Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 600 Records) |
| Query Trace: Disease and TAG[original query] |
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| Association of rs2072446 in the NGFR gene with the risk of Alzheimer's disease and amyloid-? deposition in the brain. CNS neuroscience & therapeutics 2022 Sep . He Chen-Yang, Wang Zuo-Teng, Shen Ying-Ying, Shi An-Yu, Li Hui-Yun, Chen Dong-Wan, Zeng Gui-Hua, Tan Cheng-Rong, Yu Jin-Tai, Zeng Fan, Wang Yan-Jiang, |
| Association of CDK6 gene polymorphisms with Behcet's disease in a Han Chinese population. Experimental eye research 2022 Jul 223 109203. Cai Shiya, Zhang Jun, Zhou Chunya, Shi Wenjian, Gao Yingying, Chang Rui, Tan Handan, Wang Qingfeng, Ye Xingsheng, Cao Qingfeng, Zhou Qingyun, Yang Peizeng, Hu Jianm |
| Identification of genetic variants of the IL-22 gene in association with an altered risk of COPD susceptibility. The clinical respiratory journal 2022 Jul . Wang Yan, Zhou Qipeng, Chen Lingzhu, Dong Lian, Xiong Mingmei, Xie Xiaohui, Zhao Li, Xu Jingyi, Zheng Zeguang, Wang Jian, Lu Wen |
| Crosstalk Between Gut Microflora and Vitamin D Receptor SNPs Are Associated with the Risk of Amnestic Mild Cognitive Impairment in a Chinese Elderly Population. Journal of Alzheimer's disease : JAD 2022 May . Zhang Kaixia, Ma Xiaoying, Zhang Rui, Liu Zanchao, Jiang Lei, Qin Yushi, Zhang Di, Tian Pei, Gao ZhaoYu, Zhang Nan, Shi Zhongli, Xu Shunjia |
| Tag-SNPs in Phospholipase-Related Genes Modify the Susceptibility to Nephrosclerosis and its Associated Cardiovascular Risk. Frontiers in pharmacology 2022 13 817020. González Luz M, Robles Nicolás R, Mota-Zamorano Sonia, Arévalo-Lorido José C, Valdivielso José Manuel, López-Gómez Juan, Gervasini Guiller |
| An antisense Alu transposon insertion/deletion polymorphism of ALDH1A1 may functionally associate with Parkinson's disease. BMC geriatrics 2022 05 22 (1): 427. Fan Hui-Hui, Zheng Jing, Huang Xiao-Ya, Wu Ke-Yun, Cui Lei, Dong Hao-Jia, Wang Zhen, Zhang Xiong, Zhu Jian-Ho |
| Effects of age, amyloid, sex, and APOE ?4 on the CSF proteome in normal cognition. Alzheimer's & dementia (Amsterdam, Netherlands) 2022 5 14 (1): e12286. Wesenhagen Kirsten E J, Gobom Johan, Bos Isabelle, Vos Stephanie J B, Martinez-Lage Pablo, Popp Julius, Tsolaki Magda, Vandenberghe Rik, Freund-Levi Yvonne, Verhey Frans, Lovestone Simon, Streffer Johannes, Dobricic Valerija, Bertram Lars, , Blennow Kaj, Pikkarainen Maria, Hallikainen Merja, Kuusisto Johanna, Laakso Markku, Soininen Hilkka, Scheltens Philip, Zetterberg Henrik, Teunissen Charlotte E, Visser Pieter Jelle, Tijms Betty |
| Associations between NKX2-5 gene polymorphisms and congenital heart disease in the Chinese Tibetan population. American journal of translational research 2022 12 14 (11): 8407-8415. Ma Qiang, Yang Yingzhong, Liu Yongni |
| Genome-wide association study reveals ethnicity-specific SNPs associated with ankylosing spondylitis in the Taiwanese population. Journal of translational medicine 2022 12 20 (1): 589. Ko Ching-Lung, Lin Wei-Zhi, Lee Meng-Ting, Chang Yu-Tien, Lin Hung-Che, Wu Yi-Syuan, Lin Jun-Fu, Pan Ke-Ting, Chang Yu-Chuan, Lee Ko-Han, Lee Yi-Lun, Hsieh Tsung-Ting, Huang Jia-Hsin, Wang Chih-Hung, Yang Sung-Sen, Chen Hsiang-Cheng, Chu Chi-Mi |
| Genetic variants in promoter region of TFR2 is associated with the risk of non-alcoholic fatty liver disease in a Chinese Han population: a case-control study. Gastroenterology report 2022 11 10 goac060. Pan Xinting, Peng Hewei, Zhang Junchao, Wu Yunli, Hu Zhijian, Peng Xian |
| The Roles of MTRR and MTHFR Gene Polymorphisms in Colorectal Cancer Survival. Nutrients 2022 11 14 (21): . Wang Yu, Du Meizhi, Vallis Jillian, Shariati Matin, Parfrey Patrick S, Mclaughlin John R, Wang Peizhong Peter, Zhu Y |
Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke.
Neurology 2022 Aug . Jaworek Thomas, Xu Huichun, Gaynor Brady J, Cole John W, Rannikmae Kristiina, Stanne Tara M, Tomppo Liisa, Abedi Vida, Amouyel Philippe, Armstrong Nicole D, Attia John, Bell Steven, Benavente Oscar R, Boncoraglio Giorgio B, Butterworth Adam, , Carcel-Marquez Jara, Chen Zhengming, Chong Michael, Cruchaga Carlos, Cushman Mary, Danesh John, Debette Stephanie, Duggan David J, Durda Jon Peter, Engstrom Gunnar, Enzinger Chris, Faul Jessica D, Fecteau Natalie S, Fernandez-Cadenas Israel, Gieger Christian, Giese Anne-Katrin, Grewal Raji P, Grittner Ulrike, Havulinna Aki S, Heitsch Laura, Hochberg Marc C, Holliday Elizabeth, Hu Jie, Ilinca Andreea, , Irvin Marguerite R, Jackson Rebecca D, Jacob Mina A, Janssen Raquel Rabionet, Jimenez-Conde Jordi, Johnson Julie A, Kamatani Yoichiro, Kardia Sharon L, Koido Masaru, Kubo Michiaki, Lange Leslie, Lee Jin-Moo, Lemmens Robin, Levi Christopher R, Li Jiang, Li Liming, Lin Kuang, Lopez Haley, Luke Sothear, Maguire Jane, McArdle Patrick F, McDonough Caitrin W, Meschia James F, Metso Tiina, Muller-Nurasyid Martina, O'Connor Timothy D, O'Donnell Martin, Peddareddygari Leema R, Pera Joanna, Perry James A, Peters Annette, Putaala Jukka, Ray Debashree, Rexrode Kathryn, Ribases Marta, Rosand Jonathan, Rothwell Peter M, Rundek Tatjana, Ryan Kathleen A, Sacco Ralph L, Salomaa Veikko, Sanchez-Mora Cristina, Schmidt Reinhold, Sharma Pankaj, Slowik Agnieszka, Smith Jennifer A, Smith Nicholas L, Wassertheil-Smoller Sylvia, Soederholm Martin, Stine O C, Strbian Daniel, Sudlow Cathie L, Tatlisumak Turgut, Terao Chikashi, Thijs Vincent, Torres-Aguila Nuria P, Tregouet David-Alexandre, Tuladhar Anil M, Veldink Jan H, Walters Robin G, Weir David R, Woo Daniel, Worrall Bradford B, Hong Charles C, Ross Owen, Zand Ramin, Leeuw Frank-Erik de, Lindgren Arne G, Pare Guillaume, Anderson Christopher D, Markus Hugh S, Jern Christina, Malik Rainer, Dichgans Martin, Mitchell Braxton D, Kittner Steven J, |
| Methylation and expression quantitative trait loci rs1799971 in the OPRM1 gene and rs4654327 in the OPRD1 gene are associated with opioid use disorder. Neuroscience letters 2023 9 814 137468. Jiao Yu, Yudan Zhang, Yufeng Xun, Hua Tang, Xiaoyu Fu, Rui Zhang, Feng Zhu, Jianbo Zha |
| Associations between polymorphisms in leptin and leptin receptor genes and colorectal cancer survival. Cancer biology & medicine 2023 6 . Meizhi Du, Yu Wang, Jillian Vallis, Matin Shariati, Patrick S Parfrey, John R Mclaughlin, Peizhong Peter Wang, Yun Z |
| The ERBB2 Exonic Variant Pro1170Ala Modulates Mitogen-Activated Protein Kinase Signaling Cascades and Associates with Allergic Asthma. International archives of allergy and immunology 2023 6 1-12. Yang Yie Sio, Wei Liang Gan, Wing Shan Ng, Sri Anusha Matta, Yee-How Say, Keng Foo Teh, Yi Ru Wong, Smyrna Moti Rawanan Shah, Kavita Reginald, Fook Tim Ch |
| Effect of PRDX6 gene polymorphism on susceptibility to chronic obstructive pulmonary disease in the Chinese Han population. The clinical respiratory journal 2023 6 . Mingmei Xiong, Meihua Guo, Dongjian Huang, Jing Li, Yan Zh |
| Association between HMGB1 genetic variants and ischemic stroke susceptibility, onset age, and recurrence risk among Chinese Han individuals. American journal of translational research 2023 6 15 (5): 3326-3341. Luying Qiu, Long Li, Zhiyi He, Fang Liu, Shumin Deng, Yanzhe Wa |
| Association of ZC3HAV1 single nucleotide polymorphisms with the susceptibility of Vogt-Koyanagi-Harada Disease. BMC medical genomics 2023 5 16 (1): 113. Qiuying Wu, Zhenyu Zhong, Chunya Zhou, Qingfeng Cao, Guannan Su, Peizeng Ya |
| Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35. medRxiv : the preprint server for health sciences 2023 4 . Cullina Sinead, Wojcik Genevieve L, Shemirani Ruhollah, Klarin Derek, Gorman Bryan R, Sorokin Elena P, Gignoux Christopher R, Belbin Gillian M, Pyarajan Saiju, Asgari Samira, Tsao Phil S, Damrauer Scott M, Abul-Husn Noura S, Kenny Eimear |
| Gene-wide significant association analyses of DNMT1 genetic variants with Parkinson's disease. Frontiers in genetics 2023 3 14 1112388. Wang Jian-Yong, Cui Lei, Shi Hong-Yi, Chen Ling-Hao, Jin Ren-Wei, Jiang Xiao-Xia, Chen Zhu-Ling, Zhu Jian-Hong, Zhang Xio |
| Intergenic variants, rs1200114 and rs1200108 are genetically associated along with a decreased ATP1B1 expression in Fuchs Endothelial Corneal Dystrophy. Experimental eye research 2023 2 228 109403. Chakraborty Maynak, Jandhyam Harithalakshmi, Basak Samar Kumar, Das Sujata, Alone Debasmita Pank |
| Contributions of NR1H3 genetic polymorphisms to susceptibility and effects of narrowband UVB phototherapy to nonsegmental vitiligo. Scientific reports 2023 2 13 (1): 3384. Xu Meifeng, Xu Qiuyu, Liu Yan, Li Xiaoli, Wang Mei, Dong Wei, Song Yuning, Xiao Shengxia |
| SNPs-Panel Polymorphism Variations in GHRL and GHSR Genes Are Not Associated with Prostate Cancer. Biomedicines 2023 12 11 (12): . Nesrine Merabet, Nicolas Ramoz, Amel Boulmaiz, Asma Bourefis, Maroua Benabdelkrim, Omar Djeffal, Emmanuel Moyse, Virginie Tolle, Hajira Berredj |
| Evidence for involvement of the alcohol consumption WDPCP gene in lipid metabolism, and liver cirrhosis. Scientific reports 2023 11 13 (1): 20616. Felix O'Farrell, Benjamin Aleyakpo, Rima Mustafa, Xiyun Jiang, Rui Climaco Pinto, Paul Elliott, Ioanna Tzoulaki, Abbas Dehghan, Samantha H Y Loh, Jeff W Barclay, L Miguel Martins, Raha Pazo |
| An alternative method of SNP inclusion to develop a generalized polygenic risk score analysis across Alzheimer's disease cohorts. Frontiers in dementia 2024 7 2 1120206. Keeley J Brookes, Tamar Guetta-Baranes, Alan Thomas, Kevin Morg |
| Roles of Single Nucleotide Polymorphisms of C3 Gene in Patients with Coronary Artery Disease. Reviews in cardiovascular medicine 2024 7 25 (4): 147. Shajidan Abudureyimu, Chunhui He, Dilihumaer Abulaiti, Wei Xie, Halisha Airikenjiang, Haitang Qiu, Mengjia Liu, Yan Cao, Hui Li, Jian Zhang, Ying G |
| Exploring the role of vitamin D-VDR pathway in pemphigus foliaceous: a novel perspective on disease pathogenesis. Archives of dermatological research 2024 7 316 (7): 449. Safa Tahri, Nesrine Elloumi, Boudour Khabou, Rim Frikha, Hamida Turki, Nadia Mahfoudh, Emna Bahloul, Hend Hachicha, Hatem Masmoudi, Olfa Abi |
| Disparities in ABO blood type determination across diverse ancestries: a systematic review and validation in the All of Us Research Program. Journal of the American Medical Informatics Association : JAMIA 2024 6 . Kiana L Martinez, Andrew Klein, Jennifer R Martin, Chinwuwanuju U Sampson, Jason B Giles, Madison L Beck, Krupa Bhakta, Gino Quatraro, Juvie Farol, Jason H Karn |
| The protective effect of higher serum triacylglycerol (51:4) levels against Parkinson's disease. The British journal of nutrition 2024 11 1-36. Yajun Jing, Jinye Su, Honglin Zhu, Yiming Chen, Surmai Shukla, Lianghong Yu, Dezhi Kang, Dengliang Wa |
| Polymorphisms rs562556 and rs2479409 of the PCSK9 gene associated with obesity and cardiovascular disease. Central European journal of public health 2024 1 31 (Suppl 1): S82-S88. Hedviga Vašková, Janka Porá?ová, Miriama Šlebodová, So?a Kalafutová, Mária Kone?ná, Vincent Sedlák, Tatiana Kimáková, Marta Mydlárová Blaš?áko |
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