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Genome-wide association study of medication-use and associated disease in the UK Biobank

Nature communications, 2019-04, Vol.10 (1), p.1891-1891, Article 1891

2019

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Characteristics and clinical outcomes of patients with kidney failure of unknown aetiology from ANZDATA registry

PloS one, 2024-03, Vol.19 (3), p.e0300259-e0300259

2024

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The application of long-read sequencing in clinical settings

Human genomics, 2023-08, Vol.17 (1), p.73-73, Article 73

2023

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Cellular milieu in clear cell renal cell carcinoma

Frontiers in oncology, 2022-10, Vol.12, p.943583-943583

2022

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A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder

Development (Cambridge), 2020-06, Vol.147 (21)

2020

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ABO blood group relationships to kidney transplant recipient and graft outcomes

PloS one, 2020-07, Vol.15 (7), p.e0236396-e0236396

2020

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Ciliopathies and the Kidney: A Review

American journal of kidney diseases, 2021-03, Vol.77 (3), p.410-419

2021

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Functional somatic symptoms in Emergency Department frequent presenters

BMC emergency medicine, 2024-07, Vol.24 (1), p.1-8, Article 122

2024

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Editorial: Genetics and epigenetics of chronic kidney disease

Frontiers in medicine, 2023-02, Vol.10, p.1078300-1078300

2023

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Which patients with CKD will benefit from genomic sequencing? Synthesizing progress to illuminate the future

Current opinion in nephrology and hypertension, 2022-11, Vol.31 (6), p.541

Mallett, Andrew J

2022

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Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics

Kidney international reports, 2021-02, Vol.6 (2), p.272-283

2021

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Genomics in the kidney transplant clinic: the future standard of care?

Kidney international, 2024-07, Vol.106 (1), p.18-20

2024

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Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease

Scientific reports, 2021-09, Vol.11 (1), p.19425-10, Article 19425

2021

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Theory Designed Strategies to Support Implementation of Genomics in Nephrology

Genes, 2022-10, Vol.13 (10), p.1919

2022

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Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics Study

Genes, 2022-10, Vol.13 (10), p.1804

2022

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High risk clear cell renal cell carcinoma microenvironments contain protumour immunophenotypes lacking specific immune checkpoints

NPJ precision oncology, 2023-09, Vol.7 (1), p.88-88, Article 88

2023

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Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol

BMJ open, 2019-08, Vol.9 (8), p.e029541-e029541

2019

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Determining priority indicators of utility for genomic testing in rare disease: A Delphi study

Genetics in medicine, 2024-06, Vol.26 (6), p.101116, Article 101116

2024

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Spatially Resolved Transcriptomes of Mammalian Kidneys Illustrate the Molecular Complexity and Interactions of Functional Nephron Segments

Frontiers in medicine, 2022-07, Vol.9, p.873923-873923

2022

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Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families

Npj genomic medicine, 2021-03, Vol.6 (1), p.20-20, Article 20

2021

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The increasing rates of acute interstitial nephritis in Australia: a single centre case series

BMC nephrology, 2017-10, Vol.18 (1), p.329-329, Article 329

2017

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Exploring the impact and utility of genomic sequencing in established CKD

Clinical kidney journal, 2024-03, Vol.17 (3), p.sfae043-sfae043

2024

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Implementation of reimbursement for genomic testing in Australia: early successes and the pathway ahead

Internal medicine journal, 2024-04, Vol.54 (4), p.531-534

2024

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Corrigendum to Ng MS, Malacova E, Hurst C, David MC, Johnson DW, Mallett AJ. “Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study.” Kidney Int Rep. 2021;6:2481–2485

Kidney international reports, 2022-03, Vol.7 (3), p.664-664

2022

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Genome-wide association study of medication-use and associated disease in the UK Biobank

Characteristics and clinical outcomes of patients with kidney failure of unknown aetiology from ANZDATA registry

The application of long-read sequencing in clinical settings

Cellular milieu in clear cell renal cell carcinoma

A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder

ABO blood group relationships to kidney transplant recipient and graft outcomes

Ciliopathies and the Kidney: A Review

Functional somatic symptoms in Emergency Department frequent presenters

Editorial: Genetics and epigenetics of chronic kidney disease

Which patients with CKD will benefit from genomic sequencing? Synthesizing progress to illuminate the future

Attitudes and Practices of Australian Nephrologists Toward Implementation of Clinical Genomics

Genomics in the kidney transplant clinic: the future standard of care?

Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease

Theory Designed Strategies to Support Implementation of Genomics in Nephrology

Shaping the future of kidney genetics in Australia: proceedings from the KidGen policy implementation workshop 2023

Participant Choice towards Receiving Potential Additional Findings in an Australian Nephrology Research Genomics Study

High risk clear cell renal cell carcinoma microenvironments contain protumour immunophenotypes lacking specific immune checkpoints

Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol

Determining priority indicators of utility for genomic testing in rare disease: A Delphi study

Spatially Resolved Transcriptomes of Mammalian Kidneys Illustrate the Molecular Complexity and Interactions of Functional Nephron Segments

Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families

The increasing rates of acute interstitial nephritis in Australia: a single centre case series

Exploring the impact and utility of genomic sequencing in established CKD

Implementation of reimbursement for genomic testing in Australia: early successes and the pathway ahead

Corrigendum to Ng MS, Malacova E, Hurst C, David MC, Johnson DW, Mallett AJ. “Clinical Outcomes of People With Fabry Disease — ANZDATA Registry Study.” Kidney Int Rep. 2021;6:2481–2485

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