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Publications |
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Walker GJ, Indsto JO, Sood R, Faruque MU, Hu P, Pollock PM, Duray P, Holland EA, Brown K, Kefford RF, Trent JM, Mann GJ, Hayward NK.
Deletion mapping suggests that the 1p22 melanoma susceptibility gene is a tumor suppressor localized to a 9-Mb interval.
Genes Chromosomes Cancer. 2004 Sep;41(1):56-64.
PMID: 15236317
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15236317 |
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Sturm RA, Frudakis TN.
Eye colour: portals into pigmentation genes and ancestry.
Trends Genet. 2004 Aug;20(8):327-32.
PMID: 15262401
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15262401 |
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Zhu G, Evans DM, Duffy DL, Montgomery GW, Medland SE, Gillespie NA, Ewen KR, Jewell M, Liew YW, Hayward NK, Sturm RA, Trent JM, Martin NG.
A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.
Twin Res. 2004 Apr;7(2):197-210.
PMID: 15169604
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15169604 |
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Duffy DL, Box NF, Chen W, Palmer JS, Montgomery GW, James MR, Hayward NK, Martin NG, Sturm RA.
Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.
Hum Mol Genet. 2004 Feb 15;13(4):447-61.
PMID: 14709592
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=14709592 |
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Sturm RA, Duffy DL, Box NF, Newton RA, Shepherd AG, Chen W, Marks LH, Leonard JH, Martin NG.
Genetic association and cellular function of MC1R variant alleles in human pigmentation.
Ann N Y Acad Sci. 2003 Jun;994:348-58.
PMID: 12851335
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12851335 |
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Sturm RA, Duffy DL, Box NF, Chen W, Smit DJ, Brown DL, Stow JL, Leonard JH, Martin NG.
The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes.
Pigment Cell Res. 2003 Jun;16(3):266-72.
PMID: 12753400
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12753400 |
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Leonard JH, Marks LH, Chen W, Cook AL, Boyle GM, Smit DJ, Brown DL, Stow JL, Parsons PG, Sturm RA.
Screening of human primary melanocytes of defined melanocortin-1 receptor genotype: pigmentation marker, ultrastructural and UV-survival studies.
Pigment Cell Res. 2003 Jun;16(3):198-207.
PMID: 12753386
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12753386 |
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Hayward NK.
Genetics of melanoma predisposition.
Oncogene. 2003 May 19;22(20):3053-62.
PMID: 12789280
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12789280 |
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Whiteman DC, Watt P, Purdie DM, Hughes MC, Hayward NK, Green AC.
Melanocytic nevi, solar keratoses, and divergent pathways to cutaneous melanoma.
J Natl Cancer Inst. 2003 Jun 4;95(11):806-12.
PMID: 12783935
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12783935 |
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Pollock PM, Harper UL, Hansen KS, Yudt LM, Stark M, Robbins CM, Moses TY, Hostetter G, Wagner U, Kakareka J, Salem G, Pohida T, Heenan P, Duray P, Kallioniemi O, Hayward NK, Trent JM, Meltzer PS.
High frequency of BRAF mutations in nevi.
Nat Genet. 2003 Jan;33(1):19-20.
PMID: 12447372
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12447372 |
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Sturm RA.
Skin colour and skin cancer - MC1R, the genetic link.
Melanoma Res. 2002 Oct;12(5):405-16.
PMID: 12394181
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=12394181 |
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Youl P, Aitken J, Hayward N, Hogg D, Liu L, Lassam N, Martin N, Green A.
Melanoma in adolescents: a case-control study of risk factors in Queensland, Australia.
Int J Cancer. 2002 Mar 1;98(1):92-8.
PMID: 11857391
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11857391 |
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Walker GJ, Hayward NK.
p16INK4A and p14ARF tumour suppressors in melanoma: lessons from the mouse.
Lancet. 2002 Jan 5;359(9300):7-8.
PMID: 11809177
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11809177 |
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Box NF, Duffy DL, Chen W, Stark M, Martin NG, Sturm RA, Hayward NK.
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations.
Am J Hum Genet. 2001 Oct;69(4):765-73.
PMID: 11500805
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11500805 |
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Sturm RA, Teasdale RD, Box NF.
Human pigmentation genes: identification, structure and consequences of polymorphic variation.
Gene. 2001 Oct 17;277(1-2):49-62.
PMID: 11602344
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11602344 |
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Pollock PM, Stark MS, Palmer JM, Walters MK, Aitken JF, Martin NG, Hayward NK.
Mutation analysis of the CDKN2A promoter in Australian melanoma families.
Genes Chromosomes Cancer. 2001 Sep;32(1):89-94.
PMID: 11477665
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=1147766 |
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Box NF, Duffy DL, Irving RE, Russell A, Chen W, Griffyths LR, Parsons PG, Green AC, Sturm RA.
Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma.
J Invest Dermatol. 2001 Feb;116(2):224-9.
PMID: 11179997
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11179997 |
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Hayward N.
New developments in melanoma genetics.
Curr Oncol Rep. 2000 Jul;2(4):300-6.
PMID: 11122857
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11122857 |
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Palmer JS, Duffy DL, Box NF, Aitken JF, O'Gorman LE, Green AC, Hayward NK, Martin NG, Sturm RA.
Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?
Am J Hum Genet. 2000 Jan;66(1):176-86.
PMID: 10631149
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=10631149 |
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Zhu G, Duffy DL, Eldridge A, Grace M, Mayne C, O'Gorman L, Aitken JF, Neale MC, Hayward NK, Green AC, Martin NG.
A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs.
Am J Hum Genet. 1999 Aug;65(2):483-92.
PMID: 10417291
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=10417291 |
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Aitken J, Welch J, Duffy D, Milligan A, Green A, Martin N, Hayward N.
CDKN2A variants in a population-based sample of Queensland families with melanoma.
J Natl Cancer Inst. 1999 Mar 3;91(5):446-52.
PMID: 10070944
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=10070944 |
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