For: | Jeemon P, Pettigrew K, Sainsbury C, Prabhakaran D, Padmanabhan S. Implications of discoveries from genome-wide association studies in current cardiovascular practice. World J Cardiol 2011; 3(7): 230-247 [PMID: 21860704 DOI: 10.4330/wjc.v3.i7.230] |
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URL: | https://www.wjgnet.com/1949-8462/full/v3/i7/230.htm |
Number | Citing Articles |
1 |
Ping-xian WU, Jie ZHOU, Kai WANG, De-juan CHEN, Xi-di YANG, Yi-hui LIU, An-an JIANG, Lin-yuan SHEN, Long JIN, Wei-hang XIAO, Yan-zhi JIANG, Ming-zhou LI, Li ZHU, Yang-shuang ZENG, Xu XU, Xiao-tian QIU, Xue-wei LI, Guo-qing TANG. Identifying SNPs associated with birth weight and days to 100 kg traits in Yorkshire pigs based on genotyping-by-sequencing. Journal of Integrative Agriculture 2021; 20(9): 2483 doi: 10.1016/S2095-3119(20)63474-8
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2 |
Nafise Afkhami, Malihe Aghasizadeh, Somayeh Ghiasi Hafezi, Reza Zare‐Feyzabadi, Sara Saffar Soflaei, Mohammad Rashidmayvan, Arezoo Rastegarmoghadam–Ebrahimian, Khashayar Khanizadeh, Nilufar Safari, Gordon A. Ferns, Habibollah Esmaily, Reza Assaran Darban, Majid Ghayour‐Mobarhan. Evaluation of rs1748195 ANGPTL3 gene polymorphism in patients with angiographic coronary artery disease compared to healthy individuals. Molecular Genetics & Genomic Medicine 2023; 11(3) doi: 10.1002/mgg3.2105
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3 |
Yi Xu, Huafei Shen, Yuanfei Shi, Yanchun Zhao, Xiaolong Zhen, Jianai Sun, Xueying Li, De Zhou, Chunmei Yang, Jinhan Wang, Xianbo Huang, Juying Wei, Jian Huang, Haitao Meng, Wenjuan Yu, Hongyan Tong, Jie Jin, Wanzhuo Xie. Dyslipidemia in diffuse large B-cell lymphoma based on the genetic subtypes: a single-center study of 259 Chinese patients. Frontiers in Oncology 2023; 13 doi: 10.3389/fonc.2023.1172623
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4 |
Qing-Hui Zhang, Rui-Xing Yin, Wu-Xian Chen, Xiao-Li Cao, Jin-Zhen Wu. TRIB1 and TRPS1 variants, G × G and G × E interactions on serum lipid levels, the risk of coronary heart disease and ischemic stroke. Scientific Reports 2019; 9(1) doi: 10.1038/s41598-019-38765-7
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5 |
Jinyan Zhong, Xiaoying Chen, Huadan Ye, Nan Wu, Xiaomin Chen, Shiwei Duan. CDKN2A and CDKN2B methylation in coronary heart disease cases and controls. Experimental and Therapeutic Medicine 2017; doi: 10.3892/etm.2017.5310
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6 |
Huadan Ye, Qianlei Zhao, Yi Huang, Lingyan Wang, Haibo Liu, Chunming Wang, Dongjun Dai, Leiting Xu, Meng Ye, Shiwei Duan. Meta-Analysis of Low Density Lipoprotein Receptor (LDLR) rs2228671 Polymorphism and Coronary Heart Disease. BioMed Research International 2014; 2014: 1 doi: 10.1155/2014/564940
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7 |
Yi‐Jiang Zhou, Rui‐Xing Yin, Shao‐Cai Hong, Qian Yang, Xiao‐Li Cao, Wu‐Xian Chen. Association of the HNF1A polymorphisms and serum lipid traits, the risk of coronary artery disease and ischemic stroke. The Journal of Gene Medicine 2017; 19(1-2) doi: 10.1002/jgm.2941
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8 |
R Pranavchand, BM Reddy. Current status of understanding of the genetic etiology of coronary heart disease. Journal of Postgraduate Medicine 2013; 59(1): 30 doi: 10.4103/0022-3859.109492
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9 |
Muneeza Zafar, Munazza Raza Mirza, Fazli Rabbi Awan, Muhammad Tahir, Rabia Sultan, Misbah Hussain, Ahmed Bilal, Shahid Abbas, Martin R. Larsen, Muhammad Iqbal Choudhary, Imran Riaz Malik. Effect of APOB polymorphism rs562338 (G/A) on serum proteome of coronary artery disease patients: a “proteogenomic” approach. Scientific Reports 2021; 11(1) doi: 10.1038/s41598-021-02211-4
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10 |
Eralda Asllanaj, Xiaofang Zhang, Carolina Ochoa Rosales, Jana Nano, Wichor M. Bramer, Eliana Portilla-Fernandez, Kim V.E. Braun, Valentina Gonzalez-Jaramillo, Wolfgang Ahrens, Arfan Ikram, Mohsen Ghanbari, Trudy Voortman, Oscar H. Franco, Taulant Muka, Marija Glisic. Sexually dimorphic DNA-methylation in cardiometabolic health: A systematic review. Maturitas 2020; 135: 6 doi: 10.1016/j.maturitas.2020.02.005
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11 |
Stefanos Leptidis, Eleni Papakonstantinou, Kalliopi Diakou, Katerina Pierouli, Thanasis Mitsis, Konstantina Dragoumani, Flora Bacopoulou, Despina Sanoudou, George Chrousos, Dimitrios Vlachakis. Epitranscriptomics of cardiovascular diseases (Review). International Journal of Molecular Medicine 2021; 49(1) doi: 10.3892/ijmm.2021.5064
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12 |
Liu Miao, Rui-Xing Yin, Shuo Yang, Feng Huang, Wu-Xian Chen, Xiao-Li Cao. Association between single nucleotide polymorphism rs9534275 and the risk of coronary artery disease and ischemic stroke. Lipids in Health and Disease 2017; 16(1) doi: 10.1186/s12944-017-0584-5
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13 |
S. N. Zhabin, V. A. Lazarenko, Yu. E. Azarova, D. A. Bashkatov, E. Yu. Klyosova, E. G. Gneeva, M. I. Churnosov, A. V. Polonikov. Association Analysis of Polymorphism rs386000 of the LILRA3 Gene and the Risk of Atherosclerosis Obliterans: a Pilot Study. Kardiologiia 2024; 64(6): 43 doi: 10.18087/cardio.2024.6.n2365
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14 |
Lyudmila Daudovna Khidirova, Davyd Aleksandrovich Yakhontov, Vladimir Nikolaevich Maksimov. GENETIC ASPECTS OF ATRIAL FIBRILLATION ON THE BACKGROUND OF ARTERIAL HYPERTENSION IN COMBINATION WITH NONCARDIAC DISEASES. AVICENNA BULLETIN 2019; 21(2): 238 doi: 10.25005/2074-0581-2019-21-2-238-246
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15 |
Liu Miao, Rui-Xing Yin, Shang-Ling Pan, Shuo Yang, De-Zhai Yang, Wei-Xiong Lin. BCL3-PVRL2-TOMM40 SNPs, gene-gene and gene-environment interactions on dyslipidemia. Scientific Reports 2018; 8(1) doi: 10.1038/s41598-018-24432-w
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16 |
Maha Meshal AlRasheed. Evaluation of the role of CDKN2B gene in type 2 diabetes mellitus and hypertension in ethnic Saudi Arabs. Saudi Pharmaceutical Journal 2018; 26(8): 1199 doi: 10.1016/j.jsps.2018.07.009
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17 |
Ling Qiu, Rui-Xing Yin, Rong-Jun Nie, Xi-Jiang Hu, Eksavang Khounphinith, Fen-Han Zhang. The CXCL12 SNPs and their haplotypes are associated with serum lipid traits. Scientific Reports 2019; 9(1) doi: 10.1038/s41598-019-55725-3
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18 |
Ramón Cacabelos, Clara Torrellas, Iván Carrera. Opportunities in pharmacogenomics for the treatment of Alzheimer’s disease. Future Neurology 2015; 10(3): 229 doi: 10.2217/fnl.15.12
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19 |
Christian Delles, Sandosh Padmanabhan. Genetics and Hypertension: Is It Time to Change My Practice?. Canadian Journal of Cardiology 2012; 28(3): 296 doi: 10.1016/j.cjca.2012.02.004
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20 |
Liu Miao, Rui-Xing Yin, Jin-Zhen Wu, Shuo Yang, Wei-Xiong Lin, Shang-Ling Pan. The SRGAP2 SNPs, their haplotypes and G × E interactions on serum lipid traits. Scientific Reports 2017; 7(1) doi: 10.1038/s41598-017-10950-6
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21 |
Ping Huang, Rui-Xing Yin, Ke-Ke Huang, Xiao-Na Zeng, Tao Guo, Quan-Zhen Lin, Jian Wu, Dong-Feng Wu, Hui Li, Shang-Ling Pan. Association of theKLF14rs4731702 SNP and Serum Lipid Levels in the Guangxi Mulao and Han Populations. BioMed Research International 2013; 2013: 1 doi: 10.1155/2013/231515
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22 |
Fujie Zhao, Ming-Hui Zou. Role of the Mitochondrial Protein Import Machinery and Protein Processing in Heart Disease. Frontiers in Cardiovascular Medicine 2021; 8 doi: 10.3389/fcvm.2021.749756
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23 |
Kai-Guang Li, Rui-Xing Yin, Feng Huang, Wu-Xian Chen, Jin-Zhen Wu, Xiao-Li Cao. XKR6 rs7014968 SNP Increases Serum Total Cholesterol Levels and the Risk of Coronary Heart Disease and Ischemic Stroke. Clinical and Applied Thrombosis/Hemostasis 2020; 26 doi: 10.1177/1076029620902844
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24 |
Fen-Han Zhang, Rui-Xing Yin, Li-Mei Yao, Rong-Qin Yan, Li Lu, Yuan Su. Correlation Between the APOB rs1042034 SNP and Blood Lipid Characteristics of 2 Ethnic Groups in China. Clinical and Applied Thrombosis/Hemostasis 2019; 25 doi: 10.1177/1076029619892088
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25 |
Brandon Pope, Zoe Wolcott, Marissa Castillo, Jacqueline Jin, Ka-Ho Wong, Adam de Havenon, Shadi Yaghi, Eric D. Goldstein. Mutation of breast cancer susceptibility genes increases cerebral microbleeds: A pilot study. Journal of Stroke and Cerebrovascular Diseases 2022; 31(11): 106729 doi: 10.1016/j.jstrokecerebrovasdis.2022.106729
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26 |
Sophie Visvikis-Siest, Maria G Stathopoulou, Ndeye Coumba Ndiaye. Common Mutations and Polymorphisms Predicting Adverse Cardiovascular Events: Current View. Pharmacogenomics 2012; 13(16): 1875 doi: 10.2217/pgs.12.167
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27 |
Yilan Li, Lili Li, Lei Bi, Xueming Xu, Wei Cheng, Bo Yu, Yao Zhang. Lipid-associated genetic polymorphisms are associated with FBP and LDL-c levels among myocardial infarction patients in Chinese population. Gene 2018; 676: 22 doi: 10.1016/j.gene.2018.07.016
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28 |
Peng-Fei Zheng, Rui-Xing Yin, Guo-Xiong Deng, Yao-Zong Guan, Bi-Liu Wei, Chun-Xiao Liu. Association between the XKR6 rs7819412 SNP and serum lipid levels and the risk of coronary artery disease and ischemic stroke. BMC Cardiovascular Disorders 2019; 19(1) doi: 10.1186/s12872-019-1179-z
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29 |
Dilek Pirim, Zaheda H. Radwan, Xingbin Wang, Vipavee Niemsiri, John E. Hokanson, Richard F. Hamman, Eleanor Feingold, Clareann H. Bunker, F. Yesim Demirci, M. Ilyas Kamboh, Ornit Chiba-Falek. Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups. PLOS ONE 2019; 14(3): e0214060 doi: 10.1371/journal.pone.0214060
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30 |
Malihe Aghasizadeh, Reza Zare-Feyzabadi, Tooba Kazemi, Amir Avan, Gordon A. Ferns, Habibollah Esmaily, Ebrahim Miri-Moghaddam, Majid Ghayour-Mobarhan. A haplotype of the ANGPTL3 gene is associated with CVD risk, diabetes mellitus, hypertension, obesity, metabolic syndrome, and dyslipidemia. Gene 2021; 782: 145525 doi: 10.1016/j.gene.2021.145525
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31 |
Liu Miao, Rui-Xing Yin, Shang-Ling Pan, Shuo Yang, De-Zhai Yang, Wei-Xiong Lin. Association between theMVKandMMABpolymorphisms and serum lipid levels. Oncotarget 2017; 8(41): 70378 doi: 10.18632/oncotarget.19707
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32 |
WEI WANG, RUI-XING YIN, DONG-FENG WU, LYNN HTET HTET AUNG, PING HUANG, XIAO-NA ZENG, KE-KE HUANG, QUAN-ZHEN LIN, JIAN WU, TAO GUO. Phosphodiesterase 3A rs7134375 single nucleotide polymorphism and serum lipid levels. Molecular Medicine Reports 2014; 9(5): 1618 doi: 10.3892/mmr.2014.2007
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33 |
Malihe Aghasizadeh, Mina Nosrati, Maryam Saberi‐Karimian, Hamideh Safarian, Parisa Assadian, Ensieh Akbarpour, Amirhosein Sahebkar, Amir Avan, Gordon A. Ferns, Tooba Kazemi, Ebrahim Miri‐Moghaddam, Majid Ghayour‐Mobarhan. Association of ANGPTL3 polymorphisms with high‐density lipoprotein cholesterol uptake capacity in patients with cardiovascular disease. Journal of Clinical Laboratory Analysis 2021; 35(12) doi: 10.1002/jcla.23980
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34 |
Min Xu, Jun Zhao, Yu Zhang, Xu Ma, Qiaoyun Dai, Hong Zhi, Bei Wang, Lina Wang. Apolipoprotein E Gene Variants and Risk of Coronary Heart Disease: A Meta-Analysis. BioMed Research International 2016; 2016: 1 doi: 10.1155/2016/3912175
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35 |
Lynn-Htet-Htet Aung, Rui-Xing Yin, Jin-Zhen Wu, Dong-Feng Wu, Wei Wang, Hui Li. Association between the MLX Interacting Protein-Like, BUD13 Homolog and Zinc Finger Protein 259 Gene Polymorphisms and Serum Lipid Levels. Scientific Reports 2014; 4(1) doi: 10.1038/srep05565
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36 |
Guo-Xiong Deng, Rui-Xing Yin, Yao-Zong Guan, Chun-Xiao Liu, Peng-Fei Zheng, Bi-Liu Wei, Jin-Zhen Wu, Liu Miao. Association of the NCAN-TM6SF2-CILP2-PBX4-SUGP1-MAU2 SNPs and gene-gene and gene-environment interactions with serum lipid levels. Aging 2020; 12(12): 11893 doi: 10.18632/aging.103361
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37 |
Manjula Gorre, Pranavchand Rayabarapu, Sriteja Reddy Battini, Kumuda Irgam, Mohan Reddy Battini. Analysis of 61 SNPs from the CAD specific genomic loci reveals unique set of SNPs as significant markers in the Southern Indian population of Hyderabad. BMC Cardiovascular Disorders 2022; 22(1) doi: 10.1186/s12872-022-02562-4
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38 |
Tao Guo, Rui-Xing Yin, Quan-Zhen Lin, Jian Wu, Shao-Wen Shen, Jia-Qi Sun, Guang-Yuan Shi, Jin-Zhen Wu, Hui Li, Yi-Ming Wang. Polymorphism of rs873308 near the transmembrane protein 57 gene is associated with serum lipid levels. Bioscience Reports 2014; 34(2) doi: 10.1042/BSR20130131
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39 |
Wenjing Hu, Ke Li, Hongdong Han, Shan Geng, Baoyong Zhou, Xiaoyun Fan, Shangcheng Xu, Mengliu Yang, Hua Liu, Gangyi Yang, Yongsheng Liu, Jos P. Andrade. Circulating Levels of CILP2 Are Elevated in Coronary Heart Disease and Associated with Atherosclerosis. Oxidative Medicine and Cellular Longevity 2020; 2020: 1 doi: 10.1155/2020/1871984
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40 |
Rajeev Gupta, Raghubir S. Khedar, Kiran Gaur, Denis Xavier. Low quality cardiovascular care is important coronary risk factor in India. Indian Heart Journal 2018; 70: S419 doi: 10.1016/j.ihj.2018.05.002
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41 |
Qing-Hui Zhang, Rui-Xing Yin, Feng Huang, De-Zhai Yang, Wei-Xiong Lin, Shang-Ling Pan. Association between thePINX1andNAT2polymorphisms and serum lipid levels. Oncotarget 2017; 8(69): 114081 doi: 10.18632/oncotarget.23123
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42 |
Wei-Jun Li, Rui-Xing Yin, Xiao-Li Cao, Wu-Xian Chen, Feng Huang, Jin-Zhen Wu. DOCK7-ANGPTL3 SNPs and their haplotypes with serum lipid levels and the risk of coronary artery disease and ischemic stroke. Lipids in Health and Disease 2018; 17(1) doi: 10.1186/s12944-018-0677-9
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43 |
Tao Guo, Rui-Xing Yin, Feng Huang, Li-Mei Yao, Wei-Xiong Lin, Shang-Ling Pan. Association between the DOCK7, PCSK9 and GALNT2 Gene Polymorphisms and Serum Lipid levels. Scientific Reports 2016; 6(1) doi: 10.1038/srep19079
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44 |
Oscar Franzén, Raili Ermel, Katyayani Sukhavasi, Rajeev Jain, Anamika Jain, Christer Betsholtz, Chiara Giannarelli, Jason C. Kovacic, Arno Ruusalepp, Josefin Skogsberg, Ke Hao, Eric E. Schadt, Johan L.M. Björkegren. Global analysis of A-to-I RNA editing reveals association with common disease variants. PeerJ 2018; 6: e4466 doi: 10.7717/peerj.4466
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45 |
Xiao‐Jing Wang, Dao‐Lai Zhang, Zhi‐Gang Xu, Ming‐Liang Ma, Wen‐Bo Wang, Lin‐Lin Li, Xiao‐Lin Han, Yuqing Huo, Xiao Yu, Jin‐Peng Sun. Understanding cadherin EGF LAG seven‐pass G‐type receptors. Journal of Neurochemistry 2014; 131(6): 699 doi: 10.1111/jnc.12955
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46 |
Rajeev Gupta. Genetics-based risk scores for prediction of premature coronary artery disease. Indian Heart Journal 2023; 75(5): 327 doi: 10.1016/j.ihj.2023.08.003
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47 |
Itziar Lamiquiz-Moneo, Lucía Baila-Rueda, Ana M. Bea, Rocío Mateo-Gallego, Sofía Pérez-Calahorra, Victoria Marco-Benedí, Antonio Martín-Navarro, Emilio Ros, Montserrat Cofán, José Carlos Rodríguez-Rey, Miguel Pocovi, Ana Cenarro, Fernando Civeira. ABCG5/G8 gene is associated with hypercholesterolemias without mutation in candidate genes and noncholesterol sterols. Journal of Clinical Lipidology 2017; 11(6): 1432 doi: 10.1016/j.jacl.2017.09.005
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48 |
Heiko Runz. Integrated approaches to functionally characterize novel factors in lipoprotein metabolism. Current Opinion in Lipidology 2012; 23(2): 104 doi: 10.1097/MOL.0b013e328350fc3d
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49 |
Khalid Khalaf Alharbi, Imran Ali Khan, Mohammad Abdullah Alotaibi, Abdullah Saud Aloyaid, Haifa Abdulaziz Al-Basheer, Naelah Abdullah Alghamdi, Raid Saleem Al-Baradie, A.M. Al-Sulaiman. Molecular genetic studies in Saudi population; identified variants from GWAS and meta-analysis in stroke. Saudi Journal of Biological Sciences 2018; 25(1): 83 doi: 10.1016/j.sjbs.2017.08.014
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50 |
Ting-Ting Yan, Rui-Xing Yin, Qing Li, Ping Huang, Xiao-Na Zeng, Ke-Ke Huang, Dong-Feng Wu, Lynn Htet Htet Aung. Association of MYLIP rs3757354 SNP and several environmental factors with serum lipid levels in the Guangxi Bai Ku Yao and Han populations. Lipids in Health and Disease 2012; 11(1) doi: 10.1186/1476-511X-11-141
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51 |
Ping Peng, Lu Wang, Xi Yang, Xiaoyan Huang, Yanna Ba, Xiaoliang Chen, Jian Guo, Jiangfang Lian, Jianqing Zhou, William B. Coleman. A Preliminary Study of the Relationship between Promoter Methylation of the ABCG1, GALNT2 and HMGCR Genes and Coronary Heart Disease. PLoS ONE 2014; 9(8): e102265 doi: 10.1371/journal.pone.0102265
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52 |
Ramón Cacabelos, Clara Torrellas, Oscar Teijido, Juan Carlos Carril. Pharmacogenetic Considerations in the Treatment of Alzheimer’s Disease. Pharmacogenomics 2016; 17(9): 1041 doi: 10.2217/pgs-2016-0031
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