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Items where Author is "Lunke, S"
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Number of items: 5.
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.
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.
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.
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.
Sachdev, R, Field, M, Baynam, GS, Beilby, J, Berarducci, M, Berman, Y, Boughtwood, T, Cusack, MB, Fitzgerald, V, Fletcher, J, Freckmann, ML, Grainger, N, Kirk, E, Lundie, B, Lunke, S, McGregor, L, Mowat, D, Parasivam, G, Tyrell, V, Wallis, M ORCID: 0000-0002-5441-1732, White, SM and S L Ma, A 2021
, 'Paediatric genomic testing: Navigating medicare rebatable genomic testing'
, Journal of Paediatrics and Child Health, vol. 57, no. 4
, pp. 477-483
, doi: https://doi.org/10.1111/jpc.15382.
ORCID: 0000-0002-5441-1732, White, SM and S L Ma, A 2021
, 'Paediatric genomic testing: Navigating medicare rebatable genomic testing'
, Journal of Paediatrics and Child Health, vol. 57, no. 4
, pp. 477-483
, doi: https://doi.org/10.1111/jpc.15382.