ARIANI FRANCESCA

Francesca
Ariani
Dipartimento di Biotecnologie Mediche
Professore Associato

Contacts

francesca.ariani@unisi.it

Curriculum Vitae

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Teaching activities

Completion accademic year: 2025/2026

GENETICA
Course year: 1 First cycle degree (DM 270) DIETISTIC A.Y. 2025/2026
HUMAN GENETICS
Course year: 1 First cycle degree (DM 270) SPEECH AND LANGUAGE THERAPY A.Y. 2025/2026
HUMAN GENETICS
Course year: 1 First cycle degree (DM 270) ORTHOPTIC AND OPHTALMOLOGIC ASSISTANCE A.Y. 2025/2026
LABORATORY GENETICS AND OMICS APPROACHES
Course year: 1 Second cycle degree (Laurea Magistrale) GENETIC COUNSELLORS A.Y. 2025/2026
MEDICAL GENETICS
Course year: 1 First cycle degree (DM 270) Dental Hygiene A.Y. 2025/2026
TRAINING OF GENETICS
Course year: 2 Full cicle (6 years) MEDICINA E CHIRURGIA A.Y. 2024/2025
TRAINING OF GENETICS
Course year: 4 Full cicle (6 years) MEDICINE AND SURGERY A.Y. 2022/2023

Completion accademic year: 2024/2025

HUMAN GENETICS
Course year: 1 First cycle degree (DM 270) AUDIOPROTHESIC TECHNIQUES A.Y. 2024/2025
HUMAN GENETICS
Course year: 1 First cycle degree (DM 270) ORTHOPTIC AND OPHTALMOLOGIC ASSISTANCE A.Y. 2024/2025
LABORATORY GENETICS AND OMICS APPROACHES
Course year: 1 Second cycle degree (Laurea Magistrale) GENETIC COUNSELLORS A.Y. 2024/2025

Registration for exams

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
  • 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
  • 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
  • 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
  • Privitera, F., Trusso, M.A., Valentino, F., Doddato, G., Fallerini, C., Brunelli, G., et al. (2023). Heterozygosity for Neuronal Ceroid Lipofuscinosis predisposes to Bipolar Disorder. REVISTA BRASILEIRA DE PSIQUIATRIA, 45(1), 11-19 [10.47626/1516-4446-2022-2650]. - view more
All publications