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Items: 1 to 20 of 31

1.

Twins eye study in Tasmania (TEST): rationale and methodology to recruit and examine twins.

Mackey DA, Mackinnon JR, Brown SA, Kearns LS, Ruddle JB, Sanfilippo PG, Sun C, Hammond CJ, Young TL, Martin NG, Hewitt AW.

Twin Res Hum Genet. 2009 Oct;12(5):441-54. doi: 10.1375/twin.12.5.441.

2.

Rapid inexpensive genome-wide association using pooled whole blood.

Craig JE, Hewitt AW, McMellon AE, Henders AK, Ma L, Wallace L, Sharma S, Burdon KP, Visscher PM, Montgomery GW, MacGregor S.

Genome Res. 2009 Nov;19(11):2075-80. doi: 10.1101/gr.094680.109. Epub 2009 Oct 3.

3.

Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes.

Dimasi DP, Chen JY, Hewitt AW, Klebe S, Davey R, Stirling J, Thompson E, Forbes R, Tan TY, Savarirayan R, Mackey DA, Healey PR, Mitchell P, Burdon KP, Craig JE.

Hum Genet. 2010 Jan;127(1):33-44. doi: 10.1007/s00439-009-0729-3. Epub 2009 Aug 28.

PMID:
19714363
4.

The genetics of central corneal thickness.

Dimasi DP, Burdon KP, Craig JE.

Br J Ophthalmol. 2010 Aug;94(8):971-6. doi: 10.1136/bjo.2009.162735. Epub 2009 Jun 24. Review.

PMID:
19556215
5.

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies.

Howie BN, Donnelly P, Marchini J.

PLoS Genet. 2009 Jun;5(6):e1000529. doi: 10.1371/journal.pgen.1000529. Epub 2009 Jun 19.

6.

Geographical structure and differential natural selection among North European populations.

McEvoy BP, Montgomery GW, McRae AF, Ripatti S, Perola M, Spector TD, Cherkas L, Ahmadi KR, Boomsma D, Willemsen G, Hottenga JJ, Pedersen NL, Magnusson PK, Kyvik KO, Christensen K, Kaprio J, Heikkilä K, Palotie A, Widen E, Muilu J, Syvänen AC, Liljedahl U, Hardiman O, Cronin S, Peltonen L, Martin NG, Visscher PM.

Genome Res. 2009 May;19(5):804-14. doi: 10.1101/gr.083394.108. Epub 2009 Mar 5.

7.

Common sequence variants on 20q11.22 confer melanoma susceptibility.

Brown KM, Macgregor S, Montgomery GW, Craig DW, Zhao ZZ, Iyadurai K, Henders AK, Homer N, Campbell MJ, Stark M, Thomas S, Schmid H, Holland EA, Gillanders EM, Duffy DL, Maskiell JA, Jetann J, Ferguson M, Stephan DA, Cust AE, Whiteman D, Green A, Olsson H, Puig S, Ghiorzo P, Hansson J, Demenais F, Goldstein AM, Gruis NA, Elder DE, Bishop JN, Kefford RF, Giles GG, Armstrong BK, Aitken JF, Hopper JL, Martin NG, Trent JM, Mann GJ, Hayward NK.

Nat Genet. 2008 Jul;40(7):838-40. doi: 10.1038/ng.163. Epub 2008 May 18.

8.

Deleterious mutations in the Zinc-Finger 469 gene cause brittle cornea syndrome.

Abu A, Frydman M, Marek D, Pras E, Nir U, Reznik-Wolf H, Pras E.

Am J Hum Genet. 2008 May;82(5):1217-22. doi: 10.1016/j.ajhg.2008.04.001. Epub 2008 May 1.

9.

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays.

Macgregor S, Zhao ZZ, Henders A, Nicholas MG, Montgomery GW, Visscher PM.

Nucleic Acids Res. 2008 Apr;36(6):e35. doi: 10.1093/nar/gkm1060. Epub 2008 Feb 14.

10.

The heritability of optic disc parameters: a classic twin study.

Healey P, Carbonaro F, Taylor B, Spector TD, Mitchell P, Hammond CJ.

Invest Ophthalmol Vis Sci. 2008 Jan;49(1):77-80. doi: 10.1167/iovs.07-0962.

PMID:
18172077
11.

FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A.

Berry FB, Skarie JM, Mirzayans F, Fortin Y, Hudson TJ, Raymond V, Link BA, Walter MA.

Hum Mol Genet. 2008 Feb 15;17(4):490-505. Epub 2007 Nov 9.

PMID:
17993506
12.

Predictors of long-term progression in the early manifest glaucoma trial.

Leske MC, Heijl A, Hyman L, Bengtsson B, Dong L, Yang Z; EMGT Group.

Ophthalmology. 2007 Nov;114(11):1965-72. Epub 2007 Jul 12.

PMID:
17628686
13.

Intercurrent factors associated with the development of open-angle glaucoma in the European glaucoma prevention study.

Miglior S, Torri V, Zeyen T, Pfeiffer N, Vaz JC, Adamsons I; EGPS Group.

Am J Ophthalmol. 2007 Aug;144(2):266-275. Epub 2007 Jun 4.

PMID:
17543874
14.

Efficient association mapping of quantitative trait loci with selective genotyping.

Huang BE, Lin DY.

Am J Hum Genet. 2007 Mar;80(3):567-76. Epub 2007 Jan 30.

15.

Benign joint hypermobility syndrome: evaluation, diagnosis, and management.

Simpson MR.

J Am Osteopath Assoc. 2006 Sep;106(9):531-6. Review.

PMID:
17079522
16.

Principal components analysis corrects for stratification in genome-wide association studies.

Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D.

Nat Genet. 2006 Aug;38(8):904-9. Epub 2006 Jul 23.

PMID:
16862161
17.
18.

The number of people with glaucoma worldwide in 2010 and 2020.

Quigley HA, Broman AT.

Br J Ophthalmol. 2006 Mar;90(3):262-7.

19.

Structural abnormalities of the cornea and lid resulting from collagen V mutations.

Segev F, Héon E, Cole WG, Wenstrup RJ, Young F, Slomovic AR, Rootman DS, Whitaker-Menezes D, Chervoneva I, Birk DE.

Invest Ophthalmol Vis Sci. 2006 Feb;47(2):565-73.

PMID:
16431952
20.

Genetic covariation of pelvic organ and elbow mobility in twins and their sisters.

Hansell NK, Dietz HP, Treloar SA, Clarke B, Martin NG.

Twin Res. 2004 Jun;7(3):254-60.

PMID:
15193170

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