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Items where Author is "Martyn, M"

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Number of items: 6.

Article

Eratne, D, Schneider, A, Lynch, E, Martyn, M, Velakoulis, D, Fahey, M, Kwan, P, Leventer, R, Rafehi, H, Chong, B, Stark, Z, Lunke, S, Phelan, DG, O'Keefe, M, Siemering, K, West, K, Sexton, A, Jarmolowicz, A, Taylor, JA, Schultz, J, Purvis, R, Uebergang, E, Chalinor, H, Creighton, B, Gelfand, N, Saks, T, Prawer, Y, Smagarinsky, Y, Pan, T, Goranitis, I, Ademi, Z, Gaff, C, Huq, A, Walsh, M, James, PA, Krzesinski, EI, Wallis, M ORCID: 0000-0002-5441-1732, Stutterd, CA, Bahlo, M, Delatycki, MB and Berkovic, SF 2021 , 'The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective' , Journal of the Neurological Sciences, vol. 420 , doi: https://doi.org/10.1016/j.jns.2020.117260.

Eratne, D, Schneider, A, Lynch, E, Martyn, M, Velakoulis, D, Fahey, M, Kwan, P, Leventer, R, Rafehi, H, Chong, B, Stark, Z, Lunke, S, Phelan, DG, O'Keefe, M, Siemering, K, West, K, Sexton, A, Jarmolowicz, A, Taylor, JA, Schultz, J, Purvis, R, Uebergang, E, Chalinor, H, Creighton, B, Gelfand, N, Saks, T, Prawer, Y, Smagarinsky, Y, Pan, T, Goranitis, I, Ademi, Z, Gaff, C, Huq, A, Walsh, M, James, PA, Krzesinski, EI, Wallis, M ORCID: 0000-0002-5441-1732, Stutterd, CA, Bahlo, M, Delatycki, MB and Berkovic, SF 2021 , 'The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspective' , Journal of the Neurological Sciences, vol. 420 , doi: https://doi.org/10.1016/j.jns.2020.117260.

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.

Jayasinghe, K, Stark, Z, Patel, C, Mallawaarachchi, A, McCarthy, H, Faull, R, Chakera, A, Sundaram, M, Jose, M ORCID: 0000-0002-9589-0071, Kerr, P, Wu, Y, Wardrop, L, Goranitis, I, Best, S, Martyn, M, Quinlan, C and Mallett, AJ 2019 , 'Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol' , BMJ Open , pp. 1-8 , doi: https://doi.org/10.1136/bmjopen-2019-029541.

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.

This list was generated on Thu Jun 1 01:43:51 2023 AEST.
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