| Osteogenesis imperfecta JC Marini, WA Cabral Genetics of bone biology and skeletal disease, 397-420, 2018 | 863 | 2018 |
| Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta J Becker, O Semler, C Gilissen, Y Li, HJ Bolz, C Giunta, C Bergmann, ... The American Journal of Human Genetics 88 (3), 362-371, 2011 | 412 | 2011 |
| Mutations in WNT1 cause different forms of bone fragility K Keupp, F Beleggia, H Kayserili, AM Barnes, M Steiner, O Semler, ... The American Journal of Human Genetics 92 (4), 565-574, 2013 | 302 | 2013 |
| A mutation in the 5′-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus O Semler, L Garbes, K Keupp, D Swan, K Zimmermann, J Becker, S Iden, ... The American Journal of Human Genetics 91 (2), 349-357, 2012 | 302 | 2012 |
| Attenuated BMP1 function compromises osteogenesis, leading to bone fragility in humans and zebrafish PV Asharani, K Keupp, O Semler, W Wang, Y Li, H Thiele, G Yigit, E Pohl, ... The American Journal of Human Genetics 90 (4), 661-674, 2012 | 240 | 2012 |
| Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial N Bishop, S Adami, SF Ahmed, J Antón, P Arundel, CP Burren, ... The Lancet 382 (9902), 1424-1432, 2013 | 209 | 2013 |
| Measuring procedures to determine the Cobb angle in idiopathic scoliosis: a systematic review S Langensiepen, O Semler, R Sobottke, O Fricke, J Franklin, E Schönau, ... European Spine Journal 22, 2360-2371, 2013 | 208 | 2013 |
| Results of the SIOP 93-01/GPOH trial and study for the treatment of patients with unilateral nonmetastatic Wilms Tumor H Reinhard, O Semler, D Bürger, U Bode, M Flentje, U Göbel, P Gutjahr, ... Klinische Pädiatrie 216 (03), 132-140, 2004 | 183 | 2004 |
| Safety and efficacy of denosumab in children with osteogenesis imperfecta-a first prospective trial H Hoyer-Kuhn, J Franklin, G Allo, M Kron, C Netzer, P Eysel, B Hero, ... Journal of musculoskeletal & neuronal interactions 16 (1), 24, 2016 | 165 | 2016 |
| Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta L Garbes, K Kim, A Rieß, H Hoyer-Kuhn, F Beleggia, A Bevot, MJ Kim, ... The American Journal of Human Genetics 96 (3), 432-439, 2015 | 165 | 2015 |
| First use of the RANKL antibody denosumab in osteogenesis imperfecta type VI O Semler, C Netzer, H Hoyer-Kuhn, J Becker, P Eysel, E Schoenau J Musculoskelet Neuronal Interact 12 (3), 183-8, 2012 | 158 | 2012 |
| Two years’ experience with denosumab for children with osteogenesis imperfecta type VI H Hoyer-Kuhn, C Netzer, F Koerber, E Schoenau, O Semler Orphanet journal of rare diseases 9, 1-8, 2014 | 140 | 2014 |
| Preliminary results on the mobility after whole body vibration in immobilized children and adolescents O Semler, O Fricke, K Vezyroglou, C Stark, E Schoenau Journal of Musculoskeletal and Neuronal Interactions 7 (1), 77, 2007 | 118 | 2007 |
| Effect of a new physiotherapy concept on bone mineral density, muscle force and gross motor function in children with bilateral cerebral palsy C Stark, P Nikopoulou-Smyrni, A Stabrey, O Semler, E Schoenau International Society of Musculoskeletal and Neuronal Interactions, 2010 | 117 | 2010 |
| Results of a prospective pilot trial on mobility after whole body vibration in children and adolescents with osteogenesis imperfecta O Semler, O Fricke, K Vezyroglou, C Stark, A Stabrey, E Schoenau Clinical rehabilitation 22 (5), 387-394, 2008 | 109 | 2008 |
| Consensus statement on physical rehabilitation in children and adolescents with osteogenesis imperfecta B Mueller, R Engelbert, F Baratta-Ziska, B Bartels, N Blanc, E Brizola, ... Orphanet journal of rare diseases 13, 1-14, 2018 | 94 | 2018 |
| Surgery of cavoatrial tumor thrombus in nephroblastoma: a report of the SIOP/GPOH study P Szavay, T Luithle, O Semler, N Graf, J Fuchs Pediatric blood & cancer 43 (1), 40-45, 2004 | 94 | 2004 |
| A specialized rehabilitation approach improves mobility in children with osteogenesis imperfecta H Hoyer-Kuhn, O Semler, C Stark, N Struebing, O Goebel, E Schoenau J Musculoskelet Neuronal Interact 14 (4), 445-53, 2014 | 93 | 2014 |
| Wormian bones in osteogenesis imperfecta: correlation to clinical findings and genotype O Semler, MS Cheung, FH Glorieux, F Rauch American journal of medical genetics Part A 152 (7), 1681-1687, 2010 | 83 | 2010 |
| A functional copy-number variation in MAPKAPK2 predicts risk and prognosis of lung cancer B Liu, L Yang, B Huang, M Cheng, H Wang, Y Li, D Huang, J Zheng, Q Li, ... The American Journal of Human Genetics 91 (2), 384-390, 2012 | 81 | 2012 |
