Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement von Kobayashi, Hatasu, Abe, Koji, Matsuura, Tohru, Ikeda, Yoshio, Hitomi, Toshiaki, Akechi, Yuji, Habu, Toshiyuki, Liu, Wanyang, Okuda, Hiroko, Koizumi, Akio

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Distribution of Moyamoya Disease Susceptibility Polymorphism p.R4810K in RNF213 in East and Southeast Asian Populations von LIU, Wanyang, HITOMI, Toshiaki, KOBAYASHI, Hatasu, HARADA, Kouji H., KOIZUMI, Akio

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An Integrative Study of the Genetic, Social and Environmental Determinants of Chronic Kidney Disease Characterized by Tubulointerstitial Damages in the North Central Region of Sri... von Nanayakkara, Shanika, Senevirathna, STMLD, Abeysekera, Tilak, Chandrajith, Rohana, Ratnatunga, Neelakanthi, Gunarathne, EDL, Yan, Junxia, Hitomi, Toshiaki, Muso, Eri, Komiya, Toshiyuki, Harada, Kouji H., Liu, Wanyang, Kobayashi, Hatasu, Okuda, Hiroko, Sawatari, Hideyuki, Matsuda, Fumihiko, Yamada, Ryo, Watanabe, Takao, Miyataka, Hideki, Himeno, Seiichiro, Koizumi, Akio

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Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development von Liu, Wanyang, Morito, Daisuke, Takashima, Seiji, Mineharu, Yohei, Kobayashi, Hatasu, Hitomi, Toshiaki, Hashikata, Hirokuni, Matsuura, Norio, Yamazaki, Satoru, Toyoda, Atsushi, Kikuta, Ken-ichiro, Takagi, Yasushi, Harada, Kouji H, Fujiyama, Asao, Herzig, Roman, Krischek, Boris, Zou, Liping, Kim, Jeong Eun, Kitakaze, Masafumi, Miyamoto, Susumu, Nagata, Kazuhiro, Hashimoto, Nobuo, Koizumi, Akio

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Meta‐analysis of genotype and phenotype studies to confirm the predictive role of the RNF213 p.R4810K variant for moyamoya disease von Wang, Yue, Yang, Luping, Wang, Xiaotong, Zeng, Fanxin, Zhang, Kaili, Zhang, Qian, Liu, Mengwei, Liu, Shan, Shang, Mengke, Li, Qian, Yang, Yuetian, Liang, Man, Liu, Wanyang

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Short-chain chlorinated paraffins in cooking oil and related products from China von Cao, Yang, Harada, Kouji H., Liu, Wanyang, Yan, Junxia, Zhao, Can, Niisoe, Tamon, Adachi, Ayumu, Fujii, Yukiko, Nouda, Chihiro, Takasuga, Takumi, Koizumi, Akio

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The Play of Genes and Non-genetic Factors on Type 2 Diabetes von Mambiya, Michael, Shang, Mengke, Wang, Yue, Li, Qian, Liu, Shan, Yang, Luping, Zhang, Qian, Zhang, Kaili, Liu, Mengwei, Nie, Fangfang, Zeng, Fanxin, Liu, Wanyang

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RNF213 p.R4810K Polymorphism and the Risk of Moyamoya Disease, Intracranial Major Artery Stenosis/Occlusion, and Quasi-Moyamoya Disease: A Meta-Analysis von Wang, Yue, Mambiya, Michael, Li, Qian, Yang, Luping, Jia, He, Han, Yibo, Liu, Wanyang

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Association of MTHFR gene polymorphisms with pancreatic cancer: meta-analysis of 17 case–control studies von Nie, Fangfang, Yu, Mingli, Zhang, Kaili, Yang, Luping, Zhang, Qian, Liu, Shan, Liu, Mengwei, Shang, Mengke, Zeng, Fanxin, Liu, Wanyang

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Polyfluorinated telomers in indoor air of Japanese houses von Liu, Wanyang, Takahashi, Satoshi, Sakuramachi, Yui, Harada, Kouji H., Koizumi, Akio

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Whole exome sequencing and functional validation identify CAPN1 variants as a cause of Chinese moyamoya disease von Wang, Yue, Zou, Zhengxing, Yang, Zhibin, Zhang, Zhengshan, Xu, Jun, Hao, Fangbin, Shen, Juan, Han, Cong, Liu, Wanyang, Duan, Lian

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Predictive role of modifiable factors in stroke: an umbrella review von Wang, Xiaotong, Liang, Man, Zeng, Fanxin, Wang, Yue, Yang, Yuetian, Nie, Fangfang, Shang, Mengke, Ta, Na, Wen, Lu, Ou, Lanxin, Yang, Zhibin, Liu, Wanyang

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Association of polymorphisms in endothelial dysfunction-related genes with susceptibility to essential hypertension in elderly Han population in Liaoning province, China von Ta, Na, Liu, Mengwei, Wang, Yue, Zeng, Fanxin, Nie, Fangfang, Shang, Mengke, Wang, Xiaotong, Yang, Yuetian, Liang, Man, Wen, Lu, Ou, Lanxin, Yang, Zhibin, Liu, Wanyang, Liu, Xiuping

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Combined linkage analysis and exome sequencing identifies novel genes for familial goiter von Yan, Junxia, Takahashi, Tsutomu, Ohura, Toshihiro, Adachi, Hiroyuki, Takahashi, Ikuko, Ogawa, Eishin, Okuda, Hiroko, Kobayashi, Hatasu, Hitomi, Toshiaki, Liu, Wanyang, Harada, Kouji H, Koizumi, Akio

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Ablation of Rnf213 retards progression of diabetes in the Akita mouse von Kobayashi, Hatasu, Yamazaki, Satoru, Takashima, Seiji, Liu, Wanyang, Okuda, Hiroko, Yan, Junxia, Fujii, Yukiko, Hitomi, Toshiaki, Harada, Kouji H, Habu, Toshiyuki, Koizumi, Akio

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Confirmation of an Association of Single-Nucleotide Polymorphism rs1333040 on 9p21 With Familial and Sporadic Intracranial Aneurysms in Japanese Patients von HASHIKATA, Hirokuni, WANYANG LIU, MIYAMOTO, Susumu, KOIZUMI, Akio, INOUE, Kayoko, MINEHARU, Yohei, YAMADA, Shigeki, NANAYAKKARA, Shanika, MATSUURA, Norio, HITOMI, Toshiaki, TAKAGI, Yasushi, HASHIMOTO, Nobuo

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P.R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure von Koizumi, Akio, Kobayashi, Hatasu, Liu, Wanyang, Fujii, Yukiko, Senevirathna, S T M L D, Nanayakkara, Shanika, Okuda, Hiroko, Hitomi, Toshiaki, Harada, Kouji H, Takenaka, Katsunobu, Watanabe, Takao, Shimbo, Shinichiro

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Analysis of perfluoroalkyl carboxylates in vacuum cleaner dust samples in Japan von Liu, Wanyang, Chen, Shengying, Harada, Kouji H., Koizumi, Akio

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Developmental iodine deficiency and hypothyroidism impair neural development in rat hippocampus: involvement of doublecortin and NCAM-180 von Gong, Jian, Liu, Wanyang, Dong, Jing, Wang, Yi, Xu, Hongde, Wei, Wei, Zhong, Jiapeng, Xi, Qi, Chen, Jie

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A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians von WANYANG LIU, HASHIKATA, Hirokuni, ZOU, Li-Ping, FANG FANG, HERZIG, Roman, KIM, Jeong-Eun, KANG, Hyun-Seung, OH, Chang-Wan, TREGOUET, David-Alexandre, HASHIMOTO, Nobuo, KOIZUMI, Akio, INOUE, Kayoko, MATSUURA, Norio, MINEHARU, Yohei, KOBAYASHI, Hatasu, KIKUTA, Ken-Ichiro, TAKAGI, Yasushi, HITOMI, Toshiaki, KRISCHEK, Boris

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