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Results: 11

1.

Susceptibility to Invasive Meningococcal Disease: Polymorphism of Complement System Genes and Neisseria meningitidis Factor H Binding Protein.

Bradley DT, Bourke TW, Fairley DJ, Borrow R, Shields MD, Zipfel PF, Hughes AE.

PLoS One. 2015 Mar 23;10(3):e0120757. doi: 10.1371/journal.pone.0120757. eCollection 2015.

2.

The effectiveness of disaster risk communication: a systematic review of intervention studies.

Bradley DT, McFarland M, Clarke M.

PLoS Curr. 2014 Aug 22;6. pii: ecurrents.dis.349062e0db1048bb9fc3a3fa67d8a4f8. doi: 10.1371/currents.dis.349062e0db1048bb9fc3a3fa67d8a4f8.

3.

Public health risk communication by text message in response to a cluster of invasive meningococcal infection in a primary school.

Bradley DT, Johnston J, Smyth B.

PLoS Curr. 2014 May;6. pii: ecurrents.outbreaks.ba688e481f19515a472d3adfdb5143f8. doi: 10.1371/currents.outbreaks.ba688e481f19515a472d3adfdb5143f8.

4.

A variant in LDLR is associated with abdominal aortic aneurysm.

Bradley DT, Hughes AE, Badger SA, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, Grétarsdóttir S, Burnand K, Child AH, Clough RE, Cockerill G, Hafez H, Scott DJ, Ariëns RA, Johnson A, Sohrabi S, Smith A, Thompson MM, van Bockxmeer FM, Waltham M, Matthíasson SE, Thorleifsson G, Thorsteinsdottir U, Blankensteijn JD, Teijink JA, Wijmenga C, de Graaf J, Kiemeney LA, Wild JB, Edkins S, Gwilliam R, Hunt SE, Potter S, Lindholt JS, Golledge J, Norman PE, van Rij A, Powell JT, Eriksson P, Stefánsson K, Thompson JR, Humphries SE, Sayers RD, Deloukas P, Samani NJ, Bown MJ.

Circ Cardiovasc Genet. 2013 Oct;6(5):498-504. doi: 10.1161/CIRCGENETICS.113.000165. Epub 2013 Sep 17.

5.

Re: "The association between complement component 2/complement factor B polymorphisms and age-related macular degeneration: a HuGE review and meta-analysis".

Hughes AE, Bradley DT.

Am J Epidemiol. 2013 May 1;177(9):1022-4. doi: 10.1093/aje/kwt067. Epub 2013 Apr 9. No abstract available.

6.

A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.

Meng W, Butterworth J, Bradley DT, Hughes AE, Soler V, Calvas P, Malecaze F.

Invest Ophthalmol Vis Sci. 2012 Dec 5;53(13):7983-8. doi: 10.1167/iovs.12-10409.

7.

A novel GUCY2D mutation, V933A, causes central areolar choroidal dystrophy.

Hughes AE, Meng W, Lotery AJ, Bradley DT.

Invest Ophthalmol Vis Sci. 2012 Jul 12;53(8):4748-53. doi: 10.1167/iovs.12-10061.

8.

Macular degeneration genetics.

Bradley DT, Meng W, Hughes AE.

Ophthalmology. 2012 Jun;119(6):1287-8.e1; author reply 1288. doi: 10.1016/j.ophtha.2012.02.042. No abstract available.

PMID:
22656900
9.

Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.

Bown MJ, Jones GT, Harrison SC, Wright BJ, Bumpstead S, Baas AF, Gretarsdottir S, Badger SA, Bradley DT, Burnand K, Child AH, Clough RE, Cockerill G, Hafez H, Scott DJ, Futers S, Johnson A, Sohrabi S, Smith A, Thompson MM, van Bockxmeer FM, Waltham M, Matthiasson SE, Thorleifsson G, Thorsteinsdottir U, Blankensteijn JD, Teijink JA, Wijmenga C, de Graaf J, Kiemeney LA, Assimes TL, McPherson R; CARDIoGRAM Consortium; Global BPgen Consortium; DIAGRAM Consortium; VRCNZ Consortium, Folkersen L, Franco-Cereceda A, Palmen J, Smith AJ, Sylvius N, Wild JB, Refstrup M, Edkins S, Gwilliam R, Hunt SE, Potter S, Lindholt JS, Frikke-Schmidt R, Tybjærg-Hansen A, Hughes AE, Golledge J, Norman PE, van Rij A, Powell JT, Eriksson P, Stefansson K, Thompson JR, Humphries SE, Sayers RD, Deloukas P, Samani NJ.

Am J Hum Genet. 2011 Nov 11;89(5):619-27. doi: 10.1016/j.ajhg.2011.10.002. Epub 2011 Nov 4.

10.

Mutation altering the miR-184 seed region causes familial keratoconus with cataract.

Hughes AE, Bradley DT, Campbell M, Lechner J, Dash DP, Simpson DA, Willoughby CE.

Am J Hum Genet. 2011 Nov 11;89(5):628-33. doi: 10.1016/j.ajhg.2011.09.014. Epub 2011 Oct 11.

11.
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