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Journal of Endourology|October 13, 2023
Routine Urinary Biochemistry Does Not Accurately Predict Stone Type Nor Recurrence in Kidney Stone Formers: A Multicentre, Multimodel, Externally Validated Machine-Learning StudyRobert M Geraghty, Ian Wilson, Eric Olinger, et al.Kidney International Reports|December 19, 2024
UMOD Genotype and Determinants of Urinary Uromodulin in African PopulationsMichél Strauss-Kruger, Eric Olinger, Patrick Hofmann, et al.Journal of Cell Science|August 8, 2025
Urinary renal epithelial cells for NPHP1 phenotyping and personalized therapeutic responsePraveen Dhondurao Sudhindar, Eric Olinger, Zachary T Sentell, et al.Kidney International|April 17, 2016
Tubular proteinuria in patients with HNF1α mutations: HNF1α drives endocytosis in the proximal tubuleSara Terryn, Karo Tanaka, Jean-Philippe Lengelé, et al.Elife|December 18, 2015
The serine protease hepsin mediates urinary secretion and polymerisation of Zona Pellucida domain protein uromodulinMartina Brunati, Simone Perucca, Ling Han, et al.Brain Communications|August 23, 2021
Identification of LAMA1 mutations ends diagnostic odyssey and has prognostic implications for patients with presumed Joubert syndromeLaura Powell, Eric Olinger, Sarah Wedderburn, et al.Pflugers Archiv : European Journal of Physiology|December 5, 2016
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urineTanguy Corre, Eric Olinger, Sarah E Harris, et al.Hypertension (Dallas, Tex. : 1979)|July 15, 2024
Progressive Kidney Failure by Angiotensinogen Inactivation in the GermlineFlorian J Wopperer, Eric Olinger, Antje Wiesener, et al.Clinical Genetics|October 23, 2022
Biallelic variants in CEP164 cause a motile ciliopathy-like syndromeLaura A Devlin, Janice Coles, Claire L Jackson, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2017
Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndromeSmail Hadj-Rabia, Gaelle Brideau, Yasser Al-Sarraj, et al.Pageof 6