• 4 Citations
  • 1 h-Index
20182019
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Fingerprint Dive into the research topics where Michela Faleschini is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 2 Similar Profiles
Thrombocytopenia Medicine & Life Sciences
Mutation Medicine & Life Sciences
Blood Platelets Medicine & Life Sciences
Fanconi Anemia Medicine & Life Sciences
Megakaryocytes Medicine & Life Sciences
Fanconi Anemia Complementation Group Proteins Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Adenosine Monophosphate Medicine & Life Sciences

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Research Output 2018 2019

  • 4 Citations
  • 1 h-Index
  • 4 Article

Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia

Marconi, C., Di Buduo, C. A., LeVine, K., Barozzi, S., Faleschini, M., Bozzi, V., Palombo, F., McKinstry, S., Lassandro, G., Giordano, P., Noris, P., Balduini, C. L., Savoia, A., Balduini, A., Pippucci, T., Seri, M., Katsanis, N. & Pecci, A., 2019, In : Blood. 133, 12, p. 1346-1357 12 p.

Research output: Contribution to journalArticle

A new form of inherited thrombocytopenia caused by loss-of-function mutations in <em>PTPRJ</em>

Marconi, C., Di Buduo, C. A., LeVine, K., Barozzi, S., Faleschini, M., Bozzi, V., Palombo, F., McKinstry, S., Lassandro, G., Giordano, P., Noris, P., Balduini, C. L., Savoia, A., Balduini, A., Pippucci, T., Seri, M., Katsanis, N. & Pecci, A., Jan 1 2018, In : Blood. p. blood-2018-07-859496

Research output: Contribution to journalArticle

Thrombocytopenia
Blood Platelets
Mutation
Megakaryocytes
Class 3 Receptor-Like Protein Tyrosine Phosphatases

A new form of inherited thrombocytopenia caused by loss-of-function mutations in PTPRJ

Marconi, C., Di Buduo, C. A., LeVine, K., Barozzi, S., Faleschini, M., Bozzi, V., Palombo, F., McKinstry, S., Lassandro, G., Giordano, P., Noris, P., Balduini, C. L., Savoia, A., Balduini, A., Pippucci, T., Seri, M., Katsanis, N. & Pecci, A., Dec 27 2018, In : Blood.

Research output: Contribution to journalArticle

Thrombocytopenia
Blood Platelets
Mutation
Megakaryocytes
Receptor-Like Protein Tyrosine Phosphatases
4 Citations (Scopus)

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia

Bottega, R., Nicchia, E., Cappelli, E., Ravera, S., De Rocco, D., Faleschini, M., Corsolini, F., Pierri, F., Calvillo, M., Russo, G., Casazza, G., Ramenghi, U., Farruggia, P., Dufour, C. & Savoia, A., Feb 28 2018, In : Haematologica. 103, 3, p. 417-426 10 p.

Research output: Contribution to journalArticle

Fanconi Anemia
Fanconi Anemia Complementation Group Proteins
Phenotype
Mutation
Adenosine Monophosphate