Chieng Cha Pei (Cha Pei Chieng) - マイポータル

基本情報

所属: 国立研究開発法人国立循環器病研究センター研究所病態ゲノム医学部上級研究員

学位: 修士(外国)(マラヤ大学)
博士(医科学)(東京大学)

J-GLOBAL ID: 201501015343773769
researchmap会員ID: 7000012358

研究キーワード

研究分野

ライフサイエンス / ゲノム生物学 / 薬理遺伝学

学歴

- 2011年3月

東京大学大学院医学系研究科博士課程病因・病理学専攻修了

論文

Comparative whole transcriptome analysis of Parkinson's disease focusing on the efficacy of zonisamide.

Tatsuhiko Naito, Wataru Satake, Pei-Chieng Cha, Kazuhiro Kobayashi, Miho Murata, Tatsushi Toda

Journal of neurology, neurosurgery, and psychiatry 93(5) 509-512 2022年5月
TUBB3 E410K Syndrome With Childhood-Onset Nonalcoholic Steatohepatitis.

Jun Mori, Atsushi Umemura, Wataru Satake, Pei-Chieng Cha, Yutaka Suzuki, Kyoko Itoh, Tomohiro Chiyonobu

The Journal of clinical endocrinology and metabolism 107(1) e38-e43 2022年1月1日
Bardet–Biedl syndrome and related disorders in Japan

Makito Hirano, Wataru Satake, Nobuko Moriyama, Ken Saida, Nobuhiko Okamoto, Pei-Chieng Cha, Yutaka Suzuki, Susumu Kusunoki, Tatsushi Toda

Journal of Human Genetics 2020年5月25日査読有り
Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients

Pei-Chieng Cha, Wataru Satake, Yuko Ando-Kanagawa, Ken Yamamoto, Miho Murata, Tatsushi Toda

Journal of Human Genetics 2020年5月1日査読有り
In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson's disease.

Takeshi Uenaka, Wataru Satake, Pei-Chieng Cha, Hideki Hayakawa, Kousuke Baba, Shiying Jiang, Kazuhiro Kobayashi, Motoi Kanagawa, Yukinori Okada, Hideki Mochizuki …

Human molecular genetics 27(22) 3974-3985 2018年11月15日査読有り
Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium-glucose cotransporter 2 inhibitor.

Tetsushi Hamaguchi, Yushi Hirota, Takehito Takeuchi, Yasushi Nakagawa, Atsuko Matsuoka, Masaaki Matsumoto, Hiroyuki Awano, Kazumoto Iijima, Pei Chieng Cha, Wataru Satake …

Journal of diabetes investigation 9(5) 1224-1227 2018年9月査読有り
Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases A Mendelian Randomization Study

Philip C. Haycock, Stephen Burgess, Aayah Nounu, Jie Zheng, George N. Okoli, Jack Bowden, Kaitlin Hazel Wade, Nicholas J. Timpson, David M. Evans, Peter Willeit …

JAMA ONCOLOGY 3(5) 636-651 2017年5月査読有り
A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy.

Tetsuya Oda, Hui Xiong, Kazuhiro Kobayashi, Shuo Wang, Wataru Satake, Hui Jiao, Yanling Yang, Pei-Chieng Cha, Yukiko K Hayashi, Ichizo Nishino …

Human genome variation 2 15022-15022 2015年査読有り
Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels

Chih-Chieh Yu, Mari Furukawa, Kazuhiro Kobayashi, Chizuru Shikishima, Pei-Chieng Cha, Jun Sese, Hiroko Sugawara, Kazuya Iwamoto, Tadafumi Kato, Juko Ando …

PLOS ONE 7(10) e47081 2012年10月査読有り
Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA

Siew-Kee Low, Atsushi Takahashi, Pei-Chieng Cha, Hitoshi Zembutsu, Naoyuki Kamatani, Michiaki Kubo, Yusuke Nakamura

HUMAN MOLECULAR GENETICS 21(9) 2102-2110 2012年5月査読有り
A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population

Pei-Chieng Cha, Hitoshi Zembutsu, Atsushi Takahashi, Michiaki Kubo, Naoyuki Kamatani, Yusuke Nakamura

JOURNAL OF HUMAN GENETICS 57(4) 235-237 2012年4月査読有り
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids

Pei-Chieng Cha, Atsushi Takahashi, Naoya Hosono, Siew-Kee Low, Naoyuki Kamatani, Michiaki Kubo, Yusuke Nakamura

NATURE GENETICS 43(5) 447-+ 2011年5月査読有り
Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population.

Low SK, Zembutsu H, Takahashi A, Kamatani N, Cha PC, Hosono N, Kubo M, Matsuda K, Nakamura Y

Journal of human genetics 56(3) 211-216 2011年3月査読有り
Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese

Pei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, Michiaki Kubo, Shiro Minami, Naoyuki Kamatani, Yusuke Nakamura

HUMAN MOLECULAR GENETICS 19(23) 4735-4744 2010年12月査読有り
Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression

Pei-Chieng Cha, Taisei Mushiroda, Hitoshi Zembutsu, Hiromasa Harada, Noriyuki Shinoda, Shunji Kawamoto, Rai Shimoyama, Toshihiko Nishidate, Tomohisa Furuhata, Kazuaki Sasaki …

JOURNAL OF HUMAN GENETICS 54(10) 572-580 2009年10月査読有り
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

Pei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, Shigeru Saito, Hideki Shimomura, Takao Suzuki, Naoyuki Kamatani, Yusuke Nakamura

JOURNAL OF HUMAN GENETICS 52(10) 856-864 2007年10月査読有り
Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations

PC Cha, R Yamada, A Sekine, Y Nakamura, CL Koh

JOURNAL OF HUMAN GENETICS 49(10) 558-572 2004年10月査読有り

MISC

Genomic study and subsequent in silico drug discovery for Parkinson's disease

Wataru Satake, Takeshi Uenaka, Cha Pei Chieng, Yukinori Okada, Kenichi Kashihara, Shigeo Murayama, Kazuko Hasegawa, Hideki Mochizuki, Atsushi Takeda, Mitsutoshi Yamamoto …

MOVEMENT DISORDERS 31 S95-S96 2016年3月
In silico drug discovery for Parkinson's disease by using genome-wide association study (GWAS) data

T. Uenaka, W. Satake, C. P. Chieng, Y. Okada, T. Toda

MOVEMENT DISORDERS 30 S51-S51 2015年6月

講演・口頭発表等

Genomic study and subsequent in silico drug discovery for Parkinson’s disease

Satake W, Uenaka T, Cha PC, Okada Y, Kashihara K, Murayama S, Hasegawa K, Mochizuki H, Takeda A, Yamamoto M, Murata M, Hattori N, Toda T

5th Asian and Oceanian Parkinson’s Disease and Movement Disorders Congress 2016年3月 International Parkinson and Movement Disorder Society 招待有り
Exome Association study and SNP-GWAS of Parkinson’s disease

Satake W, Suzuki Y, Shigemizu D, Cha PC, Tsuji S, Tsunoda T, Kubo M, Sugano S, Matsumoto N, Toda T

The 11th International workshop on Advanced Genomics 2015年5月日本学術振興会ゲノムテクノロジー第164委員会招待有り

所属学協会

共同研究・競争的資金等の研究課題

ゲノム解析が切り拓く心房細動の新展開

日本学術振興会科学研究費助成事業基盤研究(C) 2021年4月 - 2024年3月

謝珮琴
特発性心室細動の新展開：網羅的な全エクソン解析による遺伝要因と発症機序の解明

日本学術振興会科学研究費助成事業若手研究 2019年4月 - 2021年3月

謝珮琴
特発性心室細動の新展開：網羅的な全エクソン解析による遺伝要因と発症機序の解明

日本学術振興会科学研究費助成事業若手研究 2019年4月 - 2021年3月

謝珮琴

Chieng Cha Pei

基本情報

研究キーワード

研究分野

学歴

論文

MISC

講演・口頭発表等

所属学協会

共同研究・競争的資金等の研究課題

メニュー

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