Heinrich Sticht

Overview

Best Publications

• Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.

  Anita Rauch;Dagmar Wieczorek;Elisabeth Graf;Thomas Wieland

  1163
  Citations

• The interleukin-10 family of cytokines

  Helmut Fickenscher;Simon Hör;Heide Küpers;Andrea Knappe

  480
  Citations

• Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation

  Francesca Pasutto;Heinrich Sticht;Gerhard Hammersen;Gabriele Gillessen-Kaesbach

  456
  Citations

• AMBER force-field parameters for phosphorylated amino acids in different protonation states: phosphoserine, phosphothreonine, phosphotyrosine, and phosphohistidine

  Nadine Homeyer;Anselm H. C. Horn;Harald Lanig;Heinrich Sticht

  416
  Citations

• Structure of amyloid A4-(1-40)-peptide of Alzheimer's disease.

  Heinrich Sticht;Peter Bayer;Dieter Willbold;Sonja Dames

  374
  Citations

• Human TBX1 Missense Mutations Cause Gain of Function Resulting in the Same Phenotype as 22q11.2 Deletions

  Christiane Zweier;Heinrich Sticht;Inci Aydin-Yaylagül;Christine E. Campbell

  239
  Citations

• Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6)

  Christian Templin;Jelena-Rima Ghadri;Jean-Sébastien Rougier;Alessandra Baumer

  229
  Citations

• Structure Determination of Human and Murine Beta-Defensins Reveals Structural Conservation in the Absence of Significant Sequence Similarity

  Finn Bauer;Kristian Schweimer;Enno Klüver;Jose-Ramon Conejo-Garcia

  220
  Citations

• Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders

  Miriam S. Reuter;Hasan Tawamie;Rebecca Buchert;Ola Hosny Gebril

  214
  Citations

• Allergic Cross-reactivity Made Visible SOLUTION STRUCTURE OF THE MAJOR CHERRY ALLERGEN Pru av 1

  Philipp Neudecker;Kristian Schweimer;Jörg Nerkamp;Stephan Scheurer

  209
  Citations

• The T-cell Lymphokine Interleukin-26 Targets Epithelial Cells through the Interleukin-20 Receptor 1 and Interleukin-10 Receptor 2 Chains

  Simon Hör;Simon Hör;Heide Pirzer;Laure Dumoutier;Finn Bauer

  194
  Citations

• Structural Rearrangements of HIV-1 Tat-responsive RNA upon Binding of Neomycin B

  Cornelius Faber;Heinrich Sticht;Kristian Schweimer;Paul Rösch

  190
  Citations

• Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression.

  Markus Zweier;Anne Gregor;Christiane Zweier;Hartmut Engels

  187
  Citations

• Heterozygous NTF4 Mutations Impairing Neurotrophin-4 Signaling in Patients with Primary Open-Angle Glaucoma

  Francesca Pasutto;Tomoya Matsumoto;Christian Y. Mardin;Heinrich Sticht

  187
  Citations

• The structure of iron–sulfur proteins

  Heinrich Sticht;Paul Rösch

  185
  Citations

• B cell repertoire analysis identifies new antigenic domains on glycoprotein B of human cytomegalovirus which are target of neutralizing antibodies.

  Sonja Pötzsch;Nadja Spindler;Anna-Katharina Wiegers;Tanja Fisch

  182
  Citations

• Estrogen and progesterone receptors: from molecular structures to clinical targets

  Stephan Ellmann;Heinrich Sticht;Falk Thiel;Matthias W. Beckmann

  179
  Citations

• De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability

  Anne Gregor;Martin Oti;Evelyn N. Kouwenhoven;Juliane Hoyer

  164
  Citations

• Synthetic Peptides as Protein Mimics.

  Andrea Groß;Chie Hashimoto;Heinrich Sticht;Jutta Eichler

  163
  Citations

• Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator

  Christian T. Thiel;Denise Horn;Bernhard Zabel;Arif B. Ekici

  152
  Citations