eCite Digital Repository

Author: Wallis, M (Dr Mathew Wallis)

Number of items: 10

Journal Article
Christensen, M and Wallis, M and Jessup, P and Lemelle, I and Jones, DL, Cryopyrin-associated periodic syndrome: a treatable genetic inflammatory condition, Practical Neurology ISSN 1474-7758 (2021) [Refereed Article] 
Sachdev, R and Field, M and Baynam, GS and Beilby, J and Berarducci, M and Berman, Y and Boughtwood, T and Cusack, MB and Fitzgerald, V and Fletcher, J and Freckmann, ML and Grainger, N and Kirk, E and Lundie, B and Lunke, S and McGregor, L and Mowat, D and Parasivam, G and Tyrell, V and Wallis, M and White, SM and S L Ma, A, Paediatric genomic testing: Navigating medicare rebatable genomic testing, Journal of Paediatrics and Child Health, 57, (4) pp. 477-483. ISSN 1034-4810 (2021) [Refereed Article]
Eratne, D and Schneider, A and Lynch, E and Martyn, M and Velakoulis, D and Fahey, M and Kwan, P and Leventer, R and Rafehi, H and Chong, B and Stark, Z and Lunke, S and Phelan, DG and O'Keefe, M and Siemering, K and West, K and Sexton, A and Jarmolowicz, A and Taylor, JA and Schultz, J and Purvis, R and Uebergang, E and Chalinor, H and Creighton, B and Gelfand, N and Saks, T and Prawer, Y and Smagarinsky, Y and Pan, T and Goranitis, I and Ademi, Z and Gaff, C and Huq, A and Walsh, M and James, PA and Krzesinski, EI and Wallis, M and Stutterd, CA and Bahlo, M and Delatycki, MB and Berkovic, SF, 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, 420 ISSN 0022-510X (2021) [Refereed Article] 
Jayasinghe, K and Stark, Z and Kerr, PG and Gaff, C and Martyn, M and Whitlam, J and Creighton, B and Donaldson, E and Hunter, M and Jarmolowicz, A and Johnstone, L and Krzesinski, E and Lunke, S and Lynch, E and Nicholls, K and Patel, C and Prawer, Y and Ryan, J and See, EJ and Talbot, A and Trainer, A and Tytherleigh, R and Valente, G and Wallis, M and Wardrop, L and West, KH and White, SM and Wilkins, E and Mallett, AJ and Quinlan, C, Clinical impact of genomic testing in patients with suspected monogenic kidney disease, Genetics in Medicine, 23, (1) pp. 183-191. ISSN 1098-3600 (2020) [Refereed Article]
Brailsford, G and Cash, E and Burke, J and Kirkland, G and Wallis, M and Mallett, A and Jose, MD, Genetic kidney disease in southern Tasmania, Kidney international reports, 5, (4) pp. 534-537. ISSN 2468-0249 (2020) [Refereed Article]
Palencia-Campos, A and Aoto, PC and Machal, EMF and Rivera-Barahona, A and Soto-Bielicka, P and Bertinetti, D and Baker, B and Vu, L and Piceci-Sparascio, F and Torrente, I and Boudin, E and Peeters, S and Van Hul, W and Huber, C and Bonneau, D and Hildebrand, MS and Coleman, M and Bahlo, M and Bennett, MF and Schneider, AL and Scheffer, IE and Kibaek, M and Kristiansen, BS and Issa, MY and Mehrez, MI and Ismail, S and Tenorio, J and Li, G and Skalhegg, BS and Otaify, GA and Temtamy, S and Aglan, M and Jonch, AE and De Luca, A and Mortier, G and Cormier-Daire, V and Ziegler, A and Wallis, M and Lapunzina, P and Herberg, FW and Taylor, SS and Ruiz-Perez, VL, Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome, American Journal of Human Genetics, 107, (5) pp. 977-988. ISSN 0002-9297 (2020) [Refereed Article] 
Wallis, M and Pope-Couston, R and Mansour, J and Amor, DJ and Tang, P and Stock-Myer, S, Lymphedema distichiasis syndrome may be caused by FOXC2 promoter-enhancer dissociation and disruption of a topological associated domain, American Journal of Medical Genetics. Part A pp. 1-7. ISSN 1552-4825 (2020) [Refereed Article] 
Ramchand, J and Wallis, M and Macciocca, I and Lynch, E and Farouque, O and Martyn, M and Phelan, D and Chong, B and Lockwood, S and Weintraub, R and Thompson, T and Trainer, A and Zentner, D and Vohra, J and Chetrit, M and Hare, DL and James, P, Prospective evaluation of the utility of whole exome sequencing in dilated cardiomyopathy, American Heart Association. Journal. Cardiovascular and Cerebrovascular Disease, 9, (2) pp. 1-11. ISSN 2047-9980 (2020) [Refereed Article]
Rafehi, H and Szmulewicz, DJ and Pope, K and Wallis, M and Christodoulou, J and White, SM and Delatycki, MB and Lockhart, PJ and Bahlo, M, Rapid diagnosis of spinocerebellar ataxia 36 in a three-generation family using short-read whole-genome sequencing data, Movement Disorders pp. 1-6. ISSN 0885-3185 (2020) [Refereed Article] 
Zhang, T and Wallis, M and Petrovic, V and Challis, J and Kalitsis, P and Hudson, DF, Loss of TOP3B leads to increased R-loop formation and genome instability, Open Biology, 9, (12) Article 190222. ISSN 2046-2441 (2019) [Refereed Article]

This list was generated on Fri Feb 3 00:52:12 2023.