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Items where Author is "Trainer, A"
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Number of items: 4.
Article
Benn, DE, Zhu, Y, Andrews, KA, Wilding, M, Duncan, EL, Dwight, T, Tothill, RW, Burgess, JR 
ORCID: 0000-0003-4748-9571, Crook, A, Gill, AJ, Hicks, RJ, Kim, Edward, Luxford, C, Marfan, H, Richardson, L, Robinson, B, Schlosberg, A, Susman, R, Tacon, L, Trainer, A, Tucker, K, Maher, ER, Field, M and Clifton-Bligh, RJ 2018
, 'Bayesian approach to determining penetrance of pathogenic SDH variants'
, Cancer Genetics
, pp. 1-6
, doi: https://doi.org/10.1136/jmedgenet-2018-105427.
ORCID: 0000-0003-4748-9571, Crook, A, Gill, AJ, Hicks, RJ, Kim, Edward, Luxford, C, Marfan, H, Richardson, L, Robinson, B, Schlosberg, A, Susman, R, Tacon, L, Trainer, A, Tucker, K, Maher, ER, Field, M and Clifton-Bligh, RJ 2018
, 'Bayesian approach to determining penetrance of pathogenic SDH variants'
, Cancer Genetics
, pp. 1-6
, doi: https://doi.org/10.1136/jmedgenet-2018-105427.
Jayasinghe, K, Stark, Z, Kerr, PG, Gaff, C, Martyn, M, Whitlam, J, Creighton, B, Donaldson, E, Hunter, M, Jarmolowicz, A, Johnstone, L, Krzesinski, E, Lunke, S, Lynch, E, Nicholls, K, Patel, C, Prawer, Y, Ryan, J, See, EJ, Talbot, A, Trainer, A, Tytherleigh, R, Valente, G, Wallis, M, Wardrop, L, West, KH, White, SM, Wilkins, E, Mallett, AJ and Quinlan, C 2020
, 'Clinical impact of genomic testing in patients with suspected monogenic kidney disease'
, Genetics in Medicine
, pp. 1-9
, doi: https://doi.org/10.1038/s41436-020-00963-4.
Jayasinghe, K, Stark, Z, Kerr, PG, Gaff, C, Martyn, M, Whitlam, J, Creighton, B, Donaldson, E, Hunter, M, Jarmolowicz, A, Johnstone, L, Krzesinski, E, Lunke, S, Lynch, E, Nicholls, K, Patel, C, Prawer, Y, Ryan, J, See, EJ, Talbot, A, Trainer, A, Tytherleigh, R, Valente, G, Wallis, M ORCID: 0000-0002-5441-1732, Wardrop, L, West, KH, White, SM, Wilkins, E, Mallett, AJ and Quinlan, C 2021
, 'Clinical impact of genomic testing in patients with suspected monogenic kidney disease'
, Genetics in Medicine, vol. 23, no. 1
, pp. 183-191
, doi: https://doi.org/10.1038/s41436-020-00963-4.
ORCID: 0000-0002-5441-1732, Wardrop, L, West, KH, White, SM, Wilkins, E, Mallett, AJ and Quinlan, C 2021
, 'Clinical impact of genomic testing in patients with suspected monogenic kidney disease'
, Genetics in Medicine, vol. 23, no. 1
, pp. 183-191
, doi: https://doi.org/10.1038/s41436-020-00963-4.
Ramchand, J, Wallis, M ORCID: 0000-0002-5441-1732, Macciocca, I, Lynch, E, Farouque, O, Martyn, M, Phelan, D, Chong, B, Lockwood, S, Weintraub, R, Thompson, Tina, Trainer, A, Zentner, D, Vohra, J, Chetrit, M, Hare, DL and James, P 2020
, 'Prospective evaluation of the utility of whole exome sequencing in dilated cardiomyopathy'
, American Heart Association. Journal. Cardiovascular and Cerebrovascular Disease, vol. 9, no. 2
, pp. 1-11
, doi: https://doi.org/10.1161/JAHA.119.013346.
ORCID: 0000-0002-5441-1732, Macciocca, I, Lynch, E, Farouque, O, Martyn, M, Phelan, D, Chong, B, Lockwood, S, Weintraub, R, Thompson, Tina, Trainer, A, Zentner, D, Vohra, J, Chetrit, M, Hare, DL and James, P 2020
, 'Prospective evaluation of the utility of whole exome sequencing in dilated cardiomyopathy'
, American Heart Association. Journal. Cardiovascular and Cerebrovascular Disease, vol. 9, no. 2
, pp. 1-11
, doi: https://doi.org/10.1161/JAHA.119.013346.