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Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol.
Jayasinghe K, Stark Z, Patel C, Mallawaarachchi A, McCarthy H, Faull R, Chakera A, Sundaram M, Jose M, Kerr P, Wu Y, Wardrop L, Goranitis I, Best S, Martyn M, Quinlan C, Mallett AJ. Jayasinghe K, et al. Among authors: wu y. BMJ Open. 2019 Aug 5;9(8):e029541. doi: 10.1136/bmjopen-2019-029541. BMJ Open. 2019. PMID: 31383705 Free PMC article.
Clinical genomic testing: what matters to key stakeholders?
Best S, Stark Z, Phillips P, Wu Y, Long JC, Taylor N, Braithwaite J, Christodoulou J, Goranitis I. Best S, et al. Among authors: wu y. Eur J Hum Genet. 2020 Jul;28(7):866-873. doi: 10.1038/s41431-020-0576-1. Epub 2020 Feb 5. Eur J Hum Genet. 2020. PMID: 32024983 Free PMC article.
Parental health spillover effects of paediatric rare genetic conditions.
Wu Y, Al-Janabi H, Mallett A, Quinlan C, Scheffer IE, Howell KB, Christodoulou J, Leventer RJ, Lockhart PJ, Stark Z, Boughtwood T, Goranitis I. Wu Y, et al. Qual Life Res. 2020 Sep;29(9):2445-2454. doi: 10.1007/s11136-020-02497-3. Epub 2020 Apr 7. Qual Life Res. 2020. PMID: 32266555
Response to Lombardi and Mesnard.
Wu Y, Jayasinghe K, Stark Z, Quinlan C, Patel C, McCarthy H, Mallawaarachchi AC, Kerr PG, Alexander SI, Mallett AJ, Goranitis I; KidGen Collaborative investigators. Wu Y, et al. Genet Med. 2024 Jan;26(1):100989. doi: 10.1016/j.gim.2023.100989. Epub 2023 Sep 28. Genet Med. 2024. PMID: 37777873 No abstract available.
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