| TGF-β signaling is associated with endocytosis at the pocket region of the primary cilium CA Clement, KD Ajbro, K Koefoed, ML Vestergaard, IR Veland, ... Cell reports 3 (6), 1806-1814, 2013 | 328 | 2013 |
| Of mice and men: molecular genetics of congenital heart disease TA Andersen, KLL Troelsen, LA Larsen Cellular and molecular life sciences 71, 1327-1352, 2014 | 198 | 2014 |
| High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease F Erdogan, LA Larsen, L Zhang, Z Tümer, N Tommerup, W Chen, ... Journal of medical genetics 45 (11), 704-709, 2008 | 175 | 2008 |
| Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development K Lage, SC Greenway, JA Rosenfeld, H Wakimoto, JM Gorham, AV Segrè, ... Proceedings of the National Academy of Sciences 109 (35), 14035-14040, 2012 | 169 | 2012 |
| Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives PS Andersen, O Havndrup, L Hougs, KM Sørensen, M Jensen, LA Larsen, ... Human mutation 30 (3), 363-370, 2009 | 156 | 2009 |
| Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2 LP Jakobsen, R Ullmann, SB Christensen, KE Jensen, K Mølsted, ... Journal of medical genetics 44 (6), 381-386, 2007 | 143 | 2007 |
| The primary cilium coordinates early cardiogenesis and hedgehog signaling in cardiomyocyte differentiation CA Clement, SG Kristensen, K Møllgård, GJ Pazour, BK Yoder, ... Journal of cell science 122 (17), 3070-3082, 2009 | 138 | 2009 |
| YKL-40 protein expression in the early developing human musculoskeletal system JS Johansen, PE Høyer, LA Larsen, PA Price, K Møllgård Journal of Histochemistry & Cytochemistry 55 (12), 1213-1228, 2007 | 133 | 2007 |
| Haploinsufficiency of TAB2 causes congenital heart defects in humans B Thienpont, L Zhang, AV Postma, J Breckpot, LC Tranchevent, ... The American Journal of Human Genetics 86 (6), 839-849, 2010 | 115 | 2010 |
| Recombinant adeno-associated virus-mediated microRNA delivery into the postnatal mouse brain reveals a role for miR-134 in dendritogenesis in vivo M Christensen, LA Larsen, S Kauppinen, G Schratt Frontiers in neural circuits 3, 848, 2010 | 112 | 2010 |
| Capillary electrophoresis‐based single strand DNA conformation analysis in high‐throughput mutation screening PS Andersen, C Jespersgaard, J Vuust, M Christiansen, LA Larsen Human mutation 21 (5), 455-465, 2003 | 111 | 2003 |
| Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2‐5 Mutation and a Review of the Literature SG Ellesøe, MM Johansen, JV Bjerre, VE Hjortdal, S Brunak, LA Larsen Congenital heart disease 11 (3), 283-290, 2016 | 108 | 2016 |
| Dissecting spatio‐temporal protein networks driving human heart development and related disorders K Lage, K Møllgård, S Greenway, H Wakimoto, JM Gorham, CT Workman, ... Molecular systems biology 6 (1), 381, 2010 | 103 | 2010 |
| Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen J Tyson, L Tranebjærg, M McEntagart, L Larsen, M Christiansen, ... Human genetics 107, 499-503, 2000 | 101 | 2000 |
| High‐throughput single‐strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern‐based identification of allelic … LA Larsen, M Christiansen, J Vuust, PS Andersen Human mutation 13 (4), 318-327, 1999 | 100 | 1999 |
| Hedgehog signaling in small-cell lung cancer: frequent in vivo but a rare event in vitro J Vestergaard, MW Pedersen, N Pedersen, C Ensinger, Z Tümer, ... Lung cancer 52 (3), 281-290, 2006 | 99 | 2006 |
| Cilia and coordination of signaling networks during heart development K Koefoed, IR Veland, LB Pedersen, LA Larsen, ST Christensen Organogenesis 10 (1), 108-125, 2014 | 96 | 2014 |
| Screening for Mutations and Polymorphisms in the Genes KCNH2 and KCNE2 Encoding the Cardiac HERG/MiRP1 Ion Channel: Implications for Acquired and … LA Larsen, PS Andersen, J Kanters, IH Svendsen, JR Jacobsen, J Vuust, ... Clinical chemistry 47 (8), 1390-1395, 2001 | 95 | 2001 |
| Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations PS Andersen, O Havndrup, H Bundgaard, JC Moolman-Smook, ... Journal of medical genetics 38 (12), e43-e43, 2001 | 93 | 2001 |
| Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene LA Larsen, I Fosdal, PS Andersen, JK Kanters, J Vuust, G Wettrell, ... European journal of human genetics 7 (6), 724-728, 1999 | 93 | 1999 |
Niels TommerupProfessor in Medical Genetics, University of Copenhagen在 sund.ku.dk 的电子邮件经过验证
