Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 61 Records) |
Query Trace: Stroke and NOTCH3[original query] |
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Broad phenotype of cysteine-altering NOTCH3 variants in UK Biobank: CADASIL to nonpenetrance. Neurology 2020 8 95 (13): e1835-e1843. Rutten Julie W, Hack Remco J, Duering Marco, Gravesteijn Gido, Dauwerse Johannes G, Overzier Maurice, van den Akker Erik B, Slagboom Eline, Holstege Henne, Nho Kwangsik, Saykin Andrew, Dichgans Martin, Malik Rainer, Lesnik Oberstein Saskia A |
Clinical and imaging features of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and cysteine-sparing NOTCH3 mutations. PloS one 2020 6 15 (6): e0234797. Kim Hyunjin, Lim Young-Min, Lee Eun-Jae, Oh Yeo Jin, Kim Kwang-K |
Prevalence and Atypical Clinical Characteristics of NOTCH3 Mutations Among Patients Admitted for Acute Lacunar Infarctions. Frontiers in aging neuroscience 2020 6 12 130. Okada Takashi, Washida Kazuo, Irie Kenichi, Saito Satoshi, Noguchi Michio, Tomita Tsutomu, Koga Masatoshi, Toyoda Kazunori, Okazaki Shuhei, Koizumi Takashi, Mizuta Ikuko, Mizuno Toshiki, Ihara Masafu |
Coronary microvascular function is impaired in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. European journal of neurology 2020 12 28 (11): 3809-3813. Argirò Alessia, Sciagrà Roberto, Marchi Alberto, Beltrami Matteo, Spinelli Enrico, Salvadori Emilia, Bianchi Andrea, Mascalchi Mario, Poggesi Anna, Olivotto Iacopo, Pescini Frances |
A Novel Mutation Outside of the EGFr Encoding Exons of NOTCH3 Gene in a Chinese with CADASIL. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2020 12 29 (12): 105410. Wang Wan, Ren Zhixia, Shi Yingying, Zhang Jiew |
Cysteine-Altering NOTCH3 Variants Are a Risk Factor for Stroke in the Elderly Population. Stroke 2020 11 51 (12): 3562-3569. Hack Remco J, Rutten Julie W, Person Thomas N, Li Jiang, Khan Ayesha, Griessenauer Christoph J, , Abedi Vida, Lesnik Oberstein Saskia A J, Zand Ram |
Genetic and nongenetic factors associated with CADASIL: A retrospective cohort study. Journal of the neurological sciences 2020 Oct 419 117178. Ospina Carolina, Arboleda-Velasquez Joseph F, Aguirre-Acevedo Daniel Camilo, Zuluaga-Castaño Yesica, Velilla Lina, Garcia Gloria P, Quiroz Yakeel T, Lopera Francis |
Prominent juxtacortical white matter lesion hallmarks NOTCH3-related intracerebral haemorrhage. Stroke and vascular neurology 2021 8 7 (1): 38-46. Chen Chih-Hao, Hsu Hao-Chia, Cheng Yu-Wen, Chen Ya-Fang, Tang Sung-Chun, Jeng Jiann-Shi |
Rare NOTCH3 Variants in a Chinese Population-Based Cohort and Its Relationship With Cerebral Small Vessel Disease. Stroke 2021 8 52 (12): 3918-3925. Liu Jing-Yi, Yao Ming, Dai Yi, Han Fei, Zhai Fei-Fei, Zhang Ding-Ding, Zhou Li-Xin, Ni Jun, Zhang Shu-Yang, Cui Li-Ying, Zhu Yi-Che |
Global Cardiovascular Risk Profile and Cerebrovascular Abnormalities in Presymptomatic Individuals with CADASIL or Autosomal Dominant Alzheimer's Disease. Journal of Alzheimer's disease : JAD 2021 6 82 (2): 841-853. Schoemaker Dorothee, Velilla-Jimenez Lina, Zuluaga Yesica, Baena Ana, Ospina Carolina, Bocanegra Yamile, Alvarez Sergio, Ochoa-Escudero Martin, Guzmán-Vélez Edmarie, Martinez Jairo, Lopera Francisco, Arboleda-Velasquez Joseph F, Quiroz Yakeel |
Pathogenic NOTCH3 Variants Are Frequent Among the Korean General Population. Neurology. Genetics 2021 12 7 (6): e639. Kang Chul-Hoo, Kim Young Mee, Kim Yang-Ji, Hong Su-Jeong, Kim Do Yoon, Woo Hyun Goo, Kim Young Ree, Kim Joong-Goo, Lee Jung Seok, Kong Mi Hee, Kim Hyeon Ju, Choi Jay Ch |
Mutation spectrum and genotype-phenotype correlations in 157 Korean CADASIL patients: a multicenter study. Neurogenetics 2021 Nov . Min Ji-You, Park Seo-Jin, Kang Eun-Joo, Hwang Seung-Yong, Han Sung-H |
Monogenic basis of young-onset cryptogenic stroke: a multicenter study. Annals of translational medicine 2022 May 10 (9): 512. Yuan Wei-Zhuang, Shang Liang, Tian Dai-Shi, Wu Shi-Wen, You Yong, Tian Cheng-Lin, Wu Bo, Liu Jun, Sun Qin-Jian, Liu Qing, Xu Wei-H |
Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage. European journal of neurology 2022 7 29 (11): 3243-3254. Chen Chih-Hao, Chu Yung-Tsai, Chen Ya-Fang, Ko Tzu-Yu, Cheng Yu-Wen, Lee Ming-Jen, Chen Pei-Lung, Tang Sung-Chun, Jeng Jiann-Shi |
Effect of NOTCH3 EGFr Group, Sex, and Cardiovascular Risk Factors on CADASIL Clinical and Neuroimaging Outcomes. Stroke 2022 7 53 (10): 3133-3144. Hack Remco J, Cerfontaine Minne N, Gravesteijn Gido, Tap Stephan, Hafkemeijer Anne, van der Grond Jeroen, Witjes-Ané Marie-Noëlle, Baas Frank, Rutten Julie W, Lesnik Oberstein Saskia A |
Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations. CNS neuroscience & therapeutics 2022 7 28 (11): 1779-1789. Ni Wang, Zhang Yi, Zhang Liang, Xie Juan-Juan, Li Hong-Fu, Wu Zhi-Yi |
Association of NOTCH3 Variant Position With Stroke Onset and Other Clinical Features Among Patients With CADASIL. Neurology 2022 5 99 (5): e430-9. Cho Bernard P H, Jolly Amy A, Nannoni Stefania, Tozer Daniel, Bell Steven, Markus Hugh |
Reduced macular vessel density and inner retinal thickness correlate with the severity of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). PloS one 2022 17 (5): e0268572. Lin Chao-Wen, Yang Zih-Wei, Chen Chih-Hao, Cheng Yu-Wen, Tang Sung-Chun, Jeng Jiann-Shi |
Mutation screening and association analysis of NOTCH3 p.R544C in patients with migraine with or without aura. Cephalalgia : an international journal of headache 2022 3 42 (9): 888-898. Wang Yen-Feng, Liao Yi-Chu, Tzeng Yi-Shiang, Chen Shih-Pin, Lirng Jiing-Feng, Fuh Jong-Ling, Chen Wei-Ta, Lai Kuan-Lin, Lee Yi-Chung, Wang Shuu-Ji |
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 |
Three-tiered EGFr domain risk stratification for individualized NOTCH3-small vessel disease prediction. Brain : a journal of neurology 2022 12 . Hack Remco J, Gravesteijn Gido, Cerfontaine Minne N, Santcroos Mark A, Gatti Laura, Kopczak Anna, Bersano Anna, Duering Marco, Rutten Julie W, Lesnik Oberstein Saskia A |
Exome-based gene panel analysis in a cohort of acute juvenile ischemic stroke patients:relevance of NOTCH3 and GLA variants. Journal of neurology 2022 11 . Härtl Johanna, Hartberger Julia, Wunderlich Silke, Cordts Isabell, Bafligil Cemsel, Sturm Marc, , Westphal Dominik, Haack Tobias, Hemmer Bernhard, Ikenberg Benno David, Deschauer Marc |
Genotype and Phenotype Differences in CADASIL from an Asian Perspective. International journal of molecular sciences 2022 10 23 (19): . Kim Yerim, Bae Jong Seok, Lee Ju-Young, Song Hong Ki, Lee Ju-Hun, Lee Minwoo, Kim Chulho, Lee Sang-H |
Elderly CADASIL patients with intact neurological status. Journal of stroke 2022 Sep 24 (3): 352-362. Zhang Ruiting, Ouin Elisa, Grosset Lina, Ighilkrim Karine, Lebenberg Jessica, Guey Stéphanie, François Véronique, Tournier-Lasserve Elisabeth, Jouvent Eric, Chabriat Hugu |
The cysteine-altering p.R544C variant in the NOTCH3 gene is a probable candidate for blood pressure and relevant traits in the Taiwan Biobank. Journal of neurology 2023 8 . Eugene Lin, Po-Hsiu Kuo, Yu-Li Liu, Tso-Jen Wang, Albert C Yang, Shih-Jen Ts |
Modifiable Vascular Risk Factors Contribute to Stroke in 1,080 NOTCH3 R544C Carriers in Taiwan Biobank. International journal of stroke : official journal of the International Stroke Society 2023 7 17474930231191991. Hung-Jen Lin, Chih-Hao Chen, Ming-Wei Su, Chien-Wei Lin, Yu-Wen Cheng, Sung-Chun Tang, Jiann-Shing Je |
The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay. Cell discovery 2023 7 9 (1): 75. Si Cheng, Zhe Xu, Shengzhe Bian, Xi Chen, Yanfeng Shi, Yanran Li, Yunyun Duan, Yang Liu, Jinxi Lin, Yong Jiang, Jing Jing, Zixiao Li, Yilong Wang, Xia Meng, Yaou Liu, Mingyan Fang, Xin Jin, Xun Xu, Jian Wang, Chaolong Wang, Hao Li, Siyang Liu, Yongjun Wa |
NOTCH2NLC GGC Repeat Expansion in Patients With Vascular Leukoencephalopathy. Stroke 2023 3 . Liao Yi-Chu, Wei Cheng-Yu, Chang Fu-Pang, Chou Ying-Tsen, Hsu Shao-Lun, Chung Chih-Ping, Mizuguchi Takeshi, Matsumoto Naomichi, Yet Shaw-Fang, Lee Yi-Chu |
Contribution of the APOE Genotype to Cognitive Impairment in Individuals With NOTCH3 Cysteine-Altering Variants. Journal of the American Heart Association 2023 11 e032689. Yu-Wen Cheng, Yi-Chu Liao, Chih-Hao Chen, Chih-Ping Chung, Cathy S J Fann, Chien-Ching Chang, Yi-Chung Lee, Sung-Chun Ta |
Update on the Epidemiology, Pathogenesis, and Biomarkers of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. Journal of clinical neurology (Seoul, Korea) 2023 1 19 (1): 12-27. Yamamoto Yumi, Liao Yi-Chu, Lee Yi-Chung, Ihara Masafumi, Choi Jay Ch |
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- Page last updated:Apr 22, 2024
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