Britt-Sabina Petersen

Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges

Alexander A. Morgan, Yanay Ofran, Predrag Radivojac, 2017, Human mutation.

From next-generation sequencing alignments to accurate comparison and validation of single-nucleotide variants: the pibase software

Andreas Keller, Philip Rosenstiel, Andre Franke, 2012, Nucleic acids research.

New insights into the genetics of glioblastoma multiforme by familial exome sequencing

Sabine C. Mueller, Christina Backes, Hugo A. Katus, 2014, Oncotarget.

Genetic Factors of the Disease Course After Sepsis: Rare Deleterious Variants Are Predictive

Lyn-Rouven Schirra, Florian Schmid, Ludwig Lausser, 2016, EBioMedicine.

CEACAM1 regulates TIM-3-mediated tolerance and exhaustion

Hidde L. Ploegh, Andre Franke, Yasuyuki Kondo, 2014, Nature.

Opportunities and challenges of whole-genome and -exome sequencing

Andre Franke, David Ellinghaus, Marc P Hoeppner, 2017, BMC Genetics.