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BMJ Case Reports|March 10, 2023
Delayed-Onset olanzapine-induced rhabdomyolysisJun Hua Bowen Lim, Billy Robinson, Judith Savige
Internal Medicine Journal|December 27, 2025
Acute kidney injury signals a high risk of death, readmission and cancerZena Barakat, Matthew Jose, Judith Savige, et al.
Genome Medicine|February 12, 2024
Novel genetic markers for chronic kidney disease in a geographically isolated population of Indigenous Australians: Individual and multiple phenotype genome-wide association studyVignesh Arunachalam, Rodney Lea, Wendy Hoy, et al.
Journal of the Endocrine Society|June 7, 2022
The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome SequencingMark Stevenson, Alistair T Pagnamenta, Heather G Mack, et al.
Clinical Journal of the American Society of Nephrology : CJASN|July 26, 2011
Vision-threatening retinal abnormalities in chronic kidney disease stages 3 to 5Rajeev Deva, Mohamad Afzal Alias, Deb Colville, et al.
Kidney International Reports|March 19, 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport SyndromeThomas M Oates, Moumita Barua, Susie Gear, et al.
The Journal of Pharmacology and Experimental Therapeutics|August 15, 2018
Induced Pluripotent Stem Cell-Derived Podocyte-Like Cells as Models for Assessing Mechanisms Underlying Heritable Disease Phenotype: Initial Studies Using Two Alport Syndrome Patient Lines Indicate Impaired Potassium Channel ActivityJohn M Haynes, James N Selby, Teresa H Vandekolk, et al.
Pediatric Nephrology (Berlin, Germany)|May 3, 2019
The importance of clinician, patient and researcher collaborations in Alport syndromeMichelle N Rheault, Judith Savige, Michael J Randles, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Leveraging genomic biobanks to enhance genetic testing outcomes for kidney diseaseGretchen M Urban, Kulsoom Mohammad, Lakshna Sankar, et al.
Plos One|September 15, 2016
X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype CorrelationsJudith Savige, Helen Storey, Hae Il Cheong, et al.
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