Petr Vojta

The activation of iron deficiency responses of grapevine rootstocks is dependent to the availability of the nitrogen forms

Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress

P-001: RNA-sequencing reveals transcriptomic similarity of AL amyloidosis and MGUS aberrant plasma cells along with several potential ALA target candidate genes

Development and extensive analytical validation of deep amplicon sequencing for detecting KRAS and NRAS mutations in metastatic colorectal cancer samples.

Establishing community reference samples, data and call sets for benchmarking cancer mutation detection using whole-genome sequencing

Heterogenous mutation spectrum and deregulated cellular pathways in aberrant plasma cells underline molecular pathology of light-chain amyloidosis

Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study

Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencing