Bellgard M - Search Results

1

Rare disease registries: a call to action.

Lacaze P, Millis N, Fookes M, Zurynski Y, Jaffe A, Bellgard M, Winship I, McNeil J, Bittles AH. Lacaze P, et al. Among authors: bellgard m. Intern Med J. 2017 Sep;47(9):1075-1079. doi: 10.1111/imj.13528. Intern Med J. 2017. PMID: 28891182

2

ThalInd, a β-thalassemia and hemoglobinopathies database for India: defining a model country-specific and disease-centric bioinformatics resource.

Sinha S, Black ML, Agarwal S, Das R, Bittles AH, Bellgard M. Sinha S, et al. Among authors: bellgard m. Hum Mutat. 2011 Aug;32(8):887-93. doi: 10.1002/humu.21510. Epub 2011 Jun 23. Hum Mutat. 2011. PMID: 21520336

3

A descriptive profile of β-thalassaemia mutations in India, Pakistan and Sri Lanka.

Black ML, Sinha S, Agarwal S, Colah R, Das R, Bellgard M, Bittles AH. Black ML, et al. Among authors: bellgard m. J Community Genet. 2010 Sep;1(3):149-57. doi: 10.1007/s12687-010-0026-9. Epub 2010 Oct 10. J Community Genet. 2010. PMID: 22460247 Free PMC article.

4

A modular approach to disease registry design: successful adoption of an internet-based rare disease registry.

Bellgard MI, Macgregor A, Janon F, Harvey A, O'Leary P, Hunter A, Dawkins H. Bellgard MI, et al. Hum Mutat. 2012 Oct;33(10):E2356-66. doi: 10.1002/humu.22154. Epub 2012 Jul 2. Hum Mutat. 2012. PMID: 22753342

5

Role of international registries in enhancing the care of familial hypercholesterolaemia.

Hammond E, Watts GF, Rubinstein Y, Farid W, Livingston M, Knowles JW, Lochmüller H, Bellgard M, Dawkins HJ. Hammond E, et al. Among authors: bellgard m. Int J Evid Based Healthc. 2013 Jun;11(2):134-9. doi: 10.1111/1744-1609.12023. Int J Evid Based Healthc. 2013. PMID: 23750577 Free article.

6

Design of a framework for the deployment of collaborative independent rare disease-centric registries: Gaucher disease registry model.

Bellgard MI, Napier KR, Bittles AH, Szer J, Fletcher S, Zeps N, Hunter AA, Goldblatt J. Bellgard MI, et al. Blood Cells Mol Dis. 2018 Feb;68:232-238. doi: 10.1016/j.bcmd.2017.01.013. Epub 2017 Jan 27. Blood Cells Mol Dis. 2018. PMID: 28190666 Free PMC article.

7

The role of patient registries for rare genetic lipid disorders.

Ng DM, Hooper AJ, Bellgard MI, Burnett JR. Ng DM, et al. Among authors: bellgard mi. Curr Opin Lipidol. 2018 Apr;29(2):156-162. doi: 10.1097/MOL.0000000000000485. Curr Opin Lipidol. 2018. PMID: 29351106 Review.

8

RD-RAP: beyond rare disease patient registries, devising a comprehensive data and analytic framework.

Bellgard MI, Snelling T, McGree JM. Bellgard MI, et al. Orphanet J Rare Dis. 2019 Jul 12;14(1):176. doi: 10.1186/s13023-019-1139-9. Orphanet J Rare Dis. 2019. PMID: 31300021 Free PMC article.

9

Design, development and deployment of a web-based patient registry for rare genetic lipid disorders.

Napier KR, Hooper AJ, Ng DM, Render L, Bell DA, Pang J, Watts GF, Bellgard MI, Burnett JR. Napier KR, et al. Among authors: bellgard mi. Pathology. 2020 Jun;52(4):447-452. doi: 10.1016/j.pathol.2020.02.002. Epub 2020 Apr 7. Pathology. 2020. PMID: 32276786

10

Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes.

Sinha S, Black ML, Agarwal S, Colah R, Das R, Ryan K, Bellgard M, Bittles AH. Sinha S, et al. Among authors: bellgard m. Hugo J. 2009 Dec;3(1-4):51-62. doi: 10.1007/s11568-010-9132-3. Epub 2010 Feb 10. Hugo J. 2009. PMID: 21119755 Free PMC article.

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