Declan Bradley

Jones, G. T., Tromp, G., Kuivaniemi, H., Gretarsdottir, S., Baas, A. F., Giusti, B., Strauss, E., van 't Hof, F. N., Webb, T., Erdman, R., Ritchie, M. D., Elmore, J. R., Verma, A., Pendergrass, S., Kullo, I. J., Ye, Z., Peissig, P. L., Gottesman, O., Verma, S. S., Malinowski, J. & 97 others, Rasmussen-Torvik, L. J., Borthwick, K., Smelser, D. T., Crosslin, D. R., de Andrade, M., Ryer, E. J., McCarty, C. A., Bottinger, E. P., Pacheco, J. A., Crawford, D. C., Carrell, D. S., Gerhard, G. S., Franklin, D. P., Carey, D. J., Phillips, V. L., Williams, M. J., Wei, W., Blair, R., Hill, A. A., Vasudevan, T. M., Lewis, D. R., Thomson, I. A., Krysa, J., Hill, G. B., Roake, J., Merriman, T. R., Oszkinis, G., Galora, S., Saracini, C., Abbate, R., Pulli, R., Pratesi, C., Saratzis, A., Verissimo, A., Bumpstead, S. J., Badger, S. A., Clough, R. E., Cockerill, G. W., Hafez, H., Scott, D. J., Futers, T. S., Romaine, S. P., Bridge, K., Griffin, K. J., Bailey, M. A., Smith, A., Thompson, M. M., van Bockxmeer, F., Matthiasson, S. E., Thorleifsson, G., Thorsteinsdottir, U., Blankensteijn, J. D., Teijink, J. A., Wijmenga, C., de Graaf, J., Kiemeney, L. A., Lindholt, J. S., Hughes, A. E., Bradley, D. T., Stirrups, K., Golledge, J., Norman, P. E., Powell, J. T., Humphries, S. E., Hamby, S. E., Goodall, A. H., Nelson, C. P., Sakalihasan, N., Courtois, A., Ferrell, R. E., Eriksson, P., Folkersen, L., Franco-Cereceda, A., Eicher, J. D., Johnson, A. D., Betsholtz, C., Ruusalepp, A., Franzén, O., Schadt, E., Björkegren, J. L., Lipovich, L., Drolet, A. M., Verhoeven, E., Zeebregts, C. J., Geelkerken, R. H., van Sambeek, M. R., van Sterkenburg, S. M., de Vries, J-P. P., Stefansson, K., Thompson, J. R., de Bakker, P. I., Deloukas, P., Sayers, R. D., Harrison, S., van Rij, A. M., Samani, N. J. & Bown, M. J., 29 Nov 2016, In : Circulation Research.

Research output: Contribution to journal › Article

Open Access

File

51 Citations (Scopus)

461 Downloads (Pure)

Rare CFH mutations and early-onset age-related macular degeneration

Hughes, A. E., Meng, W., Bridgett, S. & Bradley, D. T., 20 Apr 2016, In : Acta Ophthalmologica. 94, 3, p. e247-e248 2 p.

Research output: Contribution to journal › Letter

7 Citations (Scopus)

Sequence and expression of complement factor H gene cluster variants and their roles in age-related macular degeneration risk

Hughes, A. E., Bridgett, S., Meng, W., Li, M., Curcio, C. A., Stambolian, D. & Bradley, D. T., 01 May 2016, In : Investigative Ophthalmology and Visual Science. 57, 6, p. 2763-2769

Research output: Contribution to journal › Article

Open Access

File

5 Citations (Scopus)

228 Downloads (Pure)

The £ for lb. Challenge: Factors influencing effectiveness of a workplace lifestyle weight management programme

Bradley, D., McComb, A. & Owen, T., 27 Apr 2016.

Research output: Contribution to conference › Poster

The £ for lb challenge – a lose – win – win scenario. Results from a novel workplace-based, peer-led weight management programme

Bennett, D., Bradley, D., McComb, A., Kiernan, A. & Owen, T., 11 Oct 2016.

Research output: Contribution to conference › Abstract

The Effectiveness of Disaster Risk Communication: A Systematic Review of Intervention Studies

Bradley, D., McFarland, M. & Clarke, M., 2016, Effective Communication During Disasters: Making Use of Technology, Media, and Human Resources. Kapur, G., Bezek, S. & Dyal, J. (eds.). Apple Academic Press

Research output: Chapter in Book/Report/Conference proceeding › Chapter

2015

Reasons for non-participation in the Northern Ireland Bowel Cancer Screening Programme: a qualitative study

Bradley, D. T., Treanor, C., McMullan, C., Owen, T., Graham, A. & Anderson, D., 09 Sep 2015, In : BMJ Open. 5, 9, 6 p., e008266.

Research output: Contribution to journal › Article

Open Access

File

12 Citations (Scopus)

513 Downloads (Pure)

Reasons for non-participation in the Northern Ireland Bowel Cancer Screening Programme: a qualitative study

Bradley, D., 10 May 2015.

Research output: Contribution to conference › Abstract

Report of the World Health Organization flash literature review: Guidance on emergency risk communications

Allen, C., Arbuthnott, K., Bhaumik, S., Bosch-Capblanch, X., Bradley, D., Clarke, M., Eyers, J., Gupta, S., Head, K., Hill, S., Lang, S., Lewin, S., Nevitte, A., Nunn, J., Robertshaw, L. & Santos, J., 12 Jun 2015, Evidence Aid.

Research output: Book/Report › Commissioned report

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

Bradley, D. T., Bourke, T. W., Fairley, D. J., Borrow, R., Shields, M. D., Zipfel, P. F. & Hughes, A. E., 23 Mar 2015, In : PloS one. 10, 3, 12 p., e0120757.

Research output: Contribution to journal › Article

Open Access

File

10 Citations (Scopus)

200 Downloads (Pure)

2014

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

Bradley, D. T., Johnston, J. & Smyth, B., May 2014, In : PLoS Currents: Outbreaks. 6, 5 p.

Research output: Contribution to journal › Article

Open Access

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

Bradley, D. T., McFarland, M. & Clarke, M., 22 Aug 2014, In : PLoS Currents: Outbreaks. 6, 25 p.

Research output: Contribution to journal › Article

Open Access

Variation in Complement Factor H, Complement Receptor 1 and Closely Related Genes

Hughes, A., Bridgett, S., Meng, W. & Bradley, D., 2014.

Research output: Contribution to conference › Poster

2013

Abdominal Aortic Aneurysm Genomics: Systematic Review, Meta-analysis and Analysis of Research Trends

Bradley, D., Badger, S. A., Campbell, M., Lau, L. & Hughes, A., May 2013.

Research output: Contribution to conference › Poster

A Variant in LDLR is Associated with Abdominal Aortic Aneurysm

Bradley, D. T., Hughes, A. E., Badger, S. A., Jones, G. T., Harrison, S. C., Wright, B. J., Bumpstead, S., Baas, A. F., Gretarsdottir, S., Burnand, K., Child, A. H., Clough, R. E., Cockerill, G., Hafez, H., Scott, D. J. A., Ariëns, R. A. S., Johnson, A., Sohrabi, S., Smith, A., Thompson, M. M. & 28 others, van Bockxmeer, F. M., Waltham, M., Matthiasson, S. E., Thorleifsson, G., Thorsteinsdottir, U., Blankensteijn, J. D., Teijink, J. A. W., Wijmenga, C., de Graaf, J., Kiemeney, L. A., Wild, J. B., Edkins, S., Gwilliam, R., Hunt, S. E., Potter, S., Lindholt, J. S., Golledge, J., Norman, P. E., van Rij, A., Powell, J. T., Eriksson, P., Stefansson, K., Thompson, J. R., Humphries, S. E., Sayers, R. D., Deloukas, P., Samani, N. J. & Bown, M. J., 15 Oct 2013, In : Circulation. Cardiovascular genetics. 6, 5, p. 498-504 7 p.

Research output: Contribution to journal › Article

45 Citations (Scopus)

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

Hughes, A. E. & Bradley, D. T., 01 May 2013, In : American Journal of Epidemiology. 177, 9, p. 1022-4 3 p.

Research output: Contribution to journal › Letter

2 Citations (Scopus)

2012

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, D. T., Hughes, A. E., Soler, V., Calvas, P. & Malecaze, F., Dec 2012, In : Investigative Ophthalmology and Visual Science. 53, p. 7983-7988 6 p.

Research output: Contribution to journal › Article

34 Citations (Scopus)

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

Hughes, A., Meng, W., Lotery, A. J. & Bradley, D. T., Jul 2012, In : Investigative Ophthalmology and Visual Science. 53, 8, p. 4748-4753 6 p.

Research output: Contribution to journal › Article

9 Citations (Scopus)

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

Hughes, A., Meng, W., Lotery, A. J. & Bradley, D., Nov 2012.

Research output: Contribution to conference › Poster

9 Citations (Scopus)

Macular degeneration genetics

Bradley, D. T., Meng, W. & Hughes, A. E., Jun 2012, In : Ophthalmology. 119, 6, p. 1287-1288 2 p.

Research output: Contribution to journal › Letter

1 Citation (Scopus)

PHYLOGENETIC ANALYSIS OF THE Y CHROMOSOME IN ABDOMINAL AORTIC ANEURYSMS: A META-ANALYSIS OF THREE BRITISH COHORTS.

Bloomer, L. DS., Denniff, M., Christofidou, P., Debiec, R., Scott, D. J. A., Sohrabi, S., Johnson, A., Hughes, A., Bradley, D., Badger, S., Charchar, F., Thompson, J., Sayers, R., Samani, N. J., Bown, M. & Tomaszewski, M., Sep 2012.

Research output: Contribution to conference › Poster

PHYLOGENETIC ANALYSIS OF THE Y CHROMOSOME IN ABDOMINAL AORTIC ANEURYSMS: A META-ANALYSIS OF THREE BRITISH COHORTS.

Bloomer, L. DS., Denniff, M., Christofidou, P., Debiec, R., Scott, D. J. A., Sohrabi, S., Johnson, A., Hughes, A., Bradley, D., Badger, S., Charchar, F., Thompson, J., Sayers, R. D., Samani, N. J., Bown, M. J. & Tomaszewski, M., 2012, p. e37.

Research output: Contribution to conference › Poster

PHYLOGENETIC ANALYSIS OF THE Y CHROMOSOME IN ABDOMINAL AORTIC ANEURYSMS: A META-ANALYSIS OF THREE BRITISH COHORTS.

Bloomer, L. DS., Denniff, M., Christofidou, P., Debiec, R., Scott, D. J. A., Sohrabi, S., Johnson, A., Hughes, A., Bradley, D., Badger, S. A., Charchar, F., Thompson, J., Sayers, R. D., Samani, N. J., Bown, M. & Tomaszewski, M., 2012, In : Journal of Hypertension. 30, p. e37

Research output: Contribution to journal › Meeting abstract

Response to Iliff et al

Hughes, A. E., Bradley, D. T., Campbell, M., Simpson, D. A. & Willoughby, C. E., 04 May 2012, In : The American Journal of Human Genetics. 90, 5, p. 934-935 2 p.

Research output: Contribution to journal › Letter

1 Citation (Scopus)

2011

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

Bown, M., Jones, G. T., Harrison, S. C., Wright, B. J., Bumpstead, S., Bass, A. F., Gretarsdottir, S., Badger, S., Bradley, D., Burnand, K., Child, A. H., Clough, R. E., Cockerill, G., Hafez, H., Scott, D. J. A., Futers, S., Johnston, A., Sohrabi, S., Smith, A., Thompson, M. M. & 38 others, van Bockxmeer, F. M., Waltman, M., Matthiasson, S. E., Thorleifsson, G., Thorsteinsdottir, U., Blankensteijn, J. D., Teijink, J. A. W., Wijmenga, C., de Graff, J., Kiemeney, L. A., Assimes, T. L., McPherson, R., Folkersen, L., Franco-Cereceda, A., Palmen, J., Smith, A. J., Sylvius, N., Wild, J. B., Refstrup, M., Edkins, S., Gwilliam, R., Hunt, S. E., Potter, S., Lindholt, J. S., Frikke-Schmidt, R., Tybjaerg-Hensen, A., Hughes, A., Golledge, J., Norman, P. E., van Rij, A., Powel, J. T., Eriksson, P., Stefansson, K., Thompson, J. R., Humphries, S. E., Sayers, R. D., Deloukas, P. & Samani, N. J., 11 Nov 2011, In : The American Journal of Human Genetics. 89, 5, p. 619-627 9 p.

Research output: Contribution to journal › Article