| BMP signaling controls muscle mass R Sartori, E Schirwis, B Blaauw, S Bortolanza, J Zhao, E Enzo, A Stantzou, ... Nature genetics 45 (11), 1309-1318, 2013 | 500 | 2013 |
| Role of Runx genes in chondrocyte differentiation S Stricker, R Fundele, A Vortkamp, S Mundlos Developmental biology 245 (1), 95-108, 2002 | 289 | 2002 |
| Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome CG Woods, S Stricker, P Seemann, R Stern, J Cox, E Sherridan, ... The American Journal of Human Genetics 79 (2), 402-408, 2006 | 277 | 2006 |
| Activating and deactivating mutations in the receptor interaction site of GDF5 cause symphalangism or brachydactyly type A2 P Seemann, R Schwappacher, KW Kjaer, D Krakow, K Lehmann, ... The Journal of clinical investigation 115 (9), 2373-2381, 2005 | 251 | 2005 |
| Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation F Witte, J Dokas, F Neuendorf, S Mundlos, S Stricker Gene Expression Patterns 9 (4), 215-223, 2009 | 222 | 2009 |
| Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2 K Lehmann, P Seemann, S Stricker, M Sammar, B Meyer, K Süring, ... Proceedings of the National Academy of Sciences 100 (21), 12277-12282, 2003 | 195 | 2003 |
| A molecular pathogenesis for transcription factor associated poly-alanine tract expansions AN Albrecht, U Kornak, A Böddrich, K Süring, PN Robinson, AC Stiege, ... Human molecular genetics 13 (20), 2351-2359, 2004 | 193 | 2004 |
| PDE3A mutations cause autosomal dominant hypertension with brachydactyly PG Maass, A Aydin, FC Luft, C Schächterle, A Weise, S Stricker, ... Nature genetics 47 (6), 647-653, 2015 | 183 | 2015 |
| Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal γ subunit K Hoffmann, JS Müller, S Stricker, A Megarbane, A Rajab, TH Lindner, ... The American Journal of Human Genetics 79 (2), 303-312, 2006 | 174 | 2006 |
| Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders A Michalk, S Stricker, J Becker, R Rupps, T Pantzar, J Miertus, G Botta, ... The American Journal of Human Genetics 82 (2), 464-476, 2008 | 147 | 2008 |
| Multiple roles for neurofibromin in skeletal development and growth M Kolanczyk, N Kossler, J Kühnisch, L Lavitas, S Stricker, U Wilkening, ... Human molecular genetics 16 (8), 874-886, 2007 | 146 | 2007 |
| Complement activation induces excessive T cell cytotoxicity in severe COVID-19 P Georg, R Astaburuaga-García, L Bonaguro, S Brumhard, L Michalick, ... Cell 185 (3), 493-512. e25, 2022 | 144 | 2022 |
| Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia I Kurth, E Klopocki, S Stricker, J van Oosterwijk, S Vanek, J Altmann, ... Nature genetics 41 (8), 862-863, 2009 | 133 | 2009 |
| Faulty initiation of proteoglycan synthesis causes cardiac and joint defects S Baasanjav, L Al-Gazali, T Hashiguchi, S Mizumoto, B Fischer, D Horn, ... The American Journal of Human Genetics 89 (1), 15-27, 2011 | 131 | 2011 |
| A misplaced lncRNA causes brachydactyly in humans PG Maass, A Rump, H Schulz, S Stricker, L Schulze, K Platzer, A Aydin, ... The Journal of clinical investigation 122 (11), 3990-4002, 2012 | 129 | 2012 |
| Modulation of GDF5/BRI‐b signalling through interaction with the tyrosine kinase receptor Ror2 M Sammar, S Stricker, GC Schwabe, C Sieber, A Hartung, M Hanke, ... Genes to Cells 9 (12), 1227-1238, 2004 | 123 | 2004 |
| Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis E Klopocki, S Lohan, F Brancati, R Koll, A Brehm, P Seemann, K Dathe, ... The American Journal of Human Genetics 88 (1), 70-75, 2011 | 121 | 2011 |
| Mutations in GDF5 reveal a key residue mediating BMP inhibition by NOGGIN P Seemann, A Brehm, J König, C Reissner, S Stricker, P Kuss, J Haupt, ... PLoS genetics 5 (11), e1000747, 2009 | 120 | 2009 |
| Mutations in PVRL4, encoding cell adhesion molecule nectin-4, cause ectodermal dysplasia-syndactyly syndrome F Brancati, P Fortugno, I Bottillo, M Lopez, E Josselin, ... The American Journal of Human Genetics 87 (2), 265-273, 2010 | 119 | 2010 |
| A mutation in Ihh that causes digit abnormalities alters its signalling capacity and range B Gao, J Hu, S Stricker, M Cheung, G Ma, KF Law, F Witte, J Briscoe, ... Nature 458 (7242), 1196-1200, 2009 | 119 | 2009 |
Stefan MundlosInstitut für Medizinische Genetik und Humangenetik, CharitéVerified email at molgen.mpg.de
