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Author Details

Olivier Devuyst
Institute of Physiology, University of Zurich, Cliniques Universitaires Saint-Luc
1989
427
71
PMIDPaper TitleJournal TitlePublished Year
37380129The structure of megalin: shedding new light on receptor-mediated endocytosis.Kidney Int2024
38016513Uromodulin processing in DNAJB11-kidney disease.Kidney Int2024
37621073The CTNS-MTORC1 axis couples lysosomal cystine to epithelial cell fate decisions and is a targetable pathway in cystinosis.Autophagy2024
36309125On the way to translate GWAS into kidney disease mechanisms.Kidney Int2023
37885358Allelic effects on uromodulin aggregates drive autosomal dominant tubulointerstitial kidney disease.EMBO Mol Med2023
37981431Tubular handling of filtered albumin.Kidney Int2023
35612992Uromodulin and its association with urinary metabolites: the German Chronic Kidney Disease Study.Nephrol Dial Transplant2023
37085250Series introduction: drug repurposing for kidney diseases.Kidney Int2023
36948762Advances in biodesign: artificial water channels outperforming aquaporins.Kidney Int2023
37452023Lysosomal cystine export regulates mTORC1 signaling to guide kidney epithelial cell fate specialization.Nat Commun2023
36520078Fasting influences aquaporin expression, water transport and adipocyte metabolism in the peritoneal membrane.Nephrol Dial Transplant2023
36831047Uromodulin and Vesico-Ureteral Reflux: A Genetic Study.Biomedicines2023
35134221An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International.Nephrol Dial Transplant2022
35378146Tubular cell plasticity-new hope for autosomal dominant polycystic kidney disease?Kidney Int2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35446786Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases.JCI Insight2022
36825031Flank pain has a significant adverse impact on quality of life in ADPKD: the CYSTic-QoL study.Clin Kidney J2022
36411013Urine: from waste to fertilizer.Kidney Int2022
35881244UMOD and the architecture of kidney disease.Pflugers Arch2022
35947615An intermediate-effect size variant in <i>UMOD</i> confers risk for chronic kidney disease.Proc Natl Acad Sci U S A2022
35031326Kidney traits on repeat-the role of MUC1 VNTR.Kidney Int2022
35137195Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.Nephrol Dial Transplant2022
35137071Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosis.Hum Mol Genet2022
35228297Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.J Am Soc Nephrol2022
33478975Uromodulin, Salt, and 24-Hour Blood Pressure in the General Population.Clin J Am Soc Nephrol2021
33687326Proteomic and transcriptomic profiling reveal different aspects of aging in the kidney.Elife2021
33846239Receptor-Mediated Endocytosis and Differentiation in Proximal Tubule Cell Systems.J Am Soc Nephrol2021
33566673Uromodulin: Roles in Health and Disease.Annu Rev Physiol2021
33667505PIEZO2, a mechanosensor in the urinary bladder.Kidney Int2021
33811157Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.J Am Soc Nephrol2021
33888577The Effect of Tolvaptan on BP in Polycystic Kidney Disease: A <i>Post Hoc</i> Analysis of the TEMPO 3:4 Trial.J Am Soc Nephrol2021
33745545Genetic insights into rapid kidney function decline.Kidney Int2021
34670044<i>AQP1</i> Promoter Variant, Water Transport, and Outcomes in Peritoneal Dialysis.N Engl J Med2021
34634361Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease.Kidney Int2021
34105414Assessing transport across the peritoneal membrane: Precision medicine in dialysis.Perit Dial Int2021
34078418The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results.Orphanet J Rare Dis2021
34237326An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis.Kidney Int2021
34197840A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis.Kidney Int2021
31006015Renal handling of zinc in chronic kidney disease patients and the role of circulating zinc levels in renal function decline.Nephrol Dial Transplant2020
32061435Transgenic zebrafish modeling low-molecular-weight proteinuria and lysosomal storage diseases.Kidney Int2020
31910047The Antioxidative Role of Cytoglobin in Podocytes: Implications for a Role in Chronic Kidney Disease.Antioxid Redox Signal2020
32080200Impaired mitophagy links mitochondrial disease to epithelial stress in methylmalonyl-CoA mutase deficiency.Nat Commun2020
31774122Parathyroid Hormone and Plasma Phosphate Are Predictors of Soluble α-Klotho Levels in Adults of European Descent.J Clin Endocrinol Metab2020
31980075Next-generation sequencing for detection of somatic mosaicism in autosomal dominant polycystic kidney disease.Kidney Int2020
33376102Multicenter Study of Long-Term Safety of Tolvaptan in Later-Stage Autosomal Dominant Polycystic Kidney Disease.Clin J Am Soc Nephrol2020
33051259Mechanical activation of TRPV4 channels controls albumin reabsorption by proximal tubule cells.Sci Signal2020
33266431Digital Image Analysis of Picrosirius Red Staining: A Robust Method for Multi-Organ Fibrosis Quantification and Characterization.Biomolecules2020
32919786The phosphoinositide 3-kinase inhibitor alpelisib restores actin organization and improves proximal tubule dysfunction in vitro and in a mouse model of Lowe syndrome and Dent disease.Kidney Int2020
32653401Genetic variation in claudin-2, hypercalciuria, and kidney stones.Kidney Int2020
32619563Targeting chloride transport in autosomal dominant polycystic kidney disease.Cell Signal2020
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Collaborators

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Institute of Genetic Epidemiology, Medical Center-University of Freiburg
Co-authored papers 15
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Lausanne University Hospital and University of Lausanne
Co-authored papers 14
Co-authored papers 12
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Ospedale Pediatrico Bambino Gesu IRCCS
Co-authored papers 10
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Co-authored papers 10
Centre hospitalier universitaire vaudois
Co-authored papers 9
Baylor College of Medicine
Co-authored papers 9
National Institute of Diabetes and Digestive and Kidney Diseases
Co-authored papers 9
Co-authored papers 9
Center for Primary Care and Public Health (Unisante), University of Lausanne
Co-authored papers 9
University of Lausanne
Co-authored papers 8
University Medicine Greifswald
Co-authored papers 8
Co-authored papers 8
Great Ormond Street Hospital for Children, NHS Foundation Trust
Co-authored papers 8
Co-authored papers 8
Co-authored papers 8
University of Michigan School of Public Health ann arbor
Co-authored papers 7
Co-authored papers 7
Lung and Blood Institute's (NHLBI) Framingham Heart Study
Co-authored papers 7
German Research Center for Cardiovascular Disease (DZHK)
Co-authored papers 7
Institute for Biomedicine (Affiliated to the University of Lubeck)
Co-authored papers 7
University Medicine Greifswald
Co-authored papers 7
and Blood Institute
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University of Lausanne
Co-authored papers 7