Martin NG - Search Results

1

Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis.

D'Urso S, Rajbhandari D, Peach E, de Guzman E, Li Q, Medland SE, Gordon SD, Martin NG; CHARGE Inflammation Working Group; Ligthart S, Brown MA, Powell J, McArthur C, Rhodes A, Meyer J, Finfer S, Myburgh J, Blumenthal A, Cohen J, Venkatesh B, Cuellar-Partida G, Evans DM. D'Urso S, et al. Among authors: martin ng. Twin Res Hum Genet. 2020 Aug;23(4):204-213. doi: 10.1017/thg.2020.60. Epub 2020 Aug 5. Twin Res Hum Genet. 2020. PMID: 32755526

2

Special twin environments, genetic influences and their effects on the handedness of twins and their siblings.

Medland SE, Wright MJ, Geffen GM, Hay DA, Levy F, Martin NG, Duffy DL. Medland SE, et al. Among authors: martin ng. Twin Res. 2003 Apr;6(2):119-30. doi: 10.1375/136905203321536245. Twin Res. 2003. PMID: 12723998

3

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

4

Do the genetic or environmental determinants of anxiety and depression change with age? A longitudinal study of Australian twins.

Gillespie NA, Kirk KM, Evans DM, Heath AC, Hickie IB, Martin NG. Gillespie NA, et al. Among authors: martin ng. Twin Res. 2004 Feb;7(1):39-53. doi: 10.1375/13690520460741435. Twin Res. 2004. PMID: 15053853

5

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.

6

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

7

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

8

Gender diagnosticity and androgen receptor gene CAG repeat sequence.

Loehlin JC, Jönsson EG, Gustavsson JP, Schalling M, Medland SE, Montgomery GW, Martin NG. Loehlin JC, et al. Among authors: martin ng. Twin Res. 2004 Oct;7(5):456-61. doi: 10.1375/1369052042335359. Twin Res. 2004. PMID: 15527661

9

A deletion mutation in GDF9 in sisters with spontaneous DZ twins.

Montgomery GW, Zhao ZZ, Marsh AJ, Mayne R, Treloar SA, James M, Martin NG, Boomsma DI, Duffy DL. Montgomery GW, et al. Among authors: martin ng. Twin Res. 2004 Dec;7(6):548-55. doi: 10.1375/1369052042663823. Twin Res. 2004. PMID: 15607004

10

Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26.

Treloar SA, Wicks J, Nyholt DR, Montgomery GW, Bahlo M, Smith V, Dawson G, Mackay IJ, Weeks DE, Bennett ST, Carey A, Ewen-White KR, Duffy DL, O'connor DT, Barlow DH, Martin NG, Kennedy SH. Treloar SA, et al. Among authors: martin ng. Am J Hum Genet. 2005 Sep;77(3):365-76. doi: 10.1086/432960. Epub 2005 Jul 21. Am J Hum Genet. 2005. PMID: 16080113 Free PMC article.

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