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Monica Franzese

  • 4 Citations
  • 1 h-Index
20192019
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Fingerprint Dive into the research topics where Monica Franzese is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 14 Similar Profiles
Long QT Syndrome Medicine & Life Sciences
Methylation Medicine & Life Sciences
Mothers Medicine & Life Sciences
Haploinsufficiency Medicine & Life Sciences
Genetic Counseling Medicine & Life Sciences
Multigene Family Medicine & Life Sciences
Introns Medicine & Life Sciences
Chromosomes Medicine & Life Sciences

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Research Output 2019 2019

  • 4 Citations
  • 1 h-Index
  • 1 Article
4 Citations (Scopus)

Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith–Wiedemann locus

Valente, F. M., Sparago, A., Freschi, A., Hill-Harfe, K., Maas, S. M., Frints, S. G. M., Alders, M., Pignata, L., Franzese, M., Angelini, C., Carli, D., Mussa, A., Gazzin, A., Gabbarini, F., Acurzio, B., Ferrero, G. B., Bliek, J., Williams, C. A., Riccio, A. & Cerrato, F., Jan 1 2019, (Accepted/In press) In : Genetics in Medicine.

Research output: Contribution to journal › Article

Long QT Syndrome
Methylation
Mothers
Haploinsufficiency
Genetic Counseling