Publications by authors named "Jan Halbritter"

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Medical Management of Polycystic Liver Disease: A Position Statement From the European Reference Network on Hepatological Diseases.
Sophia Heinrich, Andreia Margarida Carvalho de Matos, Jordi Colmenero, Ahmed M Elsharkawy, Soňa Fraňková, Jan Halbritter

Liver Int· January 2026

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Chronic Kidney Disease of unexplained cause (CKDx): a consensus statement by the Genes & Kidney Working Group of the ERA.
Jan Halbritter, Lucile Figueres, Albertien M Van Eerde, Giovambattista Capasso, Ewout J Hoorn

Nephrol Dial Transplant· November 2025

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CKDx: simplicity matters, implementation is key.
Emilie Cornec-Le Gall, Jan Halbritter, Roman Ulrich Müller

Nephrol Dial Transplant· November 2025

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In vivo base editing reduces liver cysts in autosomal dominant polycystic kidney disease.
Antonia Ibel, Rishi Bhardwaj, Duygu Elif Yilmaz, Shuhan Kong, Sarah Wendlinger, Jan Halbritter

Mol Ther· November 2025

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Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet).
Albertien M van Eerde, Ana Teixeira, Flavia Galletti, Michal Maternik, Valentina Capone, Jan Halbritter

Pediatr Nephrol· September 2025

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10 tips on how to take a proper family history in CKD patient care.
Emilie Cornec-Le Gall, Albertien M van Eerde, Lucile Figueres, Matias Simons, Giovambattista Capasso, Jan Halbritter

Clin Kidney J· September 2025

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Valosin-containing protein in ciliary morphology: a novel target in ADPKD.
Carlotta Pioppini, Rishi Bhardwaj, Ria Schönauer, Jan Halbritter, Fatima Hassan

Am J Physiol Renal Physiol· August 2025

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KDIGO 2025 ADPKD Guideline: A commentary on diagnosis and management of hepatopancreatic manifestations by the ERA Working Group Genes & Kidney.
Roman-Ulrich Müller, Emilie Cornec-Le Gall, Jan Degenhardt, Ron Gansevoort, Jan Halbritter

Nephrol Dial Transplant· August 2025

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Structure-Activity Analysis Reveals Perturbed Cilia-Jun N-Terminal Kinase Signaling in MAPKBP1-Associated Kidney Disease.
Christin Findeisen, Maria Papazian, Linda Pöschla, Anastasia Ertel, Wenjun Jin, Jan Halbritter

Kidney Int Rep· August 2025

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CAKUT subtypes determine the rate of progression to kidney failure - an adult patient cohort study.
Charlotte Hammett, Friederike Petzold, Sarah Stopp, Carolin B Brigl, Johannes Münch, Jan Halbritter

Nephrol Dial Transplant· August 2025

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CAKUT variants in , and : implications for splicing and ciliogenesis.
Lea M Merz, Shirlee Shril, Tucker J Carrocci, Csenge K Rezi, Natalie J Zeps, Jan Halbritter

bioRxiv· July 2025

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Donor-derived cell-free DNA monitoring for early diagnosis of antibody-mediated rejection after kidney transplantation: a randomized trial.
Aylin Akifova, Klemens Budde, Kerstin Amann, Maike Buettner-Herold, Mira Choi, Jan Halbritter

Nephrol Dial Transplant· June 2025

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The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease.
Elhussein A E Elhassan, Kane E Collins, Sophia Heneghan, Edmund Gilbert, Hana Yang, Jan Halbritter

J Nephrol· June 2025

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Characterization of the Cystic Phenotype Associated with Monoallelic ALG8 and ALG9 Pathogenic Variants.
Tabinda Jawaid, Doaa E Elbarougy, Sravanthi Lavu, Guillaume Buia, Sarah R Senum, Jan Halbritter

J Am Soc Nephrol· June 2025

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The impact of the new WHO classification of renal cell carcinoma on the diagnosis of hereditary leiomyomatosis and renal cell carcinoma.
Jan Degenhardt, Yuri Tolkach, Mahul B Amin, Giovanni Mosiello, Dilek Ertoy Baydar, Jan Halbritter

Nephrol Dial Transplant· June 2025

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Epigenetic silencing and CRISPR-mediated reactivation of tight junction protein claudin10b (CLDN10B) in renal cancer.
Sarah Arroyo Villora, Yufen Zhao, Paula Castellanos Silva, Alba A Hahn, Vivien Olanin, Jan Halbritter

Clin Epigenetics· June 2025

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-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype.
Bastian M Krüger, Annika Jens, Anna Neuhaus, Jasmina Ćomić, Riccardo Berutti, Jan Halbritter

Kidney Int Rep· May 2025

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Clinical Spectrum and Prognosis of Atypical Autosomal Dominant Polycystic Kidney Disease Caused by Monoallelic Pathogenic Variants of IFT140.
Nikola Zagorec, Alizée Calamel, Margaux Delaporte, Eric Olinger, Sarah Orr, Jan Halbritter

Am J Kidney Dis· April 2025

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Nephrectomy in autosomal dominant polycystic kidney disease: a consensus statement of the ERA Genes & Kidney Working Group.
Paul Geertsema, Ron T Gansevoort, Mustafa Arici, Giovambattista Capasso, Emilie Cornec-Le Gall, Jan Halbritter

Nephrol Dial Transplant· April 2025

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Integrated Use of Autosomal Dominant Polycystic Kidney Disease Prediction Tools for Risk Prognostication.
Constantin A Wolff, Valeria Aiello, Elhussein A E Elhassan, Carlotta Cristalli, Sarah Lerario, Jan Halbritter

Clin J Am Soc Nephrol· March 2025

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base editing reduces liver cysts in autosomal dominant polycystic kidney disease.
Antonia Ibel, Rishi Bhardwaj, Duygu Elif Yilmaz, Shuhan Kong, Sarah Wendlinger, Jan Halbritter

bioRxiv· February 2025

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Kidney transplantation in patients with polycystic kidney disease: increased risk of infection does not compromise graft and patient survival.
Johannes Waiser, Jens Klotsche, Petra Glander, Danilo Schmidt, Marcel Naik, Jan Halbritter

Clin Kidney J· December 2024

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Disrupted uromodulin trafficking is rescued by targeting TMED cargo receptors.
Silvana Bazua-Valenti, Matthew R Brown, Jason Zavras, Magdalena Riedl Khursigara, Elizabeth Grinkevich, Jan Halbritter

J Clin Invest· December 2024

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SGLT2-Inhibition in Patients With Alport Syndrome.
Jan Boeckhaus, Daniel P Gale, James Simon, Jie Ding, Yanqin Zhang, Jan Halbritter

Kidney Int Rep· December 2024

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