Martin NG - Search Results

1

Human twinning is not linked to the region of chromosome 4 syntenic with the sheep twinning gene FecB.

Duffy DL, Montgomery GW, Hall J, Mayne C, Healey SC, Brown J, Boomsma DI, Martin NG. Duffy DL, et al. Among authors: martin ng. Am J Med Genet. 2001 May 1;100(3):182-6. doi: 10.1002/ajmg.1255. Am J Med Genet. 2001. PMID: 11343301

2

Genetic contribution to DZ twinning.

Lewis CM, Healey SC, Martin NG. Lewis CM, et al. Among authors: martin ng. Am J Med Genet. 1996 Jan 22;61(3):237-46. doi: 10.1002/(SICI)1096-8628(19960122)61:3<237::AID-AJMG7>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8741868

3

Is fragile X syndrome a risk factor for dizygotic twinning?

Healey SC, Duffy DL, Martin NG, Turner G. Healey SC, et al. Among authors: martin ng. Am J Med Genet. 1997 Oct 17;72(2):245-6. doi: 10.1002/(sici)1096-8628(19971017)72:2<245::aid-ajmg24>3.0.co;2-m. Am J Med Genet. 1997. PMID: 9382153 No abstract available.

4

Mendelian segregation of normal CAG trinucleotide repeat alleles at three autosomal loci.

MacMillan JC, Voisey J, Healey SC, Martin NG. MacMillan JC, et al. Among authors: martin ng. J Med Genet. 1999 Mar;36(3):258-9. J Med Genet. 1999. PMID: 10204858 Free PMC article.

5

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.

Zhu G, Duffy DL, Eldridge A, Grace M, Mayne C, O'Gorman L, Aitken JF, Neale MC, Hayward NK, Green AC, Martin NG. Zhu G, et al. Among authors: martin ng. Am J Hum Genet. 1999 Aug;65(2):483-92. doi: 10.1086/302494. Am J Hum Genet. 1999. PMID: 10417291 Free PMC article.

6

Dizygotic twinning is not linked to variation at the alpha-inhibin locus on human chromosome 2.

Montgomery GW, Duffy DL, Hall J, Haddon BR, Kudo M, McGee EA, Palmer JS, Hsueh AJ, Boomsma DI, Martin NG. Montgomery GW, et al. Among authors: martin ng. J Clin Endocrinol Metab. 2000 Sep;85(9):3391-5. doi: 10.1210/jcem.85.9.6831. J Clin Endocrinol Metab. 2000. PMID: 10999839 Clinical Trial.

7

Genetic time-series analysis identifies a major QTL for in vivo alcohol metabolism not predicted by in vitro studies of structural protein polymorphism at the ADH1B or ADH1C loci.

Birley AJ, Whitfield JB, Neale MC, Duffy DL, Heath AC, Boomsma DI, Martin NG. Birley AJ, et al. Among authors: martin ng. Behav Genet. 2005 Sep;35(5):509-24. doi: 10.1007/s10519-005-3851-6. Behav Genet. 2005. PMID: 16184481 Clinical Trial.

8

Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task.

Hansell NK, Medland SE, Ferreira MA, Geffen GM, Zhu G, Montgomery GW, Duffy DL, Wright MJ, Martin NG. Hansell NK, et al. Among authors: martin ng. Behav Genet. 2006 Jan;36(1):29-44. doi: 10.1007/s10519-005-9002-2. Epub 2005 Dec 6. Behav Genet. 2006. PMID: 16331531

9

Genome-wide scan of IQ finds significant linkage to a quantitative trait locus on 2q.

Luciano M, Wright MJ, Duffy DL, Wainwright MA, Zhu G, Evans DM, Geffen GM, Montgomery GW, Martin NG. Luciano M, et al. Among authors: martin ng. Behav Genet. 2006 Jan;36(1):45-55. doi: 10.1007/s10519-005-9003-1. Epub 2005 Dec 9. Behav Genet. 2006. PMID: 16341610

10

Genomewide scans of red cell indices suggest linkage on chromosome 6q23.

Iliadou A, Evans DM, Zhu G, Duffy DL, Frazer IH, Montgomery GW, Martin NG. Iliadou A, et al. Among authors: martin ng. J Med Genet. 2007 Jan;44(1):24-30. doi: 10.1136/jmg.2006.043521. Epub 2006 Sep 1. J Med Genet. 2007. PMID: 16950815 Free PMC article.

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