Coronary Artery Aneurysm
What's New
Last Posted: Jul 04, 2024
- Coronary arteriopathy in a patient with Noonan phenotype: Case report.
Simran Jain, et al. Annals of pediatric cardiology 2024 0 (1) 70-73 - ITPKC polymorphism (rs7251246 T > C), coronary artery aneurysms, and thrombosis in patients with Kawasaki disease in a Southern Han Chinese population.
Jie Liu, et al. Frontiers in immunology 2023 0 1184162 - Protective Effect of TNFRSF11A rs7239667 G > C Gene Polymorphism on Coronary Outcome of Kawasaki Disease in Southern Chinese Population.
Zhang Linyuan, et al. Frontiers in genetics 2021 0 691282 - Two genetic variants in NEXN and ABCC6 genes found in a patient with right coronary artery to right ventricle fistula combined with giant coronary aneurysm and patent ductus arteriosus.
Peng Yongxuan, et al. Frontiers in cardiovascular medicine 2022 0 1048795 - The EIF2AK4/rs4594236 AG/GG Genotype Is a Hazard Factor of Immunoglobulin Therapy Resistance in Southern Chinese Kawasaki Disease Patients.
Yu Hongyan, et al. Frontiers in genetics 2022 0 868159 - Association study of miR-149, miR-196a2, and miR-499a polymorphisms with coronary artery aneurysm of Kawasaki disease in southern Chinese population.
Fu Lanyan, et al. The journal of gene medicine 2021 0 (4) e3405 - The Associated of the Risk of IVIG Resistance in Kawasaki Disease with ZNF112 Gene and ZNF180 Gene in a Southern Chinese Population.
Lu Zhaojin, et al. Journal of inflammation research 2022 0 5053-5062 - A machine learning model for non-invasive detection of atherosclerotic coronary artery aneurysm.
Rostam-Alilou Ali A et al. International journal of computer assisted radiology and surgery 2022 - FNDC1 Polymorphism (rs3003174 C > T) Increased the Incidence of Coronary Artery Aneurysm in Patients with Kawasaki Disease in a Southern Chinese Population.
Lin Kun, et al. Journal of inflammation research 2021 0 2633-2640 - Impact of Platelet Glycoprotein Ia/IIa C807T Gene Polymorphisms on Coronary Artery Aneurysms of KD Patients.
Li Wei, et al. Cardiology research and practice 2021 0 4895793 - Interleukin 10 and Transforming Growth Factor Beta Polymorphisms as Risk Factors for Kawasaki Disease: A Case-Control Study and Meta-Analysis.
Rahmani Farzaneh, et al. Avicenna journal of medical biotechnology 0 0 (4) 325-333 - P2RY12:rs7637803 TT variant genotype increases coronary artery aneurysm risk in Kawasaki disease in a southern Chinese population.
Lu Zhaoliang, et al. The journal of gene medicine 2019 1 (1) e3066 - An Angiotensinogen Gene Polymorphism (rs5050) Is Associated with the Risk of Coronary Artery Aneurysm in Southern Chinese Children with Kawasaki Disease.
Liu Yunfeng, et al. Disease markers 2019 0 2849695 - Identification of the TIFAB Gene as a Susceptibility Locus for Coronary Artery Aneurysm in Patients with Kawasaki Disease.
Kwon Young-Chang, et al. Pediatric cardiology 2018 9 - A PEAR1 polymorphism (rs12041331) is associated with risk of coronary artery aneurysm in Kawasaki disease.
Pi Lei, et al. Annals of human genetics 2018 9 - TBXA2R rs4523 G allele is associated with decreased susceptibility to Kawasaki disease.
Che Di, et al. Cytokine 2018 9 216-221 - Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease.
Kuo Ho-Chang, et al. PloS one 2016 0 (5) e0154943 - Consortium-Based Genetic Studies of Kawasaki Disease in Korea: Korean Kawasaki Disease Genetics Consortium.
Lee Jong-Keuk, et al. Korean circulation journal 2015 11 (6) 443-448 - Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan.
Lin Ying-Ju, et al. Scientific reports 2015 0 14762 - Genetic variants of glutamate receptor gene family in Taiwanese Kawasaki disease children with coronary artery aneurysms.
Lin Ying-Ju, et al. Cell & bioscience 2014 0 (1) 67 - Association between SRC-1 gene polymorphisms and coronary artery aneurysms formation in Taiwanese children with Kawasaki disease.
Chen Yng-Tay, et al. Journal of clinical laboratory analysis 2014 11 (6) 435-9 - Association of promoter genetic variants in interleukin-10 and Kawasaki disease with coronary artery aneurysms.
Lin Ying-Ju, et al. Journal of clinical laboratory analysis 2014 11 (6) 461-4 - Sorting nexin 24 genetic variation associates with coronary artery aneurysm severity in Kawasaki disease patients.
Lin YJ, et al. Cell & bioscience 2013 11 (1) 1 - TARC/CCL17 gene polymorphisms and expression associated with susceptibility and coronary artery aneurysm formation in Kawasaki disease.
Lee Chiu-Ping, et al. Pediatric research 2013 11 (5) 545-51 - Major histocompatibility complex class I chain-related gene polymorphisms: associated with susceptibility to Kawasaki disease and coronary artery aneurysms.
Hsieh Yao-Yuan, et al. Genetic testing and molecular biomarkers 2011 11 (11) 755-63 - Coronary artery aneurysm
From NCATS Genetic and Rare Diseases Information Center - Transforming growth factor-beta signaling pathway in patients with Kawasaki disease.
Shimizu Chisato, et al. Circulation. Cardiovascular genetics 2011 2 (1) 16-25 - Matrix metalloproteinase haplotypes associated with coronary artery aneurysm formation in patients with Kawasaki disease.
Shimizu Chisato, et al. Journal of human genetics 2010 12 (12) 779-84 - Human lymphocyte antigen B-associated transcript 2, 3, and 5 polymorphisms and haplotypes are associated with susceptibility of Kawasaki disease and coronary artery aneurysm.
Hsieh Yao-Yuan, et al. Journal of clinical laboratory analysis 2010 0 (4) 262-8 - Single nucleotide polymorphism rs2229634 in the ITPR3 gene is associated with the risk of developing coronary artery aneurysm in children with Kawasaki disease.
Huang Y-C, et al. International journal of immunogenetics 2010 12 (6) 439-43
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
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- Gaucher Disease
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- Graves Disease
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- Microcephaly
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- Phenylketonuria
- Retinitis Pigmentosa
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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