Heinrich Sticht

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

Anita Rauch, Dagmar Wieczorek, Elisabeth Graf et al. · The Lancet · 2012 · 1.1K citations · Full text

Genetic Mutations, Mendelian Disorder, Genetic Disorder +7

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 et al. · Journal of Molecular Modeling · 2005 · 418 citations

Protein Chemistry, Biochemistry, Protein Folding +10

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, G. Hammersen et al. · The American Journal of Human Genetics · 2007 · 358 citations · Full text

Developmental Anomaly, Developmental Biology, Genetic Disorder +8

The interleukin-10 family of cytokines

Helmut Fickenscher, Simon Hör, Heide Küpers et al. · Trends in Immunology · 2002 · 324 citations

Inflammation, Cytokine, Interleukin-10 Family +7

Structure of Amyloid A4‐(1–40)‐Peptide of Alzheimer's Disease

Heinrich Sticht, Peter Bayer, Dieter Willbold et al. · European Journal of Biochemistry · 1995 · 298 citations

Alzheimer's Disease, Amyloid A4‐, Biochemistry +14