Jan Halbritter

University Hospital Leipzig

Germany

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Articles (21)

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2025

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Collaborators (24)

Erika Salvi

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Cristian Pattaro

ITALY

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Michal Ruth Schweiger

Principal Investigator, Director, Professor

University Hospital Bonn

GERMANY

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Tania Attié‐Bitach

FRANCE

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Kerim Mutig

Charité - Universitätsmedizin Berlin

GERMANY

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Sebastian E. Sattui

Assistant Professor

University of Pittsburgh

UNITED STATES

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Whitney Besse

Assistant Professor

Yale University School of Medicine

UNITED STATES

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DUVURU GEETHA

ASSOCIATE PROFESSOR OF MEDICINE

Johns Hopkins University

UNITED STATES

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Peter Lanyon

Honorary Professor

University of Nottingham

UNITED KINGDOM

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Lucio Manenti

University of Parma

ITALY

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Albertien M. van Eerde

NETHERLANDS

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Sanaz Sedaghat

University of Minnesota

UNITED STATES

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Sebastian Bachmann

Charité - Universitätsmedizin Berlin

GERMANY

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Elisabet Ars

Head of Molecular Biology Laboratory

FUNDACIO PUIGVERT

SPAIN

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Jörg Piontek

GERMANY

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Tilman Breiderhoff

Facility Head

Deutsches Zentrum für Neurodegenerative Erkrankungen

GERMANY

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Adrienne Tin

Associate Professor

University of Mississippi Medical Center

UNITED STATES

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Kai-Uwe Eckardt

Professor / Director

Charité - Universitätsmedizin Berlin

GERMANY

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Angelika Rauch

Leipzig University

GERMANY

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Dwarakanathan Ranganathan

Associate Professor

Griffith University

AUSTRALIA

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Johannes Graumann

Professor of Translational Proteomics

Philipps-Universität Marburg

GERMANY

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Per Svensson

Associate professor, Senior Lecturer

Karolinska Institutet Institutionen för klinisk forskning och utbildning Södersjukhuset

SWEDEN

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Beatrice Spedicati

University of Trieste

ITALY

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Olivier Devuyst

Full Professor

University of Zurich

SWITZERLAND

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Jan Halbritter

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Articles (21)

Structure-Activity Analysis Reveals Perturbed Cilia-Jun N-Terminal Kinase Signaling in MAPKBP1-Associated Kidney Disease

COL4A5 -p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype.

Clinical Spectrum and Prognosis of Atypical Autosomal Dominant Polycystic Kidney Disease Caused by Monoallelic Pathogenic Variants of IFT140.

Deceased donor urinary Dickkopf-3 associates with future allograft function following kidney transplantation.

Efficacy and safety of avacopan in patients aged 65 years and older with ANCA-associated vasculitis: a post hoc analysis of data from the ADVOCATE trial.

Epigenetic silencing and CRISPR-mediated reactivation of tight junction protein claudin10b (CLDN10B) in renal cancer.

Real-world use of complement inhibitors for haemolytic uraemic syndrome: an analysis of the European Rare Kidney Disease Registry cohort.

Valosin-containing protein in ciliary morphology: a novel target in ADPKD.

Disrupted uromodulin trafficking is rescued by targeting TMED cargo receptors.

Clinical management of liver cyst infections: an international, modified Delphi-based clinical decision framework.

Renal Recovery for Patients with ANCA-Associated Vasculitis and Low eGFR in the ADVOCATE Trial of Avacopan

KidneyNetwork: using kidney-derived gene expression data to predict and prioritize novel genes involved in kidney disease.

Mechanisms of pathogenicity and the quest for genetic modifiers of kidney disease in branchiootorenal syndrome

Clinical and Functional Assessment of Digenicity in Renal Phosphate Wasting

Delta weight loss unlike genetic variation associates with hyperoxaluria after malabsorptive bariatric surgery.

Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantation

OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Claudin-10a Deficiency Shifts Proximal Tubular Cl<sup>-</sup> Permeability to Cation Selectivity via Claudin-2 Redistribution

Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract

Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assembly

Collaborators (24)

Erika Salvi

Cristian Pattaro

Michal Ruth Schweiger

Tania Attié‐Bitach

Kerim Mutig

Sebastian E. Sattui

Whitney Besse

DUVURU GEETHA

Peter Lanyon

Lucio Manenti

Albertien M. van Eerde

Sanaz Sedaghat

Sebastian Bachmann

Elisabet Ars

Jörg Piontek

Tilman Breiderhoff

Adrienne Tin

Kai-Uwe Eckardt

Angelika Rauch

Dwarakanathan Ranganathan

Johannes Graumann

Per Svensson

Beatrice Spedicati

Olivier Devuyst

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