Martin NG - Search Results

1

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM. Hillmer AM, et al. Among authors: martin ng. Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12. Nat Genet. 2008. PMID: 18849994

2

Linkage and association analysis of radiation damage repair genes XRCC3 and XRCC5 with nevus density in adolescent twins.

Zhu G, Duffy DL, Turner DR, Ewen KR, Montgomery GW, Martin NG. Zhu G, et al. Among authors: martin ng. Twin Res. 2003 Aug;6(4):315-21. doi: 10.1375/136905203322296683. Twin Res. 2003. PMID: 14511439

3

Dizygotic twinning is not associated with methylenetetrahydrofolate reductase haplotypes.

Montgomery GW, Zhao ZZ, Morley KI, Marsh AJ, Boomsma DI, Martin NG, Duffy DL. Montgomery GW, et al. Among authors: martin ng. Hum Reprod. 2003 Nov;18(11):2460-4. doi: 10.1093/humrep/deg441. Hum Reprod. 2003. PMID: 14585902

4

Genetic basis of male pattern baldness.

Nyholt DR, Gillespie NA, Heath AC, Martin NG. Nyholt DR, et al. Among authors: martin ng. J Invest Dermatol. 2003 Dec;121(6):1561-4. doi: 10.1111/j.1523-1747.2003.12615.x. J Invest Dermatol. 2003. PMID: 14675213 Free article. No abstract available.

5

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes.

Duffy DL, Box NF, Chen W, Palmer JS, Montgomery GW, James MR, Hayward NK, Martin NG, Sturm RA. Duffy DL, et al. Among authors: martin ng. Hum Mol Genet. 2004 Feb 15;13(4):447-61. doi: 10.1093/hmg/ddh043. Epub 2004 Jan 6. Hum Mol Genet. 2004. PMID: 14709592

6

Latent class and genetic analysis does not support migraine with aura and migraine without aura as separate entities.

Nyholt DR, Gillespie NG, Heath AC, Merikangas KR, Duffy DL, Martin NG. Nyholt DR, et al. Among authors: martin ng. Genet Epidemiol. 2004 Apr;26(3):231-44. doi: 10.1002/gepi.10311. Genet Epidemiol. 2004. PMID: 15022209

7

A genome scan for eye color in 502 twin families: most variation is due to a QTL on chromosome 15q.

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. Zhu G, et al. Among authors: martin ng. Twin Res. 2004 Apr;7(2):197-210. doi: 10.1375/136905204323016186. Twin Res. 2004. PMID: 15169604 Free article.

8

Multivariate QTL linkage analysis suggests a QTL for platelet count on chromosome 19q.

Evans DM, Zhu G, Duffy DL, Montgomery GW, Frazer IH, Martin NG. Evans DM, et al. Among authors: martin ng. Eur J Hum Genet. 2004 Oct;12(10):835-42. doi: 10.1038/sj.ejhg.5201248. Eur J Hum Genet. 2004. PMID: 15280902

9

Epidermal growth factor gene (EGF) polymorphism and risk of melanocytic neoplasia.

James MR, Hayward NK, Dumenil T, Montgomery GW, Martin NG, Duffy DL. James MR, et al. Among authors: martin ng. J Invest Dermatol. 2004 Oct;123(4):760-2. doi: 10.1111/j.0022-202X.2004.23305.x. J Invest Dermatol. 2004. PMID: 15373782 Free article.

10

Major quantitative trait locus for eosinophil count is located on chromosome 2q.

Evans DM, Zhu G, Duffy DL, Montgomery GW, Frazer IH, Martin NG. Evans DM, et al. Among authors: martin ng. J Allergy Clin Immunol. 2004 Oct;114(4):826-30. doi: 10.1016/j.jaci.2004.05.060. J Allergy Clin Immunol. 2004. PMID: 15480322

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