3D U-Net: learning dense volumetric segmentation from sparse annotation Ö Çiçek, A Abdulkadir, SS Lienkamp, T Brox, O Ronneberger Medical Image Computing and Computer-Assisted Intervention–MICCAI 2016: 19th …, 2016 | 8227 | 2016 |
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia C Bergmann, M Fliegauf, NO Brüchle, V Frank, H Olbrich, J Kirschner, ... The American Journal of Human Genetics 82 (4), 959-970, 2008 | 396 | 2008 |
Medical image computing and computer-assisted intervention–MICCAI 2016 Ö Çiçek, A Abdulkadir, SS Lienkamp, T Brox, O Ronneberger 19th International Conference, Athens, Greece, 424-432, 2016 | 379* | 2016 |
Vertebrate kidney tubules elongate using a planar cell polarity–dependent, rosette-based mechanism of convergent extension SS Lienkamp, K Liu, CM Karner, TJ Carroll, O Ronneberger, ... Nature genetics 44 (12), 1382-1387, 2012 | 259 | 2012 |
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3 S Hoff, J Halbritter, D Epting, V Frank, TMT Nguyen, J Van Reeuwijk, ... Nature genetics 45 (8), 951-956, 2013 | 221 | 2013 |
Direct reprogramming of fibroblasts into renal tubular epithelial cells by defined transcription factors MM Kaminski, J Tosic, C Kresbach, H Engel, J Klockenbusch, AL Müller, ... Nature cell biology 18 (12), 1269-1280, 2016 | 147 | 2016 |
Inversin, Wnt signaling and primary cilia S Lienkamp, A Ganner, G Walz Differentiation 83 (2), S49-S55, 2012 | 113 | 2012 |
Genetic and physical interaction between the NPHP5 and NPHP6 gene products T Schäfer, M Pütz, S Lienkamp, A Ganner, A Bergbreiter, ... Human molecular genetics 17 (23), 3655-3662, 2008 | 105 | 2008 |
Cyclin O (Ccno) functions during deuterosome‐mediated centriole amplification of multiciliated cells MC Funk, AN Bera, T Menchen, G Kuales, K Thriene, SS Lienkamp, ... The EMBO journal 34 (8), 1078-1089, 2015 | 95 | 2015 |
Mutations in TBX18 cause dominant urinary tract malformations via transcriptional dysregulation of ureter development A Vivante, MJ Kleppa, J Schulz, S Kohl, A Sharma, J Chen, S Shril, ... The American Journal of Human Genetics 97 (2), 291-301, 2015 | 93 | 2015 |
The C/EBP homologous protein CHOP (GADD153) is an inhibitor of Wnt/TCF signals M Horndasch, S Lienkamp, E Springer, A Schmitt, H Pavenstädt, G Walz, ... Oncogene 25 (24), 3397-3407, 2006 | 71 | 2006 |
Inversin relays Frizzled-8 signals to promote proximal pronephros development S Lienkamp, A Ganner, C Boehlke, T Schmidt, SJ Arnold, T Schäfer, ... Proceedings of the National Academy of Sciences 107 (47), 20388-20393, 2010 | 68 | 2010 |
The Rac1 regulator ELMO controls basal body migration and docking in multiciliated cells through interaction with Ezrin D Epting, K Slanchev, C Boehlke, S Hoff, NT Loges, T Yasunaga, L Indorf, ... Development 142 (1), 174-184, 2015 | 62 | 2015 |
Regulation of ciliary polarity by the APC/C A Ganner, S Lienkamp, T Schäfer, D Romaker, T Wegierski, TJ Park, ... Proceedings of the National Academy of Sciences 106 (42), 17799-17804, 2009 | 61 | 2009 |
The polarity protein Inturned links NPHP4 to Daam1 to control the subapical actin network in multiciliated cells T Yasunaga, S Hoff, C Schell, M Helmstädter, O Kretz, S Kuechlin, ... Journal of Cell Biology 211 (5), 963-973, 2015 | 57 | 2015 |
A dominant mutation in nuclear receptor interacting protein 1 causes urinary tract malformations via dysregulation of retinoic acid signaling A Vivante, N Mann, H Yonath, AC Weiss, M Getwan, MM Kaminski, ... Journal of the American Society of Nephrology 28 (8), 2364-2376, 2017 | 53 | 2017 |
Anks3 interacts with nephronophthisis proteins and is required for normal renal development TA Yakulov, T Yasunaga, H Ramachandran, C Engel, B Müller, S Hoff, ... Kidney international 87 (6), 1191-1200, 2015 | 42 | 2015 |
Molecular basis for autosomal-dominant renal Fanconi syndrome caused by HNF4A V Marchesin, A Pérez-Martí, G Le Meur, R Pichler, K Grand, ED Klootwijk, ... Cell reports 29 (13), 4407-4421. e5, 2019 | 41 | 2019 |
Using Xenopus to study genetic kidney diseases SS Lienkamp Seminars in cell & developmental biology 51, 117-124, 2016 | 40 | 2016 |
Network for early Onset cystic Kidney Diseases—A comprehensive Multidisciplinary Approach to Hereditary cystic Kidney Diseases in childhood JC König, A Titieni, M Konrad, Neocyst Consortium Frontiers in Pediatrics 6, 24, 2018 | 32 | 2018 |