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How has Max C. Liebau's publication output changed over time?
ScholarIQpublication output · 2005–2025
Output grew0% over the shown period — from 1 works in 2005 to 1 in 2025.
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2005201020112012201320142019202020232025
What are the most-cited papers on Max C. Liebau?
ScholarIQmost cited works
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
Moumita Chaki, Rannar Airik, Amiya K. Ghosh, Rachel H. Giles, Rui Chen, Gisela G. Slaats, Hui Wang, Toby W. Hurd, Weibin Zhou, Andrew Cluckey, Heon Yung Gee, Gokul Ramaswami, Chen‐Jei Hong, Bruce A. Hamilton, Igor Červenka, Ranjani Sri Ganji, Vı́tězslav Bryja, Heleen H. Arts, Jeroen van Reeuwijk, Machteld M. Oud, Stef J.F. Letteboer, Ronald Roepman, Hervé Husson, Oxana Ibraghimov‐Beskrovnaya, Takayuki Yasunaga, Gerd Walz, Lorraine Eley, John A. Sayer, Bernhard Schermer, Max C. Liebau, Thomas Benzing, Stéphanie Le Corre, Iain A. Drummond, Sabine Janssen, Susan J. Allen, S. Natarajan, John F. O’Toole, Massimo Attanasio, Sophie Saunier, Corinne Antignac, Robert K. Koenekoop, Huanan Ren, Irma López, Ahmet Nayır, Corinne Stoetzel, Hélène Dollfus, Rustin Massoudi, Joseph G. Gleeson, Sharon Andreoli, D Doherty, Anna Lindstrad, Christelle Golzio, Nicholas Katsanis, Lars Pape, Emad B. Abboud, Ali A. Al‐Rajhi, Richard A. Lewis, Heymut Omran, Eva Y.-H.P. Lee, Shaohui Wang, JoAnn Sekiguchi, Rudel A. Saunders, Colin A. Johnson, Elizabeth Garner, Katja Vanselow, Jens Andersen, Joseph Shlomai, Gudrun Nürnberg, Peter Nürnberg, Shawn Levy, Agata Smogorzewska, Edgar A. Otto, Friedhelm Hildebrandt
S110447773. 2012398 CitationsOPEN ACCESS
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome
Inga Ebermann, Jennifer B. Phillips, Max C. Liebau, Robert K. Koenekoop, Bernhard Schermer, Irma López, Ellen Schäfer, Anne‐Françoise Roux, Claudia Dafinger, Antje Bernd, Eberhart Zrenner, Mireille Claustres, Bernardo Blanco, Gudrun Nürnberg, Peter Nürnberg, Rebecca Ruland, Monte Westerfield, Thomas Benzing, Hanno J. Bolz
S114430552. 2010249 CitationsOPEN ACCESS
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics
Claudia Dafinger, Max C. Liebau, Solaf M. Elsayed, Yorck Hellenbroich, Eugen Boltshauser, Georg Christoph Korenke, Francesca Fabretti, Andreas Janecke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg, Hanswalter Zentgraf, Friederike Koerber, Klaus Addicks, Ezzat Elsobky, Thomas Benzing, Bernhard Schermer, Hanno J. Bolz
S114430552. 2011214 CitationsOPEN ACCESS
Consensus Expert Recommendations for the Diagnosis and Management of Autosomal Recessive Polycystic Kidney Disease: Report of an International Conference
Lisa M. Guay‐Woodford, John J. Bissler, Michael Braun, Detlef Böckenhauer, Melissa A. Cadnapaphornchai, Katherine MacRae Dell, Larissa Kerecuk, Max C. Liebau, Maria H. Alonso-Peclet, Benjamin L. Shneider, Sukru Emre, Theo Heller, Binita M. Kamath, Karen F. Murray, Kenneth J. Moise, Eric Eichenwald, Jacquelyn Evans, Roberta L. Keller, Louise Wilkins‐Haug, Carsten Bergmann, Meral Gunay‐Aygun, Stephen R. Hooper, Kristina K. Hardy, Erum A. Hartung, Randi Streisand, Ronald D. Perrone, Marva Moxey‐Mims
The Journal of Pediatrics. 2014181 CitationsOPEN ACCESS
A molecular mechanism explaining albuminuria in kidney disease
Linus Butt, David Unnersjö‐Jess, Martin Höhne, Aurélie Edwards, Julia Binz-Lotter, Dervla Reilly, Robert Hahnfeldt, Vera Ziegler, Katharina Fremter, Markus M. Rinschen, Martin Helmstädter, Lena K. Ebert, Hayo Castrop, Matthias J. Hackl, Gerd Walz, Paul T. Brinkkoetter, Max C. Liebau, Kálmán Tory, Peter F. Hoyer, Bodo B. Beck, Hjalmar Brismar, Hans Blom, Bernhard Schermer, Thomas Benzing
S4210232714. 2020170 Citations
Related on ScholarIQ
Universitätsklinikum Aachen
Institution
Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling
Paper
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome
Paper
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics
Paper
Consensus Expert Recommendations for the Diagnosis and Management of Autosomal Recessive Polycystic Kidney Disease: Report of an International Conference
Paper
A molecular mechanism explaining albuminuria in kidney disease
Paper