Hall G - Search Results

1

A paradigm shift in the delivery of services for diagnosis of inherited retinal disease.

O'Sullivan J, Mullaney BG, Bhaskar SS, Dickerson JE, Hall G, O'Grady A, Webster A, Ramsden SC, Black GC. O'Sullivan J, et al. Among authors: hall g. J Med Genet. 2012 May;49(5):322-6. doi: 10.1136/jmedgenet-2012-100847. J Med Genet. 2012. PMID: 22581970

2

Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study.

Dev Borman A, Ocaka LA, Mackay DS, Ripamonti C, Henderson RH, Moradi P, Hall G, Black GC, Robson AG, Holder GE, Webster AR, Fitzke F, Stockman A, Moore AT. Dev Borman A, et al. Among authors: hall g. Invest Ophthalmol Vis Sci. 2012 Jun 22;53(7):3927-38. doi: 10.1167/iovs.12-9548. Invest Ophthalmol Vis Sci. 2012. PMID: 22570351

3

Understanding the impact of genetic testing for inherited retinal dystrophy.

Combs R, McAllister M, Payne K, Lowndes J, Devery S, Webster AR, Downes SM, Moore AT, Ramsden S, Black G, Hall G. Combs R, et al. Among authors: hall g. Eur J Hum Genet. 2013 Nov;21(11):1209-13. doi: 10.1038/ejhg.2013.19. Epub 2013 Feb 13. Eur J Hum Genet. 2013. PMID: 23403902 Free PMC article.

4

Understanding the expectations of patients with inherited retinal dystrophies.

Combs R, Hall G, Payne K, Lowndes J, Devery S, Downes SM, Moore AT, Ramsden S, Black GC, McAllister M. Combs R, et al. Among authors: hall g. Br J Ophthalmol. 2013 Aug;97(8):1057-61. doi: 10.1136/bjophthalmol-2012-302911. Epub 2013 Jun 5. Br J Ophthalmol. 2013. PMID: 23740962

5

Valuing the benefits of genetic testing for retinitis pigmentosa: a pilot application of the contingent valuation method.

Eden M, Payne K, Combs RM, Hall G, McAllister M, Black GC. Eden M, et al. Among authors: hall g. Br J Ophthalmol. 2013 Aug;97(8):1051-6. doi: 10.1136/bjophthalmol-2012-303020. Epub 2013 Jun 6. Br J Ophthalmol. 2013. PMID: 23743435

6

A clinical molecular genetic service for United Kingdom families with choroideraemia.

Ramsden SC, O'Grady A, Fletcher T, O'Sullivan J, Hart-Holden N, Barton SJ, Hall G, Moore AT, Webster AR, Black GC. Ramsden SC, et al. Among authors: hall g. Eur J Med Genet. 2013 Aug;56(8):432-8. doi: 10.1016/j.ejmg.2013.06.003. Epub 2013 Jun 25. Eur J Med Genet. 2013. PMID: 23811034

7

Genetic testing for inherited ocular disease: delivering on the promise at last?

Gillespie RL, Hall G, Black GC. Gillespie RL, et al. Among authors: hall g. Clin Exp Ophthalmol. 2014 Jan-Feb;42(1):65-77. doi: 10.1111/ceo.12159. Epub 2013 Aug 21. Clin Exp Ophthalmol. 2014. PMID: 23845030 Review.

8

Patient expectations and attitudes towards specialist genetic eye services.

Clarke E, Combs R, Black G, Hall G. Clarke E, et al. Among authors: hall g. J Genet Couns. 2015 Apr;24(2):349-57. doi: 10.1007/s10897-014-9775-7. Epub 2014 Oct 3. J Genet Couns. 2015. PMID: 25273951

9

Variation in healthcare services for specialist genetic testing and implications for planning genetic services: the example of inherited retinal dystrophy in the English NHS.

Harrison M, Birch S, Eden M, Ramsden S, Farragher T, Payne K, Hall G, Black GC. Harrison M, et al. Among authors: hall g. J Community Genet. 2015 Apr;6(2):157-65. doi: 10.1007/s12687-014-0210-4. Epub 2015 Jan 9. J Community Genet. 2015. PMID: 25567483 Free PMC article.

10

Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with early macular involvement.

El-Asrag ME, Sergouniotis PI, McKibbin M, Plagnol V, Sheridan E, Waseem N, Abdelhamed Z, McKeefry D, Van Schil K, Poulter JA; UK Inherited Retinal Disease Consortium; Johnson CA, Carr IM, Leroy BP, De Baere E, Inglehearn CF, Webster AR, Toomes C, Ali M. El-Asrag ME, et al. Am J Hum Genet. 2015 Jun 4;96(6):948-54. doi: 10.1016/j.ajhg.2015.04.006. Epub 2015 May 14. Am J Hum Genet. 2015. PMID: 25983245 Free PMC article.

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