scholarly journals An association analysis to identify genetic variants linked to asthma and rhino-conjunctivitis in a cohort of Sicilian children

2019 ◽  
Vol 45 (1) ◽  
Author(s):  
Gianluca Sottile ◽  
Giuliana Ferrante ◽  
Marta Torregrossa ◽  
Fabio Cibella ◽  
Giovanna Cilluffo ◽  
...  
2018 ◽  
Vol 19 (3) ◽  
pp. 295-304 ◽  
Author(s):  
Nihal El Rouby ◽  
◽  
Caitrin W. McDonough ◽  
Yan Gong ◽  
Leslie A. McClure ◽  
...  

2007 ◽  
Vol 52 (7) ◽  
pp. 575-583 ◽  
Author(s):  
Keiko Yamazaki ◽  
Yoshihiro Onouchi ◽  
Masakazu Takazoe ◽  
Michiaki Kubo ◽  
Yusuke Nakamura ◽  
...  

2020 ◽  
Author(s):  
Nadezhda M. Belonogova ◽  
Irina V. Zorkoltseva ◽  
Yakov A. Tsepilov ◽  
Tatiana I. Axenovich

AbstractRecent genome-wide studies have reported about 600 genes potentially influencing neuroticism. Little is known about the mechanisms of their action. Here, we aimed to conduct a more detailed analysis of genes whose polymorphisms can regulate the level of neuroticism. Using UK Biobank-based GWAS summary statistics, we performed a gene-based association analysis using four sets of genetic variants within a gene differing in their protein coding properties. To guard against the influence of strong GWAS signals outside the gene, we used the specially designed procedure. As a result, we identified 190 genes associated with neuroticism due to their polymorphisms. Thirty eight of these genes were novel. Within all genes identified, we distinguished two slightly overlapping groups comprising genes that demonstrated association when using protein-coding and non-coding SNPs. Many genes from the first group included potentially pathogenic variants. For some genes from the second group, we found evidence of pleiotropy with gene expression. We demonstrated that the association of almost two hundred known genes could be inflated by the GWAS signals outside the gene. Using bioinformatics analysis, we prioritized the neuroticism genes and showed that the genes influencing the trait by their polymorphisms are the most appropriate candidate genes.


2010 ◽  
Vol 42 (1) ◽  
pp. 120-126 ◽  
Author(s):  
Pingyuan Gong ◽  
Anyun Zheng ◽  
Kejin Zhang ◽  
Xu Lei ◽  
Fengchao Li ◽  
...  

2009 ◽  
Vol 56 (2) ◽  
pp. 275-286 ◽  
Author(s):  
Eiji KURODA ◽  
Yukio HORIKAWA ◽  
Mayumi ENYA ◽  
Naohisa ODA ◽  
Eiji SUZUKI ◽  
...  

Cephalalgia ◽  
2006 ◽  
Vol 26 (2) ◽  
pp. 158-161 ◽  
Author(s):  
S Schwaag ◽  
S Evers ◽  
A Schirmacher ◽  
F Stögbauer ◽  
EB Ringelstein ◽  
...  

Mutations in the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Exons 3 and 4 are mutation hotspots. Migraine is a clinical hallmark of CADASIL. The objective of this study was to investigate whether genetic variants in exons 3 and 4 of the NOTCH3 gene are associated with migraine. Exons 3 and 4 of the NOTCH3 were analysed for mutations and polymorphisms by direct DNA sequencing in 97 migraineurs and the same number of control individuals. No mutations in exons 3 and 4 of the NOTCH3 gene were found in 97 patients with migraine. However, association analysis revealed significant association of the single nucleotide polymorphism (SNP) rs1043994 with migraine.


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