| Nusinersen versus sham control in later-onset spinal muscular atrophy E Mercuri, BT Darras, CA Chiriboga, JW Day, C Campbell, AM Connolly, ... New England Journal of Medicine 378 (7), 625-635, 2018 | 1240 | 2018 |
| Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction DF Gudbjartsson, US Bjornsdottir, E Halapi, A Helgadottir, P Sulem, ... Nature genetics 41 (3), 342-347, 2009 | 915 | 2009 |
| A sequence variant on 17q21 is associated with age at onset and severity of asthma E Halapi, DF Gudbjartsson, GM Jonsdottir, US Bjornsdottir, G Thorleifsson, ... European journal of human genetics 18 (8), 902-908, 2010 | 186 | 2010 |
| PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia A Stray-Pedersen, PH Backe, HS Sorte, L Mørkrid, NY Chokshi, ... The American Journal of Human Genetics 95 (1), 96-107, 2014 | 158 | 2014 |
| Impact of IL8 and IL8-Receptor alpha polymorphisms on the genetics of bronchial asthma and severe RSV infections B Puthothu, M Krueger, J Heinze, J Forster, A Heinzmann Clinical and Molecular Allergy 4, 1-6, 2006 | 141 | 2006 |
| A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma D Smith, H Helgason, P Sulem, US Bjornsdottir, AC Lim, ... PLoS genetics 13 (3), e1006659, 2017 | 132 | 2017 |
| Cord blood levels of interleukin-6 and interleukin-8 for the immediate diagnosis of early-onset infection in premature infants M Krueger, MS Nauck, S Sang, R Hentschel, H Wieland, R Berner Neonatology 80 (2), 118-123, 2001 | 118 | 2001 |
| TLR-4 and CD14 polymorphisms in respiratory syncytial virus associated disease B Puthothu, J Forster, A Heinzmann, M Krueger Disease markers 22 (5-6), 303-308, 2006 | 117 | 2006 |
| Association between Severe Respiratory Syncytial Virus Infection and IL13/IL4 Haplotypes B Puthothu, M Krueger, J Forster, A Heinzmann The Journal of infectious diseases 193 (3), 438-441, 2006 | 115 | 2006 |
| VEGF-A, VEGFR-1, VEGFR-2 and Tie2 levels in plasma of premature infants: relationship to retinopathy of prematurity C Pieh, H Agostini, C Buschbeck, M Krüger, J Schulte-Mönting, ... British journal of ophthalmology 92 (5), 689-693, 2008 | 103 | 2008 |
| Association of TNF‐α with severe respiratory syncytial virus infection and bronchial asthma B Puthothu, S Bierbaum, MV Kopp, J Forster, J Heinze, M Weckmann, ... Pediatric allergy and immunology 20 (2), 157-163, 2009 | 102 | 2009 |
| Exposure to furosemide as the strongest risk factor for nephrocalcinosis in preterm infants C Gimpel, A Krause, P Franck, M Krueger, C Von Schnakenburg Pediatrics International 52 (1), 51-56, 2010 | 87 | 2010 |
| Genetic and epidemiological risk factors in the development of bronchopulmonary dysplasia B Mailaparambil, M Krueger, U Heizmann, K Schlegel, J Heinze, ... Disease markers 29 (1), 1-9, 2010 | 78 | 2010 |
| Enterococcal colonization of infants in a neonatal intensive care unit: associated predictors, risk factors and seasonal patterns M Hufnagel, C Liese, C Loescher, M Kunze, H Proempeler, R Berner, ... BMC Infectious Diseases 7, 1-11, 2007 | 68 | 2007 |
| Interleukin (IL)-18 polymorphism 133C/G is associated with severe respiratory syncytial virus infection B Puthothu, M Krueger, J Forster, J Heinze, M Weckmann, A Heinzmann The Pediatric infectious disease journal 26 (12), 1094-1098, 2007 | 65 | 2007 |
| Surfactant protein Bpolymorphisms are associated with severe respiratory syncytial virus infection, but not with asthma B Puthothu, J Forster, J Heinze, A Heinzmann, M Krueger BMC Pulmonary Medicine 7, 1-5, 2007 | 63 | 2007 |
| Synchronous recurrence of group B streptococcal late-onset sepsis in twins R Elling, M Hufnagel, A De Zoysa, F Lander, K Zumstein, M Krueger, ... Pediatrics 133 (5), e1388-e1391, 2014 | 57 | 2014 |
| Association of a FGFR-4 gene polymorphism with bronchopulmonary dysplasia and neonatal respiratory distress M Rezvani, J Wilde, P Vitt, B Mailaparambil, R Grychtol, M Krueger, ... Disease markers 35, 633-640, 2013 | 56 | 2013 |
| Lipopolysaccharide binding protein is a potential marker for invasive bacterial infections in children KM Ubenauf, M Krueger, P Henneke, R Berner The Pediatric infectious disease journal 26 (2), 159-162, 2007 | 52 | 2007 |
| TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype S Donkervoort, M Papadaki, JM De Winter, MB Neu, J Kirschner, V Bolduc, ... Annals of neurology 78 (6), 982-994, 2015 | 49 | 2015 |
