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病態ゲノム医学部

スタッフ
CHA PEI CHIENG

スタッフ紹介 [CHA PEI CHIENG]

氏名 CHA PEI CHIENG NoPhoto
よみ チャ ペイ チェン
所属・職務 病態ゲノム医学部 上級研究員
内線番号 40356
FAX番号
Eメール genescha@ncvc.go.jp
棟/部屋番号 研究所5階 50406室
専門 ゲノム医学、薬理遺伝学、インフォマティクス
主要論文・著書

<論文>

  • Cha PC, Satake W, Ando-Kanagawa Y, Yamamoto K, Murata M, Toda T (2020) Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients. (Submitted)
  • Uenaka T, Satake W, Cha PC, Hayakawa H, Baba K, Jiang S, Kobayashi K, Kanagawa M, et al., (2018) In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson's disease. Hum Mol Genet. 2018 Aug 22. doi: 10.1093/hmg/ddy279.
  • Hamaguchi T, Hirota Y, Takeuchi T, Nakagawa Y, Matsuoka A, Matsumoto M, Awano H, Iijima K, Cha PC, et al., (2018) Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium-glucose cotransporter 2 inhibitor. J. Diabetes Investig. 9(5):1224-1227.
  • Telomeres Mendelian Randomization Collaboration, Haycock PC et al., (2017) Association between telomere length and risk of cancer and non-Neoplastic diseases: A Mendelian randomization study. JAMA Oncol. 3(5):636-651. (共著者多数のため省略)
  • Oda T, Xiong H, Kobayashi K, Wang S, Satake W, Jiao H, Yang Y, Cha PC, Hayashi Y, Nishino I, Suzuki Y, Sugano S, Wu X, Toda T (2015) A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy. Human Genome Variation 2:15022.
  • Yu CC, Furukawa M, Kobayashi K, Shikishima C, Cha PC, Sese J, Sugawara H, Iwamoto K, Kato T, Ando J, Toda T.(2012)Genome-Wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels. PLoS ONE 7(10):e47081.
  • Cha PC, Zembutsu H, Takahashi A, Kubo M, Kamatani N, Nakamura Y (2012) A genome-wide association study (GWAS) for gallbladder cancer (GC) in the Japanese population J. Hum. Genet. 57(4): 235-237.
  • Low SK, Takahashi A, Cha PC, Zembutsu H, Kamatani N, Kubo M, Nakamura Y (2012) Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA. Hum. Mol. Genet. 21(9):2102-10.
  • Cha PC, Takahashi A, Hosono N, Low SK, Kamatani N, Kubo M, Nakamura Y (2011) A genome-wide association study identifies three loci associated with susceptibility to uterine fibroid. Nat. Genet. 43(5): 447-450.
  • Low SK, Zembutsu H, Takahashi A, Kamatani N, Cha PC, Hosono N, Kubo M, Matsuda K, Nakamura Y (2011) Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population. J. Hum. Genet. 56(3): 211-216.
  • Cha PC, Mushiroda T, Takahashi A, Kubo M, Minami S, Kamatani N, Nakamura Y (2010) Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. Hum. Mol. Genet. 19(23): 4735-4744.
  • Cha PC, Mushiroda T, Zembutsu H, Harada H, Shinoda N, Kawamoto S, Shimoyama R, et al., (2009) Single nucleotide polymorphism (SNP) in ABCG2 is associated with irinotecan-induced severe myelosuppression. J. Hum. Genet. 54(10): 572-580.
  • Cha PC, Mushiroda T, Takahashi A, Saito S, Shimomura H, Suzuki T, Kamatani N, Nakamura Y (2007) High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population. J. Hum. Genet. 52(10): 856-864.
  • Cha PC, Yamada R, Sekine A, Nakamura Y, Koh CL (2004) Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 10 drug-related genes in 4 Asian populations. J. Hum. Genet. 49(10):558-572.
受賞
  • 第9回日本心臓財団入澤宏・彩記念女性研究奨励 (2018)
  • JSPS Postdoctoral Fellowship for Overseas Researchers (2012-2014)
  • Asian Youth Fellowship by Japan Foundation (2005-2006)
  • Student Fellowship Award (2004) The 5th HUGO Pacific Meeting and 6th Asia Pacific Conference on Human Genetics
学位 博士(医学)
所属学会 日本人類学会、アメリカ人類遺伝学会
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その他の活動
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最終更新日:2021年10月01日

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