Kết quả tìm kiếm - Wang, Minxian
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A Monte Carlo Permutation Test for Random Mating Using Genome Sequences Bằng Li, Ran, Wang, Minxian, Jin, Li, He, Yungang
Được phát hành 2013Text -
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Volanesorsen, Familial Chylomicronemia Syndrome, and Thrombocytopenia Bằng Khetarpal, Sumeet A., Wang, Minxian, Khera, Amit V.
Được phát hành 2019Text -
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Editorial: Machine Learning-Based Methods for RNA Data Analysis Bằng Peng, Lihong, Yang, Jialiang, Wang, Minxian, Zhou, Liqian
Được phát hành 2022Text -
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Quantifying and understanding the higher risk of atherosclerotic cardiovascular disease among South Asians — results from the UK Biobank prospective cohort study Bằng Patel, Aniruddh P., Wang, Minxian, Kartoun, Uri, Ng, Kenney, Khera, Amit V.
Được phát hành 2021Text -
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Autosomal Dominant Tubulointerstitial Kidney Disease—Uromodulin Misclassified as Focal Segmental Glomerulosclerosis or Hereditary Glomerular Disease Bằng Chun, Justin, Wang, Minxian, Wilkins, Maris S., Knob, Andrea U., Benjamin, Ava, Bu, Lihong, Pollak, Martin R.
Được phát hành 2020Text -
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Lipoprotein(a) concentrations and incident atherosclerotic cardiovascular disease: new insights from a large national biobank Bằng Patel, Aniruddh P., Wang, Minxian, Pirruccello, James P., Ellinor, Patrick T., Ng, Kenney, Kathiresan, Sekar, Khera, Amit V.
Được phát hành 2020Text -
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External validation and comparison of simple tools to screen for nonalcoholic fatty liver disease in Chinese community population Bằng Zhang, Liuxin, Zhang, Mengting, Wang, Min, Wang, Minxian, Zhang, Ru, Wang, Hongliang, Zhang, Wei, Ding, Yajie, Wang, Jie
Được phát hành 2022Text -
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Vitamin D Level and Vitamin D Receptor Genetic Variation Were Involved in the Risk of Non-Alcoholic Fatty Liver Disease: A Case-Control Study Bằng Zhang, Ru, Wang, Minxian, Wang, Min, Zhang, Liuxin, Ding, Yajie, Tang, Zongzhe, Fu, Zuqiang, Fan, Haozhi, Zhang, Wei, Wang, Jie
Được phát hành 2021Text -
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Genetic Polymorphism of Vitamin D Family Genes CYP2R1, CYP24A1, and CYP27B1 Are Associated With a High Risk of Non-alcoholic Fatty Liver Disease: A Case-Control Study Bằng Wang, Minxian, Zhang, Ru, Wang, Min, Zhang, Liuxin, Ding, Yajie, Tang, Zongzhe, Wang, Hongliang, Zhang, Wei, Chen, Yue, Wang, Jie
Được phát hành 2021Text -
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Corrigendum: Genetic Polymorphism of Vitamin D Family Genes CYP2R1, CYP24A1, and CYP27B1 Are Associated With a High Risk of Non-alcoholic Fatty Liver Disease: A Case-Control Study Bằng Wang, Minxian, Zhang, Ru, Wang, Min, Zhang, Liuxin, Ding, Yajie, Tang, Zongzhe, Wang, Hongliang, Zhang, Wei, Chen, Yue, Wang, Jie
Được phát hành 2021Text -
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Evaluating the Potential of T Cell Receptor Repertoires in Predicting the Prognosis of Resectable Non-Small Cell Lung Cancers Bằng Song, Zhengbo, Chen, Xiangbin, Shi, Yi, Huang, Rongfang, Wang, Wenxian, Zhu, Kunshou, Lin, Shaofeng, Wang, Minxian, Tian, Geng, Yang, Jialiang, Chen, Gang
Được phát hành 2020Text -
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A combined association of serum uric acid, alanine aminotransferase and waist circumference with non-alcoholic fatty liver disease: a community-based study Bằng Wang, Min, Wang, Minxian, Zhang, Ru, Zhang, Liuxin, Ding, Yajie, Tang, Zongzhe, Fan, Haozhi, Wang, Hongliang, Zhang, Wei, Chen, Yue, Wang, Jie
Được phát hành 2022Text -
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Influences of Vitamin D Levels and Vitamin D-Binding Protein Polymorphisms on Nonalcoholic Fatty Liver Disease Risk in a Chinese Population Bằng Wang, Min, Wang, Minxian, Zhang, Ru, Shen, Chao, Zhang, Liuxin, Ding, Yajie, Tang, Zongzhe, Wang, Hongliang, Zhang, Wei, Chen, Yue, Wang, Jie
Được phát hành 2022Text -
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Association of Pathogenic DNA Variants Predisposing to Cardiomyopathy With Cardiovascular Disease Outcomes and All-Cause Mortality Bằng Patel, Aniruddh P., Dron, Jacqueline S., Wang, Minxian, Pirruccello, James P., Ng, Kenney, Natarajan, Pradeep, Lebo, Matthew, Ellinor, Patrick T., Aragam, Krishna G., Khera, Amit V.
Được phát hành 2022Text -
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Disease-causing mutation in α-actinin-4 promotes podocyte detachment through maladaptation to periodic stretch Bằng Feng, Di, Notbohm, Jacob, Benjamin, Ava, He, Shijie, Wang, Minxian, Ang, Lay-Hong, Bantawa, Minaspi, Bouzid, Mehdi, Del Gado, Emanuela, Krishnan, Ramaswamy, Pollak, Martin R.
Được phát hành 2018Text -
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