| Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner Syndrome Meeting CH Gravholt, NH Andersen, GS Conway, OM Dekkers, ME Geffner, ... European journal of endocrinology 177 (3), G1-G70, 2017 | 1032 | 2017 |
| Diagnosis, genetics, and therapy of short stature in children: a growth hormone research society international perspective PF Collett-Solberg, G Ambler, PF Backeljauw, M Bidlingmaier, BMK Biller, ... Hormone research in paediatrics 92 (1), 1-14, 2019 | 265 | 2019 |
| Mechanisms of growth hormone (GH) action: identification of conserved Stat5 binding sites that mediate GH-induced insulin-like growth factor-I gene activation J Woelfle, DJ Chia, P Rotwein Journal of Biological Chemistry 278 (51), 51261-51266, 2003 | 224 | 2003 |
| Acute control of insulin-like growth factor-I gene transcription by growth hormone through Stat5b J Woelfle, J Billiard, P Rotwein Journal of Biological Chemistry 278 (25), 22696-22702, 2003 | 222 | 2003 |
| Fibroblast growth factor 21 (FGF-21) and its relation to obesity, metabolic syndrome, and nonalcoholic fatty liver in children: a longitudinal analysis T Reinehr, J Woelfle, R Wunsch, CL Roth The Journal of Clinical Endocrinology & Metabolism 97 (6), 2143-2150, 2012 | 201 | 2012 |
| Peptide YY is a regulator of energy homeostasis in obese children before and after weight loss CL Roth, PJ Enriori, K Harz, J Woelfle, MA Cowley, T Reinehr The Journal of Clinical Endocrinology & Metabolism 90 (12), 6386-6391, 2005 | 181 | 2005 |
| Detection of collagens by multispectral optoacoustic tomography as an imaging biomarker for Duchenne muscular dystrophy AP Regensburger, LM Fonteyne, J Jüngert, AL Wagner, T Gerhalter, ... Nature medicine 25 (12), 1905-1915, 2019 | 164 | 2019 |
| Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes V Mihaylova, JS Müller, JJ Vilchez, MA Salih, MM Kabiraj, A D’Amico, ... Brain 131 (3), 747-759, 2008 | 162 | 2008 |
| Basal inhibin B and the testosterone response to human chorionic gonadotropin correlate in prepubertal boys K Kubini, M Zachmann, N Albers, O Hiort, M Bettendorf, J Wölfle, ... The Journal of Clinical Endocrinology & Metabolism 85 (1), 134-138, 2000 | 150 | 2000 |
| Growth and puberty in German children: is there still a positive secular trend? B Gohlke, J Woelfle Deutsches Ärzteblatt International 106 (23), 377, 2009 | 139 | 2009 |
| In vivo regulation of growth hormone-stimulated gene transcription by STAT5b J Woelfle, P Rotwein American Journal of Physiology-Endocrinology and Metabolism 286 (3), E393-E401, 2004 | 133 | 2004 |
| Characterization of distinct Stat5b binding sites that mediate growth hormone-stimulated IGF-I gene transcription DJ Chia, M Ono, J Woelfle, M Schlesinger-Massart, H Jiang, P Rotwein Journal of Biological Chemistry 281 (6), 3190-3197, 2006 | 112 | 2006 |
| Cantú Syndrome Resulting from Activating Mutation in the KCNJ8 Gene PE Cooper, H Reutter, J Woelfle, H Engels, DK Grange, G van Haaften, ... Human mutation 35 (7), 809-813, 2014 | 111 | 2014 |
| Testicular growth and spermatogenesis: new goals for pubertal hormone replacement in boys with hypogonadotropic hypogonadism?‐a multicentre prospective study of hCG/rFSH … J Rohayem, BP Hauffa, M Zacharin, S Kliesch, M Zitzmann, ... Clinical endocrinology 86 (1), 75-87, 2017 | 108 | 2017 |
| In Vivo Transcript Profiling and Phylogenetic Analysis Identifies Suppressor of Cytokine Signaling 2 as a Direct Signal Transducer and Activator of Transcription 5b … OM Vidal, R Merino, E Rico-Bautista, L Fernandez-Perez, DJ Chia, ... Molecular endocrinology 21 (1), 293-311, 2007 | 95 | 2007 |
| Microvascular complications in childhood-onset type 1 diabetes and celiac disease: a multicenter longitudinal analysis of 56,514 patients from the German-Austrian DPV database TR Rohrer, J Wolf, S Liptay, KP Zimmer, E Fröhlich-Reiterer, N Scheuing, ... Diabetes Care 38 (5), 801-807, 2015 | 92 | 2015 |
| Lack of association between apelin, insulin resistance, cardiovascular risk factors, and obesity in children: a longitudinal analysis T Reinehr, J Woelfle, CL Roth Metabolism 60 (9), 1349-1354, 2011 | 83 | 2011 |
| Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counselling F Haverkamp, J Wölfle, M Aretz, A Krämer, B Höhmann, H Fahnenstich, ... European journal of pediatrics 158, 474-478, 1999 | 76 | 1999 |
| DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations A Sharma, MA Jamil, N Nuesgen, F Schreiner, L Priebe, P Hoffmann, ... Clinical epigenetics 7, 1-15, 2015 | 75 | 2015 |
| Complete virilization in congenital adrenal hyperplasia: clinical course, medical management and disease‐related complications J Woelfle, W Hoepffner, WG Sippell, JH Brämswig, P Heidemann, D Deiss, ... Clinical Endocrinology 56 (2), 231-238, 2002 | 75 | 2002 |
