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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. Among authors: macmillan j. Pharmacogenet Genomics. 2009 Jun;19(6):422-8. doi: 10.1097/FPC.0b013e32832af5a3. Pharmacogenet Genomics. 2009. PMID: 19384265 Clinical Trial.
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. 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
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort.
Maher BH, Kerr M, Cox HC, MacMillan JC, Brimage PJ, Esposito T, Gianfrancesco F, Haupt LM, Nyholt DR, Lea RA, Griffiths LR. Maher BH, et al. Among authors: macmillan jc. Neurogenetics. 2012 Feb;13(1):97-101. doi: 10.1007/s10048-011-0312-7. Neurogenetics. 2012. PMID: 22294494
Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine.
Menon S, Buteri J, Roy B, Murrell M, Quinlan S, Macmillan JC, Lea RA, Haupt LM, Griffiths LR. Menon S, et al. Among authors: macmillan jc. Brain Res. 2011 Mar 10;1378:119-24. doi: 10.1016/j.brainres.2010.12.072. Epub 2010 Dec 31. Brain Res. 2011. PMID: 21195698
A population genomics overview of the neuronal nitric oxide synthase (nNOS) gene and its relationship to migraine susceptibility.
Johnson MP, Lea RA, Colson NJ, Macmillan JC, Griffiths LR. Johnson MP, et al. Among authors: macmillan jc. Cell Mol Biol (Noisy-le-grand). 2005 Sep 5;51(3):285-92. Cell Mol Biol (Noisy-le-grand). 2005. PMID: 16191396
Association of a Notch 3 gene polymorphism with migraine susceptibility.
Menon S, Cox HC, Kuwahata M, Quinlan S, MacMillan JC, Haupt LM, Lea RA, Griffiths LR. Menon S, et al. Among authors: macmillan jc. Cephalalgia. 2011 Feb;31(3):264-70. doi: 10.1177/0333102410381143. Epub 2010 Sep 2. Cephalalgia. 2011. PMID: 20813781
Investigation of the NOTCH3 and TNFSF7 genes on C19p13 as candidates for migraine.
Smith RA, Curtain R, Ovcaric M, Tajouri L, Macmillan J, Griffiths L. Smith RA, et al. Among authors: macmillan j. Open Neurol J. 2008;2:1-7. doi: 10.2174/1874205X00802010001. Epub 2008 Apr 23. Open Neurol J. 2008. PMID: 19018300 Free PMC article.
Association analysis of chromosome 1 migraine candidate genes.
Fernandez F, Curtain RP, Colson NJ, Ovcaric M, MacMillan J, Griffiths LR. Fernandez F, et al. Among authors: macmillan j. BMC Med Genet. 2007 Aug 29;8:57. doi: 10.1186/1471-2350-8-57. BMC Med Genet. 2007. PMID: 17727731 Free PMC article.
No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree.
Curtain R, Tajouri L, Lea R, MacMillan J, Griffiths L. Curtain R, et al. Among authors: macmillan j. Eur J Med Genet. 2006 Jan-Feb;49(1):57-62. doi: 10.1016/j.ejmg.2005.01.015. Epub 2005 Feb 12. Eur J Med Genet. 2006. PMID: 16473310
Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility.
Curtain R, Sundholm J, Lea R, Ovcaric M, MacMillan J, Griffiths L. Curtain R, et al. Among authors: macmillan j. BMC Med Genet. 2005 Sep 14;6:32. doi: 10.1186/1471-2350-6-32. BMC Med Genet. 2005. PMID: 16162291 Free PMC article.
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