Genome-wide association study in Guillain-Barre syndrome

Blum, Stefan, Ji, Ying, , , , McCombe, Pamela, & (2018) Genome-wide association study in Guillain-Barre syndrome. Journal of Neuroimmunology, 323, pp. 109-114.

View at publisher

Description

Guillain-Barre syndrome (GBS) is considered to have an immune-mediated basis, but the genetic contribution to GBS is unclear. We conducted a GWAS involving 215 GBS patients and 1,105 healthy controls. No significant associations of individual SNPs or imputed HLA types were observed. We performed a genome-wide complex trait analysis for evaluation of the heritability of GBS, and found that common SNPs contribute up to 25% of susceptibility to the disease. Genetic risk score analysis showed no evidence of overlap in genetic susceptibility factors of GBS and multiple sclerosis. Given the unexplained heritability of the trait further larger GWAS are indicated.

Impact and interest:

16 citations in Scopus
18 citations in Web of Science®
Search Google Scholar™

Citation counts are sourced monthly from Scopus and Web of Science® citation databases.

These databases contain citations from different subsets of available publications and different time periods and thus the citation count from each is usually different. Some works are not in either database and no count is displayed. Scopus includes citations from articles published in 1996 onwards, and Web of Science® generally from 1980 onwards.

Citations counts from the Google Scholar™ indexing service can be viewed at the linked Google Scholar™ search.

Full-text downloads:

275 since deposited on 07 Jan 2019
25 in the past twelve months

Full-text downloads displays the total number of times this work’s files (e.g., a PDF) have been downloaded from QUT ePrints as well as the number of downloads in the previous 365 days. The count includes downloads for all files if a work has more than one.

ID Code: 124009
Item Type: Contribution to Journal (Journal Article)
Refereed: Yes
ORCID iD:
Li, Zhixiuorcid.org/0000-0002-2924-9120
Leo, Paulorcid.org/0000-0001-8325-4134
Brown, Mattorcid.org/0000-0003-0538-8211
Measurements or Duration: 6 pages
Keywords: Case-control study, Genetic risk score, Genome-wide association study, Guillain-Barre syndrome, Heritability, Human leukocyte antigen (HLA) genes
DOI: 10.1016/j.jneuroim.2018.07.016
ISSN: 0165-5728
Pure ID: 33384653
Divisions: Past > QUT Faculties & Divisions > Faculty of Health
Past > Institutes > Institute of Health and Biomedical Innovation
Funding:
Copyright Owner: Consult author(s) regarding copyright matters
Copyright Statement: This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au
Deposited On: 07 Jan 2019 13:33
Last Modified: 13 Nov 2025 03:43