Quinlan S - Search Results

1

Analysis of the MTHFR C677T variant with migraine phenotypes.

Liu A, Menon S, Colson NJ, Quinlan S, Cox H, Peterson M, Tiang T, Haupt LM, Lea RA, Griffiths LR. Liu A, et al. Among authors: quinlan s. BMC Res Notes. 2010 Jul 28;3:213. doi: 10.1186/1756-0500-3-213. BMC Res Notes. 2010. PMID: 20663228 Free PMC article.

2

No role for estrogen receptor 1 gene intron 1 Pvu II and exon 4 C325G polymorphisms in migraine susceptibility.

Colson NJ, Lea RA, Quinlan S, Griffiths LR. Colson NJ, et al. Among authors: quinlan s. BMC Med Genet. 2006 Feb 28;7:12. doi: 10.1186/1471-2350-7-12. BMC Med Genet. 2006. PMID: 16504171 Free PMC article.

3

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: quinlan s. Pharmacogenet Genomics. 2009 Jun;19(6):422-8. doi: 10.1097/FPC.0b013e32832af5a3. Pharmacogenet Genomics. 2009. PMID: 19384265 Free article. Clinical Trial.

4

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. Among authors: quinlan s. Neurogenetics. 2002 Mar;4(1):17-22. doi: 10.1007/s10048-001-0125-1. Neurogenetics. 2002. PMID: 12030327

5

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups.

Colson NJ, Lea RA, Quinlan S, MacMillan J, Griffiths LR. Colson NJ, et al. Among authors: quinlan s. Neurogenetics. 2004 Jun;5(2):129-33. doi: 10.1007/s10048-004-0181-4. Epub 2004 May 7. Neurogenetics. 2004. PMID: 15133719

6

Investigation of hormone receptor genes in migraine.

Colson NJ, Lea RA, Quinlan S, MacMillan J, Griffiths LR. Colson NJ, et al. Among authors: quinlan s. Neurogenetics. 2005 Feb;6(1):17-23. doi: 10.1007/s10048-004-0205-0. Epub 2005 Jan 15. Neurogenetics. 2005. PMID: 15654614

7

The role of vascular and hormonal genes in migraine susceptibility.

Colson NJ, Lea RA, Quinlan S, Griffiths LR. Colson NJ, et al. Among authors: quinlan s. Mol Genet Metab. 2006 Jun;88(2):107-13. doi: 10.1016/j.ymgme.2005.11.013. Epub 2006 Jan 5. Mol Genet Metab. 2006. PMID: 16403664 Review.

8

Association between a 19 bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura.

Fernandez F, Lea RA, Colson NJ, Bellis C, Quinlan S, Griffiths LR. Fernandez F, et al. Among authors: quinlan s. J Neurol Sci. 2006 Dec 21;251(1-2):118-23. doi: 10.1016/j.jns.2006.09.013. Epub 2006 Nov 7. J Neurol Sci. 2006. PMID: 17095019

9

Association between migraine and a functional polymorphism at the dopamine beta-hydroxylase locus.

Fernandez F, Colson N, Quinlan S, MacMillan J, Lea RA, Griffiths LR. Fernandez F, et al. Among authors: quinlan s. Neurogenetics. 2009 Jul;10(3):199-208. doi: 10.1007/s10048-009-0176-2. Epub 2009 Feb 14. Neurogenetics. 2009. PMID: 19219470

10

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: quinlan s. Cephalalgia. 2011 Feb;31(3):264-70. doi: 10.1177/0333102410381143. Epub 2010 Sep 2. Cephalalgia. 2011. PMID: 20813781

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