Peter Leemans

CADD v1.7: using protein language models, regulatory CNNs and other nucleotide-level scores to improve genome-wide variant predictions

Diagnosis and management of subarachnoid haemorrhage

Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12

ECG abnormalities in predicting secondary cerebral ischemia after subarachnoid haemorrhage