HuGE Literature Finder
Records 1-30
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RNF213 rare variants and cerebral arteriovenous malformation in a Chinese population.
Clinical neurology and neurosurgery 2021 Apr 203 106582. Liu Junyu, Hu Chongyu, Zhou Jilin, Li Bingyang, Liao Xin, Liu Songlin, Li Yifeng, Yuan Dun, Jiang Weixi, Yan Junx |
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Association of genetic variants of RNF213 with ischemic stroke risk in Koreans.
Genes & genomics 2021 Feb . Park Young Seok, Park Hyeon Woo, Park Han Sung, Ryu Chang Soo, Lee Jeong Yong, Ko Eun Ju, Sung Jung Hoon, Kim Jinkwon, Kim Ok Joon, Kim Nam Ke |
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Prolonged/delayed cerebral hyperperfusion in adult patients with moyamoya disease with RNF213 gene polymorphism c.14576G>A (rs112735431) after superficial temporal artery-middle cerebral artery anastomosis.
Journal of neurosurgery 2020 Oct 1-8. Tashiro Ryosuke, Fujimura Miki, Katsuki Masahito, Nishizawa Taketo, Tomata Yasutake, Niizuma Kuniyasu, Tominaga Tei |
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Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosis.
Scientific reports 2020 Jul 10 (1): 11942. Hongo Hiroki, Miyawaki Satoru, Imai Hideaki, Shimizu Masahiro, Yagi Shinichi, Mitsui Jun, Ishiura Hiroyuki, Yoshimura Jun, Doi Koichiro, Qu Wei, Teranishi Yu, Okano Atsushi, Ono Hideaki, Nakatomi Hirofumi, Shimizu Tsuneo, Morishita Shinichi, Tsuji Shoji, Saito Nobuhi |
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RNF213 gene polymorphism rs9916351 and rs8074015 significantly associated with moyamoya disease in Chinese population.
Annals of translational medicine 2020 Jul 8 (14): 851. Zhu Bin, Liu Xingju, Zhen Xueke, Li Xixi, Wu Mingfen, Zhang Yan, Zhao Zhigang, Zhang Dong, Zhao Jizo |
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Association of Genetic Variants With Moyamoya Disease in 13 000 Individuals: A Meta-Analysis.
Stroke 2020 May STROKEAHA120029527. Wang Xiaotong, Wang Yue, Nie Fangfang, Li Qian, Zhang Kaili, Liu Mengwei, Yang Luping, Zhang Qian, Liu Shan, Zeng Fanxin, Shang Mengke, Liang Man, Yang Yuetian, Liu Xiuping, Liu Wanya |
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Genetic analysis of ring finger protein 213 (RNF213) c.14576G>A polymorphism in patients with vertebral artery dissection: a comparative study with moyamoya disease.
Neurological research 2019 May 1-6. Tashiro Ryosuke, Fujimura Miki, Sakata Hiroyuki, Endo Hidenori, Tomata Yasutake, Sato-Maeda Mika, Niizuma Kuniyasu, Tominaga Tei |
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Novel missense variants in the RNF213 gene from a European family with Moyamoya disease.
Human genome variation 2019 6 35. Gagunashvili Andrey N, Ocaka Louise, Kelberman Daniel, Munot Pinki, Bacchelli Chiara, Beales Philip L, Ganesan Vije |
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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.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2018 May . Wang Yue, Mambiya Michael, Li Qian, Yang Luping, Jia He, Han Yibo, Liu Wanya |
Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.
Stroke 2018 Jan 49 (1): 11-18. Duan Lian, Wei Ling, Tian Yanghua, Zhang Zhengshan, Hu Panpan, Wei Qiang, Liu Sugang, Zhang Jun, Wang Yuyang, Li Desheng, Yang Weizhong, Zong Rui, Xian Peng, Han Cong, Bao Xiangyang, Zhao Feng, Feng Jie, Liu Wei, Cao Wuchun, Zhou Guoping, Zhu Chunyan, Yu Fengqiong, Yang Weimin, Meng Yu, Wang Jingye, Chen Xianwen, Wang Yu, Shen Bing, Zhao Bing, Wan Jinghai, Zhang Fengyu, Zhao Gang, Xu Aimin, Zhang Xuejun, Liu Jianjun, Zuo Xianbo, Wang K |
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Increased serum production of soluble CD163 and CXCL5 in patients with moyamoya disease: Involvement of intrinsic immune reaction in its pathogenesis.
Brain research 2018 01 1679 39-44. Fujimura Miki, Fujimura Taku, Kakizaki Aya, Sato-Maeda Mika, Niizuma Kuniyasu, Tomata Yasutake, Aiba Setsuya, Tominaga Tei |
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Novel and recurrent RNF213 variants in Japanese pediatric patients with moyamoya disease.
Human genome variation 2018 5 17060. Akagawa Hiroyuki, Mukawa Maki, Nariai Tadashi, Nomura Shunsuke, Aihara Yasuo, Onda Hideaki, Yoneyama Taku, Kudo Takumi, Sumita Kazutaka, Maehara Taketoshi, Kawamata Takakazu, Kasuya Hidetos |
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Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1.
PloS one 2018 13 (7): e0200446. Santoro Claudia, Giugliano Teresa, Kraemer Markus, Torella Annalaura, Schwitalla Jan Claudius, Cirillo Mario, Melis Daniela, Berlit Peter, Nigro Vincenzo, Perrotta Silverio, Piluso Giul |
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The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea.
International journal of molecular sciences 2017 Nov 18 (11): . Park Young Seok, An Hui Jeong, Kim Jung Oh, Kim Won Seop, Han In Bo, Kim Ok Joon, Kim Nam Keun, Kim Dong-Se |
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Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan.
Neurologia medico-chirurgica 2017 Sep . Takamatsu Yuichiro, Higashimoto Ken, Maeda Toshiyuki, Kawashima Masatou, Matsuo Muneaki, Abe Tatsuya, Matsushima Toshio, Soejima Hideno |
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Genetic Analysis of Ring Finger Protein 213 (RNF213) c.14576G>A in Intracranial Atherosclerosis of the Anterior and Posterior Circulations.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2017 Aug . Shinya Yuki, Miyawaki Satoru, Imai Hideaki, Hongo Hiroki, Ono Hideaki, Takenobu Atsumi, Nakatomi Hirofumi, Teraoka Akira, Saito Nobuhi |
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RNF213 p.R4810K Variant and Intracranial Arterial Stenosis or Occlusion in Relatives of Patients with Moyamoya Disease.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2017 May . Matsuda Yoshiko, Mineharu Yohei, Kimura Mitsuru, Takagi Yasushi, Kobayashi Hatasu, Hitomi Toshiaki, Harada Kouji H, Uchihashi Yoshito, Funaki Takeshi, Miyamoto Susumu, Koizumi Ak |
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Genetic analysis of RNF213 p.R4810K variant in non-moyamoya intracranial artery stenosis/occlusion disease in a Chinese population.
Environmental health and preventive medicine 2017 Apr 22 (1): 41. Zhang Tong, Guo Congrong, Liao Xin, Xia Jian, Wang XiaoXiao, Deng Jing, Yan Junx |
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RNF213 rs112735431 polymorphism in intracranial artery steno-occlusive disease and moyamoya disease in Koreans.
Journal of the neurological sciences 2017 Apr 375 331-334. Park Min-Gyu, Shin Jin-Hong, Lee Sang Weon, Park Hae Rim, Park Kyung-P |
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The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.
World neurosurgery 2017 Mar 99 701-708.e1. Zhang Qian, Liu Yaping, Yu Lebao, Duan Ran, Ma Yonggang, Ge Peicong, Zhang Dong, Zhang Yan, Wang Rong, Wang Shuo, Zhao Yuanli, Cao Yong, Liu Xingju, Deng Xiaofeng, Zhao Jizong, Zhang X |
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Frequency and significance of rare RNF213 variants in patients with adult moyamoya disease.
PloS one 2017 12 (6): e0179689. Jang Mi-Ae, Chung Jong-Won, Yeon Je Young, Kim Jong-Soo, Hong Seung Chyul, Bang Oh Young, Ki Chang-Se |
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Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease.
PloS one 2017 12 (4): e0175649. Morimoto Takaaki, Mineharu Yohei, Ono Koh, Nakatochi Masahiro, Ichihara Sahoko, Kabata Risako, Takagi Yasushi, Cao Yang, Zhao Lanying, Kobayashi Hatasu, Harada Kouji H, Takenaka Katsunobu, Funaki Takeshi, Yokota Mitsuhiro, Matsubara Tatsuaki, Yamamoto Ken, Izawa Hideo, Kimura Takeshi, Miyamoto Susumu, Koizumi Ak |
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Moyamoya vasculopathy shows a genetic mutational gradient decreasing from East to West.
Journal of neurosurgical sciences 2016 Oct . Raso Alessandro, Biassoni Roberto, Mascelli Samantha, Nozza Paolo, Ugolotti Elisabetta, DI Marco Eddi, DE Marco Patrizia, Merello Elisa, Cama Armando, Pavanello Marco, Capra Valer |
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RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population.
American journal of human genetics 2016 Sep . Zhou Sirui, Ambalavanan Amirthagowri, Rochefort Daniel, Xie Pingxing, Bourassa Cynthia V, Hince Pascale, Dionne-Laporte Alexandre, Spiegelman Dan, Gan-Or Ziv, Mirarchi Cathy, Zaharieva Vessela, Dupré Nicolas, Kobayashi Hatasu, Hitomi Toshiaki, Harada Kouji, Koizumi Akio, Xiong Lan, Dion Patrick A, Rouleau Guy |
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Association between the rs112735431 polymorphism of the RNF213 gene and moyamoya disease: A case-control study and meta-analysis.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2016 Aug . Huang Yanlan, Cheng Daobin, Zhang Jiede, Zhao Weij |
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Nonatheroscleotic Isolated Middle Cerebral Artery Disease May Be Early Manifestation of Moyamoya Disease.
Stroke; a journal of cerebral circulation 2016 Aug . Kim Yeon-Jung, Lee Joo Kyung, Ahn Sung-Ho, Kim Bum Joon, Kang Dong-Wha, Kim Jong S, Kwon Sun |
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Caveolin-1, Ring finger protein 213, and endothelial function in Moyamoya disease.
International journal of stroke : official journal of the International Stroke Society 2016 Jul . Bang Oh Young, Chung Jong-Won, Kim Suk Jae, Oh Mi Jeong, Kim Soo Yoon, Cho Yeon Hee, Cha Jihoon, Yeon Je Young, Kim Keon Ha, Kim Gyeong-Moon, Chung Chin-Sang, Lee Kwang Ho, Ki Chang-Seok, Jeon Pyoung, Kim Jong-Soo, Hong Seung Chyul, Moon Gyeong Jo |
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Significant Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2016 Jul . Morimoto Takaaki, Mineharu Yohei, Kobayashi Hatasu, Harada Kouji H, Funaki Takeshi, Takagi Yasushi, Sakai Nobuyuki, Miyamoto Susumu, Koizumi Ak |
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RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients.
PloS one 2016 11 (10): e0164759. Kobayashi Hatasu, Brozman Miroslav, Kyselová Kate?ina, Viszlayová Daša, Morimoto Takaaki, Roubec Martin, Školoudík David, Petrovi?ová Andrea, Juskani? Dominik, Strauss Jozef, Halaj Marián, Kurray Peter, Hranai Marián, Harada Kouji H, Inoue Sumiko, Yoshida Yukako, Habu Toshiyuki, Herzig Roman, Youssefian Shohab, Koizumi Ak |
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The association between the ring finger protein 213 gene R4810K variant and intracranial major artery stenosis/occlusion in the Han Chinese population and high-resolution magnetic resonance imaging findings.
Brain circulation 0 4 (1): 33-39. Xue Sufang, Cheng Weiyang, Wang Wanqian, Song Xiaowei, Wu Jian, Song Haiqi |
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- Page last updated:Sep 16, 2021
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