HuGE Literature Finder
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| Possible association between a polymorphism of EPAS1 gene and persistent pulmonary hypertension of the newborn: a case-control study. Jornal de pediatria 2021 Oct . Nakwan Narongsak, Mahasirimongkol Surakameth, Satproedprai Nusara, Chaiyasung Tassamonwan, Kunhapan Punna, Charoenlap Cheep, Singkhamanan Kamonnut, Charalsawadi Chariyaw |
| Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
| Effect of gene-gene and gene-environment interaction on the risk of first-ever stroke and poststroke death. Molecular genetics & genomic medicine 2019 Jul e846. Feng Congrui, Yang Yunyun, Yang Shujun, Tu Xin, Wang Yibo, Song Yiqing, Hui Rutai, Zhang Wei |
| Association of Notch3 single-nucleotide polymorphisms and lacunar infarctions in patients. Experimental and therapeutic medicine 2016 Jan 11 (1): 28-32. Li Ying, Liu Nan, Chen Hui, Huang Yonghua, Zhang Weiw |
| Common NOTCH3 Variants and Cerebral Small-Vessel Disease. Stroke; a journal of cerebral circulation 2015 Jun 46 (6): 1482-7. Rutten-Jacobs Loes C A, Traylor Matthew, Adib-Samii Poneh, Thijs Vincent, Sudlow Cathie, Rothwell Peter M, Boncoraglio Giorgio, Dichgans Martin, Bevan Steve, Meschia James, Levi Christopher, Rost Natalia S, Rosand Jonathan, Hassan Ahamad, Markus Hugh |
| Mutations of NOTCH3 in childhood pulmonary arterial hypertension. Molecular genetics & genomic medicine 2014 May 2 (3): 229-39. Chida Ayako, Shintani Masaki, Matsushita Yoshihisa, Sato Hiroki, Eitoku Takahiro, Nakayama Tomotaka, Furutani Yoshiyuki, Hayama Emiko, Kawamura Yoichi, Inai Kei, Ohtsuki Shinichi, Saji Tsutomu, Nonoyama Shigeaki, Nakanishi Tosh |
| Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease. Brain : a journal of neurology 2011 Nov 134 (Pt 11): 3384-97. Schmidt Helena, Zeginigg Marion, Wiltgen Marco, Freudenberger Paul, Petrovic Katja, Cavalieri Margherita, Gider Pierre, Enzinger Christian, Fornage Myriam, Debette Stephanie, Rotter Jerome I, Ikram Mohammad A, Launer Lenore J, Schmidt Reinhold, |
| Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals. Stroke; a journal of cerebral circulation 2010 Apr 41 (4): 630-4. Adib-Samii Poneh, Brice Glen, Martin Roswell J, Markus Hugh |
| Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese. Journal of neurology 2009 Feb 256 (2): 249-55. Lee Yi-Chung, Liu Chin-San, Chang Ming-Hong, Lin Kon-Ping, Fuh Jong-Ling, Lu Yi-Chu, Liu Ya-Fen, Soong Bing-W |
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