Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Disease and ZEB2[original query] |
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Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
Human molecular genetics 2013 Dec 22 (25): 5288-94. Khor Chiea Chuen, Miyake Masahiro, Chen Li Jia, Shi Yi, Barathi Veluchamy A, Qiao Fan, Nakata Isao, Yamashiro Kenji, Zhou Xin, Tam Pancy O S, Cheng Ching-Yu, Tai E Shyong, Vithana Eranga N, Aung Tin, Teo Yik-Ying, Wong Tien-Yin, Moriyama Muka, Ohno-Matsui Kyoko, Mochizuki Manabu, Matsuda Fumihiko, , Yong Rita Y Y, Yap Eric P H, Yang Zhenglin, Pang Chi Pui, Saw Seang-Mei, Yoshimura Nagahi |
| Effects of a functional variant c.353T>C in snai1 on risk of two contextual diseases. Chronic obstructive pulmonary disease and lung cancer. American journal of respiratory and critical care medicine 2014 Jan 189 (2): 139-48. Yang Lei, Yang Xiaorong, Ji Weidong, Deng Jieqiong, Qiu Fuman, Yang Rongrong, Fang Wenxiang, Zhang Lisha, Huang Dongsheng, Xie Chenli, Zhang Haibo, Zhong Nanshan, Ran Pixin, Zhou Yifeng, Lu Jiach |
| 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 |
| Sleep disturbance in Mowat-Wilson syndrome. American journal of medical genetics. Part A 2015 Dec . Evans Elizabeth, Mowat David, Wilson Meredith, Einfeld Stewa |
| De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients. NPJ genomic medicine 2016 1 16033. Mak Christopher C Y, Chow Pak Cheong, Liu Anthony P Y, Chan Kelvin Y K, Chu Yoyo W Y, Mok Gary T K, Leung Gordon K C, Yeung Kit San, Chau Adolphus K T, Lowther Chelsea, Scherer Stephen W, Marshall Christian R, Bassett Anne S, Chung Brian H |
| Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns. Genome medicine 2017 Oct 9 (1): 95. Li Alexander H, Hanchard Neil A, Furthner Dieter, Fernbach Susan, Azamian Mahshid, Nicosia Annarita, Rosenfeld Jill, Muzny Donna, D'Alessandro Lisa C A, Morris Shaine, Jhangiani Shalini, Parekh Dhaval R, Franklin Wayne J, Lewin Mark, Towbin Jeffrey A, Penny Daniel J, Fraser Charles D, Martin James F, Eng Christine, Lupski James R, Gibbs Richard A, Boerwinkle Eric, Belmont John |
| Targeted Sequencing Study to Uncover Shared Genetic Susceptibility Between Peripheral Artery Disease and Coronary Heart Disease-Brief Report. Arteriosclerosis, thrombosis, and vascular biology 2019 Apr ATVBAHA118312128. Safarova Maya S, Fan Xiao, Austin Erin E, van Zuydam Natalie, Hopewell Jemma, Schaid Daniel J, Kullo Iftikhar |
| Multiple independent mechanisms link gene polymorphisms in the region of ZEB2 with risk of coronary artery disease. Atherosclerosis 2020 9 311 20-29. Ma Lijiang, Chandel Nirupama, Ermel Raili, Sukhavasi Katyayani, Hao Ke, Ruusalepp Arno, Björkegren Johan L M, Kovacic Jason |
| Genetics of type 2 diabetes and coronary artery disease and their associations with twelve cardiometabolic traits in the United Arab Emirates population. Gene 2020 5 750 144722. Osman Wael, Hassoun Ahmed, Jelinek Herbert F, Almahmeed Wael, Afandi Bachar, Tay Guan K, Alsafar Habi |
| Genotype-phenotype analysis in Mowat-Wilson syndrome associated with two novel and two recurrent
variants. Experimental and therapeutic medicine 2020 Dec 20 (6): 263. Zou Dongfang, Wang Lin, Wen Feiqiu, Xiao Hongdou, Duan Jing, Zhang Tongda, Yin Zhenzhen, Dong Qiwen, Guo Jian, Liao Jianxia |
| Identification of ZEB2 as an Immune-Associated Gene in Endometrial Carcinoma and Associated with Macrophage Infiltration by Bioinformatic Analysis. Journal of healthcare engineering 2021 12 2021 4372373. Zhu Yuanyuan, Lin Xinchao, Zang Yuanlong, Yang Qiaoh |
| Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic Review. Frontiers in genetics 2022 6 13 853183. Fu Youqing, Xu Wanfang, Wang Qingming, Lin Yangyang, He Peiqing, Liu Yanhui, Yuan Haimi |
| HOXB9 Overexpression Promotes Colorectal Cancer Progression and Is Associated with Worse Survival in Liver Resection Patients for Colorectal Liver Metastases. International journal of molecular sciences 2022 2 23 (4): . Martinou Eirini, Moller-Levet Carla, Karamanis Dimitrios, Bagwan Izhar, Angelidi Angeliki |
| Genetic diagnosis of fetal microcephaly at a single tertiary center in China. Frontiers in genetics 2023 5 14 1112153. You Wang, Fang Fu, Tingying Lei, Li Zhen, Qiong Deng, Hang Zhou, Chunling Ma, Ken Cheng, Ruibin Huang, Ru Li, Qiuxia Yu, Lushan Li, Jin Han, Xin Yang, Dongzhi Li, Can Li |
| Molecular mechanisms of coronary artery disease risk at the PDGFD locus. bioRxiv : the preprint server for biology 2023 2 . Kim Hyun-Jung, Cheng Paul, Travisano Stanislao, Weldy Chad, Monteiro Jo O P, Kundu Ramendra, Nguyen Trieu, Sharma Disha, Shi Huitong, Lin Yi, Liu Boxiang, Haldar Saptarsi, Jackson Simon, Quertermous Thom |
| Clarifying Chronic Obstructive Pulmonary Disease Genetic Associations Observed in Biobanks via Mediation Analysis of Smoking. AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science 2024 6 2024 499-508. Katrina Bazemore, Jaehyun Joo, Wei-Ting Hwang, Blanca E Him |
| Genetic Association and Differential RNA Expression of Histone (De)Acetylation-Related Genes in Pemphigus Foliaceus-A Possible Epigenetic Effect in the Autoimmune Response. Life (Basel, Switzerland) 2024 1 14 (1): . Maiara Sulzbach Denardin, Valéria Bumiller-Bini Hoch, Amanda Salviano-Silva, Sara Cristina Lobo-Alves, Gabriel Adelman Cipolla, Danielle Malheiros, Danillo G Augusto, Michael Wittig, Andre Franke, Claudia Pföhler, Margitta Worm, Nina van Beek, Matthias Goebeler, Miklós Sárdy, Saleh Ibrahim, Hauke Busch, Enno Schmidt, Jennifer Elisabeth Hundt, Maria Luiza Petzl-Erler, Angelica Beate Winter Bol |
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