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Rchr
J-GLOBAL ID：201501015343773769
Update date: Jun. 25, 2024 Chieng Cha Pei
チャ ペイチェン | Chieng Cha Pei
ClipsPapers (17)
- Tatsuhiko Naito, Wataru Satake, Pei-Chieng Cha, Kazuhiro Kobayashi, Miho Murata, Tatsushi Toda. Comparative whole transcriptome analysis of Parkinson's disease focusing on the efficacy of zonisamide. Journal of neurology, neurosurgery, and psychiatry. 2022. 93. 5. 509-512
- Jun Mori, Atsushi Umemura, Wataru Satake, Pei-Chieng Cha, Yutaka Suzuki, Kyoko Itoh, Tomohiro Chiyonobu. TUBB3 E410K Syndrome With Childhood-Onset Nonalcoholic Steatohepatitis. The Journal of clinical endocrinology and metabolism. 2022. 107. 1. e38-e43
- Makito Hirano, Wataru Satake, Nobuko Moriyama, Ken Saida, Nobuhiko Okamoto, Pei-Chieng Cha, Yutaka Suzuki, Susumu Kusunoki, Tatsushi Toda. Bardet-Biedl syndrome and related disorders in Japan. Journal of Human Genetics. 2020
- Pei-Chieng Cha, Wataru Satake, Yuko Ando-Kanagawa, Ken Yamamoto, Miho Murata, Tatsushi Toda. Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients. Journal of Human Genetics. 2020
- Takeshi Uenaka, Wataru Satake, Pei-Chieng Cha, Hideki Hayakawa, Kousuke Baba, Shiying Jiang, Kazuhiro Kobayashi, Motoi Kanagawa, Yukinori Okada, Hideki Mochizuki, et al. In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson's disease. Human molecular genetics. 2018. 27. 22. 3974-3985
- Tetsushi Hamaguchi, Yushi Hirota, Takehito Takeuchi, Yasushi Nakagawa, Atsuko Matsuoka, Masaaki Matsumoto, Hiroyuki Awano, Kazumoto Iijima, Pei Chieng Cha, Wataru Satake, et al. Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium-glucose cotransporter 2 inhibitor. Journal of diabetes investigation. 2018. 9. 5. 1224-1227
- 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, et al. Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases A Mendelian Randomization Study. JAMA ONCOLOGY. 2017. 3. 5. 636-651
- Tetsuya Oda, Hui Xiong, Kazuhiro Kobayashi, Shuo Wang, Wataru Satake, Hui Jiao, Yanling Yang, Pei-Chieng Cha, Yukiko K Hayashi, Ichizo Nishino, et al. A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy. Human genome variation. 2015. 2. 15022-15022
- Chih-Chieh Yu, Mari Furukawa, Kazuhiro Kobayashi, Chizuru Shikishima, Pei-Chieng Cha, Jun Sese, Hiroko Sugawara, Kazuya Iwamoto, Tadafumi Kato, Juko Ando, et al. Genome-Wide DNA Methylation and Gene Expression Analyses of Monozygotic Twins Discordant for Intelligence Levels. PLOS ONE. 2012. 7. 10. e47081
- Siew-Kee Low, Atsushi Takahashi, Pei-Chieng Cha, Hitoshi Zembutsu, Naoyuki Kamatani, Michiaki Kubo, Yusuke Nakamura. Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA. HUMAN MOLECULAR GENETICS. 2012. 21. 9. 2102-2110
- Pei-Chieng Cha, Hitoshi Zembutsu, Atsushi Takahashi, Michiaki Kubo, Naoyuki Kamatani, Yusuke Nakamura. A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population. JOURNAL OF HUMAN GENETICS. 2012. 57. 4. 235-237
- Pei-Chieng Cha, Atsushi Takahashi, Naoya Hosono, Siew-Kee Low, Naoyuki Kamatani, Michiaki Kubo, Yusuke Nakamura. A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NATURE GENETICS. 2011. 43. 5. 447-+
- Siew-Kee Low, Hitoshi Zembutsu, Atsushi Takahashi, Naoyuki Kamatani, Pei-Chieng Cha, Naoya Hosono, Michiaki Kubo, Koichi Matsuda, Yusuke Nakamura. Impact of LIMK1, MMP2 and TNF-alpha variations for intracranial aneurysm in Japanese population. JOURNAL OF HUMAN GENETICS. 2011. 56. 3. 211-216
- Pei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, Michiaki Kubo, Shiro Minami, Naoyuki Kamatani, Yusuke Nakamura. Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. HUMAN MOLECULAR GENETICS. 2010. 19. 23. 4735-4744
- Pei-Chieng Cha, Taisei Mushiroda, Hitoshi Zembutsu, Hiromasa Harada, Noriyuki Shinoda, Shunji Kawamoto, Rai Shimoyama, Toshihiko Nishidate, Tomohisa Furuhata, Kazuaki Sasaki, et al. Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression. JOURNAL OF HUMAN GENETICS. 2009. 54. 10. 572-580
- Pei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, Shigeru Saito, Hideki Shimomura, Takao Suzuki, Naoyuki Kamatani, Yusuke Nakamura. 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. JOURNAL OF HUMAN GENETICS. 2007. 52. 10. 856-864
- PC Cha, R Yamada, A Sekine, Y Nakamura, CL Koh. Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations. JOURNAL OF HUMAN GENETICS. 2004. 49. 10. 558-572
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