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The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic.
Stafford F, Krishnan N, Richardson E, Butters A, Hespe S, Burns C, Gray B, Medi C, Nowak N, Isbister JC, Raju H, Richmond D, Ryan MP, Singer ES, Sy RW, Yeates L, Bagnall RD, Semsarian C, Ingles J. Stafford F, et al. Among authors: nowak n. Genome Med. 2022 Dec 28;14(1):145. doi: 10.1186/s13073-022-01149-0. Genome Med. 2022. PMID: 36578016 Free PMC article.
Genetic architecture of left ventricular noncompaction in adults.
Ross SB, Singer ES, Driscoll E, Nowak N, Yeates L, Puranik R, Sy RW, Rajagopalan S, Barratt A, Ingles J, Bagnall RD, Semsarian C. Ross SB, et al. Among authors: nowak n. Hum Genome Var. 2020 Oct 15;7:33. doi: 10.1038/s41439-020-00120-y. eCollection 2020. Hum Genome Var. 2020. PMID: 33082984 Free PMC article.
Genetic Basis of Childhood Cardiomyopathy.
Bagnall RD, Singer ES, Wacker J, Nowak N, Ingles J, King I, Macciocca I, Crowe J, Ronan A, Weintraub RG, Semsarian C. Bagnall RD, et al. Among authors: nowak n. Circ Genom Precis Med. 2022 Dec;15(6):e003686. doi: 10.1161/CIRCGEN.121.003686. Epub 2022 Oct 11. Circ Genom Precis Med. 2022. PMID: 36252119 Free article.
A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship.
Austin R, Brown JS, Casauria S, Madelli EO, Mattiske T, Boughtwood T, Metke A, Davis A, Horton AE, Winlaw D, Das D, Soka M, Giannoulatou E, Rath EM, Haan E, Blue GM, Vohra J, Atherton JJ, van Spaendonck-Zwarts K, Cox K, Burnett L, Wallis M, Haas M, Quinn MCJ, Pachter N, Poplawski NK, Stark Z, Bagnall RD, Weintraub RG, Pantaleo SJ, Lunke S, De Fazio P, Thompson T, James P, Chang Y, Fatkin D, Macciocca I, Ingles J, Dunwoodie SL, Semsarian C, McGaughran J; Australian Genomics Cardiovascular Disorders Flagship. Austin R, et al. Genet Med Open. 2024 Mar 25;2:101842. doi: 10.1016/j.gimo.2024.101842. eCollection 2024. Genet Med Open. 2024. PMID: 39669597 Free PMC article.
Intrauterine blood transfusion causes dose- and time-dependent signal alterations in the liver and the spleen on fetal magnetic resonance imaging.
Schwarz M, Schmidbauer VU, Malik J, Nowak NM, Kienast P, Watzenboeck M, Stuempflen M, Schwarz C, Kittinger J, Bettelheim D, Haberl C, Binder J, Kiss H, Reiberger T, Prayer D, Kasprian G. Schwarz M, et al. Among authors: nowak nm. Eur Radiol. 2024 Dec 11. doi: 10.1007/s00330-024-11228-y. Online ahead of print. Eur Radiol. 2024. PMID: 39663265
309 results