Björn Brändl

The paper identifies ampliconic sequences in mouse t-haplotypes as drivers of selfish transmission, showing their evolutionary relationship to sex chromosome dynamics.

This study uses long-read sequencing to identify novel structural variants in Prader-Willi syndrome patients, linking them to psychiatric traits and challenging current genetic hypotheses.

The paper generates a chromosome-level genome assembly for the functionally extinct northern white rhinoceros and compares it to the southern white rhinoceros.

This paper develops a Cas12a-based enrichment strategy and algorithm for nanopore sequencing to quantify repeat expansions and their methylation status.