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Fingerprint Dive into the research topics where Francesca Cortini is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 4 Similar Profiles
Frontotemporal Lobar Degeneration Medicine & Life Sciences
Alzheimer Disease Medicine & Life Sciences
Multiple Sclerosis Medicine & Life Sciences
Ehlers-Danlos Syndrome Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Genetic Association Studies Medicine & Life Sciences

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Research Output 2007 2019

  • 991 Citations
  • 19 h-Index
  • 42 Article
  • 4 Review article
2 Citations (Scopus)

Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's disease

Cortini, F., Roma, F. & Villa, C., Mar 1 2019, In : Ageing Research Reviews. 50, p. 19-26 8 p.

Research output: Contribution to journalReview article

Long Noncoding RNA
Alzheimer Disease
Biological Phenomena
Untranslated RNA
Complex networks
2 Citations (Scopus)

Understanding the basis of Ehlers–Danlos syndrome in the era of the next-generation sequencing

Cortini, F., Villa, C., Marinelli, B., Combi, R., Pesatori, A. C. & Bassotti, A., May 6 2019, In : Archives of Dermatological Research. 311, 4, p. 265-275 11 p.

Research output: Contribution to journalReview article

Joint Instability
Genetic Techniques
Molecular Pathology
Connective Tissue
Extracellular Matrix
1 Citation (Scopus)
External Carotid Artery
Carotid Arteries
Aneurysm
Stroke
Endovascular Procedures

Ehlers-danlos syndrome caused by the c.934C>T, p. Arg312Cys mutation in COL1A1 gene: An Italian family without cardio-vascular events

Cortini, F., Marinelli, B., Seia, M., Seresini, A. & Bassotti, A., Jul 1 2018, In : Dermatology Online Journal. 24, 7, 9.

Research output: Contribution to journalArticle

Ehlers-Danlos Syndrome
Blood Vessels
Missense Mutation
Mutation
Collagen Type V

Ehlers-Danlos Syndrome classical type: A novel COL5A2 missense mutation with possible additive effect of a COL5A1 stop-gain mutation in a strongly correlated phenotype

Cortini, F., Villa, C., Marinelli, B., Franchetti, S., Seia, M., Pesatori, A. C., Montano, N. & Bassotti, A., Dec 1 2018, In : Meta Gene. 18, p. 132-136 5 p.

Research output: Contribution to journalArticle

Ehlers-Danlos Syndrome
Missense Mutation
Collagen Type V
Phenotype
Mutation