Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and WDR35[original query] |
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| Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Nature genetics 2012 Aug 44 (8): 890-4. Lu Xiangfeng, Wang Laiyuan, Chen Shufeng, He Lin, Yang Xueli, Shi Yongyong, Cheng Jing, Zhang Liang, Gu C Charles, Huang Jianfeng, Wu Tangchun, Ma Yitong, Li Jianxin, Cao Jie, Chen Jichun, Ge Dongliang, Fan Zhongjie, Li Ying, Zhao Liancheng, Li Hongfan, Zhou Xiaoyang, Chen Lanying, Liu Donghua, Chen Jingping, Duan Xiufang, Hao Yongchen, Wang Ligui, Lu Fanghong, Liu Zhendong, Yao Cailiang, Shen Chong, Pu Xiaodong, Yu Lin, Fang Xianghua, Xu Lihua, Mu Jianjun, Wu Xianping, Zheng Runping, Wu Naqiong, Zhao Qi, Li Yun, Liu Xiaoli, Wang Mengqin, Yu Dahai, Hu Dongsheng, Ji Xu, Guo Dongshuang, Sun Dongling, Wang Qianqian, Yang Ying, Liu Fangchao, Mao Qunxia, Liang Xiaohua, Ji Jingfeng, Chen Panpan, Mo Xingbo, Li Dianjiang, Chai Guoping, Tang Yida, Li Xiangdong, Du Zhenhan, Liu Xuehui, Dou Chenlong, Yang Zili, Meng Qingjie, Wang Dong, Wang Renping, Yang Jun, Schunkert Heribert, Samani Nilesh J, Kathiresan Sekar, Reilly Muredach P, Erdmann Jeanette, , Peng Xiaozhong, Wu Xigui, Liu Depei, Yang Yuejin, Chen Runsheng, Qiang Boqin, Gu Dongfe |
| Association study of genetic variants at TTC32-WDR35 gene cluster with coronary artery disease in Chinese Han population. Journal of clinical laboratory analysis 2020 10 35 (2): e23594. Xu Ying, Zhuo Yang, Ye Mengliang, Li Mengmeng, Tang Xiaojun, Zhou |
| WDR35 variants in a cranioectodermal dysplasia patient with early onset end-stage renal disease and retinal dystrophy. American journal of medical genetics. Part A 2022 7 188 (10): 3071-3077. Walczak-Sztulpa Joanna, Wawrocka Anna, Sikora Weronika, Pawlak Marta, Bukowska-Olech Ewelina, Kopaczewski Bart?omiej, Urzykowska Agnieszka, Arts Heleen H, Gotz-Wi?ckowska Anna, Grenda Ryszard, Latos-Biele?ska Anna, Glazar Rena |
| Ciliary phenotyping in renal epithelial cells in a cranioectodermal dysplasia patient with WDR35 variants. Frontiers in molecular biosciences 2024 1 10 1285790. Joanna Walczak-Sztulpa, Anna Wawrocka, ?ukasz Kuszel, Paulina Pietras, Marta Le?niczak-Staszak, Miros?aw Andrusiewicz, Maciej R Krawczy?ski, Anna Latos-Biele?ska, Marta Pawlak, Ryszard Grenda, Anna Materna-Kiryluk, Machteld M Oud, Witold Szaflars |
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