Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 41 Records) |
Query Trace: Stroke and RNF213[original query] |
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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 |
Cav-1 (Caveolin-1) and Arterial Remodeling in Adult Moyamoya Disease. Stroke 2018 10 49 (11): 2597-2604. Chung Jong-Won, Kim Dong Hee, Oh Mi Jeong, Cho Yeon Hee, Kim Eun Hee, Moon Gyeong Joon, Ki Chang-Seok, Cha Jihoon, Kim Keon Ha, Jeon Pyoung, Yeon Je Young, Kim Gyeong-Moon, Kim Jong-Soo, Hong Seung Chyul, Bang Oh You |
Prevalence of RNF213 p.R4810K Variant in Early-Onset Stroke With Intracranial Arterial Stenosis. Stroke 2019 5 50 (6): 1561-1563. Kamimura Teppei, Okazaki Shuhei, Morimoto Takaaki, Kobayashi Hatasu, Harada Kouji, Tomita Tsutomu, Higashiyama Aya, Yoshimoto Takeshi, Takahashi Jun C, Nakagawara Jyoji, Koga Masatoshi, Toyoda Kazunori, Maruyama Hirofumi, Koizumi Akio, Ihara Masafu |
Genotype-Phenotype Correlation in Long-Term Cohort of Japanese Patients with Moyamoya Disease. Cerebrovascular diseases (Basel, Switzerland) 2019 Apr 1-7. Nomura Shunsuke, Yamaguchi Koji, Akagawa Hiroyuki, Kawashima Akitsugu, Moteki Yosuke, Ishikawa Tatsuya, Aihara Yasuo, Saito Taiichi, Okada Yoshikazu, Kawamata Takaka |
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 |
Are Genetic Variants Associated with the Location of Cerebral Arterial Lesions in Stroke Patients? Cerebrovascular diseases (Basel, Switzerland) 2020 Jun 1-7. Kim Yeon-Jung, Kim Bum Joon, Lee Min Hwan, Lee Han-Bin, Lee Ji Sung, Chang Dae-Il, Choi-Kwon Smi, Chun Sail, Lee Jong-Keuk, Kang Dong-Wha, Kwon Sun U, Kim Jong |
Genetic Risk Factors of Intracranial Atherosclerosis. Current atherosclerosis reports 2020 5 22 (4): 13. Liu Minghua, Gutierrez Jo |
Distribution of Intracranial Major Artery Stenosis/Occlusion According to RNF213 Polymorphisms. International journal of molecular sciences 2020 3 21 (6): . Kim Jinkwon, Park Young Seok, Woo Min-Hee, An Hui Jeong, Kim Jung Oh, Park Han Sung, Ryu Chang Soo, Kim Ok Joon, Kim Nam Ke |
Prevalence of RNF213 variants in symptomatic intracranial arterial stenosis/occlusion in China. Molecular genetics and genomics : MGG 2020 Feb . Sun Xunsha, Luo Man, Li Jiaoxing, Lai Rong, Lin Jing, Wang Yufang, Xu Xiaowei, Wu Shaoqing, Sheng Wen |
Global Assessment of Mendelian Stroke Genetic Prevalence in 101 635 Individuals From 7 Ethnic Groups. Stroke 2020 Feb STROKEAHA119028840. Grami Nickrooz, Chong Michael, Lali Ricky, Mohammadi-Shemirani Pedrum, Henshall David E, Rannikmäe Kristiina, Paré Guillau |
Rare genetic variants in patients with cervical artery dissection. European stroke journal 2020 1 4 (4): 355-362. Traenka Christopher, Kloss Manja, Strom Tim, Lyrer Philippe, Brandt Tobias, Bonati Leo H, Grond-Ginsbach Caspar, Engelter Stef |
Clinical Usefulness of Genetic Testing For Patients with Moyamoya Disease: A Systematic Review. World neurosurgery 2021 6 152 198-205.e1. Shlobin Nathan A, Hoffman Steven C, Clark Jeffrey R, Du Rebecca Y, Lam San |
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 |
RNF213 p.R4810K Variant Carriers with Intracranial Arterial Stenosis Have a Low Atherosclerotic Burden. Journal of atherosclerosis and thrombosis 2021 12 29 (11): 1655-1662. Ohara Mariko, Yoshimoto Takeshi, Okazaki Shuhei, Gon Yasufumi, Todo Kenichi, Sasaki Tsutomu, Takasugi Junji, Ohara Nobuyuki, Ihara Masafumi, Mochizuki Hide |
The association between the Moyamoya disease susceptible gene RNF213 variant and incident cardiovascular disease in a general population: the Nagahama study. Journal of hypertension 2021 Dec 39 (12): 2521-2526. Tabara Yasuharu, Yamada Hitomi, Setoh Kazuya, Matsukawa Manami, Takahashi Meiko, Kawaguchi Takahisa, Nakayama Takeo, Matsuda Fumihiko, Kosugi Shin |
RNF213 p.Arg4810Lys Heterozygosity in Moyamoya Disease Indicates Early Onset and Bilateral Cerebrovascular Events. Translational stroke research 2021 Oct . Ishigami Daiichiro, Miyawaki Satoru, Imai Hideaki, Shimizu Masahiro, Hongo Hiroki, Dofuku Shogo, Ohara Kenta, Teranishi Yu, Shimada Daisuke, Koizumi Satoshi, Ono Hideaki, Hirano Yudai, Segawa Masafumi, Nakatomi Hirofumi, Saito Nobuhi |
First Report: Rare RNF213 Variant Associated with Familial Moyamoya Disease in an African American Family. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2021 10 30 (12): 106123. Sunmonu N Abimbola, Ambati Naveen Kumar, Thomas Matthew J, Ulep Robin D, Worrall Bradfo |
Genome-Wide Association Study of Intracranial Artery Stenosis Followed by Phenome-Wide Association Study.
Translational stroke research 2022 Jun . Dofuku Shogo, Sonehara Kyuto, Miyawaki Satoru, Sakaue Saori, Imai Hideaki, Shimizu Masahiro, Hongo Hiroki, Shinya Yuki, Ohara Kenta, Teranishi Yu, Okano Atsushi, Ono Hideaki, Nakatomi Hirofumi, Teraoka Akira, Yamamoto Kenichi, Maeda Yuichi, Nii Takuro, Kishikawa Toshihiro, Suzuki Ken, Hirata Jun, Takahashi Meiko, Matsuda Koichi, Kumanogoh Atsushi, Matsuda Fumihiko, Okada Yukinori, Saito Nobuhi |
Moyamoya disease: diagnosis and interventions. The Lancet. Neurology 2022 5 21 (8): 747-758. Ihara Masafumi, Yamamoto Yumi, Hattori Yorito, Liu Wanyang, Kobayashi Hatasu, Ishiyama Hiroyuki, Yoshimoto Takeshi, Miyawaki Satoru, Clausen Tim, Bang Oh Young, Steinberg Gary K, Tournier-Lasserve Elisabeth, Koizumi Ak |
Genetic determinants of intracranial large artery stenosis in the northern Manhattan study. Journal of the neurological sciences 2022 3 436 120218. Liu Minghua, Sariya Sanjeev, Khasiyev Farid, Tosto Giuseppe, Dueker Nicole D, Cheung Ying Kuen, Wright Clinton B, Sacco Ralph L, Rundek Tatjana, Elkind Mitchell S V, Gutierrez Jo |
Prevalence of Mutations in Mendelian Stroke Genes in Early Onset Stroke Patients. Annals of neurology 2022 12 . Park Hong-Kyun, Lee Keon-Joo, Park Jong-Moo, Kang Kyusik, Lee Soo Joo, Kim Jae Guk, Cha Jae-Kwan, Kim Dae-Hyun, Han Moon-Ku, Kang Jihoon, Kim Beom Joon, Park Tai Hwan, Park Moo-Seok, Lee Kyung Bok, Lee Jun, Hong Keun-Sik, Cho Yong-Jin, Lee Byung-Chul, Yu Kyung-Ho, Oh Mi Sun, Kim Joon-Tae, Choi Kang-Ho, Kim Dong-Eog, Ryu Wi-Sun, Choi Jay Chol, Kwon Jee-Hyun, Kim Wook-Joo, Shin Dong-Ick, Sohn Sung Il, Hong Jeong-Ho, Lee Juneyoung, Lee Kyunghoon, Song Junghan, Bae Joon Seol, Cheong Hyun Sub, Debette Stéphanie, Bae Hee-Jo |
Effect of the RNF213 p.R4810K Variant on the Progression of Intracranial Artery Stenosis: A 15-Year Follow-up Study. Neurology. Genetics 2022 11 8 (5): e200029. Okazaki Shuhei, Yoshimoto Takeshi, Ohara Mariko, Takagaki Masatoshi, Nakamura Hajime, Watanabe Kotaro, Gon Yasufumi, Todo Kenichi, Sasaki Tsutomu, Araki Hiroyuki, Yamada Tomomi, Manabe Shirou, Kishima Haruhiko, Ihara Masafumi, Mochizuki Hide |
Hypertensive disorders of pregnancy in moyamoya disease: A single institution experience. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2023 9 32 (11): 107377. Hirohisa Yajima, Satoru Miyawaki, Seisuke Sayama, Keiichi Kumasawa, Masako Ikemura, Hideaki Imai, Hiroki Hongo, Yudai Hirano, Daiichiro Ishigami, Seiei Torazawa, Satoshi Kiyofuji, Satoshi Koizumi, Nobuhito Sai |
Association of thyroid peroxidase antibody with the RNF213 p.R4810K variant in ischemic stroke/transient ischemic attack. Atherosclerosis 2023 9 382 117281. Takeshi Yoshimoto, Hiroyuki Ishiyama, Yorito Hattori, Kunihiro Nishimura, Yoko Okada, Hideaki Watanabe, Yasumasa Ohyagi, Yasuhisa Akaiwa, Tomoyuki Miyamoto, Michi Kawamoto, Masahiko Ichijo, Hiroyasu Inoue, Noriyuki Matsukawa, Toshiki Mizuno, Hirofumi Matsuyama, Hidekazu Tomimoto, Daisuke Kawakami, Kazunori Toyoda, Masatoshi Koga, Masafumi Iha |
Meta-analysis of the association between RNF213 polymorphisms and clinical features of moyamoya disease in Asian population. Clinical neurology and neurosurgery 2023 6 231 107801. Xiaolong Jiang, Li Liu, Sijin Ai, Xinrui Xie, Jiajun Deng, Zeshen Jiang, Bin Teng, Chengjiang Liu, Haiying Hua |
Detailed phenotype of RNF213 p.R4810K variant identified by the Chinese patients with acute ischaemic stroke or transient ischaemic attack. Stroke and vascular neurology 2023 5 . Hongyu Zhou, Jing Jing, Yuehua Pu, Wei Li, Xia Meng, Anxin Wang, Yingting Zuo, Zhe Xu, Qin Xu, Yue Suo, Hao Li, Yongjun Wa |
A long-term study of posterior circulation changes after revascularization in patients with moyamoya disease. Journal of neurosurgery 2023 4 1-6. Bao Xiang-Yang, Tong Huai-Yu, Wang Qian-Nan, Wang Xiao-Peng, Gao Gan, Zhang Qian, Zou Zheng-Xing, Duan Li |
The genetic landscape and clinical implication of pediatric Moyamoya angiopathy in an international cohort. European journal of human genetics : EJHG 2023 4 . Zanoni Paolo, Steindl Katharina, Sticht Heinrich, Oneda Beatrice, Joset Pascal, Ivanovski Ivan, Horn Anselm H C, Cabello Elena M, Laube Julia, Zweier Markus, Baumer Alessandra, Rauch Anita, Khan Nad |
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke. Genetics in medicine : official journal of the American College of Medical Genetics 2023 11 101013. Theresa Brunet, Benedikt Zott, Victoria Lieftüchter, Dominic Lenz, Axel Schmidt, Philipp Peters, Robert Kopajtich, Malin Zaddach, Hanna Zimmermann, Irina Hüning, Diana Ballhausen, Christian Staufner, Alyssa Bianzano, Joanne Hughes, Robert W Taylor, Robert McFarland, Anita Devlin, Mihaela Mihaljevi?, Nina Bariši?, Meino Rohlfs, Sibylle Wilfling, Neal Sondheimer, Stacy Hewson, Nikolaos M Marinakis, Konstantina Kosma, Joanne Traeger-Synodinos, Miriam Elbracht, Matthias Begemann, Sonja Trepels-Kottek, Dimah Hasan, Marcello Scala, Valeria Capra, Federico Zara, Amelie T van der Ven, Joenna Driemeyer, Christian Apitz, Johannes Krämer, Alanna Strong, Hakon Hakonarson, Deborah Watson, Johannes A Mayr, Holger Prokisch, Thomas Meitinger, Ingo Borggraefe, Juliane Spiegler, Ivo Baric, Marco Paolini, Lucia Gerstl, Matias Wagn |
A Case of Multiple Intracranial Major Artery Stenoses With Coexisting PCSK9 p.E32K and RNF213 p.R4810K Variants. Neurology. Genetics 2024 1 9 (5): e200099. Kotaro Noda, Yorito Hattori, Mika Hori, Mariko Harada-Shiba, Masafumi Iha |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
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