Cargando…

Systematic analyses of genetic variants in chromatin interaction regions identified four novel lung cancer susceptibility loci

Genome-wide association studies (GWAS) have reported 45 single-nucleotide polymorphisms (SNPs) that may contribute to the susceptibility of lung cancer, with the majority in non-coding regions. However, no study has ever systematically evaluated the association between SNPs in physical chromatin int...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ji, Pei, Ding, Dongsheng, Qin, Na, Wang, Cheng, Zhu, Meng, Li, Yuancheng, Dai, Juncheng, Jin, Guangfu, Hu, Zhibin, Shen, Hongbing, Chen, Liang, Ma, Hongxia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Ivyspring International Publisher 2020
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959073/ https://www.ncbi.nlm.nih.gov/pubmed/31956354 http://dx.doi.org/10.7150/jca.35127

Ejemplares similares

Systematical analyses of variants in CTCF-binding sites identified a novel lung cancer susceptibility locus among Chinese population
por: Dai, Juncheng, et al.
Publicado: (2015)

Cross-Cancer Pleiotropic Analysis Reveals Novel Susceptibility Loci for Lung Cancer
por: Wang, Lijuan, et al.
Publicado: (2020)

Genome-wide analysis of runs of homozygosity identifies new susceptibility regions of lung cancer in Han Chinese
por: Wang, Cheng, et al.
Publicado: (2013)

Genetic variants in regulatory regions of microRNAs are associated with lung cancer risk
por: Xie, Kaipeng, et al.
Publicado: (2016)

Fine Mapping in Chromosome 3q28 Identified Two Variants Associated with Lung Cancer Risk in Asian Population
por: Wen, Yang, et al.
Publicado: (2019)

Genetic Variants in the Promoter Region of miR-10b and the Risk of Breast Cancer
por: Chen, Jiaping, et al.
Publicado: (2017)

Systematic identification of long non-coding RNAs with cancer-testis expression patterns in 14 cancer types
por: Qin, Na, et al.
Publicado: (2017)

A novel plasma circular RNA circFARSA is a potential biomarker for non‐small cell lung cancer
por: Hang, Dong, et al.
Publicado: (2018)

Evaluation of functional genetic variants at 6q25.1 and risk of breast cancer in a Chinese population
por: Wang, Yanru, et al.
Publicado: (2014)

A causal variant rs3769823 in 2q33.1 involved in apoptosis pathway leading to a decreased risk of non-small cell lung cancer
por: Zhang, Xu, et al.
Publicado: (2022)

A germline variant N375S in MET and gastric cancer susceptibility in a Chinese population
por: Liu, Yao, et al.
Publicado: (2012)

Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women
por: Dai, Juncheng, et al.
Publicado: (2012)

Telomere length, genetic variants and risk of squamous cell carcinoma of the head and neck in Southeast Chinese
por: Gu, Yayun, et al.
Publicado: (2016)

Identification of Recurrent Variants in BRCA1 and BRCA2 across Multiple Cancers in the Chinese Population
por: Jiang, Yue, et al.
Publicado: (2020)

Cumulative Effect and Predictive Value of Genetic Variants Associated with Type 2 Diabetes in Han Chinese: A Case-Control Study
por: Qian, Yun, et al.
Publicado: (2015)

A functional variant in miR-155 regulation region contributes to lung cancer risk and survival
por: Xie, Kaipeng, et al.
Publicado: (2015)

The known genetic loci for telomere length may be involved in the modification of telomeres length after birth
por: Weng, Qiao, et al.
Publicado: (2016)

Polygenic score: An anchor holding the whole life course
por: Jin, Guangfu, et al.
Publicado: (2023)

Genetic variants at 9p21.3 are associated with risk of esophageal squamous cell carcinoma in a Chinese population
por: Lin, Xiaoming, et al.
Publicado: (2017)

Genetic Variants at 1p11.2 and Breast Cancer Risk: A Two-Stage Study in Chinese Women
por: Jiang, Yue, et al.
Publicado: (2011)

Integration of GWAS and eQTL Analysis to Identify Risk Loci and Susceptibility Genes for Gastric Cancer
por: Ni, Jing, et al.
Publicado: (2020)

Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
por: Chen, Jiaping, et al.
Publicado: (2014)

Analysis of the interaction effect of 48 SNPs and obesity on type 2 diabetes in Chinese Hans
por: Liu, Jia, et al.
Publicado: (2020)

Genetic variants at 8q24 are associated with risk of esophageal squamous cell carcinoma in a Chinese population
por: Dai, Ningbin, et al.
Publicado: (2014)

Association analyses identify 31 new risk loci for colorectal cancer susceptibility
por: Law, Philip J., et al.
Publicado: (2019)

Genetic variants at 10q23.33 are associated with plasma lipid levels in a Chinese population
por: Liu, Sijun, et al.
Publicado: (2014)

Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: a population-based exome-wide association study
por: Li, Zhihua, et al.
Publicado: (2018)

Prognostic assessment of apoptotic gene polymorphisms in non-small cell lung cancer in Chinese
por: Cao, Songyu, et al.
Publicado: (2013)

The eQTL-missense polymorphisms of APOBEC3H are associated with lung cancer risk in a Han Chinese population
por: Zhu, Meng, et al.
Publicado: (2015)

Blood groups A and AB are associated with increased gastric cancer risk: evidence from a large genetic study and systematic review
por: Mao, Yingying, et al.
Publicado: (2019)

Genetic Variations in miR-30 Family Member Regulatory Regions Are Associated with Breast Cancer Risk in a Chinese Population
por: Zhou, Jing, et al.
Publicado: (2020)

Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo
por: Jin, Ying, et al.
Publicado: (2012)

Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease
por: Maguire, Lillias H., et al.
Publicado: (2018)

Meta-Analyses of Splicing and Expression Quantitative Trait Loci Identified Susceptibility Genes of Glioma
por: Patro, C. Pawan K., et al.
Publicado: (2021)

Genetic variant in fat mass and obesity-associated gene associated with type 2 diabetes risk in Han Chinese
por: Qian, Yun, et al.
Publicado: (2013)

Fine-mapping of Parkinson’s disease susceptibility loci identifies putative causal variants
por: Schilder, Brian M, et al.
Publicado: (2021)

Genetic Variants at 12p11 and 12q24 Are Associated with Breast Cancer Risk in a Chinese Population
por: Qin, Zhenzhen, et al.
Publicado: (2013)

Mitochondrial DNA copy number is associated with risk of head and neck squamous cell carcinoma in Chinese population
por: Wang, Lihua, et al.
Publicado: (2018)

Comprehensive characterization of functional eRNAs in lung adenocarcinoma reveals novel regulators and a prognosis-related molecular subtype
por: Qin, Na, et al.
Publicado: (2020)

Circulating Tumor Cells Enriched by the Depletion of Leukocytes with Bi-Antibodies in Non-Small Cell Lung Cancer: Potential Clinical Application
por: Yin, Jian, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_kdfjufu3t2g7h78pt3g7s4r7hv