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Clinical impact of genomic testing in patients with suspected monogenic kidney disease.
Genet Med. 2021 Jan;23(1):183-191. doi: 10.1038/s41436-020-00963-4. Epub 2020 Sep 17.
Genet Med. 2021.
PMID: 32939031
Free PMC article.
Renal genetics in Australia: Kidney medicine in the genomic age.
Jayasinghe K, Quinlan C, Stark Z, Patel C, Mallawaarachchi A, Wardrop L, Kerr PG, Trnka P, Mallett AJ; KidGen Collaborative.
Jayasinghe K, et al. Among authors: wardrop l.
Nephrology (Carlton). 2019 Mar;24(3):279-286. doi: 10.1111/nep.13494. Epub 2018 Oct 18.
Nephrology (Carlton). 2019.
PMID: 30239064
Free PMC article.
Review.
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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: wardrop l.
BMJ Open. 2019 Aug 5;9(8):e029541. doi: 10.1136/bmjopen-2019-029541.
BMJ Open. 2019.
PMID: 31383705
Free PMC article.
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The HIDDEN Protocol: An Australian Prospective Cohort Study to Determine the Utility of Whole Genome Sequencing in Kidney Failure of Unknown Aetiology.
Soraru J, Jahan S, Quinlan C, Simons C, Wardrop L, O'Shea R, Wood A, Mallawaarachchi A, Patel C, Stark Z, Mallett AJ.
Soraru J, et al. Among authors: wardrop l.
Front Med (Lausanne). 2022 May 26;9:891223. doi: 10.3389/fmed.2022.891223. eCollection 2022.
Front Med (Lausanne). 2022.
PMID: 35721054
Free PMC article.
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Data resource profile: The Child LAnguage REpository (CLARE).
Reilly S, Cini E, Gold L, Goldfeld S, Law J, Levickis P, Mensah F, Morgan A, Nicholson JM, Le HND, Pezic A, Tomblin B, Wake M, Wardrop L.
Reilly S, et al. Among authors: wardrop l.
Int J Epidemiol. 2018 Jun 1;47(3):688-688j. doi: 10.1093/ije/dyy034.
Int J Epidemiol. 2018.
PMID: 29562305
No abstract available.
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