Sham PC - Search Results

1

Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth Cohort.

Hysi PG, Simpson CL, Fok YK, Gerrelli D, Webster AR, Bhattacharya SS, Hammond CJ, Sham PC, Rahi JS. Hysi PG, et al. Among authors: sham pc. Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):440-7. doi: 10.1167/iovs.10-5640. Invest Ophthalmol Vis Sci. 2012. PMID: 22110064

2

MaGIC: a program to generate targeted marker sets for genome-wide association studies.

Simpson CL, Hansen VK, Sham PC, Collins A, Powell JF, Al-Chalabi A. Simpson CL, et al. Among authors: sham pc. Biotechniques. 2004 Dec;37(6):996-9. doi: 10.2144/04376BIN03. Biotechniques. 2004. PMID: 15597550 Free article.

3

A central resource for accurate allele frequency estimation from pooled DNA genotyped on DNA microarrays.

Simpson CL, Knight J, Butcher LM, Hansen VK, Meaburn E, Schalkwyk LC, Craig IW, Powell JF, Sham PC, Al-Chalabi A. Simpson CL, et al. Among authors: sham pc. Nucleic Acids Res. 2005 Feb 8;33(3):e25. doi: 10.1093/nar/gni028. Nucleic Acids Res. 2005. PMID: 15701753 Free PMC article.

4

The Roles of PAX6 and SOX2 in Myopia: lessons from the 1958 British Birth Cohort.

Simpson CL, Hysi P, Bhattacharya SS, Hammond CJ, Webster A, Peckham CS, Sham PC, Rahi JS. Simpson CL, et al. Among authors: sham pc. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4421-5. doi: 10.1167/iovs.07-0231. Invest Ophthalmol Vis Sci. 2007. PMID: 17898260

5

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.

Simpson CL, Lemmens R, Miskiewicz K, Broom WJ, Hansen VK, van Vught PW, Landers JE, Sapp P, Van Den Bosch L, Knight J, Neale BM, Turner MR, Veldink JH, Ophoff RA, Tripathi VB, Beleza A, Shah MN, Proitsi P, Van Hoecke A, Carmeliet P, Horvitz HR, Leigh PN, Shaw CE, van den Berg LH, Sham PC, Powell JF, Verstreken P, Brown RH Jr, Robberecht W, Al-Chalabi A. Simpson CL, et al. Among authors: sham pc. Hum Mol Genet. 2009 Feb 1;18(3):472-81. doi: 10.1093/hmg/ddn375. Epub 2008 Nov 7. Hum Mol Genet. 2009. PMID: 18996918 Free PMC article.

6

Major genetic effects in glaucoma: commingling analysis of optic disc parameters in an older Australian population.

van Koolwijk LM, Healey PR, Hitchings RA, Mitchell P, Sham PC, McGuffin P, Viswanathan AC. van Koolwijk LM, et al. Among authors: sham pc. Invest Ophthalmol Vis Sci. 2009 Nov;50(11):5275-80. doi: 10.1167/iovs.08-3065. Epub 2009 May 20. Invest Ophthalmol Vis Sci. 2009. PMID: 19458335

7

Commingling analyses of central corneal thickness and adjusted intraocular pressure in an older Australian population.

Rahman ML, Bunce C, Healey PR, Mitchell P, Sham PC, McGuffin P, Viswanathan AC. Rahman ML, et al. Among authors: sham pc. Invest Ophthalmol Vis Sci. 2010 May;51(5):2512-8. doi: 10.1167/iovs.09-4270. Epub 2010 Jan 13. Invest Ophthalmol Vis Sci. 2010. PMID: 20071671

8

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

Hysi PG, Young TL, Mackey DA, Andrew T, Fernández-Medarde A, Solouki AM, Hewitt AW, Macgregor S, Vingerling JR, Li YJ, Ikram MK, Fai LY, Sham PC, Manyes L, Porteros A, Lopes MC, Carbonaro F, Fahy SJ, Martin NG, van Duijn CM, Spector TD, Rahi JS, Santos E, Klaver CC, Hammond CJ. Hysi PG, et al. Among authors: sham pc. Nat Genet. 2010 Oct;42(10):902-5. doi: 10.1038/ng.664. Epub 2010 Sep 12. Nat Genet. 2010. PMID: 20835236 Free PMC article.

9

The future of association studies: gene-based analysis and replication.

Neale BM, Sham PC. Neale BM, et al. Among authors: sham pc. Am J Hum Genet. 2004 Sep;75(3):353-62. doi: 10.1086/423901. Epub 2004 Jul 22. Am J Hum Genet. 2004. PMID: 15272419 Free PMC article.

10

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population.

Li T, Ma X, Sham PC, Sun X, Hu X, Wang Q, Meng H, Deng W, Liu X, Murray RM, Collier DA. Li T, et al. Among authors: sham pc. Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):13-5. doi: 10.1002/ajmg.b.30049. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15274030

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