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537 results
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The effects of vitamin supplementation and MTHFR (C677T) genotype on homocysteine-lowering and migraine disability.
Lea R, Colson N, Quinlan S, Macmillan J, Griffiths L. Lea R, et al. Pharmacogenet Genomics. 2009 Jun;19(6):422-8. doi: 10.1097/FPC.0b013e32832af5a3. Pharmacogenet Genomics. 2009. PMID: 19384265 Clinical Trial.
Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity.
Nyholt DR, Lea RA, Goadsby PJ, Brimage PJ, Griffiths LR. Nyholt DR, et al. Among authors: lea ra. Neurology. 1998 May;50(5):1428-32. doi: 10.1212/wnl.50.5.1428. Neurology. 1998. PMID: 9596000
Evidence for allelic association of the dopamine beta-hydroxylase gene (DBH) with susceptibility to typical migraine.
Lea RA, Dohy A, Jordan K, Quinlan S, Brimage PJ, Griffiths LR. Lea RA, et al. Neurogenetics. 2000 Sep;3(1):35-40. doi: 10.1007/pl00022977. Neurogenetics. 2000. PMID: 11085595
No evidence for involvement of the human inducible nitric oxide synthase (iNOS) gene in susceptibility to typical migraine.
Lea RA, Curtain RP, Shepherd AG, Brimage PJ, Griffiths LR. Lea RA, et al. Am J Med Genet. 2001 Jan 8;105(1):110-3. Am J Med Genet. 2001. PMID: 11424980
Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.
McCarthy LC, Hosford DA, Riley JH, Bird MI, White NJ, Hewett DR, Peroutka SJ, Griffiths LR, Boyd PR, Lea RA, Bhatti SM, Hosking LK, Hood CM, Jones KW, Handley AR, Rallan R, Lewis KF, Yeo AJ, Williams PM, Priest RC, Khan P, Donnelly C, Lumsden SM, O'Sullivan J, See CG, Smart DH, Shaw-Hawkins S, Patel J, Langrish TC, Feniuk W, Knowles RG, Thomas M, Libri V, Montgomery DS, Manasco PK, Xu CF, Dykes C, Humphrey PP, Roses AD, Purvis IJ. McCarthy LC, et al. Among authors: lea ra. Genomics. 2001 Dec;78(3):135-49. doi: 10.1006/geno.2001.6647. Genomics. 2001. PMID: 11735220
Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility.
Lea RA, Curtain RP, Hutchins C, Brimage PJ, Griffiths LR. Lea RA, et al. Am J Med Genet. 2001 Dec 8;105(8):707-12. doi: 10.1002/ajmg.1609. Am J Med Genet. 2001. PMID: 11803518
A typical migraine susceptibility region localizes to chromosome 1q31.
Lea RA, Shepherd AG, Curtain RP, Nyholt DR, Quinlan S, Brimage PJ, Griffiths LR. Lea RA, et al. Neurogenetics. 2002 Mar;4(1):17-22. doi: 10.1007/s10048-001-0125-1. Neurogenetics. 2002. PMID: 12030327
Dopamine receptor genes and migraine with and without aura: an association study.
Shepherd AG, Lea RA, Hutchins C, Jordan KL, Brimage PJ, Griffiths LR. Shepherd AG, et al. Among authors: lea ra. Headache. 2002 May;42(5):346-51. doi: 10.1046/j.1526-4610.2002.02105.x. Headache. 2002. PMID: 12047334
The GSTM1 null genotype confers an increased risk for solar keratosis development in an Australian Caucasian population.
Carless MA, Lea RA, Curran JE, Appleyard B, Gaffney P, Green A, Griffiths LR. Carless MA, et al. Among authors: lea ra. J Invest Dermatol. 2002 Dec;119(6):1373-8. doi: 10.1046/j.1523-1747.2002.19646.x. J Invest Dermatol. 2002. PMID: 12485442
An investigation of the 5-HT2C receptor gene as a migraine candidate gene.
Johnson MP, Lea RA, Curtain RP, MacMillan JC, Griffiths LR. Johnson MP, et al. Among authors: lea ra. Am J Med Genet B Neuropsychiatr Genet. 2003 Feb;117B(1):86-9. doi: 10.1002/ajmg.b.10007. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12555241
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