Foote SJ - Search Results

1

Linkage to 10q22 for maximum intraocular pressure and 1p32 for maximum cup-to-disc ratio in an extended primary open-angle glaucoma pedigree.

Charlesworth JC, Dyer TD, Stankovich JM, Blangero J, Mackey DA, Craig JE, Green CM, Foote SJ, Baird PN, Sale MM. Charlesworth JC, et al. Among authors: foote sj. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3723-9. doi: 10.1167/iovs.05-0312. Invest Ophthalmol Vis Sci. 2005. PMID: 16186355

2

Evidence for a novel glaucoma locus at chromosome 3p21-22.

Baird PN, Foote SJ, Mackey DA, Craig J, Speed TP, Bureau A. Baird PN, et al. Among authors: foote sj. Hum Genet. 2005 Jul;117(2-3):249-57. doi: 10.1007/s00439-005-1296-x. Epub 2005 May 20. Hum Genet. 2005. PMID: 15906098

3

Analysis of 15 primary open-angle glaucoma families from Australia identifies a founder effect for the Q368STOP mutation of myocilin.

Baird PN, Craig JE, Richardson AJ, Ring MA, Sim P, Stanwix S, Foote SJ, Mackey DA. Baird PN, et al. Among authors: foote sj. Hum Genet. 2003 Feb;112(2):110-6. doi: 10.1007/s00439-002-0865-5. Epub 2002 Nov 21. Hum Genet. 2003. PMID: 12522550

4

Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus.

Perera D, Stankovich J, Butzkueven H, Taylor BV, Foote SJ, Kilpatrick TJ, Rubio JP. Perera D, et al. Among authors: foote sj. J Neuroimmunol. 2009 Jun 25;211(1-2):105-9. doi: 10.1016/j.jneuroim.2009.03.010. Epub 2009 Apr 17. J Neuroimmunol. 2009. PMID: 19375175

5

Anticipation in familial hematologic malignancies.

Tegg EM, Thomson RJ, Stankovich JM, Banks A, Marsden KA, Lowenthal RM, Foote SJ, Dickinson JL. Tegg EM, et al. Among authors: foote sj. Blood. 2011 Jan 27;117(4):1308-10. doi: 10.1182/blood-2010-07-296475. Epub 2010 Nov 29. Blood. 2011. PMID: 21115977 Free article.

6

A retrospective examination of mean relative telomere length in the Tasmanian Familial Hematological Malignancies Study.

Blackburn NB, Charlesworth JC, Marthick JR, Tegg EM, Marsden KA, Srikanth V, Blangero J, Lowenthal RM, Foote SJ, Dickinson JL. Blackburn NB, et al. Among authors: foote sj. Oncol Rep. 2015 Jan;33(1):25-32. doi: 10.3892/or.2014.3568. Epub 2014 Oct 24. Oncol Rep. 2015. PMID: 25351806 Free PMC article.

7

A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis.

Field J, Browning SR, Johnson LJ, Danoy P, Varney MD, Tait BD, Gandhi KS, Charlesworth JC, Heard RN; Australia and New Zealand Multiple Sclerosis Genetics Consortium; Stewart GJ, Kilpatrick TJ, Foote SJ, Bahlo M, Butzkueven H, Wiley J, Booth DR, Taylor BV, Brown MA, Rubio JP, Stankovich J. Field J, et al. Among authors: foote sj. PLoS One. 2010 Oct 26;5(10):e13454. doi: 10.1371/journal.pone.0013454. PLoS One. 2010. PMID: 21049023 Free PMC article.

8

Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes.

Tegg EM, Thomson RJ, Stankovich J, Banks A, Flowers C, McWhirter R, Panton J, Piaszczyk A, Bahlo M, Marsden KA, Lowenthal RM, Foote SJ, Dickinson JL. Tegg EM, et al. Among authors: foote sj. Br J Haematol. 2010 Aug;150(4):456-62. doi: 10.1111/j.1365-2141.2010.08267.x. Epub 2010 Jun 15. Br J Haematol. 2010. PMID: 20560968 Free article.

9

Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.

Bahlo M, Stankovich J, Speed TP, Rubio JP, Burfoot RK, Foote SJ. Bahlo M, et al. Among authors: foote sj. Hum Genet. 2006 Mar;119(1-2):38-50. doi: 10.1007/s00439-005-0114-9. Epub 2005 Dec 14. Hum Genet. 2006. PMID: 16362347

10

No maternally inherited diabetes and deafness mutations in a sample of 193 Tasmanian diabetics with glaucoma.

Symons RC, Turakulov R, Foote SJ, Craig JE, McCartney PJ, Mackey DA. Symons RC, et al. Among authors: foote sj. Ophthalmic Genet. 2007 Mar;28(1):39-41. doi: 10.1080/13816810701201971. Ophthalmic Genet. 2007. PMID: 17454746 No abstract available.

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