The University of Siena PhD Course in
Genetics, Oncology and Clinical Medicine


PhD Graduate

Chiara FALLERINI  

PhD Program years: 2010 - 2014







PUBLICATIONS DURING THE PHD PROGRAM
  1. Advances in Alport syndrome diagnosis using next-generation sequencing.
    Artuso R, Fallerini C, Dosa L, Scionti F, Clementi M, Garosi G, Massella L, Epistolato MC, Mancini R, Mari F, Longo I, Ariani F, Renieri A, Bruttini M.
    Eur J Hum Genet. 2011 Sep 7.

  2. A Unique Patient Presenting with Concomitant Klinefelter Syndrome, Alport Syndrome and Craniopharyngioma.
    Rotondi M, Fallerini C, Pirali B, Longo I, Pasquali D, Rampino T, Chiovato L, Mari F, Renieri A.
    J Androl. 2012 Apr 19.

  3. Prognostic value of glomerular collagen IV immunofluorescence studies in male patients with X-linked Alport syndrome.
    Massella L, Gangemi C, Giannakakis K, Crisafi A, Faraggiana T, Fallerini C, Renieri A, Muda AO, Emma F.
    Clin J Am Soc Nephrol. 2013 May;8(5):749-55

  4. Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases.
    Fallerini C, Dosa L, Tita R, Del Prete D, Feriozzi S, Gai G, Clementi M, La Manna A, Miglietti N, Mancini R, Mandrile G, Ghiggeri G, Piaggio G, Brancati F, Diano L, Frate E, Pinciaroli A, Giani M, Castorina P, Bresin E, Giachino D, De Marchi M, Mari F, Bruttini M, Renieri A, Ariani F.
    Clin Genet. 2013 Sep 4

ABSTRACTS OF CONFERENCE DURING THE PHD PROGRAM
  1. Advances in Alport syndrome diagnosis using next generation sequencing. (ESHG 28-31 May 2011-07-21 Amsterdam)

  2. Next Generation Sequencing applied to Alport syndrome diagnosis. (ASHG 11-15 October 2011, Montreal, Quebec)
    Ariani F, Artuso R, Fallerini C, Dosa L, Scionti F, Massella L, Mancini R, Mari F , Longo I, Bruttini M

  3. Applicazione della tecnologia “Next generation sequencing”alla diagnosi molecolare della sindrome di Alport (SIGU 13-16 November 2011, Milano
    C Fallerini, R Artuso, L Dosa, M Clementi, G Garosi, L Massella, R Mancini, F Mari, I Longo, F Ariani, M Bruttini, A Renieri.

  4. Alport syndrome: simultaneous mutation analysis of COL4A3, COL4A4 and COL4A5 genes in 81 unrelated patients by a benchtop Next Generation
    Sequencer (XV Congresso Nazionale SIGU, Sorrento, 21-24 November 2012)
    Fallerini C, Dosa L, Seri A, Del Prete D, Feriozzi S, Gai G, Clementi M, La Manna A, Miglietti N, Mancini R, Mandrile G, Ghiggeri M, Brancati F, Frate E, Pinciaroli A R, Giani M, Giachino D, De Marchi M, Mari F, Bruttini M, Ariani F, Renieri A

  5. Next Generation Sequencing analysis of COL4A3, COL4A4 and COL4A5 genes in 100 unrelated Alport syndrome patients: diagnostic implications and
    identification of 41 novel mutations (ASHG 2013 Annual Meeting, Boston, 22-26 October 2013)
    Fallerini C, Dosa L, Tita R, Baldassarri M, Del Prete D, Feriozzi S, Gai G, Clementi M, La Manna A, Miglietti N, Mancini R, Mandrile G, Artuso R, Ghiggeri G M, Piaggio G, Brancati F, Diano L, Frate E, Pinciaroli A R, Giani M, Castorina P, Bresin E, Giachino D, De Marchi M, Seri M, Izzi C, Briuglia S, Mari F, Bruttini M, Renieri A, Ariani F.

  6. Introduzionedella tecnologia Next Generaton Sequencing nello screening mutazionale dei geni BRCA1/BRCA2: effetti dell'improvement tecnologico sull'attività clinica. (XVI Congresso Nazionale SIGU, Rome, 25-28 September 2013)
    M.A. Mencarelli, C. Fallerini, A. Marozza, L. Dosa, C. Lo Rizzo, C. Di Marco, S. Crispino, A. Falzetta, C. Liberatore, A. Grasso, S. Marsili, M. Crociani, A. Stella, A.
    Tripodi, F. Fantozzi, A. Giusti, L. Mantovani, A. Fausto, A. Neri, A. Bernini, L. Grimaldi, T. Megha, A. Disanto, A. Basile, S. Rossi, G. Carignani, M. Baldassarri, M.G. Lolli, M. Bruttini, F. Mari, F. Ariani, A. Renieri
ACTIVITY DURING THE PHD PROGRAM

TRAINING PERIOD ABROAD
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  • Hosting Institution Name
    Location
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