Silke Appenzeller

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Arvid Suls, Johanna A. Jaehn, Angéla Kecskés et al. · The American Journal of Human Genetics · 2013 · 219 citations · Full text

Chd2 Cause, Dravet Syndrome, Molecular Neuroscience +8

Single-cell RNA-seq ties macrophage polarization to growth rate of intracellular Salmonella

Antoine‐Emmanuel Saliba, Lei Li, Alexander J. Westermann et al. · Nature Microbiology · 2016 · 202 citations

Single Cell Sequencing, Growth Rate, Medicine +9

Targeted Molecular Analysis in Adrenocortical Carcinomas: A Strategy Toward Improved Personalized Prognostication

Juliane Lippert, Silke Appenzeller, Raimunde Liang et al. · The Journal of Clinical Endocrinology & Metabolism · 2018 · 117 citations · Full text

Whole transcriptome profiling reveals the RNA content of motor axons

Michael Briese, Lena Saal, Silke Appenzeller et al. · Nucleic Acids Research · 2015 · 116 citations · Full text

Genetics, Whole Transcriptome Profiling, Total Rna +18

Polymorphisms in the glial glutamate transporter <i>SLC1A2</i> are associated with essential tremor

Sandra Thier, Delia Lorenz, Michael Nothnagel et al. · Neurology · 2012 · 111 citations · Full text