| Physical exercise–induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic β cells T Otonkoski, H Jiao, N Kaminen-Ahola, I Tapia-Paez, MS Ullah, LE Parton, ... The American Journal of Human Genetics 81 (3), 467-474, 2007 | 268 | 2007 |
| Long-term follow-up of 114 patients with congenital hyperinsulinism T Meissner, U Wendel, P Burgard, S Schaetzle, E Mayatepek European journal of endocrinology 149 (1), 43-52, 2003 | 244 | 2003 |
| Favorable acceptance of mini-tablets compared with syrup: a randomized controlled trial in infants and preschool children V Klingmann, N Spomer, C Lerch, I Stoltenberg, C Frömke, HM Bosse, ... The Journal of pediatrics 163 (6), 1728-1732. e1, 2013 | 213 | 2013 |
| Acceptance of uncoated mini-tablets in young children: results from a prospective exploratory cross-over study N Spomer, V Klingmann, I Stoltenberg, C Lerch, T Meissner, J Breitkreutz Archives of disease in childhood 97 (3), 283-286, 2012 | 203 | 2012 |
| Characterization of pancreatic NMDA receptors as possible drug targets for diabetes treatment J Marquard, S Otter, A Welters, A Stirban, A Fischer, J Eglinger, ... Nature medicine 21 (4), 363-372, 2015 | 183 | 2015 |
| Propionic acidemia: clinical course and outcome in 55 pediatric and adolescent patients SC Grünert, S Müllerleile, L De Silva, M Barth, M Walter, K Walter, ... Orphanet journal of rare diseases 8 (1), 1-9, 2013 | 174 | 2013 |
| Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin release T Otonkoski, N Kaminen, J Ustinov, R Lapatto, T Meissner, E Mayatepek, ... Diabetes 52 (1), 199-204, 2003 | 168 | 2003 |
| Increased DNA methylation variability in type 1 diabetes across three immune effector cell types DS Paul, AE Teschendorff, MAN Dang, R Lowe, MI Hawa, S Ecker, ... Nature communications 7 (1), 1-11, 2016 | 156 | 2016 |
| Biallelic mutations in DNAJC12 cause hyperphenylalaninemia, dystonia, and intellectual disability Y Anikster, TB Haack, T Vilboux, B Pode-Shakked, B Thöny, N Shen, ... The American Journal of Human Genetics 100 (2), 257-266, 2017 | 149 | 2017 |
| Acceptability of uncoated mini-tablets in neonates—a randomized controlled trial V Klingmann, A Seitz, T Meissner, J Breitkreutz, A Moeltner, HM Bosse The Journal of pediatrics 167 (4), 893-896. e2, 2015 | 148 | 2015 |
| Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype J Rohayem, C Ehlers, B Wiedemann, R Holl, K Oexle, O Kordonouri, ... Diabetes care 34 (7), 1503-1510, 2011 | 138 | 2011 |
| Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany S Kölker, SF Garbade, N Boy, EM Maier, T Meissner, C Mühlhausen, ... Pediatric research 62 (3), 357-363, 2007 | 128 | 2007 |
| Mild trimethylaminuria caused by common variants in FM03 gene J Zschocke, D Kohlmueller, E Quak, T Meissner, GF Hoffmann, ... The Lancet 354 (9181), 834-835, 1999 | 126 | 1999 |
| Interventions for the prevention of nutritional rickets in term born children C Lerch, T Meissner Cochrane Database of Systematic Reviews, 2007 | 113 | 2007 |
| Propionic acidemia: neonatal versus selective metabolic screening SC Grünert, S Müllerleile, L De Silva, M Barth, M Walter, K Walter, ... Journal of inherited metabolic disease 35 (1), 41-49, 2012 | 101 | 2012 |
| Long-term medical treatment in congenital hyperinsulinism: a descriptive analysis in a large cohort of patients from different clinical centers A Welters, C Lerch, S Kummer, J Marquard, B Salgin, E Mayatepek, ... Orphanet journal of rare diseases 10 (1), 150, 2015 | 97 | 2015 |
| Inborn errors of carbohydrate metabolism E Mayatepek, B Hoffmann, T Meissner Best Practice & Research Clinical Gastroenterology 24 (5), 607-618, 2010 | 77 | 2010 |
| Is disordered eating behavior more prevalent in adolescents with early‐onset type 1 diabetes than in their representative peers? C Baechle, K Castillo, K Strassburger, A Stahl‐Pehe, T Meissner, RW Holl, ... International Journal of Eating Disorders 47 (4), 342-352, 2014 | 76 | 2014 |
| Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome R Santer, M Kinner, M Passarge, A Superti-Furga, E Mayatepek, ... Human genetics 108 (1), 66-71, 2001 | 75 | 2001 |
| Exercise induced hypoglycaemic hyperinsulinism T Meissner, T Otonkoski, R Feneberg, B Beinbrech, S Apostolidou, I Sipilä, ... Archives of disease in childhood 84 (3), 254-257, 2001 | 70 | 2001 |
