Sam Hawarden

Mulligan, M. R., Mulhall, H., Hawarden, S. R. A., Davies-Payne, D., Heller, R., & Bicknell, L. S. (2026). Strømme syndrome: The clinical and molecular spectrum associated with variants in CENPF. European Journal of Human Genetics. Advance online publication. doi: 10.1038/s41431-026-02187-7 Journal - Research Article

Schoch, K., Ruegg, M. S. G., Fellows, B. J., Cao, J., Uhrig, S., Einsele-Scholz, S., … Hawarden, S. R. A., … Brown, C. M., … Bicknell, L. S. (2024). A second hotspot for pathogenic exon-skipping variants in CDC45. European Journal of Human Genetics, 32, 786-794. doi: 10.1038/s41431-024-01583-1 Journal - Research Article