ARIANI FRANCESCA

Curriculum Vitae

Teaching activities

Completion accademic year: 2026/2027

Course year: 1 First cycle degree (DM 270) DIETISTICA (ABILITANTE ALLA PROFESSIONE SANITARIA DI DIETISTA) A.Y. 2026/2027
Course year: 1 First cycle degree (DM 270) ORTHOPTIC AND OPHTALMOLOGIC ASSISTANCE A.Y. 2026/2027
Course year: 1 First cycle degree (DM 270) LOGOPEDIA (ABILITANTE ALLA PROFESSIONE SANITARIA DI LOGOPEDISTA) A.Y. 2026/2027
Course year: 1 Second cycle degree (Laurea Magistrale) GENETIC COUNSELLORS A.Y. 2026/2027
Course year: 1 First cycle degree (DM 270) DENTAL HYGIENE A.Y. 2026/2027
Course year: 4 Full cicle (6 years) MEDICINA E CHIRURGIA A.Y. 2023/2024

Completion accademic year: 2025/2026

Course year: 1 First cycle degree (DM 270) DIETISTIC A.Y. 2025/2026
Course year: 1 First cycle degree (DM 270) SPEECH AND LANGUAGE THERAPY A.Y. 2025/2026
Course year: 1 First cycle degree (DM 270) ORTHOPTIC AND OPHTALMOLOGIC ASSISTANCE A.Y. 2025/2026
Course year: 1 Second cycle degree (Laurea Magistrale) GENETIC COUNSELLORS A.Y. 2025/2026

Research

Ultime pubblicazioni:

  • Daga, S., Loberti, L., Rollo, G., Adamo, L., Colavecchio, O.L., Brunelli, G., et al. (2025). Slowly progressive autosomal dominant Alport Syndrome due to COL4A3 splicing variant. EUROPEAN JOURNAL OF HUMAN GENETICS, 33(4), 461-467 [10.1038/s41431-024-01706-8]. - view more
  • Innamorato, S., Basso, S.L., Belakhdar, O., Bruttini, M., Fallerini, C., Huseynli, H., et al. (2025). A Complex Case of Retinoblastoma Solved by the Combined Approach of Humor/Plasma cfDNA-NGS and LR-WGS. GENES, 16(12) [10.3390/genes16121399]. - view more
  • Minnai, F., Biscarini, F., Esposito, M., Dragani, T.A., Bujanda, L., Rahmouni, S., et al. (2024). A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death. SCIENTIFIC REPORTS, 14(1) [10.1038/s41598-024-53310-x]. - view more
  • Serio, V.B., Palmieri, M., Innamorato, S., Loberti, L., Fallerini, C., Ariani, F., et al. (2023). Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors. FRONTIERS IN GENETICS, 14 [10.3389/fgene.2023.1213283]. - view more
  • Ronzoni, L., Mureddu, M., Malvestiti, F., Moretti, V., Bianco, C., Periti, G., et al. (2023). Liver Involvement in Patients with Rare MBOAT7 Variants and Intellectual Disability: A Case Report and Literature Review. GENES, 14(8) [10.3390/genes14081633]. - view more