Watkins H - Search Results

1

"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.

Ormondroyd E, Mackley MP, Blair E, Craft J, Knight JC, Taylor JC, Taylor J, Watkins H. Ormondroyd E, et al. Among authors: watkins h. Genet Med. 2018 Mar;20(3):320-328. doi: 10.1038/gim.2017.157. Epub 2017 Oct 26. Genet Med. 2018. PMID: 29261176 Free PMC article.

2

Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.

Blair E, Redwood C, de Jesus Oliveira M, Moolman-Smook JC, Brink P, Corfield VA, Ostman-Smith I, Watkins H. Blair E, et al. Among authors: watkins h. Circ Res. 2002 Feb 22;90(3):263-9. doi: 10.1161/hh0302.104532. Circ Res. 2002. PMID: 11861413

3

Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.

Ashrafian H, Redwood C, Blair E, Watkins H. Ashrafian H, et al. Among authors: watkins h. Trends Genet. 2003 May;19(5):263-8. doi: 10.1016/S0168-9525(03)00081-7. Trends Genet. 2003. PMID: 12711218 Review.

4

Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy.

Crilley JG, Boehm EA, Blair E, Rajagopalan B, Blamire AM, Styles P, McKenna WJ, Ostman-Smith I, Clarke K, Watkins H. Crilley JG, et al. Among authors: watkins h. J Am Coll Cardiol. 2003 May 21;41(10):1776-82. doi: 10.1016/s0735-1097(02)03009-7. J Am Coll Cardiol. 2003. PMID: 12767664 Free article.

5

Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Blair E, Redwood C, Watkins H. Blair E, et al. Among authors: watkins h. Circulation. 2003 Jul 29;108(4):e24-5; author reply e24-5. doi: 10.1161/01.CIR.0000081440.49766.A6. Circulation. 2003. PMID: 12885737 No abstract available.

6

Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.

Oliveira SM, Ehtisham J, Redwood CS, Ostman-Smith I, Blair EM, Watkins H. Oliveira SM, et al. Among authors: watkins h. J Mol Cell Cardiol. 2003 Oct;35(10):1251-5. doi: 10.1016/s0022-2828(03)00237-2. J Mol Cell Cardiol. 2003. PMID: 14519435

7

Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype.

Ashrafian H, Watkins H. Ashrafian H, et al. Among authors: watkins h. J Am Coll Cardiol. 2007 Mar 27;49(12):1251-64. doi: 10.1016/j.jacc.2006.10.073. Epub 2007 Mar 9. J Am Coll Cardiol. 2007. PMID: 17394955 Free article. Review.

8

Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy.

Carballo S, Robinson P, Otway R, Fatkin D, Jongbloed JD, de Jonge N, Blair E, van Tintelen JP, Redwood C, Watkins H. Carballo S, et al. Among authors: watkins h. Circ Res. 2009 Aug 14;105(4):375-82. doi: 10.1161/CIRCRESAHA.109.196055. Epub 2009 Jul 9. Circ Res. 2009. PMID: 19590045

9

DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model.

Wordsworth S, Leal J, Blair E, Legood R, Thomson K, Seller A, Taylor J, Watkins H. Wordsworth S, et al. Among authors: watkins h. Eur Heart J. 2010 Apr;31(8):926-35. doi: 10.1093/eurheartj/ehq067. Epub 2010 Mar 18. Eur Heart J. 2010. PMID: 20299350 Review.

10

Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications.

Ormondroyd E, Oates S, Parker M, Blair E, Watkins H. Ormondroyd E, et al. Among authors: watkins h. Eur J Hum Genet. 2014 Jan;22(1):88-93. doi: 10.1038/ejhg.2013.81. Epub 2013 May 1. Eur J Hum Genet. 2014. PMID: 23632793 Free PMC article.

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