NEOCYST - Netzwerk für frühkindliche zystische Nierenerkrankungen
Was sind zystische Nierenerkrankungen?
Erbliche zystische Nierenerkrankungen zählen zu den häufigsten Ursachen für ein chronisches Nierenversagen im Kindesalter. Hinter dem Begriff „zystische Nierenerkrankungen“ verbergen sich unterschiedliche Erkrankungsentitäten, welche alle durch einen zumeist langsam fortschreitenden Nierenfunktionsverlust gekennzeichnet sind und darüber hinaus weitere Organe betreffen können. Als wichtigste Vertreter sind die autosomal rezessive polyzystische Nierenerkrankung (ARPKD), die Nephronophthise (NPH) und Nephronophthise-assoziierte Zilienerkrankungen (NPH-RC) sowie die sog. HNF1b Nephropathie zu nennen.
Auf molekularer Ebene liegen den Erkrankungen Genveränderungen in sogenannten Ziliengenen zugrunde, welche wiederum Auswirkungen auf unterschiedliche biologische Prozesse und Signalwege haben. Die allermeisten der genannten Erkrankungen manifestieren sich bereits in der frühen Kindheit, zum Teil sogar vorgeburtlich. Obgleich jede einzelne der genannten Erkrankungsentitäten sehr selten ist, sind in ihrer Gesamtheit deutschlandweit ca. 500-700 Kinder und Jugendliche betroffen.
Weltweite Forschungsaktivitäten haben in den vergangenen Jahren zu einem deutlich verbesserten Verständnis der molekularen Krankheitsmechanismen geführt – nicht zuletzt durch den Beitrag des NEOCYST-Forschungsverbunds. Weiterhin fehlen jedoch zuverlässige und belastbare Prognose-Modell für den zu erwartenden Krankheitsverlauf individueller Personen sowie insbesondere kausale Therapieoptionen.
Gemeinsame Forschung im NEOCYST Verbund
NEOCYST ist ein 2016 gegründetes multidisziplinäres Experten-Netzwerk an verschiedenen Standorten in Deutschland, welches sich der umfassenden Erforschung zystischer Nierenerkrankungen im Kindesalter widmet und so an einem verbesserten Krankheitsverständnis und der Identifikation möglicher Therapieansätze arbeitet. Durch neue Forschungsergebnisse und das Erreichen einer optimierten individuellen Beratung soll eine bessere Patientenversorgung erreicht werden.
Im Rahmen der ersten vom Bundesministerium für Bildung und Forschung (BMBF) geförderten Projektphase (2016-2019) konnten ein Webportal, eine Biobank sowie ein Online-Patientenregister aufgebaut werden, welche mittlerweile auf mehr als 700 registrierte Patient:innen sowie über 3.500 Bioproben angewachsen sind. Die erhobenen Daten waren Grundlage für viele wissenschaftliche Arbeiten innerhalb des NEOCYST-Verbunds und haben neben der Identifikation bislang unbekannter genetischer Ursachen vor allem zu einer detaillierten phänotypischen Charakterisierung sowie der Erarbeitung von Genotyp-Phänotyp-Korrelationen beitragen können.
Die aktuellen Arbeiten des Forschungsverbunds werden auch weiterhin vom BMBF gefördert. Die Schwerpunkte der aktuellen Förderphase werden dabei sowohl auf einer verbesserten Vorhersagbarkeit individueller Krankheitsverläufe mittels innovativer prognostischer Werkzeuge und Biomarker als auch auf der Identifikation therapeutischer Angriffspunkte liegen. Insgesamt ist es das Ziel, die Grundlagen für zeitnahe klinische Therapiestudien zu schaffen.
Auch international ist der NEOCYST Verbund umfassend vernetzt und unter anderem aktiver Partner des Europäischen Referenznetzwerks für Seltene Nierenerkrankungen (ERKNet) sowie des europäischen Forschungsnetzwerkes THERACIL.
Projekte- Koordinationszentrum & NEOCYST-Register: Dr. Jens König, Westfälische Wilhelms-Universität Münster – Universitätsklinikum Münster.
- Erstellung prädiktiver Erkrankungsmodelle und Etablierung Patienten-orientierter Outcome Parameter: Dr. Jens König, Mareike Dahmer-Heath und PD Joachim Gerß, Westfälische Wilhelms-Universität Münster – Universitätsklinikum Münster.
- Evaluation von Störungen aus dem Autismus Spektrum: Prof. Stefanie Weber, Prof. Katja Becker und Prof. Inge Kamp-Becker; Philipps-Universität Marburg – Uniklinikum Gießen und Marburg.
- Etablierung und Validierung patientenzentrierter Outcomeparameter (PCOMs): PD Dr. Charlotte Gimpel und Prof. Franz Schaefer, Ruprecht-Karls-Universität Heidelberg – Medizinische Fakultät und Universitätsklinikum
- Patienten-orientierte Aufklärung und Informationsverbreitung mittels DigiCYST-App sowie umfassende sonografische Evaluation: Dr. Metin Cetiner, Prof. Lars Pape, Universitätsklinikum Essen.
- Infrastruktur und Vernetzung der NEOCYST-Plattform: Dr. Jessica Vasseur, Dr. Holger Storf, Institut für Medizininformatik – IMI, Johann-Wolfgang-Goethe Universität Frankfurt.
- Next-Level Molekulare Genetik: Prof. Carsten Bergmann, Limbach Genetics, Medizinische Genetik, Mainz.
- Verbesserung des pathophysiologischen Verständnisses von Ziliopathien und Entwicklung therapeutischer Strategien und Interventionen: Prof. Max Christoph Liebau und Prof. Bernhard Schermer, Universitätsklinikum Köln; Prof. Heymut Omran und Dr. Petra Pennekamp, Westfälische Wilhelms-Universität Münster; Prof. Dieter Haffner. Dr. Jens Drube und Dr. Wolfgang Ziegler, Medizinische Hochschule Hannover (MHH); Prof. Franz Schaefer, Ruprecht-Karls-Universität Heidelberg – Medizinische Fakultät und Universitätsklinikum sowie Prof. Carsten Bergmann, Universitätsklinikum Freiburg.
- Integrative Analyse und Auswertung klinischer, genetischer und molekularer Informationen: Dr. Philipp Anczak, Zentrum für Molekulare Medizin an der Universität zu Köln.
- NEOCYST Zentrale Biobank: Dr. Norman Klopp und Prof. Thomas Illig, Medizinische Hochschule Hannover (MHH), Hannover Unified Biobank (HUB).
Universitätskinderklinik Münster
Allgemeine Pädiatrie, Pädiatrische Nephrologie
Waldeyerstrasse 22
48149 Münster
Deutschland
Tel: +49-251-83 56 213
E-mail: jens.koenig@uni-muenster.de
Website: www.neocyst.de
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12. November 2024 (NEOCYST)
Ultrasound evaluation of kidney and liver involvement in Bardet-Biedl syndromeOrphanet J Rare Dis. 2024 Nov 12. >>Pubmed-Link<<
Metin Cetiner, Ilja Finkelberg, Felix Schiepek, Lars Pape, Raphael Hirtz, Anja K Büscher
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31. Juli 2024 (NEOCYST)
Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendationsEur J Hum Genet. 2024 Jul 31. >>Pubmed-Link<<
Hélène Dollfus, Marc R Lilien, Pietro Maffei, Alain Verloes, Jean Muller, Giacomo M Bacci, Metin Cetiner, Erica L T van den Akker, Monika Grudzinska Pechhacker, Francesco Testa, Didier Lacombe, Marijn F Stokman, Francesca Simonelli, Aurélie Gouronc, Amélie Gavard, Mieke M van Haelst, Jens Koenig, Sylvie Rossignol, Carsten Bergmann, Miriam Zacchia, Bart P Leroy, Héléna Mosbah, Albertien M Van Eerde, Djalila Mekahli, Aude Servais, Christine Poitou, Diana Valverde
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1. Juni 2024 (NEOCYST)
Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tractPediatr Nephrol. 2024 Jun. >>Pubmed-Link<<
Marcin Kołbuc, Mateusz F Kołek, Rafał Motyka, Beata Bieniaś, Sandra Habbig, Kathrin Burgmaier, Larisa Prikhodina, Svetlana Papizh, Velibor Tasic, Christine Okorn, Maria Szczepańska, Katarzyna Kiliś-Pstrusińska, Anna Wasilewska, Piotr Adamczyk, Marcin Tkaczyk, Małgorzata Pańczyk-Tomaszewska, Monika Miklaszewska, Krzysztof Pawlaczyk, Ewelina Bukowska-Olech, Aleksander Jamsheer, Augustina Jankauskiene, Jens König, Hae Il Cheong, Yo Han Ahn, Sophie Kaspar, Przemysław Sikora, Bodo B Beck, Marcin Zaniew
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27. Mai 2024 (NEOCYST)
Pathogenic PHIP Variants are Variably Associated With CAKUTKidney Int Rep. 2024 May 27. eCollection 2024 Aug. >>Pubmed-Link<<
Jonathan de Fallois, Tobias Sieckmann, Ria Schönauer, Friederike Petzold, Johannes Münch, Melissa Pauly, Georgia Vasileiou, Christin Findeisen, Antje Kampmeier, Alma Kuechler, André Reis, Eva Decker, Carsten Bergmann, Konrad Platzer, Velibor Tasic, Karin Michaela Kirschner, Shirlee Shril, Friedhelm Hildebrandt, Wendy K Chung, Jan Halbritter
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16. Mai 2024 (NEOCYST)
Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 MicrodeletionsKidney Int Rep. 2024 May 16. eCollection 2024 Aug. >>Pubmed-Link<<
Bénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, Stefanie Weber, Jens König, Laurence Heidet, Nabila Moussaoui, Jeanne-Pierrette Vu, Stanislas Faguer, Audrey Casemayou, Richa Prakash, Véronique Baudouin, Julien Hogan, Demi Alexandrou, Detlef Bockenhauer, Justine Bacchetta, Bruno Ranchin, Stepanka Pruhova, Jakub Zieg, Annie Lahoche, Christine Okorn, Violetta Antal-Kónya, Denis Morin, Francesca Becherucci, Sandra Habbig, Max C Liebau, Mathilde Mauras, Tom Nijenhuis, Brigitte Llanas, Djalila Mekahli, Julia Thumfart, Burkhard Tönshoff, Laura Massella, Philippe Eckart, Sylvie Cloarec , Alejandro Cruz, Ludwig Patzer, Gwenaelle Roussey, Isabelle Vrillon, Olivier Dunand, Lucie Bessenay, Francesca Taroni, Marcin Zaniew, Ferielle Louillet, Carsten Bergmann, Franz Schaefer, Albertien M van Eerde, Joost P Schanstra, Stéphane Decramer; HNF1B variant study group
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1. Mai 2024 (NEOCYST)
Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver DiseaseGastroenterology. 2024 May. >>PubMed-Link<<
Ria Schönauer, Dana Sierks, Melissa Boerrigter, Tabinda Jawaid, Lea Caroff, Marie-Pierre Audrezet, Anja Friedrich, Melissa Shaw, Jan Degenhardt, Mirjam Forberger, Jonathan de Fallois, Hendrik Bläker, Carsten Bergmann, Juliana Gödiker, Philipp Schindler, Bernhard Schlevogt, Roman-U Müller, Thomas Berg, Ilse Patterson, William J Griffiths, John A Sayer; Genomics England Research Consortium; Bernt Popp, Vicente E Torres, Marie C Hogan, Stefan Somlo, Terry J Watnick, Frederik Nevens, Whitney Besse, Emilie Cornec-Le Gall, Peter C Harris, Joost P H Drenth, Jan Halbritter
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26. April 2024 (NEOCYST)
Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubulesScience. 2024 Apr 26. >>Pubmed-Link<<
Daniel O Dodd, Sabrina Mechaussier, Patricia L Yeyati, Fraser McPhie, Jacob R Anderson, Chen Jing Khoo, Amelia Shoemark, Deepesh K Gupta, Thomas Attard, Maimoona A Zariwala, Marie Legendre, Diana Bracht, Julia Wallmeier, Miao Gui, Mahmoud R Fassad, David A Parry, Peter A Tennant, Alison Meynert, Gabrielle Wheway, Lucas Fares-Taie, Holly A Black, Rana Mitri-Frangieh, Catherine Faucon, Josseline Kaplan, Mitali Patel, Lisa McKie, Roly Megaw, Christos Gatsogiannis, Mai A Mohamed, Stuart Aitken, Philippe Gautier, Finn R Reinholt, Robert A Hirst, Chris O’Callaghan, Ketil Heimdal, Mathieu Bottier, Estelle Escudier, Suzanne Crowley, Maria Descartes, Ethylin W Jabs, Priti Kenia, Jeanne Amiel, Giacomo Maria Bacci, Claudia Calogero, Viviana Palazzo, Lucia Tiberi, Ulrike Blümlein, Andrew Rogers, Jennifer A Wambach, Daniel J Wegner, Anne B Fulton, Margaret Kenna, Margaret Rosenfeld, Ingrid A Holm, Alan Quigley, Emma A Hall, Laura C Murphy, Diane M Cassidy, Alex von Kriegsheim; Scottish Genomes Partnership; Genomics England Research Consortium; Undiagnosed Diseases Network; Jean-François Papon, Laurent Pasquier, Marlène S Murris, James D Chalmers, Claire Hogg, Kenneth A Macleod, Don S Urquhart, Stefan Unger, Timothy J Aitman, Serge Amselem, Margaret W Leigh, Michael R Knowles, Heymut Omran, Hannah M Mitchison, Alan Brown, Joseph A Marsh, Julie P I Welburn, Shih-Chieh Ti, Amjad Horani, Jean-Michel Rozet, Isabelle Perrault, Pleasantine Mill
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1. April 2024 (NEOCYST)
Ibrutinib-associated focal segmental glomerulosclerosis and the impact of podocin mutations in chronic lymphocytic leukemiaKidney Int. 2024 Apr. >>PubMed-Link<<
Jan Czogalla, Simon Schliffke, Shun Lu, Maria Schwerk, Helena Petereit, Tianran Zhang, Shuya Liu, Bernhard Dumoulin, Sydney Gies, Guochao Wu, Sonja Hänzelmann, Marlies Bode, Florian Grahammer, Markus Gödel, Minna Voigtländer, Linus Butt, Carsten Bokemeyer, Carsten Bergmann, Thomas Benzing, Thorsten Wiech, Victor G Puelles, Tobias B Huber
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11. März 2024 (NEOCYST)
Defects of renal tubular homeostasis and cystogenesis in the Pkhd1 knockoutiScience. 2024 Mar 11. >>PubMed-Link<<
Julia C Fox, Susanne T Hahnenstein, Fatima Hassan, Andrea Grund, Dieter Haffner, Wolfgang H Ziegler
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8. März 2024 (NEOCYST)
Verbesserte Versorgungs-und Behandlungsoptionen für Patienten mit Hyperphagie-assoziierter Adipositas bei Bardet-Biedl-Syndrom [Improved Care and Treatment Options for Patients with Hyperphagia-Associated Obesity in Bardet-Biedl Syndrome]Klin Padiatr. 2024 Mar 8. >>PubMed-Link<<
Metin Cetiner, Carsten Bergmann, Markus Bettendorf, Johanna Faust, Anja Gäckler, Bernarda Gillissen, Matthias Hansen, Maximilian Kerber, Günter Klaus, Jens König, Laura Kühlewein, Jun Oh, Annette Richter-Unruh, Julia von Schnurbein, Martin Wabitsch, Susann Weihrauch-Blüher, Lars Pape
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6. November 2023 (NEOCYST)
Kif21a deficiency leads to impaired glomerular filtration barrier functionSci Rep. 2023 Nov 6. >>PubMed-Link<<
Hanna Riedmann, Séverine Kayser, Martin Helmstädter, Daniel Epting, Carsten Bergmann
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17. Oktober 2023 (NEOCYST)
A novel role for the chloride intracellular channel protein Clic5 in ciliary functionSci Rep. 2023 Oct 17. >>PubMed-Link<<
Elisabeth Ott, Sylvia Hoff, Lara Indorf, Franck Anicet Ditengou, Julius Müller, Gina Renschler, Soeren S Lienkamp, Albrecht Kramer-Zucker, Carsten Bergmann, Daniel Epting
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25. September 2023 (NEOCYST)
Emerging principles of primary cilia dynamics in controlling tissue organization and functionEMBO J. 2023 Sep 25. >>PubMed-Link<<
Jay Gopalakrishnan, Kerstin Feistel, Benjamin M Friedrich, Anne Grapin-Botton, Nathalie Jurisch-Yaksi, Elvira Mass, David U Mick, Roman-Ulrich Müller, Helen May-Simera, Bernhard Schermer, Miriam Schmidts, Peter Walentek, Dagmar Wachten
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1. September 2023 (NEOCYST)
Autosomal Recessive Polycystic Kidney Disease: Diagnosis, Prognosis, and ManagementAdv Kidney Dis Health. 2023 Sep. >>PubMed-Link<<
Kathrin Burgmaier, Ilse J Broekaert, Max C Liebau
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17. April 2023 (NEOCYST)
Validation of attenuation imaging coefficient, shear wave elastography, and dispersion as emerging tools for non-invasive evaluation of liver tissue in childrenFront Pediatr. 2023 Apr 17. >>PubMed-Link<<
Metin Cetiner, Felix Schiepek, Ilja Finkelberg, Raphael Hirtz, Anja K Büscher
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13. April 2023 (NEOCYST)
Clinical Characteristics and Courses of Patients With Autosomal Recessive Polycystic Kidney Disease-Mimicking PhenocopiesKidney Int Rep. 2023 Apr 13 >>PubMed-Link<<
Abdul A Halawi, Kathrin Burgmaier, Anja K Buescher, Ismail Dursun, Florian Erger, Matthias Galiano, Michaela Gessner, Ibrahim Gökce, Djalila Mekahli, Sevgi Mir, Lukasz Obrycki, Rukshana Shroff, Stella Stabouli, Maria Szczepanska, Ana Teixeira, Lutz T Weber, Andrea Wenzel Elke Wühl, Katarzyna Zachwieja, Jörg Dötsch, Franz Schaefer, Max C Liebau
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1. März 2023 (NEOCYST)
A Low-Cost Sequencing Platform for Rapid Genotyping in ADPKD and its Impact on Clinical CareKidney Int Rep. 2023 Mar. >>PubMed-Link<<
Christoph Heinrich Lindemann, Andrea Wenzel, Florian Erger, Lea Middelmann, Julika Borde, Eric Hahnen, Denise Krauß, Simon Oehm, Sita Arjune, Polina Todorova, Kathrin Burgmaier, Max Christoph Liebau, Franziska Grundmann, Bodo B Beck, Roman-Ulrich Müller
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1. September 2022 (NEOCYST)
Refining Kidney Survival in 383 Genetically Characterized Patients With NephronophthisisKidney Int Rep. 2022 Jun 16. >>PubMed-Link<<
Jens Christian König, Rebeka Karsay, Joachim Gerß, Karl-Peter Schlingmann, Mareike Dahmer-Heath, Anna-Katharina Telgmann, Sabine Kollmann, Gema Ariceta, Valentine Gillion, Detlef Bockenhauer, Aurélia Bertholet-Thomas, Antonio Mastrangelo, Olivia Boyer, Marc Lilien, Stéphane Decramer, Joost P Schanstra, Martin Pohl, Raphael Schild, Stefanie Weber, Julia Hoefele, Jens Drube, Metin Cetiner, Matthias Hansen, Julia Thumfart, Burkhard Tönshoff, Sandra Habbig, Max Christoph Liebau, Martin Bald, Carsten Bergmann, Petra Pennekamp and Martin Konrad on behalf of the NEOCYST consortium
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23. August 2022 (NEOCYST)
Perspectives on Drug Development in Autosomal Recessive Polycystic Kidney DiseaseClin J Am Soc Nephrol. 2022 Aug 23. >>PubMed-Link<<
Max C Liebau, Erum A Hartung, Ronald D Perrone
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4. August 2022 (NEOCYST)
Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assemblyGenes Dis. 2022 Aug 4. >>PubMed-Link<<
Sebastian Sewerin, Jörg Piontek, Ria Schönauer, Sonja Grunewald, Angelika Rauch, Steffen Neuber, Carsten Bergmann, Dorothee Günzel, Jan Halbritter
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1. Juli 2022 (NEOCYST)
Phenotypic Variability in Siblings With Autosomal Recessive Polycystic Kidney DiseaseKidney Int Rep. 2022 Jul 1. >>PubMed-Link<<
Ramona Ajiri, Kathrin Burgmaier, Nurver Akinci, Ilse Broekaert, Anja Büscher, Ismail Dursun, Ali Duzova, Loai Akram Eid, Marc Fila, Michaela Gessner, Ibrahim Gokce, Laura Massella, Antonio Mastrangelo, Monika Miklaszewska, Larisa Prikhodina, Bruno Ranchin, Nadejda Ranguelov, Rina Rus, Lale Sever, Julia Thumfart, Lutz Thorsten Weber, Elke Wühl, Alev Yilmaz, Jörg Dötsch, Franz Schaefer, Max Christoph Liebau
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30. Juni 2022 (NEOCYST)
Definition, diagnosis, and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet working group on Kidney MalformationsNephrol Dial Transplant. 2022 Jun 30. >>PubMed-Link<<
Stefan Kohl, Fred E Avni, Peter Boor, Valentina Capone, William L Clapp, Diego De Palma, Tess Harris, Laurence Heidet, Alina C Hilger, Helen Liapis, Marc Lilie, Gianantonio Manzoni, Giovanni Montini, Susanna Negrisolo, Marie-Jeanne Pierrat, Ann Raes, Heiko Reutter, Michiel F Schreuder, Stefanie Weber, Paul J D Winyard, Adrian S Woolf, Franz Schaefer, Max C Liebau
joint publication NEOCYST/STOP-FSGS
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25. Mai 2022 (NEOCYST)
Crosstalk between cilia and autophagy: implication for human diseasesAutophagy. 2022 May 25. >>PubMed-Link<<
Manuela Morleo, Helena L A Vieira, Petra Pennekamp, Alessandro Palma, Liliana Bento-Lopes, Heymut Omran, Susana S Lopes, Duarte C Barral, Brunella Franco
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5. Mai 2022 (NEOCYST)
Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutationsAm J Hum Genet. 2022 May 5. >>PubMed-Link<<
John Devane, Elisabeth Ott, Eric G Olinger, Daniel Epting, Eva Decker, Anja Friedrich, Nadine Bachmann, Gina Renschler, Tobias Eisenberger, Andrea Briem-Richter, Enke Freya Grabhorn, Laura Powell, Ian J Wilson, Sarah J Rice, Colin G Miles, Katrina Wood, Genomics England Research Consortium; Palak Trivedi, Gideon Hirschfield, Andrea Pietrobattista, Elizabeth Wohler, Anya Mezina, Nara Sobreira, Emanuele Agolini, Giuseppe Maggiore, Mareike Dahmer-Heath, Ali Yilmaz, Melanie Boerries, Patrick Metzger, Christoph Schell, Inga Grünewald, Martin Konrad, Jens König, Bernhard Schlevogt, John A Sayer, Carsten Bergmann
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5. Mai 2022 (NEOCYST)
Potential Therapeutic Effects of Long-Term Stem Cell Administration: Impact on the Gene Profile and Kidney Function of PKD/Mhm (Cy/ plus ) RatsJ Clin Med. 2022 May 5. >>PubMed-Link<<
Daniela Nardozi, Stefania Palumbo, Arif Ul Maula Khan, Carsten Sticht, Karen Bieback, Samar Sadeghi, Mark Andreas Kluth, Michael Keese, Norbert Gretz
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1. Mai 2022 (NEOCYST)
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tractKidney Int. 2022 May. >>PubMed-Link<<
Johannes Münch, Marie Engesser, Ria Schönauer, J Austin Hamm, Christin Hartig, Elena Hantmann, Gulsen Akay, Davut Pehlivan, Tadahiro Mitani, Zeynep Coban Akdemir, Beyhan Tüysüz, Toshihiko Shirakawa, Sumito Dateki, Laura R Claus, Albertien M van Eerde, Genomics England Research Consortium; Thomas Smol, Louise Devisme, Hélène Franquet, Tania Attié-Bitach, Timo Wagner, Carsten Bergmann, Anne Kathrin Höhn, Shirlee Shril, Ari Pollack, Tara Wenger, Abbey A Scott, Sarah Paolucci, Jillian Buchan, George C Gabriel, Jennifer E Posey, James R Lupski, Florence Petit, Andrew A McCarthy, Gregory J Pazour, Cecilia W Lo, Bernt Popp, Jan Halbritter
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9. März 2022 (NEOCYST)
Primary URECs: a source to better understand the pathology of renal tubular epithelia in pediatric hereditary cystic kidney diseasesOrphanet J Rare Dis. 2022 Mar 9. >>PubMed-Link<<
Wolfgang H Ziegler, Sarah Lüdiger, Fatima Hassan, Margarita E Georgiadis, Kathrin Swolana, Amrit Khera, Arne Mertens, Doris Franke, Kai Wohlgemuth, Mareike Dahmer-Heath, Jens König, Claudia Dafinger, Max C Liebau, Metin Cetiner, Carsten Bergmann, Birga Soetje, Dieter Haffner
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6. Februar 2022 (NEOCYST)
The ciliary transition zone protein TMEM218 synergistically interacts with the NPHP module and its reduced dosage leads to a wide range of syndromic ciliopathiesHum Mol Genet. 2022 Feb 6. >>PubMed-Link<<
Daniel Epting, Eva Decker, Elisabeth Ott, Tobias Eisenberger, Ingrid Bader, Nadine Bachmann, Carsten Bergmann
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2. Februar 2022 (NEOCYST)
Interstitial Nephritis: A Change in Diagnosis With Next-Generation SequencingKidney Int Rep. 2022 Feb 2. >>PubMed-Link<<
Mira Choi, Anne Rübsam, Marten Schulz, Eva Decker, Anja Friedrich, Eva Schrezenmeier, Fabian Halleck, Kai-Uwe Eckardt, Carsten Bergmann
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25. Januar 2022 (NEOCYST)
Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practiceNephrol Dial Transplant. 2022 Jan 25. >>PubMed-Link<<
Nine Knoers, Corinne Antignac, Carsten Bergmann, Karin Dahan, Sabrina Giglio, Laurence Heidet, Beata S Lipska-Ziętkiewicz, Marina Noris, Giuseppe Remuzzi, Rosa Vargas-Poussou, Franz Schaefer
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4. November 2021 (NEOCYST)
Early childhood height-adjusted total kidney volume as a risk marker of kidney survival in ARPKDSci Rep. 2021 Nov 4. >>PubMed-Link<<
Kathrin Burgmaier, Samuel Kilian, Klaus Arbeiter, Bahriye Atmis, Anja Büscher, Ute Derichs, Ismail Dursun, Ali Duzova, Loai Akram Eid, Matthias Galiano, Michaela Gessner, Ibrahim Gokce, Karsten Haeffner, Nakysa Hooman, Augustina Jankauskiene, Friederike Körber, Germana Longo, Laura Massella, Djalila Mekahli, Gordana Miloševski-Lomić, Hulya Nalcacioglu, Rina Rus, Rukshana Shroff , Stella Stabouli, Lutz T Weber, Simone Wygoda, Alev Yilmaz, Katarzyna Zachwieja, Ilona Zagozdzon, Jörg Dötsch, Franz Schaefer, Max Christoph Liebau, ARegPKD Consortium
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1. November 2021 (NEOCYST)
NPHP1 gene-associated nephronophthisis is associated with an occult retinopathyKidney Int. 2021 Nov. >>PubMed-Link<<
Johannes Birtel, Georg Spital, Marius Book, Sandra Habbig, Sören Bäumner, Vera Riehmer, Bodo B Beck, David Rosenkranz, Hanno J Bolz, Mareike Dahmer-Heath, Philipp Herrmann, Jens König, Peter Charbel Issa
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18. Oktober 2021 (NEOCYST)
Generation of an induced pluripotent stem cell line (DHMCi006-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a compound heterozygous missense mutation in the fibrocystin encoding PKHD1 geneStem Cell Res. 2021 Oct 18. >>PubMed-Link<<
Theresa Leonie Fluhr, Mansoureh Tabatabaeifar, Hanna Syring, Gudrun Göhring, Franz Schaefer, Sabine Jung-Klawitter
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16. Oktober 2021 (NEOCYST)
Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 geneStem Cell Res. 2021 Oct 16. >>PubMed-Link<<
Mansoureh Tabatabaeifar, Theresa Leonie Fluhr, Hanna Syring, Gudrun Göhring, Franz Schaefer, Sabine Jung-Klawitter
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5. Oktober 2021 (NEOCYST)
Is There a Functional Role of Mitochondrial Dysfunction in the Pathogenesis of ARPKD?Front Med (Lausanne). 2021 Oct 5. >>PubMed-Link<<
Max Christoph Liebau
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1. September 2021 (NEOCYST)
Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variantsKidney Int. 2021 Sep. >>PubMed-Link<<
Burgmaier, K., Brinker, L., Erger, F., Beck, B. B., Benz, M. R., Bergmann, C., Boyer, O., Collard, L., Dafinger, C., Fila, M., Kowalewska, C., Lange-Sperandio, B., Massella, L., Mastrangelo, A., Mekahli, D., Miklaszewska, M., Ortiz-Bruechle, N., Patzer, L., Prikhodina, L., Ranchin, B., Ranguelov, N., Schild, R., Seeman, T., Sever, L., Sikora, P., Szczepanska, M., Teixeira, A., Thumfart, J., Uetz, B., Weber, L. T., Wuhl, E., Zerres, K., Dotsch, J., Schaefer, F., Liebau, M. C., Escape Study Grp, G. P. N. Study Grp, A. RegPKD Consortium
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1. September 2021 (NEOCYST)
Systematic evaluation of olfaction in patients with hereditary cystic kidney diseases/renal ciliopathiesJ Med Genet. 2021 Sep. >>PubMed-Link<<
Mareike Dahmer-Heath, Valentin Schriever, Sabine Kollmann, Carolin Schleithoff, Andrea Titieni, Metin Cetiner, Ludwig Patzer, Burkhard Tönshoff, Matthias Hansen, Petra Pennekamp, Joachim Gerß, Martin Konrad, Jens König
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12. August 2021 (NEOCYST)
Systematic review on outcomes used in clinical research on autosomal recessive polycystic kidney disease-are patient-centered outcomes our blind spot?Pediatr Nephrol. 2021 Aug 12. >>PubMed-Link<<
Gimpel, C., Liebau, M. C., Schaefer, F.
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6. Juli 2021 (NEOCYST)
DLG5 variants are associated with multiple congenital anomalies including ciliopathy phenotypesJ Med Genet. 2021 Jul. >>PubMed-Link<<
Jonathan Marquez, Nina Mann, Kathya Arana, Engin Deniz, Weizhen Ji, Monica Konstantino, Emily K Mis, Charu Deshpande, Lauren Jeffries, Julie McGlynn, Hannah Hugo, Eugen Widmeier, Martin Konrad, Velibor Tasic, Raffaella Morotti , Julia Baptista, Sian Ellard, Saquib Ali Lakhani, Friedhelm Hildebrandt, Mustafa K Khokha
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1. Juli 2021 (NEOCYST)
Diagnosis and Management of Renal Cystic Disease of the Newborn: Core Curriculum 2021Am J Kidney Dis. 2021 Jul. >>PubMed-Link<<
Rupesh Raina, Ronith Chakraborty, Sidharth K Sethi, Deepak Kumar, Kelly Gibson, Carsten Bergmann
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26. März 2021 (NEOCYST)
Collagen IV alpha 345 dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture’s and Alport diseasesJ Biol Chem. Jan-Jun 2021. >>PubMed-Link<<
Pokidysheva, E. N., Seeger, H., Pedchenko, V., Chetyrkin, S., Bergmann, C., Abrahamson, D., Cui, Z. W., Delpire, E., Fervenza, F. C., Fidler, A. L., Fogo, A. B., Gaspert, A., Grohmann, M., Gross, O., Haddad, G., Harris, . C., Kashtan, C., Kitching, A. R., Lorenzen, J. M., McAdoo, S., Pusey, C. D., Segelmark, M., Simmons, A., Voziyan, P. A., Wagner, T., Wuthrich, R. P., Zhao, M. H., Boudko, S. P., Kistler, A. D., Hudson, B. G.
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7. März 2021 (NEOCYST)
The wind of change in the management of autosomal dominant polycystic kidney disease in childhoodPediatr Nephrol. 2021 Mar 7. >>PubMed-Link<<
Charlotte Gimpel, Carsten Bergmann, Djalila Mekahli
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12. Februar 2021 (NEOCYST)
Targeted deletion of Ruvbl1 results in severe defects of epidermal development and perinatal mortalityMol Cell Pediatr. 2021 Feb 12. >>PubMed-Link<<
Claudia Dafinger, Thomas Benzing, Jörg Dötsch, Bernhard Schermer, Max C Liebau
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12. November 2020 (NEOCYST)
Occurrence of Portal Hypertension and Its Clinical Course in Patients With Molecularly Confirmed Autosomal Recessive Polycystic Kidney Disease (ARPKD)Front Pediatr. 2020 Nov 12. [Epub ahead of print] >>PubMed-Link<<
Dorota Wicher, Ryszard Grenda, Mikołaj Teisseyre, Marek Szymczak, Paulina Halat-Wolska, Dorota Jurkiewicz, Max Christoph Liebau, Elżbieta Ciara, Małgorzata Rydzanicz, Joanna Kosińska, Krystyna Chrzanowska, Irena Jankowska
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1. November 2020 (NEOCYST)
Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndromeHum Mutat. 2020 Nov 1. [Epub ahead of print] >>PubMed-Link<<
Daniel Epting, Lokuliyange D S Senaratne, Elisabeth Ott, Asbjørn Holmgren, Dulika Sumathipala, Selma M Larsen, Julia Wallmeier, Diana Bracht, Kari-Anne M Frikstad, Suzanne Crowley, Alma Sikiric, Tuva Barøy, Barbara Käsmann-Kellner, Eva Decker, Christian Decker, Nadine Bachmann, Sebastian Patzke, Ian G Phelps, Nicholas Katsanis, Rachel Giles, Miriam Schmidts, Manuela Zucknick, Soeren S Lienkamp, Heymut Omran, Erica E Davis, Dan Doherty, Petter Strømme, Eirik Frengen, Carsten Bergmann, Doriana Misceo
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28. Oktober 2020 (NEOCYST)
The carboxy-terminus of the human ARPKD protein fibrocystin can control STAT3 signalling by regulating SRC-activationJ Cell Mol Med. 2020 Oct 28. [Epub ahead of print] >>PubMed-Link<<
Claudia Dafinger, Amrei M Mandel, Alina Braun, Heike Göbel, Kathrin Burgmaier, Laura Massella, Antonio Mastrangelo, Jörg Dötsch, Thomas Benzing, Thomas Weimbs, Bernhard Schermer, Max C Liebau
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1. Oktober 2020 (NEOCYST)
Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitmentKidney Int. 2020 Oct. [Epub ahead of print] >>PubMed-Link<<
Ria Schönauer, Wenjun Jin, Anastasia Ertel, Melanie Nemitz-Kliemchen, Nydia Panitz, Elena Hantmann, Anna Seidel, Daniela A Braun, Shirlee Shril, Matthias Hansen, Khurrum Shahzad, Richard Sandford, Sophie Saunier, Alexandre Benmerah, Carsten Bergmann, Friedhelm Hildebrandt, Jan Halbritter
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29. September 2020 (NEOCYST)
Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD)Sci Rep. 2020 Sep 29. [Epub ahead of print] >>PubMed-Link<<
Kathrin Burgmaier, Gema Ariceta, Martin Bald, Anja Katrin Buescher, Mathias Burgmaier, Florian Erger, Michaela Gessner, Ibrahim Gokce, Jens König, Claudia Kowalewska, Laura Massella, Antonio Mastrangelo, Djalila Mekahli, Lars Pape, Ludwig Patzer, Alexandra Potemkina, Gesa Schalk, Raphael Schild, Rukshana Shroff, Maria Szczepanska, Katarzyna Taranta-Janusz, Marcin Tkaczyk, Lutz Thorsten Weber, Elke Wühl, Donald Wurm, Simone Wygoda, Ilona Zagozdzon, Jörg Dötsch, Jun Oh, Franz Schaefer, Max Christoph Liebau
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1. September 2020 (NEOCYST)
Nierenzysten und zystische Nierenerkrankungen bei Kindern (AWMF S2k-Leitlinie) [Kidney Cysts and Cystic Nephropathies in Children – A Consensus Guideline by 10 German Medical Societies]Klin Padiatr. 2020 Sep. >>PubMed-Link<<
Charlotte Gimpel, Carsten Bergmann, Florian Brinkert, Metin Cetiner, Ulrich Gembruch, Dieter Haffner, Markus Kemper, Jens König, Max Liebau, Rolf Felix Maier, Jun Oh, Lars Pape, Silke Riechardt, Udo Rolle, Rainer Rossi, Joachim Stegmann, Udo Vester, Constantin von Kaisenberg, Stefanie Weber, Franz Schaefer
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24. August 2020 (NEOCYST)
Metabolic Changes in Polycystic Kidney Disease as a Potential Target for Systemic TreatmentInt J Mol Sci. 2020 Aug 24. [Epub ahead of print] >>PubMed-Link<<
Sophie Haumann, Roman-Ulrich Müller, Max C Liebau
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1. August 2020 (NEOCYST)
Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genesGenet Med. 2020 Aug. [Epub ahead of print] >>PubMed-Link<<
Ria Schönauer, Sebastian Baatz, Melanie Nemitz-Kliemchen, Valeska Frank, Friederike Petzold, Sebastian Sewerin, Bernt Popp, Johannes Münch, Steffen Neuber, Carsten Bergmann, Jan Halbritter
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20. Juli 2020 (NEOCYST)
Fibrocystin is Essential to Cellular Control of Adhesion and Epithelial MorphogenesisInt J Mol Sci. 2020 Jul 20. >>PubMed-Link<<
Wolfgang H Ziegler, Birga Soetje, Lisa P Marten, Jana Wiese, Mithila Burute, Dieter Haffner
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25. Mai 2020 (NEOCYST)
Maintenance Peritoneal Dialysis in Children With Autosomal Recessive Polycystic Kidney Disease: A Comparative Cohort Study of the International Pediatric Peritoneal Dialysis Network RegistryAm J Kidney Dis. 2020 Mar. [Epub ahead of print] >>PubMed-Link<<
Abdelaziz Akarkach, Kathrin Burgmaier, Anja Sander, Nakysa Hooman, Lale Sever, Francisco Cano, Pedro Zambrano, Ilmay Bilge, Joseph T Flynn, Onder Yavascan, Patricia G Vallés , Reyner Loza Munarriz, Hiren P Patel, Erkin Serdaroglu, Vera H Koch, Angela Del Carmen Suarez, Monica Galanti, Claudia Gonzalez Celedon, Anabella Rébori, Jameela A Kari, Cynthia J Wong, Ewa Elenberg, Luisa F Rojas, Bradley A Warady, Max C Liebau, Franz Schaefer, IPPN Registry
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20. April 2020 (NEOCYST)
STAT Signaling in Polycystic Kidney DiseaseCell Signal. 2020 Apr 20. [Epub ahead of print] >>PubMed-Link<<
Sebastian Strubl, Jacob A Torres, Alison K Spindt, Hannah Pellegrini, Max C Liebau, Thomas Weimbs
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1. Dezember 2019 (NEOCYST)
TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic SyndromeJ Am Soc Nephrol. 2019 Dec. [Epub ahead of print] >>PubMed-Link<<
Lina L Kampf, Ronen Schneider, Lea Gerstner, Roland Thünauer , Mengmeng Chen, Martin Helmstädter, Ali Amar, Ana C Onuchic-Whitford, Reyner Loza Munarriz, Afig Berdeli, Dominik Mülle, Eva Schrezenmeier, Klemens Budde, Shrikant Mane, Kristen M Laricchia, Heidi L Rehm, Daniel G MacArthur, Richard P Lifton, Gerd Walz, Winfried Römer, Carsten Bergmann, Friedhelm Hildebrandt, Tobias Hermle
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15. Oktober 2019 (NEOCYST)
Human C-terminal CUBN variants associate with chronic proteinuria and normal renal functionJ Clin Invest. 2019 Oct 15. [Epub ahead of print] >>PubMed-Link<<
Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaudé L, Tête MJ, Cambier A, Hogan J, Baudouin V, Krid S, Bensman A, Lammens F, Louillet F, Ranchin B, Vigneau C, Bouteau I, Isnard-Bagnis C, Mache CJ, Schäfer T, Pape L, Gödel M, Huber TB, Benz M, Klaus G, Hansen M, Latta K, Gribouval O, Morinière V, Tournant C, Grohmann M, Kuhn E, Wagner T, Bole-Feysot C, Jabot-Hanin F, Nitschké P, Ahluwalia TS, Köttgen A, Brix Folsted Andersen C, Bergmann C, Antignac C, Simons M.
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5. September 2019 (NEOCYST)
Autosomal dominant tubulointerstitial kidney diseaseNat Rev Dis Primers. 2019 Sep 5. [Epub ahead of print] >>PubMed-Link<<
Olivier Devuyst, Eric Olinger, Stefanie Weber, Kai-Uwe Eckardt, Stanislav Kmoch , Luca Rampoldi, Anthony J Bleyer
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28. Mai 2019 (NEOCYST)
Clinical courses and complications of young adults with Autosomal Recessive Polycystic Kidney Disease (ARPKD)Sci Rep. 2019 May 28. [Epub ahead of print] >>PubMed-Link<<
Burgmaier K, Kilian S, Bammens B, Benzing T, Billing H, Büscher A, Galiano M, Grundmann F, Klaus G, Mekahli D, Michel-Calemard L, Milosevski-Lomic G, Ranchin B, Sauerstein K, Schaefer S, Shroff R, Sterenborg R, Verbeeck S, Weber LT, Wicher D, Wühl E, Dötsch J, Schaefer F, Liebau MC
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22. Mai 2019 (NEOCYST)
International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease (ADPKD) in children and young peopleNat Rev Nephrol. 2019 May 22.[Epub ahead of print] >>PubMed-Link<<
C. Gimpel, C. Bergmann, D.Bockenhauer, L. Breysem, M. Cadnapaphornchai, M.Cetiner, J. Dudley, F Emma, M. Konrad, T. Harris, P. Harris, J. König, M.Liebau, M. Marlais, D.Mekahli, A.Metcalfe, J. Oh, R. Perrone, M. Sinha, A. Titieni, R. Torra, S. Weber, P. Winyard, and F.Schaefer
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1. April 2019 (NEOCYST)
Inactivation of Apoptosis Antagonizing Transcription Factor in tubular epithelial cells induces accumulation of DNA damage and nephronophthisisKidney Int. 2019 Apr;. [Epub ahead of print] >>PubMed-Link<<
Manaswita Jain, Rainer W J Kaiser, Katrin Bohl, Martin Hoehne, Heike Göbel, Malte P Bartram, Sandra Habbig, Roman-Ulrich Müller, Agnes B Fogo, Thomas Benzing, Bernhard Schermer, Katja Höpker, Gisela G Slaats
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1. März 2019 (NEOCYST)
Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus StatementRadiology. 2019 Mar. [Epub ahead of print] >>PubMed-Link<<
Charlotte Gimpel, E Fred Avni, Luc Breysem, Kathrin Burgmaier, Anna Caroli, Metin Cetiner, Dieter Haffner, Erum A Hartung, Doris Franke, Jens König, Max C Liebau, Djalila Mekahli, Albert C M Ong, Lars Pape, Andrea Titieni, Roser Torra, Paul J D Winyard, Franz Schaefer
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18. Februar 2019 (NEOCYST)
Urinary proteome signature of Renal Cysts and Diabetes syndrome in childrenSci Rep. 2019 Feb 18. [Epub ahead of print] >>PubMed-Link<<
Ricci P, Magalhães P, Krochmal M, Pejchinovski M, Daina E, Caruso MR, Goea L, Belczacka I, Remuzzi G, Umbhauer M, Drube J, Pape L, Mischak H, Decramer S, Schaefer F, Schanstra JP, Cereghini S, Zürbig P.
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30. Januar 2019 (NEOCYST)
Management of ciliopathies in childhood and adolescenceDer Nephrologe 2019, doi.org/10.1007/s11560-019-0312-4
J. König, S. Habbig, M.C. Liebau
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21. Januar 2019 (NEOCYST)
HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood RegistryPediatr Nephrol. 2019 Jan 21. [Epub ahead of print] >>PubMed-Link<<
Okorn C, Goertz A, Vester U, Beck BB, Bergmann C, Habbig S, König J, Konrad M, Müller D, Oh J, Ortiz-Brüchle N, Patzer L, Schild R, Seeman T, Staude H, Thumfart J, Tönshoff B, Walden U, Weber L, Zaniew M, Zappel H, Hoyer PF, Weber S.
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10. Januar 2019 (NEOCYST)
Diagnostic Utility of Exome Sequencing for Kidney DiseaseN Engl J Med. 2019 Jan 10. [Epub ahead of print] >>PubMed-Link<<
Emily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, Slavé Petrovski, Vimla S Aggarwa, Hila Milo-Rasouly, Yifu Li, Junying Zhang, Jordan Nestor, Priya Krithivasan, Wan Yee Lam, Adele Mitrotti, Stacy Piva, Byum H Kil, Debanjana Chatterjee, Rachel Reingold, Drew Bradbury, Michael DiVecchia, Holly Snyder, Xueru Mu, Karla Mehl, Olivia Balderes, David A Fasel, Chunhua Weng, Jai Radhakrishnan, Pietro Canetta, Gerald B Appel, Andrew S Bomback, Wooin Ahn, Natalie S Uy 1 , Shumyle Alam, David J Cohen, Russell J Crew, Geoffrey K Dube, Maya K Rao, Sitharthan Kamalakaran, Brett Copeland, Zhong Ren, Joshua Bridgers, Colin D Malone, Caroline M Mebane, Neha Dagaonkar, Bengt C Fellström, Carolina Haefliger, Sumit Mohan, Simone Sanna-Cherchi, Krzysztof Kiryluk, Jan Fleckner, Ruth March, Adam Platt, David B Goldstein, Ali G Gharavi
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19. Dezember 2018 (NEOCYST)
Editorial: Genetic kidney diseases of childhoodFrontiers in Pediatrics 2018 Dec 19. [Epub ahead of print] >>PubMed-Link<<
Schmidts M, Liebau MC.
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17. Dezember 2018 (NEOCYST)
Unmet needs and challenges for follow-up and treatment of ADPKD: the pediatric perspectiveClin Kidney J. 2018 Dec. [Epub ahead of print] >>PubMed-Link<<
De Rechter S, Bammens B, Schaefer F, Liebau MC, Mekahli D,
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6. Dezember 2018 (NEOCYST)
Polycystic kidney diseaseNat Rev Dis Primers. 2018 Dec 6. [Epub ahead of print] >>PubMed-Link<<
Carsten Bergmann, Lisa M Guay-Woodford, Peter C Harris, Shigeo Horie, Dorien J M Peters, Vicente E Torres
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3. Dezember 2018 (NEOCYST)
Nephronophthisis and related ciliopathiesmedgen, https://doi.org/10.1007/s11825-018-0213-3 Biol Chem, 2018.
Titieni A, König J
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25. Oktober 2018 (NEOCYST)
Early and Severe Polycystic Kidney Disease and Related Ciliopathies: An Emerging Field of InterestNephron. 2018 Oct 25. [Epub ahead of print] >>PubMed-Link<<
Bergmann C.
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17. August 2018 (NEOCYST)
Homozygosity for the c.428delG variant in KIAA0586 in a healthy individual: implications for molecular testing in patients with Joubert syndrome.J Med Genet. 2018 Aug 17. pii: jmedgenet-2018-105470. doi: 10.1136/jmedgenet-2018-105470.
Pauli S, Altmüller J, Schröder S, Ohlenbusch A, Dreha-Kulaczewski S, Bergmann C, Nürnberg P, Thiele H, Li Y, Wollnik B, Brockmann K
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12. Juli 2018 (NEOCYST)
Human urine-derived renal epithelial cells provide insights into kidney-specific alternate splicing variantsEur J Hum Genet. 12 July 2018. [Epub ahead of print] >>PubMed-Link<<
Molinari E, Decker E, Mabillard H, Tellez J, Srivastava S, Raman S, Wood K, Kempf C, Alkanderi S, Ramsbottom SA, Miles CG, Johnson CA, Hildebrandt F, Bergmann C, Sayer JA.
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1. Juli 2018 (NEOCYST)
Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140Hum Mutat. 2018 Jul. [Epub ahead of print] >>PubMed-Link<<
Véronique Geoffroy, Corinne Stoetzel, Sophie Scheidecker , Elise Schaefer, Isabelle Perrault, Séverine Bär, Ariane Kröll, Marion Delbarre, Manuela Antin, Anne-Sophie Leuvrey, Charline Henry, Hélène Blanché, Eva Decker, Katja Kloth, Günter Klaus, Christoph Mache, Dominique Martin-Coignard, Steven McGinn, Anne Boland, Jean-François Deleuze, Sylvie Friant, Sophie Saunier, Jean-Michel Rozet, Carsten Bergmann, Hélène Dollfus, Jean Muller
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28. Juni 2018 (NEOCYST)
Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalusExp Mol Med. 2018 Jun 28. [Epub ahead of print] >>PubMed-Link<<
Dafinger C, Rinschen MM, Borgal L, Ehrenberg C, Basten SG, Franke M, Höhne M, Rauh M, Göbel H, Bloch W, Wunderlich FT, Peters DJM, Tasche D, Mishra T, Habbig S, Dötsch J, Müller RU, Brüning JC, Persigehl T, Giles RH, Benzing T, Schermer B, Liebau MC.
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4. Juni 2018 (NEOCYST)
Gastrostomy tube insertion in pediatric patients with autosomal recessive polycystic kidney disease (ARPKD): current practiceFrontiers in Pediatrics. 2018 Jun 4. [Epub ahead of print] >>PubMed-Link<<
Burgmaier K, Brandt J, Shroff R, Witters P, Weber LT, Dötsch J, Schaefer F, Mekahli D, Liebau MC.
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22. Mai 2018 (NEOCYST)
A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate GenesCell Rep. 2018 May 22. [Epub ahead of print] >>PubMed-Link<<
Markus M Rinschen, Markus Gödel, Florian Grahammer, Stefan Zschiedrich, Martin Helmstädter, Oliver Kretz, Mostafa Zarei, Daniela A Braun, Sebastian Dittrich, Caroline Pahmeyer, Patricia Schroder, Carolin Teetzen, HeonYung Gee, Ghaleb Daouk , Martin Pohl, Elisa Kuhn, Bernhard Schermer, Victoria Küttner, Melanie Boerries, Hauke Busch, Mario Schiffer, Carsten Bergmann, Marcus Krüger, Friedhelm Hildebrandt, Joern Dengjel, Thomas Benzing, Tobias B Huber
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9. Mai 2018 (NEOCYST)
Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney DiseaseJ Pediatr. 2018 May 9. [Epub ahead of print] >>PubMed-Link<<
Burgmaier K, Kunzmann K, Ariceta G, Bergmann C, Buescher AK, Burgmaier M, Dursun I, Duzova A, Eid L, Erger F, Feldkoetter M, Galiano M, Geßner M, Goebel H, Gokce I, Haffner D, Hooman N, Hoppe B, Jankauskiene A, Klaus G, König J, Litwin M, Massella L, Mekahli D, Melek E, Mir S, Pape L, Prikhodina L, Ranchin B, Schild R, Seeman T, Sever L, Shroff R, Soliman NA, Stabouli S, Stanczyk M, Tabel Y, Taranta-Janusz K, Testa S, Thumfart J, Topaloglu R, Weber LT, Wicher D, Wühl E, Wygoda S, Yilmaz A, Zachwieja K, Zagozdzon I, Zerres K; ESCAPE Study Group; GPN Study Group, Dötsch J, Schaefer F, Liebau MC; ARegPKD consortium.
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3. Mai 2018 (NEOCYST)
An optimized electroporation approach for efficient CRISPR/Cas9 genome editing in murine zygotesPLoS One. 2018 May 3. [Epub ahead of print] >>PubMed-Link<<
Simon E Tröder, Lena K Ebert, Linus Butt, Sonja Assenmacher, Bernhard Schermer, Branko Zevnik
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9. März 2018 (NEOCYST)
Single-nephron proteomes connect morphology and function in proteinuric kidney diseaseKidney International 2018 Mar 9. [Epub ahead of print] >>PubMed-Link<<
Höhne M, Frese CK, Grahammer F, Dafinger C, Ciarimboli G, Butt L, Binz J, Hackl MJ, Rahmatollahi M, Kann M, Schneider S, Altintas MM, Schermer B, Reinheckel T, Göbel H, Reiser J, Huber TB, Kramann R, Seeger-Nukpezah T, Liebau MC, Beck BB, Benzing T, Beyer A, Rinschen MM
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13. Februar 2018 (NEOCYST)
Network for Early Onset Cystic Kidney Diseases-A Comprehensive Multidisciplinary Approach to Hereditary Cystic Kidney Diseases in Childhood.Front Pediatr. 2018 Feb 13. [Epub ahead of print] >>PubMed-Link<<
König JC, Titieni A, Konrad M
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9. Februar 2018 (NEOCYST)
Genetics of Autosomal Recessive Polycystic Kidney Disease and Its Differential DiagnosesFront Pediatr. 2018 Feb 9. [Epub ahead of print] >>PubMed-Link<<
Bergmann C.
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17. Dezember 2017 (NEOCYST)
Recent advances in the molecular diagnosis of polycystic kidney diseaseExpert Rev Mol Diagn 2017 Dec. [Epub ahead of print] >>PubMed-Link<<
Bergmann C.
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1. Dezember 2017 (NEOCYST)
Magnetic resonance T2 mapping and diffusion-weighted imaging for early detection of cystogenesis and response to therapy in a mouse model of polycystic kidney diseaseKidney Int. 2017 Dec. [Epub ahead of print] >>PubMed-Link<<
Franke M, Baeßler B, Vechtel J, Dafinger C, Höhne M, Borgal L, Göbel H, Koerber F, Maintz D, Benzing T, Schermer B, Persigehl T.
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30. November 2017 (NEOCYST)
No general treatment recommendation for nephrectomy in prenatal suspicion of ARPKDDer Urologe, 2017 Nov;56,(11), 1465–1466.
Ebner K.,Liebau MC.
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27. November 2017 (NEOCYST)
Perinatal diagnosis, management, and follow-up of cystic renal diseases – a clinical practice recommendation with systematic literature reviewsJAMA Pediatr. 2018 Jan 1. [Epub ahead of print] >>PubMed-Link<<
Gimpel C., Avni F.E., Bergmann C., Cetiner M., Habbig S., Haffner D., König J., Konrad M., Liebau MC., Pape L, Rellensmann G., Titieni A., Kaiserberg von C., Weber S., Winyard P. J.D., Schaefer F.
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16. November 2017 (NEOCYST)
Phenotypic Spectrum of Children with Nephronophthisis and Related CiliopathiesClin J Am Soc Nephrol 2017 Nov 16. [Epub ahead of print] >>PubMed-Link<<
König J., Kranz B., König S., Schlingmann K. P., Titieni A., Tönshoff B., Habbig S., Pape L., Häffner K., Hansen M., Büscher A., Bald M., Billing H., Schild R´., Walden U., Hampel T., Staude H., Riedl M., Gretz N., Lablans M., Bergmann C., Hildebrandt F., Omran H., Konrad M. for the Gesellschaft für Pädiatrische Nephrologie (GPN)
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29. September 2017 (NEOCYST)
Clinicians‘ attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney disease.PLoS One. 2017 Sep 29. [Epub ahead of print] >>PubMed-Link<<
De Rechter S, Kringen J, Janssens P, Liebau MC, Devriendt K, Levtchenko E, Bergmann C, Jouret F, Bammens B, Borry P, Schaefer F, Mekahli D.
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17. Juli 2017 (NEOCYST)
Mutations in DZIP1L, which encodes a ciliary transition zone protein, cause autosomal recessive polycystic kidney diseaseNat Genet. 2017 Jul. [Epub ahead of print] >>PubMed-Link<<
Lu H, Galeano MCR, Ott E, Kaeslin G, Kausalya PJ, Kramer C, Ortiz-Brüchle N, Hilger N, Metzis V, Hiersche M, Tay SY,
Tunningley R, Vij S, Courtney AD, Whittle B, Wühl E, Vester U, Hartleben B, Neuber S, Frank V, Little MH, Epting D, Papathanasiou P, Perkins AC, Wright GD, Hunziker W, Gee HY, Otto EA, Zerres K, Hildebrandt F, Roy S, Wicking C, Bergmann C -
14. Juli 2017 (NEOCYST)
The ciliary membrane-associated proteome reveals actin-binding proteins as key components of ciliaEMBO reports 2017 Jul 14. [Epub ahead of print] >>PubMed-Link<<
Priyanka Kohli, Martin Höhne, Christian Jüngst, Sabine Bertsch, Lena K Ebert, Astrid C Schauss, Thomas Benzing, Markus M Rinschen& Bernhard Schermer
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7. Juli 2017 (NEOCYST)
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutationsPediatr Nephrol. 2017 Jul. [Epub ahead of print] >>PubMed-Link<<
Ebner K, Dafinger C, Ortiz-Bruechle N, Koerber F, Schermer B, Benzing T, Dötsch J, Zerres K, Weber LT, Beck BB, Liebau MC.
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7. Juli 2017 (NEOCYST)
Advances in renal genetic diagnosisCell Tissue Res 2017 Jul. >>PubMed-Link<<
Bergmann C.
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15. Mai 2017 (NEOCYST)
A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndromeClin Nephrol. 2017 May 15. [Epub ahead of print] >>PubMed-Link<<
Ebner K, Reintjes N, Feldkötter M, Körber F, Nagel M, Dötsch J, Hoppe B, Weber LT, Beck BB, Liebau MC.
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28. April 2017 (NEOCYST)
Expanding the role of vasopressin antagonism in polycystic kidney diseases: from adult to children?Pediatric Nephrology 2017 Apr 28. [Epub ahead of print] >>PubMed-Link<<
Janssens P.,Weydert C. ,De Rechter S., Wissing KM.,Liebau MC, Mekahli D.
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27. März 2017 (NEOCYST)
Application and Comparison of Supervised Learning Strategies to Classify Polarity of Epithelial Cell Spheroids in 3D CultureFront Genet. 2020 Mar 27. [Epub ahead of print] >>PubMed-Link<<
Birga Soetje, Joachim Fuellekrug, Dieter Haffner, Wolfgang H Ziegler
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16. Februar 2017 (NEOCYST)
ARegPKD Consortium. Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney DiseaseFront Pediatr. 2017 Feb 16;5:18. doi: 10.3389/fped.2017.00018. eCollection 2017.
Ebner K, Schaefer F, Liebau MC; ARegPKD Consortium -
16. Februar 2017 (NEOCYST)
Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney DiseaseFront Pediatr. 2017 Feb 16. [Epub ahead of print] >>PubMed-Link<<
Kathrin Ebner, Franz Schaefer, Max Christoph Liebau, ARegPKD Consortium
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20. Januar 2017 (NEOCYST)
Neues zu ZystennierenDer Nephrologe 01/2017
Liebau MC; Kidney Week 2016
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7. November 2016 (NEOCYST)
Aktuelle Forschung auf dem Gebiet der seltenen Nierenerkrankungen am Beispiel der Autosomal Rezessiven Polyzystischen Nierenerkrankung (ARPKD)Nieren- und Hochdruckkrankheiten, Jahrgang 45, Nr. 11/2016, S. 425-431
K. Ebner, K. Zerres und M.C. Liebau
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1. August 2016 (NEOCYST)
MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosumEur J Med Genet. 2016 Aug.
Bader I, Decker E, Mayr JA, Lunzer V, Koch J, Boltshauser E, Sperl W, Pietsch P, Ertl-Wagner B, Bolz H, Bergmann C, Rittinger O.
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1. Januar 2016 (NEOCYST)
Polycystic Kidney Disease: ADPKD and ARPKDDOI: 10.1007/978-3-662-52972-0_12
In book: Pediatric Kidney Disease, pp.333-367 (Schaefer, Geary)
Patiententage 2021: AKPRD Nierenzysten (online!)
Patiententag 2021: Bardet-Biedl-Syndrom
Format (Online- oder Präsenzveranstaltung) noch offen.