Heinz Lauffer

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 589 citations · Full text

Increased dorsolateral prefrontal cortex activation in obese children during observation of food stimuli

Saarah F. G. Davids, Heinz Lauffer, K Thoms et al. · International Journal of Obesity · 2009 · 160 citations

Obesity, Childhood Obesity, Cognitive Science +12

Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseases

Matthias Baumann, Eva-Maria Hennes, Kathrin Schanda et al. · Multiple Sclerosis Journal · 2016 · 157 citations

Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy

Sabine Rudnik‐Schöneborn, H. H. Goebel, W. Schlote et al. · Neurology · 2003 · 112 citations

Symbolic Analysis of High-Dimensional Time Series

Karsten Keller, Heinz Lauffer · International Journal of Bifurcation and Chaos · 2003 · 108 citations

Cognitive Science, Engineering, Information Theory +15