Publications and communications of Sabrina BERTOLI

Kukor, L., BERTOLI, S., CREVECOEUR, J., Bours, V., & BULK, S. (21 April 2022). What does a Genetic Counsellor do in the University Hospital of Liège ? [Poster presentation]. BeSHG/NVHG Annual Genetics Symposium 2022.

BERTOLI, S., VAN CASTEREN, L., Bours, V., & BULK, S. (16 February 2018). The cardiogenetics consultation : an inventorisation of the Liege population [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium.

KUKOR, L., BERTOLI, S., Bours, V., BULK, S., & DOCAMPO MARTINEZ, E. (16 February 2018). Ehlers-Danlos syndrome in the University Hospital of Liege [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium.

Manard, M., François, S., Bahri, M. A., Phillips, C., BOURS, V., BERTOLI, S., DIDEBERG, V., Salmon, E., & Collette, F. (10 May 2016). The influence of COMT single nucleotide polymorphism (rs4680) on the neural substrates of working memory representations maintenance in healthy aging [Poster presentation]. IUAP Annual meeting.

Dideberg, V., Louis, E., Farnir, F., Bertoli, S., Vermeire, S., Rutgeerts, P., De Vos, M., Van Gossum, A., Belaiche, J., & Bours, V. (May 2006). Lymphotoxin alpha gene in Crohn's disease patients: absence of implication in the response to infliximab in a large cohort study. Pharmacogenetics and Genomics, 16 (5), 369-373. doi:10.1097/01.fpc.0000204993.91806.b1