Carless MA - Search Results

1

Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits.

Benton MC, Lea RA, Macartney-Coxson D, Carless MA, Göring HH, Bellis C, Hanna M, Eccles D, Chambers GK, Curran JE, Harper JL, Blangero J, Griffiths LR. Benton MC, et al. Among authors: carless ma. Am J Hum Genet. 2013 Dec 5;93(6):1087-99. doi: 10.1016/j.ajhg.2013.11.004. Am J Hum Genet. 2013. PMID: 24314549 Free PMC article.

2

Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate.

Cox HC, Lea RA, Bellis C, Carless M, Dyer T, Blangero J, Griffiths LR. Cox HC, et al. J Headache Pain. 2011 Dec;12(6):603-8. doi: 10.1007/s10194-011-0392-7. Epub 2011 Oct 22. J Headache Pain. 2011. PMID: 22030984 Free PMC article.

3

An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12.

Maher BH, Lea RA, Benton M, Cox HC, Bellis C, Carless M, Dyer TD, Curran J, Charlesworth JC, Buring JE, Kurth T, Chasman DI, Ridker PM, Schürks M, Blangero J, Griffiths LR. Maher BH, et al. PLoS One. 2012;7(5):e37903. doi: 10.1371/journal.pone.0037903. Epub 2012 May 29. PLoS One. 2012. PMID: 22666411 Free PMC article.

4

A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility.

Cox HC, Lea RA, Bellis C, Carless M, Dyer TD, Curran J, Charlesworth J, Macgregor S, Nyholt D, Chasman D, Ridker PM, Schürks M, Blangero J, Griffiths LR. Cox HC, et al. Neurogenetics. 2012 Aug;13(3):261-6. doi: 10.1007/s10048-012-0325-x. Epub 2012 Jun 8. Neurogenetics. 2012. PMID: 22678113 Free PMC article.

5

Common polygenic variation contributes to risk of migraine in the Norfolk Island population.

Rodriguez-Acevedo AJ, Ferreira MA, Benton MC, Carless MA, Goring HH, Curran JE, Blangero J, Lea RA, Griffiths LR. Rodriguez-Acevedo AJ, et al. Among authors: carless ma. Hum Genet. 2015 Oct;134(10):1079-87. doi: 10.1007/s00439-015-1587-9. Epub 2015 Jul 29. Hum Genet. 2015. PMID: 26220684

6

A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers.

Benton MC, Lea RA, Macartney-Coxson D, Hanna M, Eccles DA, Carless MA, Chambers GK, Bellis C, Goring HH, Curran JE, Harper JL, Gibson G, Blangero J, Griffiths LR. Benton MC, et al. Among authors: carless ma. PLoS Genet. 2015 Oct 16;11(10):e1005593. doi: 10.1371/journal.pgen.1005593. eCollection 2015 Oct. PLoS Genet. 2015. PMID: 26474483 Free PMC article.

7

Serum bilirubin concentration is modified by UGT1A1 haplotypes and influences risk of type-2 diabetes in the Norfolk Island genetic isolate.

Benton MC, Lea RA, Macartney-Coxson D, Bellis C, Carless MA, Curran JE, Hanna M, Eccles D, Chambers GK, Blangero J, Griffiths LR. Benton MC, et al. Among authors: carless ma. BMC Genet. 2015 Dec 2;16:136. doi: 10.1186/s12863-015-0291-z. BMC Genet. 2015. PMID: 26628212 Free PMC article.

8

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. J Invest Dermatol. 2002 Dec;119(6):1373-8. doi: 10.1046/j.1523-1747.2002.19646.x. J Invest Dermatol. 2002. PMID: 12485442 Free article.

9

Cytogenetics of melanoma and nonmelanoma skin cancer.

Carless MA, Griffiths LR. Carless MA, et al. Adv Exp Med Biol. 2008;624:227-40. doi: 10.1007/978-0-387-77574-6_18. Adv Exp Med Biol. 2008. PMID: 18348460 Review.

10

Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease.

Johansson A, Curran JE, Johnson MP, Freed KA, Fenstad MH, Bjørge L, Eide IP, Carless MA, Rainwater DL, Goring HH, Austgulen R, Moses EK, Blangero J. Johansson A, et al. Among authors: carless ma. Eur J Hum Genet. 2011 Jul;19(7):796-800. doi: 10.1038/ejhg.2011.19. Epub 2011 Feb 23. Eur J Hum Genet. 2011. PMID: 21343950 Free PMC article.

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