Ricarda Flöttmann

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

Insights and implications of sexual dimorphism in osteoporosis

A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia

Microduplications encompassing the Sonic hedgehog limb enhancer ZRS are associated with Haas‐type polysyndactyly and Laurin‐Sandrow syndrome