Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 38 Records) |
| Query Trace: Disease and JUN[original query] |
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| Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes. Archives of neurology 2010 Dec 67 (12): 1473-84. Jun Gyungah, Naj Adam C, Beecham Gary W, Wang Li-San, Buros Jacqueline, Gallins Paul J, Buxbaum Joseph D, Ertekin-Taner Nilufer, Fallin M Daniele, Friedland Robert, Inzelberg Rivka, Kramer Patricia, Rogaeva Ekaterina, St George-Hyslop Peter, , Cantwell Laura B, Dombroski Beth A, Saykin Andrew J, Reiman Eric M, Bennett David A, Morris John C, Lunetta Kathryn L, Martin Eden R, Montine Thomas J, Goate Alison M, Blacker Deborah, Tsuang Debby W, Beekly Duane, Cupples L Adrienne, Hakonarson Hakon, Kukull Walter, Foroud Tatiana M, Haines Jonathan, Mayeux Richard, Farrer Lindsay A, Pericak-Vance Margaret A, Schellenberg Gerard |
| The nine-repeat DC-SIGNR isoform is associated with increased HIV-RNA loads and HIV sexual transmission. Journal of clinical immunology 2010 May 30 (3): 402-7. Xu Lijun, Li Qinguang, Ye Hanhui, Zhang Qiyun, Chen Huicong, Huang Fan, Chen Ronghua, Zhou Rui, Zhou Wen, Xia Pincang, Chen Yi, Pan Ch |
| Confirmation of an association between single nucleotide polymorphisms in the VDR gene with respiratory syncytial virus related disease in South African children. Journal of medical virology 2011 Oct 83 (10): 1834-40. Kresfelder T L, Janssen R, Bont L, Pretorius M, Venter |
| Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. PloS one 2013 8 (4): e61805. Yiu Wai Chi, Yap Maurice K H, Fung Wai Yan, Ng Po Wah, Yip Shea Pi |
| Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data. Circulation research 2014 Oct 115 (10): 884-96. Glessner Joseph T, Bick Alexander G, Ito Kaoru, Homsy Jason G, Rodriguez-Murillo Laura, Fromer Menachem, Mazaika Erica, Vardarajan Badri, Italia Michael, Leipzig Jeremy, DePalma Steven R, Golhar Ryan, Sanders Stephan J, Yamrom Boris, Ronemus Michael, Iossifov Ivan, Willsey A Jeremy, State Matthew W, Kaltman Jonathan R, White Peter S, Shen Yufeng, Warburton Dorothy, Brueckner Martina, Seidman Christine, Goldmuntz Elizabeth, Gelb Bruce D, Lifton Richard, Seidman Jonathan, Hakonarson Hakon, Chung Wendy |
| Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls. Scientific reports 2014 4 7311. Xuan Chao, Li Hui, Zhao Jin-Xia, Wang Hong-Wei, Wang Yi, Ning Chun-Ping, Liu Zhen, Zhang Bei-Bei, He Guo-Wei, Lun Li-M |
| Associations between interleukin-1 gene polymorphisms and sepsis risk: a meta-analysis. BMC medical genetics 2014 15 (1): 8. Zhang An-Qiang, Pan Wei, Gao Jun-Wei, Yue Cai-Li, Zeng Ling, Gu Wei, Jiang Jian-X |
| MicroRNA biogenesis pathway genes polymorphisms and cancer risk: a systematic review and meta-analysis. PeerJ 2016 4 e2706. He Jieyu, Zhao Jun, Zhu Wenbo, Qi Daxun, Wang Lina, Sun Jinfang, Wang Bei, Ma Xu, Dai Qiaoyun, Yu Xiaoj |
| Lack of association between the Angiogenin (ANG) rs11701 polymorphism and amyotrophic lateral sclerosis risk: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 Jan . Pan Li-Shou, Deng Xin-Bo, Wang Zheng, Leng Hui-Lin, Zhu Xue-Peng, Ding D |
| [Clinical-based study of ovarian cancer patients with and without BRCA1/2 genes mutation: clinical features and pedigree analysis]. Zhonghua fu chan ke za zhi 2017 Jan 52 (1): 20-25. Tao T, Yang J X, Shen K, Cao D |
| Haplotype Analysis of PPAR? Gene Polymorphisms and the Lipoprotein (a) Level. Iranian journal of public health 2018 Jul 47 (7): 973-979. Shen Chao, Fan Wei, Xie Hui-Jian, Wu Ming, Zhou Zheng-Yuan, Guo Zhi-Rong, Dong Ch |
| Intensive genetic analysis for Chinese patients with very high triglyceride levels: Relations of mutations to triglyceride levels and acute pancreatitis. EBioMedicine 2018 Dec 38 171-177. Jin Jing-Lu, Sun Di, Cao Ye-Xuan, Zhang Hui-Wen, Guo Yuan-Lin, Wu Na-Qiong, Zhu Cheng-Gang, Gao Ying, Dong Qiu-Ting, Liu Geng, Dong Qian, Li Jian-J |
| Syndecan-1 (sCD138) levels in chronic lymphocytic leukemia: clinical and hematological correlations. Blood research 2018 10 53 (3): 205-209. Sharma Monica, Tyagi Seema, Tripathi Preeti, Seth Tuli |
| Molecular Basis for Dysregulated Activation of NKX2-5 in the Vascular Remodeling of Systemic Sclerosis. Arthritis & rheumatology (Hoboken, N.J.) 2018 1 70 (6): 920-931. Dritsoula Athina, Papaioannou Ioannis, Guerra Sandra G, Fonseca Carmen, Martin Javier, Herrick Ariane L, Abraham David J, Denton Christopher P, Ponticos Markel |
| APOE Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of APOE ?4 on Alzheimer's Disease Risk in a Multiracial Sample. Journal of clinical medicine 2019 8 8 (8): . Choi Kyu Yeong, Lee Jang Jae, Gunasekaran Tamil Iniyan, Kang Sarang, Lee Wooje, Jeong Jangho, Lim Ho Jae, Zhang Xiaoling, Zhu Congcong, Won So-Yoon, Choi Yu Yong, Seo Eun Hyun, Lee Seok Cheol, Gim Jungsoo, Chung Ji Yeon, Chong Ari, Byun Min Soo, Seo Sujin, Ko Pan-Woo, Han Ji-Won, McLean Catriona, Farrell John, Lunetta Kathryn L, Miyashita Akinori, Hara Norikazu, Won Sungho, Choi Seong-Min, Ha Jung-Min, Jeong Jee Hyang, Kuwano Ryozo, Song Min Kyung, An Seong Soo A, Lee Young Min, Park Kyung Won, Lee Ho-Won, Choi Seong Hye, Rhee Sangmyung, Song Woo Keun, Lee Jung Sup, Mayeux Richard, Haines Jonathan L, Pericak-Vance Margaret A, Choo I L Han, Nho Kwangsik, Kim Ki-Woong, Lee Dong Young, Kim SangYun, Kim Byeong C, Kim Hoowon, Jun Gyungah R, Schellenberg Gerard D, Ikeuchi Takeshi, Farrer Lindsay A, Lee Kun Ho, Neuroimaging Initative Alzheimer's Disea |
| Hydrogen Sulfide Ameliorates Homocysteine-Induced Cardiac Remodeling and Dysfunction. Frontiers in physiology 2019 10 598. Kar Sumit, Shahshahan Hamid R, Kambis Tyler N, Yadav Santosh K, Li Zhen, Lefer David J, Mishra Paras |
| Rare non-coding Desmoglein-2 variant contributes to Arrhythmogenic right ventricular cardiomyopathy. Journal of molecular and cellular cardiology 2019 5 131 164-170. Christensen Alex Hørby, Andersen Claus B, Wassilew Katharina, Svendsen Jesper Hastrup, Bundgaard Henning, Brand Stefan-Martin, Schmitz Bor |
| Mechanical activation of noncoding-RNA-mediated regulation of disease-associated phenotypes in human cardiomyocytes. Nature biomedical engineering 2019 3 3 (2): 137-146. Kumar Aditya, Thomas Stephanie K, Wong Kirsten C, Lo Sardo Valentina, Cheah Daniel S, Hou Yang-Hsun, Placone Jesse K, Tenerelli Kevin P, Ferguson William C, Torkamani Ali, Topol Eric J, Baldwin Kristin K, Engler Adam |
| A functional variant alters binding of activating protein 1 regulating expression of FGF7 gene associated with chronic obstructive pulmonary disease. BMC medical genetics 2019 Feb 20 (1): 33. Zhang Xiaomei, Guo Yongxin, Yang Jing, Niu Jianlou, Du Lina, Li Haiyan, Li Xiaok |
| A Study of the Relationship between the Polymorphism and Mutation of rs682429 and rs3781590 in the LRP5 Gene and Bone Metabolism in Postmenopausal Type 2 Diabetic Women in Xinjiang. Journal of diabetes research 2020 2020 3071217. Li Jun, Li SiYuan, Zhao HuiRong, Li JiaJia, Wang Shuang, Shi YanQ |
| Serum resistin levels and resistin gene polymorphism in patients with acne vulgaris: does it correlate with disease severity? International journal of dermatology 2021 Jul . Shehata Wafaa A, Maraee Alaa, Wahab Tagreed A A, Azmy Ran |
| Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype. Canadian journal of gastroenterology & hepatology 2021 5 2021 6610434. Xie Li-Jun, Ruan Dan-Dan, Zhang Jian-Hui, Li Yi, Chen Li, Yan Mao-Lin, Yu Ming-Dian, Luo Jie-Wei, Zhang Hui-Zh |
| Association of apolipoprotein B XbaI (rs693) polymorphism and gallstone disease risk based on a comprehensive analysis. Genes and environment : the official journal of the Japanese Environmental Mutagen Society 2021 5 43 (1): 17. Zhu Haifeng, Yu Linhai, Feng Linso |
| Efficacy, safety, and genetic analysis of furmonertinib (AST2818) in patients with EGFR T790M mutated non-small-cell lung cancer: a phase 2b, multicentre, single-arm, open-label study. The Lancet. Respiratory medicine 2021 Mar . Shi Yuankai, Hu Xingsheng, Zhang Shucai, Lv Dongqing, Wu Lin, Yu Qitao, Zhang Yiping, Liu Li, Wang Xiang, Cheng Ying, Ma Zhiyong, Niu Hongrui, Wang Dong, Feng Jifeng, Huang Cheng, Liu Chunling, Zhao Hui, Li Jingzhang, Zhang Xiaodong, Jiang Yong, Gu Chu |
| EGFR and PDL1: A Match (Not) Made in Heaven-A Real-World Retrospective Analysis of PDL1 Expression in EGFR-Mutated NSCLC. Advances in therapy 2021 2 38 (4): 1791-1800. Batra Ullas, Sharma Mansi, Nathany Shrinidhi, Bansal Abhishek, Pasricha Sunil, Jain Parveen, Mehta Anurag, Singh Harkir |
| Multimodal single-cell/nucleus RNA sequencing data analysis uncovers molecular networks between disease-associated microglia and astrocytes with implications for drug repurposing in Alzheimer's disease. Genome research 2021 2 31 (10): 1900-1912. Xu Jielin, Zhang Pengyue, Huang Yin, Zhou Yadi, Hou Yuan, Bekris Lynn M, Lathia Justin, Chiang Chien-Wei, Li Lang, Pieper Andrew A, Leverenz James B, Cummings Jeffrey, Cheng Feixio |
| Meta-Analysis of miRNA Variants Associated with Susceptibility to Autoimmune Disease. Disease markers 2021 10 2021 9978460. Zhang Jun, Tan Handan, Cao Qingfeng, Su Guannan, Yang Peize |
| The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia. Nature communications 2022 6 13 (1): 3690. Nehme Ralda, Pietiläinen Olli, Artomov Mykyta, Tegtmeyer Matthew, Valakh Vera, Lehtonen Leevi, Bell Christina, Singh Tarjinder, Trehan Aditi, Sherwood John, Manning Danielle, Peirent Emily, Malik Rhea, Guss Ellen J, Hawes Derek, Beccard Amanda, Bara Anne M, Hazelbaker Dane Z, Zuccaro Emanuela, Genovese Giulio, Loboda Alexander A, Neumann Anna, Lilliehook Christina, Kuismin Outi, Hamalainen Eija, Kurki Mitja, Hultman Christina M, Kähler Anna K, Paulo Joao A, Ganna Andrea, Madison Jon, Cohen Bruce, McPhie Donna, Adolfsson Rolf, Perlis Roy, Dolmetsch Ricardo, Farhi Samouil, McCarroll Steven, Hyman Steven, Neale Ben, Barrett Lindy E, Harper Wade, Palotie Aarno, Daly Mark, Eggan Kev |
| NFKB1 Gene Mutant Was Associated with Prognosis of Coronary Artery Disease and Exacerbated Endothelial Mitochondrial Fission and Dysfunction. Oxidative medicine and cellular longevity 2022 11 2022 9494926. Luo Jun-Yi, Liu Fen, Fang Bin-Bin, Tian Ting, Li Yan-Hong, Zhang Tong, Li Xiao-Mei, Yang Yi-Ni |
| Results of the phase IIa study to evaluate the efficacy and safety of rezivertinib (BPI-7711) for the first-line treatment of locally advanced or metastatic/recurrent NSCLC patients with EGFR mutation from a phase I/IIa study. BMC medicine 2023 1 21 (1): 11. Shi Yuankai, Zhou Jianying, Zhao Yanqiu, Zhu Bo, Zhang Liangming, Li Xingya, Fang Jian, Shi Jianhua, Zhuang Zhixiang, Yang Sheng, Wang Donglin, Yu Huiqing, Zhang Longzhen, Zheng Rongsheng, Greco Michael, Wang Tingti |
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