• 424 Citations
  • 9 h-Index
20092019
If you made any changes in Pure these will be visible here soon.

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

  • 12 Similar Profiles
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Parkinson Disease Medicine & Life Sciences
Tetralogy of Fallot Medicine & Life Sciences
Neural Cell Adhesion Molecule L1 Medicine & Life Sciences
Genetic Databases Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Congenital Heart Defects Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2009 2019

  • 424 Citations
  • 9 h-Index
  • 26 Article
  • 1 Review article
Mitochondrial DNA
Immune System
Brain
Cerebrospinal Fluid
Biomarkers
glucocorticoids
catecholamine
gene expression
Corticosterone
markers

Methamphetamine persistently increases alpha-synuclein and suppresses gene promoter methylation within striatal neurons

Biagioni, F., Ferese, R., Limanaqi, F., Madonna, M., Lenzi, P., Gambardella, S. & Fornai, F., Sep 15 2019, In : Brain Research. 1719, p. 157-175 19 p.

Research output: Contribution to journalArticle

Corpus Striatum
alpha-Synuclein
Methamphetamine
Methylation
Neurons
3 Citations (Scopus)

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect

Ferese, R., Bonetti, M., Consoli, F., Guida, V., Sarkozy, A., Lepri, F. R., Versacci, P., Gambardella, S., Calcagni, G., Margiotti, K., Piceci Sparascio, F., Hozhabri, H., Mazza, T., Digilio, M. C., Dallapiccola, B., Tartaglia, M., Marino, B., Hertog, J. D. & De Luca, A., Oct 1 2018, In : Human Mutation. 39, 10, p. 1428-1441 14 p.

Research output: Contribution to journalArticle

Missense Mutation
Calcineurin
Mutation
Atrioventricular Septal Defect
Zebrafish

Heterozygous missense mutations in NFATC1 are associated with atrioventricular septal defect

Ferese, R., Bonetti, M., Consoli, F., Guida, V., Sarkozy, A., Lepri, F. R., Versacci, P., Gambardella, S., Calcagni, G., Margiotti, K., Piceci Sparascio, F., Hozhabri, H., Mazza, T., Digilio, M. C., Dallapiccola, B., Tartaglia, M., Marino, B., Hertog, J. D. & De Luca, A., Oct 2018, In : Human Mutation. 39, 10, p. 1428-1441 14 p.

Research output: Contribution to journalArticle

Missense Mutation
Calcineurin
Mutation
Atrioventricular Septal Defect
Zebrafish