl. S355-S355
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野本 順子, 田中 真生, 辻 省次, 小林 幸夫. 日本人高齢者リンパ性腫瘍に特徴的なゲノム異常. 国際医療福祉大学学会誌. 2022. 27. 抄録号. 151-151
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MISC (43)：
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辻省次, 佐藤奈穂子, 田中真生, 野本順子. Comprehensive genome analysis for establishment of molecular diagnosis of genetic diseases. 月刊皮膚科. 2024. 5. 1
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辻省次, 田中真生, 野本順子, 佐藤奈穂子. 遺伝性疾患のゲノム解析研究のミッションと改正医療法下の遺伝学的検査. 日本遺伝子診療学会大会プログラム・抄録集. 2022. 29th
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田中真生, 野本順子, 佐藤奈穂子, 佐藤奈穂子, 辻省次, 辻省次. 次世代シーケンサーを用いたクリニカルシーケンスの実施にあたって必要となるプログラム群およびパイプラインに関する検討. 日本人類遺伝学会大会プログラム・抄録集. 2022. 67th (CD-ROM)
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佐藤奈穂子, 田中真生, 野本順子, 西垣昌和, 辻省次, 辻省次. 次世代シーケンサーを用いたクリニカルシーケンスの診療体制の構築. 日本人類遺伝学会大会プログラム・抄録集. 2022. 67th (CD-ROM)
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野本順子, 小林幸夫, 田中真生, 辻省次. 二次性白血病発症に関わる遺伝子変異の経時的なゲノム解析. 国際医療福祉大学学会誌. 2020. 25
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Professional career (1)：
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