Williams GA - Search Results

1

Replication of the recessive STBMS1 locus but with dominant inheritance.

Rice A, Nsengimana J, Simmons IG, Toomes C, Hoole J, Willoughby CE, Cassidy F, Williams GA, George ND, Sheridan E, Young TL, Hunter TI, Barrett BT, Elliott DB, Bishop DT, Inglehearn CF. Rice A, et al. Among authors: williams ga. Invest Ophthalmol Vis Sci. 2009 Jul;50(7):3210-7. doi: 10.1167/iovs.07-1631. Epub 2009 Feb 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19218600

2

Macular dystrophy associated with the Arg172Trp substitution in peripherin/RDS: genotype-phenotype correlation.

Anand S, Sheridan E, Cassidy F, Inglehearn C, Williams G, Springell K, Allgar V, Kelly TL, McKibbin M. Anand S, et al. Retina. 2009 May;29(5):682-8. doi: 10.1097/IAE.0b013e318198dbed. Retina. 2009. PMID: 19262438

3

CFH, VEGF and HTRA1 promoter genotype may influence the response to intravitreal ranibizumab therapy for neovascular age-related macular degeneration.

McKibbin M, Ali M, Bansal S, Baxter PD, West K, Williams G, Cassidy F, Inglehearn CF. McKibbin M, et al. Br J Ophthalmol. 2012 Feb;96(2):208-12. doi: 10.1136/bjo.2010.193680. Epub 2011 May 10. Br J Ophthalmol. 2012. PMID: 21558292

4

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.

Ali M, Buentello-Volante B, McKibbin M, Rocha-Medina JA, Fernandez-Fuentes N, Koga-Nakamura W, Ashiq A, Khan K, Booth AP, Williams G, Raashid Y, Jafri H, Rice A, Inglehearn CF, Zenteno JC. Ali M, et al. Mol Vis. 2010 Jun 23;16:1162-8. Mol Vis. 2010. PMID: 20664696 Free PMC article.

5

Evidence for a role of HLA DRB1 alleles in the control of IgE levels, strengthened by interacting TCR A/D marker alleles.

Mansur AH, Williams GA, Bishop DT, Markham AF, Lewis S, Britton J, Morrison JF. Mansur AH, et al. Among authors: williams ga. Clin Exp Allergy. 2000 Oct;30(10):1371-8. doi: 10.1046/j.1365-2222.2000.00944.x. Clin Exp Allergy. 2000. PMID: 10998012

6

Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis.

Ramprasad VL, Soumittra N, Nancarrow D, Sen P, McKibbin M, Williams GA, Arokiasamy T, Lakshmipathy P, Inglehearn CF, Kumaramanickavel G. Ramprasad VL, et al. Among authors: williams ga. Mol Vis. 2008 Mar 10;14:481-6. Mol Vis. 2008. PMID: 18334959 Free PMC article.

7

Association between - 308 tumour necrosis factor promoter polymorphism and bronchial hyperreactivity in asthma.

Li Kam Wa TC, Mansur AH, Britton J, Williams G, Pavord I, Richards K, Campbell DA, Morton N, Holgate ST, Morrison JF. Li Kam Wa TC, et al. Clin Exp Allergy. 1999 Sep;29(9):1204-8. doi: 10.1046/j.1365-2222.1999.00638.x. Clin Exp Allergy. 1999. PMID: 10469028

8

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.

den Hollander AI, Koenekoop RK, Mohamed MD, Arts HH, Boldt K, Towns KV, Sedmak T, Beer M, Nagel-Wolfrum K, McKibbin M, Dharmaraj S, Lopez I, Ivings L, Williams GA, Springell K, Woods CG, Jafri H, Rashid Y, Strom TM, van der Zwaag B, Gosens I, Kersten FF, van Wijk E, Veltman JA, Zonneveld MN, van Beersum SE, Maumenee IH, Wolfrum U, Cheetham ME, Ueffing M, Cremers FP, Inglehearn CF, Roepman R. den Hollander AI, et al. Among authors: williams ga. Nat Genet. 2007 Jul;39(7):889-95. doi: 10.1038/ng2066. Epub 2007 Jun 3. Nat Genet. 2007. PMID: 17546029

9

Platelet activation during hand vibration.

Kent PJ, Williams GA, Kester RC. Kent PJ, et al. Among authors: williams ga. Br J Surg. 1994 Jun;81(6):815-8. doi: 10.1002/bjs.1800810608. Br J Surg. 1994. PMID: 8044590

10

Chromosome-level genome assembly of the common chiton, Liolophura japonica (Lischke, 1873).

Hong Kong Biodiversity Genomics Consortium. Hong Kong Biodiversity Genomics Consortium. GigaByte. 2024 Apr 25;2024:gigabyte123. doi: 10.46471/gigabyte.123. eCollection 2024. GigaByte. 2024. PMID: 38707631 Free PMC article.

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