• 2205 Citations
  • 25 h-Index
19962019
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Fingerprint Dive into the research topics where Caterina Cancrini is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles
T-Lymphocytes Medicine & Life Sciences
Mutation Medicine & Life Sciences
B-Lymphocytes Medicine & Life Sciences
DiGeorge Syndrome Medicine & Life Sciences
HIV-1 Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Genes Medicine & Life Sciences
Autoimmunity Medicine & Life Sciences

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Research Output 1996 2019

  • 2205 Citations
  • 25 h-Index
  • 103 Article
  • 3 Review article
  • 2 Letter

Autosomal dominant Hyper IgE syndrome is associated with appearance of infections early in life and/or neonatal rash: evidence from the Italian cohort of 61 patients with elevated IgE

Lorenzini, T., Giacomelli, M., Scomodon, O., Cortesi, M., Rivellini, V., Dotta, L., Soresina, A., Dellepiane, R. M., Carrabba, M., Cossu, F., Cancrini, C., Specchia, F., Giardino, G., Pignata, C., Plebani, A., Pietrogrande, M. C. & Badolato, R., Feb 20 2019, In : Journal of Allergy and Clinical Immunology: In Practice.

Research output: Contribution to journalArticle

Clinical, Immunological, and Molecular Features of Typical and Atypical Severe Combined Immunodeficiency: Report of the Italian Primary Immunodeficiency Network

Cirillo, E., Cancrini, C., Azzari, C., Martino, S., Martire, B., Pession, A., Tommasini, A., Naviglio, S., Finocchi, A., Consolini, R., Pierani, P., D'Alba, I., Putti, M. C., Marzollo, A., Giardino, G., Prencipe, R., Esposito, F., Grasso, F., Scarselli, A., Di Matteo, G. & 15 others, Attardi, E., Ricci, S., Montin, D., Specchia, F., Barzaghi, F., Cicalese, M. P., Quaremba, G., Lougaris, V., Giliani, S., Locatelli, F., Rossi, P., Aiuti, A., Badolato, R., Plebani, A. & Pignata, C., 2019, In : Frontiers in Immunology. 10, p. 1908

Research output: Contribution to journalArticle

Severe Combined Immunodeficiency
Phenotype
Genetic Heterogeneity
Genetic Association Studies
Cell- and Tissue-Based Therapy

Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

Cifaldi, C., Brigida, I., Barzaghi, F., Zoccolillo, M., Ferradini, V., Petricone, D., Cicalese, M. P., Lazarevic, D., Cittaro, D., Omrani, M., Attardi, E., Conti, F., Scarselli, A., Chiriaco, M., Di Cesare, S., Licciardi, F., Davide, M., Ferrua, F., Canessa, C., Pignata, C. & 20 others, Giliani, S., Ferrari, S., Fousteri, G., Barera, G., Merli, P., Palma, P., Cesaro, S., Gattorno, M., Trizzino, A., Moschese, V., Chini, L., Villa, A., Azzari, C., Finocchi, A., Locatelli, F., Rossi, P., Sangiuolo, F., Aiuti, A., Cancrini, C. & Di Matteo, G., 2019, In : Frontiers in Immunology. 10, p. 1184

Research output: Contribution to journalArticle

Genetic Testing
Genetic Association Studies
corrigendum
Inflammatory Bowel Diseases
Bone Marrow
Transplants
Phenotype