Cargando…

Exome-Wide Association Study Reveals Several Susceptibility Genes and Pathways Associated With Acute Coronary Syndromes in Han Chinese

Genome-wide association studies have identified more than 150 susceptibility loci for coronary artery disease (CAD); however, there is still a large proportion of missing heritability remaining to be investigated. This study sought to identify population-based genetic variation associated with acute...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zheng, Qiwen, Zhang, Yan, Jiang, Jie, Jia, Jia, Fan, Fangfang, Gong, Yanjun, Wang, Zhi, Shi, Qiuping, Chen, Dafang, Huo, Yong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2020
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7160370/ https://www.ncbi.nlm.nih.gov/pubmed/32328087 http://dx.doi.org/10.3389/fgene.2020.00336

Ejemplares similares

Exome-Wide Association Study Identifies East Asian-Specific Missense Variant MTHFR C136T Influencing Homocysteine Levels in Chinese Populations RH: ExWAS of tHCY in a Chinese Population
por: Liu, Tianzi, et al.
Publicado: (2021)

Association of SGK1 Polymorphisms With Susceptibility to Coronary Heart Disease in Chinese Han Patients With Comorbid Depression
por: Han, Wenxiu, et al.
Publicado: (2019)

Association of SLC11A1 Polymorphisms With Tuberculosis Susceptibility in the Chinese Han Population
por: Hu, Baoping, et al.
Publicado: (2022)

Association Between GSDMB Gene Polymorphism and Cervical Cancer in the Northeast Chinese Han Population
por: Li, Songxue, et al.
Publicado: (2022)

Use of whole-exome sequencing to identify novel monogenic gene mutations and genotype–phenotype correlations in Chinese Han children with urolithiasis
por: Wang, Zhi, et al.
Publicado: (2023)

Corrigendum: Association between GSDMB gene polymorphism and cervical cancer in the Northeast Chinese Han population
por: Li, Songxue, et al.
Publicado: (2023)

Validation of Susceptibility Loci for Vitiligo Identified by GWAS in the Chinese Han Population
por: Cheng, Lu, et al.
Publicado: (2020)

The Integrated Landscape of Biological Candidate Causal Genes in Coronary Artery Disease
por: Zheng, Qiwen, et al.
Publicado: (2020)

Altered Expression of Brain-specific Autism-Associated miRNAs in the Han Chinese Population
por: Wang, Ziqi, et al.
Publicado: (2022)

Genetic predisposition to type 2 diabetes is associated with severity of coronary artery disease in patients with acute coronary syndromes
por: Zheng, Qiwen, et al.
Publicado: (2019)

Replication of Putative Susceptibility Loci from Genome-Wide Association Studies Associated with Coronary Atherosclerosis in Chinese Han Population
por: Xie, Fang, et al.
Publicado: (2011)

ACTB Variants Confer the Genetic Susceptibility to Diabetic Kidney Disease in a Han Chinese Population
por: Li, Mengxia, et al.
Publicado: (2019)

The cis-Regulatory Element of SNCA Intron 4 Modulates Susceptibility to Parkinson’s Disease in Han Chinese
por: Zhu, Shi-Guo, et al.
Publicado: (2020)

Autoimmune Disease Associated CLEC16A Variants Convey Risk of Parkinson’s Disease in Han Chinese
por: Fan, Hui-Hui, et al.
Publicado: (2022)

Variants in the SMARCA4 gene was associated with coronary heart disease susceptibility in Chinese han population
por: Guo, Xuan, et al.
Publicado: (2016)

Association of endothelial lipase gene−384A/C with coronary artery disease in Han Chinese people
por: Xie, Liang, et al.
Publicado: (2015)

Polymorphisms in ERAP1 and ERAP2 Genes Are Associated With Tuberculosis in the Han Chinese
por: Zhang, Shuqiong, et al.
Publicado: (2020)

Association of the CACNA2D2 gene with schizophrenia in Chinese Han population
por: Fu, Yingli, et al.
Publicado: (2020)

Intercellular Adhesion Molecule-1 Gene Polymorphisms and Susceptibility to Cervical Cancer in the Northern Chinese Han Population
por: Feng, Yanan, et al.
Publicado: (2021)

Genome-wide association study and identification of systemic comorbidities in development of age-related macular degeneration in a hospital-based cohort of Han Chinese
por: Shih, Chien-Hung, et al.
Publicado: (2023)

The Same Chromosome 9p21.3 Locus Is Associated With Type 2 Diabetes and Coronary Artery Disease in a Chinese Han Population
por: Cheng, Xiang, et al.
Publicado: (2011)

Novel Mutations Associated With Various Types of Corneal Dystrophies in a Han Chinese Population
por: Zhang, Jing, et al.
Publicado: (2019)

Sex-Specific Associations of MIR137 Polymorphisms With Schizophrenia in a Han Chinese Cohort
por: Yin, Jingwen, et al.
Publicado: (2021)

Promoter Specific Methylation of SSTR4 is Associated With Alcohol Dependence in Han Chinese Males
por: Zhao, Rongrong, et al.
Publicado: (2022)

An Exome-Wide Sequencing Study of the GOLDN Cohort Reveals Novel Associations of Coding Variants and Fasting Plasma Lipids
por: Geng, Xin, et al.
Publicado: (2019)

Whole‐exome sequencing and genome‐wide association studies identify novel sarcopenia risk genes in Han Chinese
por: Ran, Shu, et al.
Publicado: (2020)

Association between the g.296596G > A genetic variant of RELN gene and susceptibility to autism in a Chinese Han population
por: Fu, Xiaoyan, et al.
Publicado: (2013)

Association between PPAP2B gene polymorphisms and coronary heart disease susceptibility in Chinese Han males and females
por: Sun, Yu-Xiao, et al.
Publicado: (2017)

Targeted re-sequencing on 1p22 among non-syndromic orofacial clefts from Han Chinese population
por: Li, Mu-Jia, et al.
Publicado: (2022)

Whole Exome Sequencing Identifies Genes Associated With Non-Obstructive Azoospermia
por: Zhang, Hongguo, et al.
Publicado: (2022)

A Genetic Polymorphism in the WDR72 Gene is Associated With Calcium Nephrolithiasis in the Chinese Han Population
por: Wang, Lujia, et al.
Publicado: (2022)

Association of Variants in PLD1, 3p24.1, and 10q11.21 Regions With Hirschsprung’s Disease in Han Chinese Population
por: Niu, Wei-Bo, et al.
Publicado: (2020)

Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort
por: Xiang, Huifen, et al.
Publicado: (2021)

Candidate Gene Polymorphisms Influence the Susceptibility to Salt Sensitivity of Blood Pressure in a Han Chinese Population: Risk Factors as Mediators
por: Xie, Yunyi, et al.
Publicado: (2021)

Replication of the Association Between Keratoconus and Polymorphisms in PNPLA2 and MAML2 in a Han Chinese Population
por: Zhang, Jing, et al.
Publicado: (2020)

A Polymorphism in the BDNF Gene (rs11030101) is Associated With Negative Symptoms in Chinese Han Patients With Schizophrenia
por: Ping, Junjiao, et al.
Publicado: (2022)

Association study of WNK1 genetic variants and essential hypertension risk in the Northern Han Chinese in Beijing
por: Liu, Kuo, et al.
Publicado: (2023)

Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases
por: Zhu, Xiaobo, et al.
Publicado: (2023)

Association of a SNP in SLC35F3 Gene with the Risk of Hypertension in a Chinese Han Population
por: Zang, Xiao-Li, et al.
Publicado: (2016)

Association Study Confirmed Susceptibility Loci with Keloid in the Chinese Han Population
por: Zhu, Fei, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_dtrh3jvnj8r9cbknnqmvp2pav2