Harvard Catalyst Profiles

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Viola Fanfani, Ph.D.

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Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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  1. Zátopková M, Ševcíková T, Fanfani V, Chyra Z, Ríhová L, Bezdeková R, Žihala D, Growková K, Filipová J, Cerná L, Broskevicova L, Kryukov F, Minarík J, Smejkalová J, Maisnar V, Harvanová L, Pour L, Jungova A, Popková T, Bago JR, Anilkumar Sithara A, Hrdinka M, Jelínek T, Šimícek M, Stracquadanio G, Hájek R. Mutation landscape of multiple myeloma measurable residual disease: identification of targets for precision medicine. Blood Adv. 2022 Jan 25; 6(2):368-372. PMID: 34500459.
    Citations:    Fields:    
  2. Fanfani V, Citi L, Harris AL, Pezzella F, Stracquadanio G. The Landscape of the Heritable Cancer Genome. Cancer Res. 2021 05 15; 81(10):2588-2599. PMID: 33731442.
    Citations: 1     Fields:    Translation:Humans
  3. Fanfani V, Cassano F, Stracquadanio G. PyGNA: a unified framework for geneset network analysis. BMC Bioinformatics. 2020 Oct 22; 21(1):476. PMID: 33092528.
    Citations:    Fields:    
  4. Draberova H, Janusova S, Knizkova D, Semberova T, Pribikova M, Ujevic A, Harant K, Knapkova S, Hrdinka M, Fanfani V, Stracquadanio G, Drobek A, Ruppova K, Stepanek O, Draber P. Systematic analysis of the IL-17 receptor signalosome reveals a robust regulatory feedback loop. EMBO J. 2020 09 01; 39(17):e104202. PMID: 32696476.
    Citations:    Fields:    Translation:HumansCells
  5. Fanfani V, Zatopkova M, Harris AL, Pezzella F, Stracquadanio G. Dissecting the heritable risk of breast cancer: From statistical methods to susceptibility genes. Semin Cancer Biol. 2021 07; 72:175-184. PMID: 32569822.
    Citations: 1     Fields:    Translation:Humans
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.