| Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study A Rauch, D Wieczorek, E Graf, T Wieland, S Endele, T Schwarzmayr, ... The Lancet 380 (9854), 1674-1682, 2012 | 1047 | 2012 |
| The interleukin-10 family of cytokines H Fickenscher, S Hör, H Küpers, A Knappe, S Wittmann, H Sticht Trends in immunology 23 (2), 89-96, 2002 | 463 | 2002 |
| Structure of amyloid A4‐(1–40)‐peptide of Alzheimer's disease H Sticht, P Bayer, D Willbold, S Dames, C Hilbich, K Beyreuther, ... European Journal of Biochemistry 233 (1), 293-298, 1995 | 355 | 1995 |
| Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia … F Pasutto, H Sticht, G Hammersen, G Gillessen-Kaesbach, DR FitzPatrick, ... The American Journal of Human Genetics 80 (3), 550-560, 2007 | 351 | 2007 |
| AMBER force-field parameters for phosphorylated amino acids in different protonation states: phosphoserine, phosphothreonine, phosphotyrosine, and phosphohistidine N Homeyer, AHC Horn, H Lanig, H Sticht Journal of molecular modeling 12 (3), 281-289, 2006 | 326 | 2006 |
| Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11. 2 deletions C Zweier, H Sticht, I Aydin-Yaylagül, CE Campbell, A Rauch The American Journal of Human Genetics 80 (3), 510-517, 2007 | 221 | 2007 |
| Structure determination of human and murine β‐defensins reveals structural conservation in the absence of significant sequence similarity F Bauer, K Schweimer, E Klüver, JR Conejo‐Garcia, WG Forssmann, ... Protein Science 10 (12), 2470-2479, 2001 | 213 | 2001 |
| Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6) C Templin, JR Ghadri, JS Rougier, A Baumer, V Kaplan, M Albesa, ... European heart journal 32 (9), 1077-1088, 2011 | 201 | 2011 |
| Allergic cross-reactivity made visible: solution structure of the major cherry allergen Pru av 1 P Neudecker, K Schweimer, J Nerkamp, S Scheurer, S Vieths, H Sticht, ... Journal of Biological Chemistry 276 (25), 22756-22763, 2001 | 199 | 2001 |
| Structural rearrangements of HIV-1 Tat-responsive RNA upon binding of neomycin B C Faber, H Sticht, K Schweimer, P Rösch Journal of Biological Chemistry 275 (27), 20660-20666, 2000 | 177 | 2000 |
| Estrogen and progesterone receptors: from molecular structures to clinical targets S Ellmann, H Sticht, F Thiel, MW Beckmann, R Strick, PL Strissel Cellular and Molecular Life Sciences 66 (15), 2405-2426, 2009 | 172 | 2009 |
| Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma F Pasutto, T Matsumoto, CY Mardin, H Sticht, JH Brandstätter, ... The American Journal of Human Genetics 85 (4), 447-456, 2009 | 170 | 2009 |
| The T-cell lymphokine interleukin-26 targets epithelial cells through the interleukin-20 receptor 1 and interleukin-10 receptor 2 chains S Hör, H Pirzer, L Dumoutier, F Bauer, S Wittmann, H Sticht, JC Renauld, ... Journal of Biological Chemistry 279 (32), 33343-33351, 2004 | 168 | 2004 |
| The structure of iron–sulfur proteins H Sticht, P Rösch Progress in biophysics and molecular biology 70 (2), 95-136, 1998 | 165 | 1998 |
| Mutations in MEF2C from the 5q14. 3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression M Zweier, A Gregor, C Zweier, H Engels, H Sticht, E Wohlleber, ... Human mutation 31 (6), 722-733, 2010 | 163 | 2010 |
| B cell repertoire analysis identifies new antigenic domains on glycoprotein B of human cytomegalovirus which are target of neutralizing antibodies S Pötzsch, N Spindler, AK Wiegers, T Fisch, P Rücker, H Sticht, N Grieb, ... PLoS pathogens 7 (8), e1002172, 2011 | 150 | 2011 |
| Diagnostic yield and novel candidate genes by exome sequencing in 152 consanguineous families with neurodevelopmental disorders MS Reuter, H Tawamie, R Buchert, OH Gebril, T Froukh, C Thiel, S Uebe, ... JAMA psychiatry 74 (3), 293-299, 2017 | 143 | 2017 |
| Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator CT Thiel, D Horn, B Zabel, AB Ekici, K Salinas, E Gebhart, F Rüschendorf, ... The American Journal of Human Genetics 77 (5), 795-806, 2005 | 139 | 2005 |
| De novo mutations in the genome organizer CTCF cause intellectual disability A Gregor, M Oti, EN Kouwenhoven, J Hoyer, H Sticht, AB Ekici, ... The American Journal of Human Genetics 93 (1), 124-131, 2013 | 128 | 2013 |
| Structural analysis of the protein phosphatase 1 docking motif: molecular description of binding specificities identifies interacting proteins H Meiselbach, H Sticht, R Enz Chemistry & biology 13 (1), 49-59, 2006 | 125 | 2006 |
