Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: 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 |
Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors. Cancer causes & control : CCC 2014 Jun 25 (6): 759-69. Huhn Stefanie, Bevier Melanie, Pardini Barbara, Naccarati Alessio, Vodickova Ludmila, Novotny Jan, Vodicka Pavel, Hemminki Kari, Försti As |
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 |
Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathies. PloS one 2017 7 12 (7): e0181842. Forleo Cinzia, D'Erchia Anna Maria, Sorrentino Sandro, Manzari Caterina, Chiara Matteo, Iacoviello Massimo, Guaricci Andrea Igoren, De Santis Delia, Musci Rita Leonarda, La Spada Antonino, Marangelli Vito, Pesole Graziano, Favale Stefa |
A comprehensive genomic meta-analysis identifies confirmatory role of OBSCN gene in breast tumorigenesis. Oncotarget 2017 12 8 (60): 102263-102276. Rajendran Barani Kumar, Deng Chu-X |
Mutation analysis of adenomas and carcinomas of the colon: Early and late drivers. Genes, chromosomes & cancer 2018 Mar . Wolff Roger K, Hoffman Michael D, Wolff Erica C, Herrick Jennifer S, Sakoda Lori C, Samowitz Wade S, Slattery Martha |
Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. Journal of cardiovascular development and disease 2018 1 4 (2): . Serie Daniel J, Crook Julia E, Necela Brian M, Axenfeld Bianca C, Dockter Travis J, Colon-Otero Gerardo, Perez Edith A, Thompson E Aubrey, Norton Nadi |
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 |
A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug Reactions. Pharmacogenomics and personalized medicine 2020 3 13 59-70. Calderon-Ospina Carlos Alberto, Hernández-Sómerson Mario, García Ana María, Mejia Adriana, Tamayo-Agudelo Caroll, Laissue Paul, Fonseca Mendoza Dora Jane |
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 |
Discovering novel driver mutations from pan-cancer analysis of mutational and gene expression profiles. PloS one 2020 11 15 (11): e0242780. Tegally Houriiyah, Kensler Kevin H, Mungloo-Dilmohamud Zahra, Ghoorah Anisah W, Rebbeck Timothy R, Baichoo Shakunta |
Identification of germline and somatic mutations in pancreatic adenosquamous carcinoma using whole exome sequencing. Cancer biomarkers : section A of Disease markers 2020 Jan . Ma Hongyun, Song Bin, Guo Shiwei, Li Gang, Jin Ga |
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 |
Mucin 4 mutation is associated with tumor mutation burden and promotes antitumor immunity in colon cancer patients. Aging 2021 Mar 13 (6): 9043-9055. Peng Linglong, Li Yang, Gu Haitao, Xiang Ling, Xiong Yongfu, Wang Rong, Zhou He, Wang Jiji |
Establishing and Validating an Aging-Related Prognostic Four-Gene Signature in Colon Adenocarcinoma. BioMed research international 2021 11 2021 4682589. Zheng Lian, Yang Yang, Cui Xiaoro |
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 |
Integrative Genomic and Transcriptomic Analysis of Primary Malignant Gliomas Revealed Different Patterns Between Grades and Somatic Mutations Related to Glioblastoma Prognosis. Frontiers in molecular biosciences 2022 7 9 873042. Jin Huawei, Yu Zhenhua, Tian Tian, Shen Guoping, Chen Weian, Fan Miao, He Qun, Dai Dandan, Zhang Xuan, Liu Daw |
Whole-exome sequencing of transforming oral lichen planus reveals mutations in DNA damage repair and apoptosis pathway genes. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2022 Feb . Xie Fangyi, Gleue Casey A, Deschaine Maria, Dasari Surendra, Lau Julie S, Sartori-Valinotti Julio C, Meves Alexander, Lehman Julia |
Genomic analyses reveal SCN7A is associated with the prognosis of esophageal squamous cell carcinoma. Esophagus : official journal of the Japan Esophageal Society 2022 1 19 (2): 303-315. Yuan Ping, Rao Wenqing, Lin Zheng, Liu Shuang, Lin Xiuquan, Wu Chaofeng, Lin Xu, Hu Zhijian, Ye Weim |
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 |
Tumour genotypes account for survival differences in right- and left-sided colon cancers. Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland 2022 Jan . Ward Thomas M, Cauley Christy E, Stafford Caitlin E, Goldstone Robert N, Bordeianou Liliana G, Kunitake Hiroko, Berger David L, Ricciardi Roc |
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 |
Association analyses of predicted loss-of-function variants prioritized 15 genes as blood pressure regulators. The Canadian journal of cardiology 2023 7 . Estelle Lecluze, Guillaume Lett |
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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- Page last updated:Apr 16, 2024
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