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 · 221 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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 · 215 citations

Life Sciences, Microbiology, Molecular Biology +16

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 · 119 citations · Full text

Medicine, Molecular Genetics, Oncology +17

Whole transcriptome profiling reveals the RNA content of motor axons

Michael Briese, Lena Saal, Silke Appenzeller et al. · Nucleic Acids Research · 2015 · 118 citations · Full text

Life Sciences, Neurobiology, Neuroscience +15

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

Life Sciences, Genetics, Neuroscience +17