Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and OBSCN[original query] |
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| Contribution of the OBSCN nonsynonymous variants to aspirin exacerbated respiratory disease susceptibility in Korean population. DNA and cell biology 2012 Jun 31 (6): 1001-9. Kim Jeong-Hyun, Park Byung-Lae, Pasaje Charisse Flerida A, Kim Yongha, Bae Joon Seol, Park Jong Sook, Uh Soo-Taek, Kim Yong-Hoon, Kim Mi-Kyeong, Choi Inseon S, Cho Sang Heon, Choi Byoung Whui, Koh InSong, Park Choon-Sik, Shin Hyoung D |
| Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing. G3 (Bethesda, Md.) 2015 Nov . Shoemaker Lorelei D, Clark Michael J, Patwardhan Anil, Chandratillake Gemma, Garcia Sarah, Chen Rong, Morgan Alexander A, Leng Nan, Kirk Scott, Chen Richard, Cook Douglas J, Snyder Michael, Steinberg Gary |
| Reevaluation of genetic variants previously associated with arrhythmogenic right ventricular cardiomyopathy integrating population-based cohorts and proteomics data. Clinical genetics 2019 8 96 (6): 506-514. Ye Johan Z, Delmar Mario, Lundby Alicia, Olesen Morten |
The Genetic Makeup of the Electrocardiogram.
Cell systems 2020 Sep 11 (3): 229-238.e5. Verweij Niek, Benjamins Jan-Walter, Morley Michael P, van de Vegte Yordi J, Teumer Alexander, Trenkwalder Teresa, Reinhard Wibke, Cappola Thomas P, van der Harst P |
| Integrated characterisation of cancer genes identifies key molecular biomarkers in stomach adenocarcinoma. Journal of clinical pathology 2020 2 73 (9): 579-586. Wang Haifeng, Shen Liyijing, Li Yaoqing, Lv Jieqi |
| The Phenomenon of Gene Rearrangement is Frequently Associated with TP53 Mutations and Poor Disease-Free Survival in Hepatocellular Carcinoma. Pharmacogenomics and personalized medicine 2021 6 14 723-736. He Fu, Song Kangjian, Guan Ge, Huo Junyu, Xin Yang, Li Tianxiang, Liu Chao, Zhu Qingwei, Fan Ning, Guo Yuan, Wu Liq |
| Truncating Variants in OBSCN Gene Associated With Disease-Onset and Outcomes of Hypertrophic Cardiomyopathy. Circulation. Genomic and precision medicine 2021 10 14 (5): e003401. Wu Guixin, Liu Jie, Liu Minghao, Huang Qiya, Ruan Jieyun, Zhang Channa, Wang Dong, Sun Xiaolu, Jiang Wen, Kang Lianming, Wang Jizheng, Song L |
| Identification of Survival-Specific Genes in Clear Cell Renal Cell Carcinoma Using a Customized Next-Generation Sequencing Gene Panel. Journal of personalized medicine 2022 Jan 12 (1): . Hwang Jia, Kim Heeeun, Han Jinseon, Lee Jieun, Hong Sunghoo, Kim Saewoong, Yoon Sungjoo Kim, Choi Keonwoo, Yang Jihoon, Park Unsang, Kim Kwangjoong, Yim Kwangil, Kim Yuil, Choi Yeongj |
| Large-scale exome sequence analysis identifies sex- and age-specific determinants of obesity. Cell genomics 2023 8 3 (8): 100362. Lena R Kaisinger, Katherine A Kentistou, Stasa Stankovic, Eugene J Gardner, Felix R Day, Yajie Zhao, Alexander Mörseburg, Christopher J Carnie, Guido Zagnoli-Vieira, Fabio Puddu, Stephen P Jackson, Stephen O'Rahilly, I Sadaf Farooqi, Laura Dearden, Lucas C Pantaleão, Susan E Ozanne, Ken K Ong, John R B Per |
| Rare genetic variants impact muscle strength. Nature communications 2023 6 14 (1): 3449. Yunfeng Huang, Dora Bodnar, Chia-Yen Chen, Gabriela Sanchez-Andrade, Mark Sanderson, , Jun Shi, Katherine G Meilleur, Matthew E Hurles, Sebastian S Gerety, Ellen A Tsai, Heiko Ru |
| Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients. Frontiers in genetics 2023 2 14 1075349. Hu Huan, Geng Zilong, Zhang Shasha, Xu Yuejuan, Wang Qingjie, Chen Sun, Zhang Bing, Sun Kun, Lu Yan |
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