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Ion channelopathies and migraine pathogenesis.
Albury CL, Stuart S, Haupt LM, Griffiths LR. Albury CL, et al. Among authors: stuart s. Mol Genet Genomics. 2017 Aug;292(4):729-739. doi: 10.1007/s00438-017-1317-1. Epub 2017 Apr 7. Mol Genet Genomics. 2017. PMID: 28389699 Review.
Investigation of lymphotoxin α genetic variants in migraine.
Oikari LE, Stuart S, Okolicsanyi RK, Cox HC, Dixit S, Lea RA, Haupt LM, Griffiths LR. Oikari LE, et al. Among authors: stuart s. Gene. 2013 Jan 10;512(2):527-31. doi: 10.1016/j.gene.2012.09.116. Epub 2012 Oct 7. Gene. 2013. PMID: 23051989 Free article.
Tiered analysis of whole-exome sequencing for epilepsy diagnosis.
Dunn PJ, Maher BH, Albury CL, Stuart S, Sutherland HG, Maksemous N, Benton MC, Smith RA, Haupt LM, Griffiths LR. Dunn PJ, et al. Among authors: stuart s. Mol Genet Genomics. 2020 May;295(3):751-763. doi: 10.1007/s00438-020-01657-x. Epub 2020 Mar 7. Mol Genet Genomics. 2020. PMID: 32146541
Ion torrent high throughput mitochondrial genome sequencing (HTMGS).
Harvey NR, Albury CL, Stuart S, Benton MC, Eccles DA, Connell JR, Sutherland HG, Allcock RJN, Lea RA, Haupt LM, Griffiths LR. Harvey NR, et al. Among authors: stuart s. PLoS One. 2019 Nov 15;14(11):e0224847. doi: 10.1371/journal.pone.0224847. eCollection 2019. PLoS One. 2019. PMID: 31730669 Free PMC article.
The role of the MTHFR gene in migraine.
Stuart S, Cox HC, Lea RA, Griffiths LR. Stuart S, et al. Headache. 2012 Mar;52(3):515-20. doi: 10.1111/j.1526-4610.2012.02106.x. Epub 2012 Feb 29. Headache. 2012. PMID: 22375693 Free article. Review.
Detection of a novel mutation in the CACNA1A gene.
Stuart S, Roy B, Davies G, Maksemous N, Smith R, Griffiths LR. Stuart S, et al. Twin Res Hum Genet. 2012 Feb;15(1):120-5. doi: 10.1375/twin.15.1.120. Twin Res Hum Genet. 2012. PMID: 22784462 Free article.
543 results