Cargando…

Systematic Confirmation Study of GWAS-Identified Genetic Variants for Kawasaki Disease in A Chinese Population

Genome-wide association studies (GWASs) have identified multiple single nucleotide polymorphisms (SNPs) associated with Kawasaki disease (KD). In this study, we replicated the associations of 10 GWAS-identified SNPs with KD in a Han Chinese population. Odds ratios (ORs) and 95% confidence intervals...

Descripción completa

Detalles Bibliográficos
Autores principales:	Lou, Jiao, Zhong, Rong, Shen, Na, Lu, Xu-zai, Ke, Jun-tao, Duan, Jia-yu, Qi, Yan-qi, Wang, Yu-jia, Zhang, Qing, Wang, Wei, Gong, Fang-qi, Miao, Xiao-ping
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group 2015
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314627/ https://www.ncbi.nlm.nih.gov/pubmed/25645453 http://dx.doi.org/10.1038/srep08194

Ejemplares similares

The Roles of Ca(2+)/NFAT Signaling Genes in Kawasaki Disease: Single- and Multiple-Risk Genetic Variants
por: Wang, Wei, et al.
Publicado: (2014)

8p22–23-rs2254546 as a Susceptibility Locus for Kawasaki Disease: a Case-control Study and a Meta-analysis
por: Wang, Wei, et al.
Publicado: (2014)

A Genetic Variant rs1801274 in FCGR2A as a Potential Risk Marker for Kawasaki Disease: A Case-Control Study and Meta-Analysis
por: Duan, Jiayu, et al.
Publicado: (2014)

Replication and Meta-Analysis of GWAS Identified Susceptibility Loci in Kawasaki Disease Confirm the Importance of B Lymphoid Tyrosine Kinase (BLK) in Disease Susceptibility
por: Chang, Chia-Jung, et al.
Publicado: (2013)

The precision relationships between eight GWAS-identified genetic variants and breast cancer in a Chinese population
por: Chen, Yazhen, et al.
Publicado: (2016)

Evaluation of GWAS-Identified Genetic Variants for Gastric Cancer Survival
por: Gu, Dongying, et al.
Publicado: (2018)

Fifty Years On: GWAS Confirms the Role of a Rare Variant in Lung Disease
por: Turner, Alice M.
Publicado: (2013)

New insights from GWAS for the cleft palate among han Chinese population
por: Duan, Shi-Jun, et al.
Publicado: (2017)

Two GWAS-identified variants are associated with lumbar spinal stenosis and Gasdermin-C expression in Chinese population
por: Jiang, Hua, et al.
Publicado: (2020)

Exploration and detection of potential regulatory variants in refractive error GWAS
por: Liao, Xuan, et al.
Publicado: (2016)

Identifying genetic variants associated with amphotericin B (AMB) resistance in Aspergillus fumigatus via k-mer-based GWAS
por: Chen, Meng-Meng, et al.
Publicado: (2023)

Environmental factors, seven GWAS‐identified susceptibility loci, and risk of gastric cancer and its precursors in a Chinese population
por: Cai, Meng, et al.
Publicado: (2017)

Identification of a Potential Regulatory Variant for Colorectal Cancer Risk Mapping to Chromosome 5q31.1: A Post-GWAS Study
por: Ke, Juntao, et al.
Publicado: (2015)

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

Evaluating GWAS-Identified SNPs for Age at Natural Menopause among Chinese Women
por: Shen, Chong, et al.
Publicado: (2013)

A Post-GWAS Replication Study Confirming the PTK2 Gene Associated with Milk Production Traits in Chinese Holstein
por: Wang, Haifei, et al.
Publicado: (2013)

MicrobiomeGWAS: A Tool for Identifying Host Genetic Variants Associated with Microbiome Composition
por: Hua, Xing, et al.
Publicado: (2022)

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility
por: Zhang, Xing, et al.
Publicado: (2023)

Biallelic SORD pathogenic variants cause Chinese patients with distal hereditary motor neuropathy
por: Dong, Hai-Lin, et al.
Publicado: (2021)

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
por: Pairo-Castineira, Erola, et al.
Publicado: (2023)

Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations
por: Chang, Jiang, et al.
Publicado: (2018)

Case report: Novel DGUOK variants associated with idiopathic non-cirrhotic portal hypertension in a Han Chinese child
por: Li, Jia-Qi, et al.
Publicado: (2023)

Associations between Two Genetic Variants in NKX2-5 and Risk of Congenital Heart Disease in Chinese Population: A Meta-Analysis
por: Wang, Zhenling, et al.
Publicado: (2013)

Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants
por: Ng, Bernard, et al.
Publicado: (2021)

Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease
por: Chen, Mei-Jiao, et al.
Publicado: (2022)

Genome-wide Association Study (GWAS) of Germline Copy Number Variations (CNVs) Reveal Genetic Risks of Prostate Cancer in Chinese population
por: Wu, Yishuo, et al.
Publicado: (2018)

Whole exome sequencing identifies a novel variant in an apoptosis-inducing factor gene associated with X-linked recessive hearing loss in a Chinese family
por: Wang, Qi, et al.
Publicado: (2019)

Compound heterozygous variants in MAN2B2 identified in a Chinese child with congenital disorders of glycosylation
por: Tian, Qi, et al.
Publicado: (2022)

A post-GWAS confirming effects of PRKG1 gene on milk fatty acids in a Chinese Holstein dairy population
por: Shi, Lijun, et al.
Publicado: (2019)

Study of 11 BMI-Associated Loci Identified in GWAS for Associations with Central Obesity in the Chinese Children
por: Xi, Bo, et al.
Publicado: (2013)

A replication study confirms the association of GWAS-identified SNPs at MICB and PLCE1 in Thai patients with dengue shock syndrome
por: Dang, Tran Ngoc, et al.
Publicado: (2014)

Meta-Analysis Indicates That the European GWAS-Identified Risk SNP rs1344706 within ZNF804A Is Not Associated with Schizophrenia in Han Chinese Population
por: Li, Ming, et al.
Publicado: (2013)

Genetic Variations of GWAS-Identified Genes and Neuroblastoma Susceptibility: a Replication Study in Southern Chinese Children()()()
por: He, Jing, et al.
Publicado: (2017)

Dataset of GWAS-identified variants underlying venous thromboembolism susceptibility and linkage to cancer aggressiveness
por: Tavares, Valéria, et al.
Publicado: (2020)

Author Correction: GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19
por: Pairo-Castineira, Erola, et al.
Publicado: (2023)

New biomarkers of Kawasaki disease identified by urine proteomic analysis
por: Hu, Hui‐Min, et al.
Publicado: (2018)

New pathogenic variants of ALMS1 gene in two Chinese families with Alström Syndrome
por: Cheng, Wan-Yu, et al.
Publicado: (2022)

Reverse GWAS: Using genetics to identify and model phenotypic subtypes
por: Dahl, Andy, et al.
Publicado: (2019)

Association of PECAM-1 Gene Polymorphisms with Kawasaki Disease in Chinese Children
por: Li, Zhuoying, et al.
Publicado: (2017)

GWAS for Interleukin-1β levels in gingival crevicular fluid identifies IL37 variants in periodontal inflammation
por: Offenbacher, Steven, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_d6gp9nvocafuhhh3bjkrt3ksb1