Dr Thomas Ohnesorg
- 2023Oxford medical case reports10.1093/omcr/omad005
Hyper-IgM and acquired C1q complement deficiency in a patient with mutation.
- 2021Genome medicine10.1186/s13073-021-00841-x
ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
- 2021European journal of human genetics : EJHG10.1038/s41431-020-00796-4
Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing.