• 4078 Citations
  • 38 h-Index
1987 …2019
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Fingerprint Dive into the research topics where Patrizia Noris is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 12 Similar Profiles
Blood Platelets Medicine & Life Sciences
Thrombocytopenia Medicine & Life Sciences
Mutation Medicine & Life Sciences
Bernard-Soulier Syndrome Medicine & Life Sciences
Platelet Aggregation Medicine & Life Sciences
Platelet Count Medicine & Life Sciences
Megakaryocytes Medicine & Life Sciences
Hemorrhage Medicine & Life Sciences

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Research Output 1987 2019

  • 4078 Citations
  • 38 h-Index
  • 121 Article
  • 2 Letter
  • 1 Review 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

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

Platelets
Thrombocytopenia
Blood Platelets
Mutation
Megakaryocytes

Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC

BAT-VAL study investigators, Jan 1 2019, (Accepted/In press) In : Journal of Thrombosis and Haemostasis.

Research output: Contribution to journalArticle

2 Citations (Scopus)

ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia

Faleschini, M., Melazzini, F., Marconi, C., Giangregorio, T., Pippucci, T., Cigalini, E., Pecci, A., Bottega, R., Ramenghi, U., Siitonen, T., Seri, M., Pastore, A., Savoia, A. & Noris, P., Jan 1 2018, (Accepted/In press) In : British Journal of Haematology.

Research output: Contribution to journalArticle

Thrombocytopenia
Blood Platelets
Mutation
Genetic Databases
Actinin

ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia

Faleschini, M., Melazzini, F., Marconi, C., Giangregorio, T., Pippucci, T., Cigalini, E., Pecci, A., Bottega, R., Ramenghi, U., Siitonen, T., Seri, M., Pastore, A., Savoia, A. & Noris, P., 2018, In : British Journal of Haematology. 183, 2, p. 276-288 13 p.

Research output: Contribution to journalArticle