Heinrich Sticht
Heinrich Sticht
Professor für Bioinformatik, FAU Erlangen-Nürnberg
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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
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
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
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, 281-289, 2006
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
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
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
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
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
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
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
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
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
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, 2405-2426, 2009
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
The structure of iron–sulfur proteins
H Sticht, P Rösch
Progress in biophysics and molecular biology 70 (2), 95-136, 1998
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
Synthetic peptides as protein mimics
A Groß, C Hashimoto, H Sticht, J Eichler
Frontiers in bioengineering and biotechnology 3, 211, 2016
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
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
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